WO2020032069A1 - Absorbent article - Google Patents

Absorbent article Download PDF

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Publication number
WO2020032069A1
WO2020032069A1 PCT/JP2019/030997 JP2019030997W WO2020032069A1 WO 2020032069 A1 WO2020032069 A1 WO 2020032069A1 JP 2019030997 W JP2019030997 W JP 2019030997W WO 2020032069 A1 WO2020032069 A1 WO 2020032069A1
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WO
WIPO (PCT)
Prior art keywords
display unit
absorbent article
excrement
wearer
color
Prior art date
Application number
PCT/JP2019/030997
Other languages
French (fr)
Japanese (ja)
Inventor
裕哉 鈴木
Original Assignee
ユニ・チャーム株式会社
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from JP2018148036A external-priority patent/JP7154060B2/en
Priority claimed from JP2018148035A external-priority patent/JP7064992B2/en
Application filed by ユニ・チャーム株式会社 filed Critical ユニ・チャーム株式会社
Priority to CN201980051299.4A priority Critical patent/CN112512471B/en
Publication of WO2020032069A1 publication Critical patent/WO2020032069A1/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators

Definitions

  • the present invention relates to an absorbent article.
  • FIG. 1 of Patent Document 1 discloses an absorbent article provided with an inspection member for inspecting a wearer's health condition.
  • the inspection member has a display unit that displays the health condition of the wearer.
  • the display unit includes a color indicator based on a detection target contained in the excrement. For this reason, when the excrement includes the detection target, the color of the display unit changes due to the color reaction of the indicator.
  • the wearer can confirm the health condition by visually recognizing the display unit.
  • the absorbent article is provided with the inspection member, the wearer can easily inspect the health condition.
  • the inspection member is disposed at the center in the front-rear direction and the width direction. Accordingly, the excrement of the wearer is easily excreted toward the inspection member, and at least a part of the inspection member may be covered by the excrement of the wearer.
  • the wearer cannot visually recognize the display unit and cannot check the health condition. Further, even if the wearer can visually recognize the display unit via the excrement, there is a possibility that the color of the display unit is erroneously recognized based on the color of the excrement. Thus, there is a possibility that the wearer may not be able to grasp the exact health condition based on the excrement.
  • the absorbent article according to the present disclosure includes a front-rear direction, a width direction orthogonal to the front-rear direction, a thickness direction orthogonal to the front-rear direction and the width direction, an absorbent core including an absorbent material, and an absorbent core.
  • a top sheet having an absorption region that is arranged on the skin surface side and overlaps the absorption core in the thickness direction, and an inspection member for inspecting a health condition of a wearer.
  • the inspection member has a contact portion for contacting the excrement of the wearer and a display portion for displaying a health condition of the wearer.
  • the display unit includes an indicator that changes color based on a detection target included in the excrement contacted with the contact unit. At least a part of the contact portion is arranged in a range where the excrement excreted in the absorption region reaches. At least a part of the display unit does not overlap with the absorbing core in the thickness direction.
  • the absorbent article according to the present disclosure has a front-rear direction, a width direction orthogonal to the front-rear direction, a thickness direction orthogonal to the front-rear direction and the width direction, and a horizontal direction parallel to the front-rear direction and the width direction.
  • a direction an absorbent core containing an absorbent material, a backsheet arranged on a non-skin side than the absorbent core, and an inspection member for inspecting a health condition of a wearer.
  • the inspection member is arranged on the skin surface side of the back sheet in the thickness direction.
  • the inspection member has a display unit including an indicator that changes color based on a detection target included in the excrement.
  • the display unit is visible from the back sheet side.
  • a hydrophobic portion having hydrophobicity is arranged in an extension region extending from the display portion in the thickness direction and the horizontal direction on the skin surface side of the back sheet.
  • the absorbent article includes a front-rear direction, a width direction perpendicular to the front-rear direction, a thickness direction perpendicular to the front-rear direction and the width direction, an absorbent core including an absorbent material, and A top sheet having an absorption region that is arranged on the skin surface side and overlaps the absorption core in the thickness direction, and an inspection member for inspecting a health condition of a wearer.
  • the inspection member has a contact portion for contacting the excrement of the wearer and a display portion for displaying a health condition of the wearer.
  • the display unit includes an indicator that changes color based on a detection target included in the excrement contacted with the contact unit. At least a part of the contact portion is arranged in a range where the excrement excreted in the absorption region reaches. At least a part of the display unit does not overlap with the absorbing core in the thickness direction.
  • the excrement can be brought into contact with the contact portion.
  • the indicator contained in the display unit can be colored, and the display unit can display the health condition.
  • the wearer since at least part of the display unit does not overlap with the absorbent core, the wearer can easily view the display unit without blocking at least part of the display unit with the absorbent core.
  • most excrement is absorbed by the absorbent core, at least a part of the display does not overlap with the absorbent core, so that at least a part of the display does not easily come into contact with excrement.
  • the contact portion contacts the absorbent core. Since the excrement is excreted in the absorbent core, more excretion can be brought into contact with the contact portion by contacting at least a part of the contact portion with the absorbent core.
  • the indicator can be colored based on many detection targets, and the inspection accuracy can be improved.
  • the contact portion overlaps the absorbent core in the thickness direction. Since the excrement is excreted in the absorbent core, at least a part of the contact portion overlaps with the absorbent core, so that more excrement can be brought into contact with the contact portion.
  • the indicator can be colored based on many detection targets, and the inspection accuracy can be improved.
  • the absorbent article has a guiding portion for guiding the excrement to at least a part of the contact portion. Since the excrement is guided to at least a part of the contact portion by the guide portion, more excrement can be brought into contact with the contact portion. Thus, the indicator can be colored based on many detection targets, and the inspection accuracy can be improved.
  • the absorbent article has a main body having the absorbent core and a non-skin surface of the wearing article that extends from the main body to the outside in the width direction and is attached to the wearing article. And a pair of wings fixed to the side. At least a part of the display unit is disposed on one of the pair of wings in the thickness direction. Since the wing is fixed to the non-skin side of the wearing article when attached to the wearing article (for example, underwear), the excrement excreted from the skin side hardly adheres to the wing. This makes it difficult for at least a part of the display unit to be covered with the excrement, and makes it easier for the wearer to visually recognize the display unit without being affected by the excrement.
  • the wing is fixed to the non-skin side of the wearing article, when the wearer wears the absorbent article, at least a part of the display section and the wearer's skin are in the thickness direction. There is a wearing article. For this reason, at the time of wearing the absorbent article, it is difficult for at least a part of the display unit to touch the wearer's skin. Even if the indicator contained in the display unit can damage the skin, the safety of the wearer can be improved.
  • At least a portion of the display unit extends from an outer edge of the absorbent core in the front-rear direction.
  • the excrement is more likely to be excreted toward the center than the end in the front-rear direction of the absorbent article, so that it is difficult for the excrement to spread beyond the outer edge of the absorbent core in the front-rear direction.
  • At least a portion of the display unit extends from the outer edge of the absorbent core in the front-rear direction, so that the display unit is not easily covered with excrement, and the wearer can easily view the display unit without being affected by the excrement. .
  • the absorbent article has an absorbent article main body composed of members other than the inspection member.
  • the display unit extends from an outer edge of the absorbent article main body. Since at least a part of the display unit extends from the outer edge of the absorbent article main body, at least a part of the display unit is arranged at a position where excrement cannot be diffused. Thereby, it can suppress that at least one copy of a display part is covered with excrement.
  • the wearer since at least a part of the display unit extends from the outer edge of the absorbent article main body, the wearer can directly visually recognize the display unit. Therefore, it is possible for the wearer to easily grasp the correct health condition.
  • the absorbent article has a plurality of inspection members whose detection targets are different from each other.
  • the display units of each of the plurality of inspection members are arranged at different positions in the thickness direction. Since the detection target is provided with a plurality of inspection members different from each other, a plurality of items indicating the health condition can be confirmed with one absorbent article. Since the display units included in each of the plurality of inspection members are arranged at positions different from each other in the thickness direction, the wearer can easily recognize each of the display units, and it is possible to suppress oversight of some of the display units.
  • the inspection member is arranged on a non-skin side than the top sheet. Since the inspection member is arranged on the non-skin side than the top sheet, it is possible to suppress the inspection member from directly touching the wearer's skin. Thereby, the discomfort at the time of wearing due to the inspection member directly hitting the skin of the wearer can be suppressed. Furthermore, even if the indicator can give irritation to the skin, it becomes difficult for the indicator to touch the skin of the wearer, and the safety of the wearer can be enhanced.
  • the contact portion is arranged on a non-skin side with respect to the absorbent core.
  • the absorption core has an opening penetrating the absorption core in the thickness direction.
  • the contact portion does not overlap with the opening in the thickness direction.
  • the excrement is more likely to reach the non-skin side of the absorbent core where the contact portion is arranged by passing through the opening than through the gap between the fibers constituting the absorbent member of the absorbent core. Therefore, the time required to reach the contact portion can be reduced, and a large amount of excrement can reach the contact portion. Thereby, the inspection accuracy can be improved. Further, when the contact portion contains the indicator, the indicator may be dissolved in the excrement reaching the contact portion.
  • the contact portion does not overlap the opening in the thickness direction, it is difficult for the excrement to reach the non-skin surface side of the absorbent core through the opening. For this reason, even if the indicator can stimulate the skin, it is difficult for the excrement containing the indicator to reach the non-skin side of the top sheet, and the safety of the wearer can be improved.
  • the absorbent article has a front-rear direction, a width direction perpendicular to the front-rear direction, a thickness direction perpendicular to the front-rear direction and the width direction, and a horizontal direction parallel to the front-rear direction and the width direction.
  • a direction an absorbent core containing an absorbent material, a backsheet arranged on a non-skin side than the absorbent core, and an inspection member for inspecting a health condition of a wearer.
  • the inspection member is arranged on the skin surface side of the back sheet in the thickness direction.
  • the inspection member has a display unit including an indicator that changes color based on a detection target included in the excrement. The display unit is visible from the back sheet side.
  • a hydrophobic portion having hydrophobicity is arranged in an extension region extending from the display portion in the thickness direction and the horizontal direction on the skin surface side of the back sheet.
  • Japanese Patent Application Publication No. 2002-538890 discloses an absorbent article provided with an inspection member for inspecting a wearer's health condition.
  • the inspection member has a display unit that displays the health condition of the wearer.
  • the display unit includes a color indicator based on a detection target contained in the excrement. After the excrement of the difference in wearing reaches the inspection member, if the excrement includes the detection target, the color of the display unit changes due to the color reaction of the indicator.
  • the inspection member is placed in contact with the inner surface of the liquid impermeable film.
  • the display portion can be visually recognized from a transparent area forming a viewing window.
  • the wearer can confirm the health condition by visually recognizing the display unit.
  • the excrement of the wearer reaches at least one of the inspection members when the excrement of the wearer reaches the inspection member. And may overlap.
  • the wearer cannot visually recognize the display unit and cannot check the health condition.
  • the wearer can visually recognize the display unit via the excrement that overlaps the display unit, there is a possibility that the color of the display unit is erroneously recognized based on the color of the excrement.
  • the wearer may not be able to grasp the exact health condition based on the excrement.
  • the hydrophobic part when the hydrophobic part is disposed in the extension area extending in the thickness direction from the display part, the excrement excreted on the skin side of the absorbent article has a thickness.
  • the hydrophobic part exists on the diffusion path that diffuses toward the display part in the direction. Since the hydrophobic part has hydrophobicity, it is easy to suppress the water-soluble excrement from diffusing to the display part side.
  • the hydrophobic portion is disposed in an extension region extending in the horizontal direction from the display portion, on the diffusion path in which the excrement diffused inside the absorbent article is diffused in the horizontal direction toward the display portion, There is a hydrophobic part.
  • the hydrophobic part can easily prevent the water-soluble excrement from diffusing to the display part side. Further, even when the display unit is not arranged in a range where the excrement reaches while the absorbent article is worn, the excrement may reach the display unit due to unexpected movement of the wearer. is there. Even in such a case, it is easy to suppress the excrement from reaching the display unit by the hydrophobic part arranged in the extension area. As described above, it is easy to suppress the excrement from covering or overlapping the display unit, and it is easy to ensure the visibility of the display unit. Accordingly, when the wearer visually recognizes the display unit from the back seat side, the wearer can easily grasp the correct health condition.
  • the absorbent article has a top sheet that is arranged on the skin surface side of the absorbent core and has an absorbent region overlapping the absorbent core in the thickness direction.
  • the hydrophobic part disposed in the extension region is disposed in a range where the excrement discharged in the absorption region reaches. This can prevent the excrement reaching the hydrophobic part from being diffused to the display part side, so that the visibility of the display part can be easily secured. Accordingly, when the wearer visually recognizes the display unit from the back seat side, the wearer can easily grasp the correct health condition.
  • the hydrophobic part is in contact with the display part. Thereby, it is possible to suppress the excrement from reaching the display unit. Thereby, the visibility of the display unit can be secured, and the wearer can easily grasp the correct health condition.
  • the hydrophobic portion is in contact with the surface on the skin surface side of the display unit. Therefore, it is possible to suppress the excrement diffusing from the skin surface side to the non-skin surface side from reaching the display unit. Thereby, the visibility of the display unit can be secured, and the wearer can easily grasp the correct health condition.
  • the hydrophobic portion is in contact with a surface on the non-skin side of the display unit.
  • the inspection member is arranged between the absorbent core and the back sheet in the thickness direction.
  • a sheet-like sheet member is arranged as the hydrophobic portion between the absorbing core and the display unit. Since the sheet member is disposed between the absorbent core and the display unit, it is possible to suppress the excrement diffused from the skin surface side to the non-skin surface side from reaching the display unit. Thereby, the visibility of the display unit can be secured, and the wearer can easily grasp the correct health condition.
  • the absorbent article 1 has an excretion port contact portion that contacts the excretion port of the wearer.
  • the hydrophobic portion is closer to the center of the excretion opening contact portion than the display portion. Since the hydrophobic part is closer to the center of the excretion port contact part than the display part, the hydrophobic part exists on the diffusion path in which the excrement excreted in the excretion port contact part diffuses toward the display part. The hydrophobic part can suppress the excrement diffused from the excretion opening contact part toward the display part from reaching the display part. Thereby, the visibility of the display unit can be secured, and the wearer can easily grasp the correct health condition.
  • the absorbent article 1 has a skin-side member disposed closer to the skin than the display unit.
  • the skin surface side member is a region that does not overlap with the display unit in the thickness direction, and has a background region that is visible from the back sheet side.
  • the color of the display unit is a color having a hue difference of 120 degrees or more in a hue circle with respect to the color of the background area.
  • the display portion is visually recognized by being emphasized by the color of the background region. This makes it easier for the wearer to visually recognize the display unit, so that the wearer can easily grasp the correct health condition.
  • the color of the display unit is a color having a hue difference of 120 degrees or more in terms of a hue circle with respect to the color of the excrement.
  • the display portion is visually recognized with the display portion highlighted by the color of the excrement. This makes it easier for the wearer to visually recognize the display unit, so that the wearer can easily grasp the correct health condition.
  • the absorbent article 1 has a skin-side member disposed closer to the skin than the display unit.
  • the skin surface side member is a region that does not overlap with the display unit in the thickness direction, and has a background region that is visible from the back sheet side.
  • the color of the background area is a color having a hue difference of 45 degrees or less in the hue circle with respect to the color of the excrement. Even if the excrement permeates the skin-side member, the color of the background area is a color whose hue difference is not more than 45 degrees in the hue circle angle with respect to the color of the excrement, so that the excrement is inconspicuous. This makes it easier for the wearer to visually recognize the display unit without being distracted by the color of the excrement, thereby making it easier to grasp an accurate health condition.
  • the absorbent article may be an absorbent article such as a sanitary napkin, panty liner, incontinence pad, stool pad.
  • the absorbent article may be an article used by being attached to the inside of a wearing article such as underwear.
  • the absorbent article 1 of the present embodiment is a sanitary napkin.
  • FIG. 1 is a plan view of the absorbent article according to the first embodiment viewed from the skin side.
  • FIG. 2 is a cross-sectional view of the absorbent article according to the first embodiment.
  • FIG. 2A is a cross-sectional view along the line AA shown in FIG. Drawing 2B is a sectional view of an absorptive article in the state where it was attached to a wearing article (underwear).
  • FIG. 3 is a diagram for explaining the absorbent article according to the first embodiment.
  • FIG. 3A is a cross-sectional view illustrating an example (part 1) of removing the absorbent article from the wearing article.
  • FIG. 3B is a cross-sectional view illustrating an example (part 2) of removing the absorbent article from the wearing article.
  • skin side corresponds to the side facing the wearer's skin during wearing (during use).
  • Non-skin side corresponds to the side that is turned away from the wearer's skin during wearing (during use).
  • the absorbent article 1 has a front-rear direction L and a width direction W.
  • the front-rear direction L is a direction extending from the front side (abdominal side) to the rear side (back side) of the wearer, or a direction extending from the rear side of the wearer to the front side.
  • the width direction W is a direction orthogonal to the front-rear direction L.
  • the absorbent article has a thickness direction T extending to the skin side T1 and the non-skin side T2. Note that the absorbent article may have a horizontal direction that is parallel to the front-rear direction L and the width direction W.
  • the outer edge is an outer edge in the width direction
  • the inner edge is an inner edge in the width direction
  • the absorbent article 1 has a central area S3, a front area S1 and a rear area S2.
  • the central area S3 is an area having an excretion port contact portion that contacts an excretion port (for example, a vaginal opening) of the wearer.
  • the central region S3 is located at the crotch of the wearing article. That is, the central region is a region located between the wearer's crotch, that is, between the wearer's feet.
  • the central region S3 is a region where the wings 14 for fastening the absorbent article 1 to the wearing article are provided.
  • the front side area S1 is located on the front side of the central area S3.
  • the rear area S2 is located behind the central area S3.
  • the absorbent article 1 may include an absorbent article main body 10 formed of members other than the inspection member 60, and the inspection member 60.
  • the absorbent article main body 10 may correspond to a general absorbent article such as a sanitary napkin that does not include the inspection member 60. That is, the absorbent article main body 10 may correspond to the absorbent article 1 having no inspection member 60.
  • the absorbent article main body 10 may be constituted by the main body 12 and a pair of wings 14.
  • the main body 12 has an absorbent core 20.
  • the main body portion 12 is a portion inside the wing 14 in the width direction W.
  • the pair of wings 14 extend from the main body 12 to the outside in the width direction W, and are fixed to the non-skin side T2 of the wearing article when attached to the wearing article.
  • the boundary between the main body 12 and the wing 14 is a fold FL extending in the front-rear direction L.
  • the absorbent article 1 includes the absorbent core 20, the top sheet 30, and the inspection member 60. Further, the absorbent article 1 may include a back sheet 40, a side sheet 50, and an adhesive section 70.
  • the absorbent core 20 includes an absorbent material that absorbs liquid.
  • Absorbent materials can be formed, for example, from hydrophilic fibers, pulp and superabsorbent polymers (SAP).
  • SAP superabsorbent polymers
  • the absorbent core 20 may be wrapped by a core wrap (not shown).
  • the core wrap only needs to cover the absorbent core 20 at least on the skin-facing surface side of the absorbent core 20.
  • the core wrap may include a sheet disposed on the skin side of the absorbent core 20 and a sheet disposed on the non-skin side of the absorbent core 20.
  • the absorbent core 20 may not be covered by the core wrap.
  • the absorbent core 20 is arranged at least in the central area S3.
  • the absorber core may extend from the central area S3 to the front area S1.
  • the absorber core may extend from the central area S3 to the rear area S2.
  • the top sheet 30 is arranged on the skin side with respect to the absorbent core 20.
  • the top sheet 30 has an absorption region AR overlapping the absorption core in the thickness direction T.
  • the top sheet 30 has liquid permeability.
  • the topsheet 30 may be made of any sheet-like material having a structure that allows liquid to pass through, such as a nonwoven fabric, a woven fabric, a perforated plastic sheet, or a mesh sheet.
  • a nonwoven fabric such as a nonwoven fabric, a woven fabric, a perforated plastic sheet, or a mesh sheet.
  • a mesh sheet such as a nonwoven fabric, a woven fabric, a perforated plastic sheet, or a mesh sheet.
  • any of natural fibers and chemical fibers can be used.
  • the back sheet 40 has liquid impermeability.
  • the back sheet 40 is made of a material such as a sheet in which a breathable resin film is joined to a nonwoven fabric such as a laminated nonwoven fabric mainly composed of polyethylene sheet or polypropylene, a breathable resin film, spunbond, or spunlace. Good.
  • the side sheet 50 may cover the outer edge of the top sheet 30.
  • the side sheet 50 may cover the outer edge of the top sheet 30 in the width direction W, and may extend outside the top sheet 30 in the width direction W. Note that the absorbent article 1 may not have the side sheet 50.
  • the side sheet 50 can be made of the same material as the top sheet 30. However, in order to prevent the bodily fluid attached to the top sheet 30 from crossing the side sheet 50 and leaking out of the absorbent article 1 in the width direction W, the side sheet 50 has hydrophobicity or water repellency. May have.
  • the side sheet 50 may be disposed on the outer edge of the absorbent core 20 in the width direction W, the wing 14 described later, and the flap portion 80 described later.
  • the inspection member 60 is a member for inspecting a wearer's health condition.
  • the inspection member 60 displays the health condition (color indicating) of the wearer with an indicator.
  • an immunochromatography method or a test paper method can be used for examining a health condition.
  • the immunochromatography method is performed by dropping excrement (eg, blood) on a member (eg, a cellulose membrane) on which labeled particles containing antibodies are spread.
  • a detection target specifically, a target component (eg, an antigen) to be detected
  • the detection target and the antibody cause an antigen-antibody reaction to form a complex.
  • the formed complex moves on the membrane by capillary action.
  • a different type of antibody (indicator) is linearly arranged at the destination of the complex.
  • the complex is colored by binding to another type of antibody.
  • the presence or absence of coloration indicates the health condition of the wearer. The wearer can confirm the health condition by visually determining the presence or absence of coloration.
  • the indicator is included in the inspection member 60 and color is generated when the indicator reacts with the detection target included in the excrement.
  • the presence or absence of coloration indicates the health condition of the wearer.
  • the wearer can visually confirm the coloration (change in the color of the indicator) by the indicator to confirm the health condition.
  • Excretions include, for example, blood, urine, stool, sweat, vaginal discharge, and the like.
  • Items indicating health status include, for example, physical condition-related (pH, iron deficiency anemia, renal function, myocardial infarction, inflammation / infection, nutritional status evaluation, etc.), pregnancy-related (physiological cycle prediction, ovulation prediction, etc.), mental-related (Depression, drugs, etc.).
  • the detection target is, for example, urine waste (urine specific gravity), leukocyte, hydrogen ion (pH), protein, glucose, ketone body, urobilinogen, bilirubin, urinary occult blood, nitrite, steroid, peptide, aromatic compound, FSH ( Follicle stimulating hormone), BUN (Urea @ nitorogen), AlB (Albumin), LPS (lipopolysaccharide), hCG (human chorionic gonadotropin), LH (luteinizing hormone), U-ALB, CRP (C-reactiv protein), Examples include myoglobin, CK-MB, troponin I, troponin T, hemoglobin, strep A, HBs antibody, HIV antibody, TP antibody, rotavirus, influenza virus, adenovirus, DNA, O-157, cocaine, marijuana, morphine and the like. No.
  • the inspection member 60 has a contact part 62 and a display part 64.
  • the contact part 62 is a part for making excretion contact.
  • the display unit 64 is a part that displays the health state (color indicating) of the wearer.
  • the display unit 64 includes an indicator that changes color based on the detection target contained in the excrement that has come into contact with the contact unit 62.
  • the indicator is a chemical substance (inorganic substance, organic substance) that is colored by reacting with a detection target or a substance derived from the detection target (for example, a complex).
  • the contact portion 62 is a portion for guiding excrement (test target) to a region where the labeled particles including the antibody are arranged.
  • the contact portion 62 may include a region where the label particles are arranged.
  • the detection target (antigen) and the antibody contained in the excretion cause an antigen-antibody reaction to form a complex.
  • the display unit 64 includes a region (detection line) in which an indicator (another type of antibody) that is colored by binding to the complex is arranged. Therefore, when the immunochromatography method is used, the contact section 62 and the display section 64 are arranged at different positions. Therefore, in this case, the contact section 62 and the display section 64 are different.
  • test member 60 may include a control line that is a color region regardless of the presence or absence of the target antigen to be detected when the test is appropriate.
  • the control line is located farther from the contact section 62 than the detection line (display section 64).
  • the contact portion 62 includes at least a region where the indicator is arranged. Since the indicator contained in the contact part 62 reacts with the detection target to give a color, the contact part 62 and the display part 64 are arranged at the same position. Therefore, in this case, the contact portion 62 and the display portion 64 are the same.
  • the contact portion 62 includes a label particle
  • the display portion 64 includes an indicator for displaying a wearer's health condition.
  • the contact part 62 that is, the display part 64, includes an indicator for displaying the health condition of the wearer.
  • the contact portion 62 may not include the indicator.
  • the inspection member 60 may be any member that can hold or contain the indicator.
  • the inspection member 60 can be made of any material such as paper, nonwoven fabric, and woven fabric.
  • the rigidity of the inspection member 60 may be equal to or less than the rigidity of the member used for the absorbent article 1. Thereby, even if the absorbent article 1 is provided with the inspection member 60, it becomes easy to suppress deterioration of the touch of the wearer.
  • the inspection member 60 may be, for example, a linear plate shape.
  • the contact portion 62 is arranged in a reach range where the excrement excreted in the absorption area AR reaches. Thereby, the excrement excreted from the wearer can be brought into contact with the contact portion 62. Therefore, the indicator contained in the display unit 64 can be colored, and the display unit 64 can display the health condition.
  • At least a part of the contact portion 62 may be in contact with the absorbent core. Since the excrement is excreted in the absorbent core 20, more excretion can be brought into contact with the contact portion 62. Thus, the indicator can be colored based on many detection targets, and the inspection accuracy can be improved. In FIG. 2A, a part of the contact portion 62 is in contact with the absorbent core 20.
  • At least a part of the contact portion 62 may overlap the absorbent core 20 in the thickness direction T. Since the excrement is excreted in the absorbent core 20, more excretion can be brought into contact with the contact portion. Thus, the indicator can be colored based on many detection targets, and the inspection accuracy can be improved.
  • a part of the contact portion 62 overlaps the absorbent core 20 in the thickness direction T. The rest of the contact portion 62 does not overlap with the absorbent core 20 in the thickness direction.
  • the reaching range may be a diffusion range of the excrement when the excrement is a liquid.
  • the reach may be a range where the excrement spreads during wear when the excrement is solid / semi-solid.
  • the maximum range of the reaching range is excreted in the absorption region AR. This is an area that overlaps with at least one of the liquid-permeable sheets that directly or indirectly comes into contact with the top sheet 30 through which excrement that can be diffused.
  • a liquid-permeable sheet that comes into “indirect” contact with the top sheet 30 means that it is in contact with the top sheet 30 via another liquid-permeable sheet.
  • the excrement excreted in the top sheet 30 can be diffused to the liquid permeable sheet via another liquid permeable sheet.
  • the maximum range of the reaching range is a range from the surface of the top sheet 30 on the skin side T1 to the surface of the back sheet 40 on the skin side T1. It is.
  • At least a part of the contact portion 62 only needs to be arranged within the maximum range of the reaching range. At least a part of the contact portion 62 is disposed at a position overlapping the top sheet 30 in the thickness direction T or at a position overlapping the absorbent core 20 so that the excrement easily reaches the contact portion 62. , May be arranged in the central area S3, or may be arranged in the range of the excretion opening contact portion that contacts the excretion opening of the wearer. Thereby, the excrement excreted from the wearer can be brought into contact with the contact portion 62. Therefore, the indicator contained in the display unit 64 can be colored, and the display unit 64 can display the health condition.
  • At least a part of the display unit 64 does not overlap with the absorbing core 20 in the thickness direction T. This makes it easier for the wearer to visually recognize the display unit 64 without blocking at least a part of the display unit 64 with the absorbent core 20. Furthermore, since most of the excrement is absorbed by the absorbent core 20, at least a part of the display unit 64 does not overlap with the absorbent core 20, so that at least a part of the display unit 64 does not easily come into contact with the excrement. This makes it difficult for at least a part of the display unit 64 to be covered with excrement, and makes it easier for the wearer to visually recognize the display unit 64 without being affected by the excrement. As described above, since the wearer can easily visually recognize the display unit 64, the wearer can easily grasp the correct health condition. In FIG. 2A, not all of the display portions 64 overlap the absorbing core 20 in the thickness direction T.
  • the absorbent member 1 includes the inspection member 60 using the test paper method
  • a part of the region of the inspection member 60 containing the indicator is disposed in the reach.
  • the display portion 64 which is the remaining region including the indicator, does not overlap with the absorbent core 20 in the thickness direction T.
  • the excrement penetrates from the area arranged in the reaching range, and the display unit 64 can display color.
  • positioned in the reaching range is the display part 64 at the same time as the contact part 62, it can color. Therefore, in this case, a part of the display unit 64 overlaps the absorbing core 20 in the thickness direction.
  • the absorbent member 1 includes the test member 60 using the immunochromatography method
  • a portion at least the contact portion 62 that guides the excrement (test target) to the region where the labeled particles including the antibody are arranged.
  • the detection line (display portion 64), which is the region where another type of antibody (indicator) that is colored by binding to the complex derived from the detection target, does not overlap with the absorption core 20 in the thickness direction T.
  • the inspection member 60 may be inserted into the exposure opening 52 formed in the side sheet 50. Thereby, at least a part of the display unit 64 may be exposed.
  • the display unit 64 may include a non-exposed portion 642 located on the non-skin side T2 than the side sheet 50 and an exposed portion 644 located on the skin side T1 than the side sheet 50.
  • the non-exposed portion 642 may be indirectly visible through the side sheet 50.
  • the exposed part 644 is directly visible.
  • the exposed part 644 may have a detection line that is at least a part of the display part 64. This allows the wearer to directly check the display section 64, and thus can easily check the health condition. Further, the exposure section 644 may have a control line without including the detection line. Thereby, the wearer can easily confirm that the inspection has been properly performed by visually recognizing the exposed portion 644.
  • the "side sheet 50" may be replaced with the "top sheet 30".
  • At least a part of the display unit 64 may be arranged on one of the pair of wings 14 in the thickness direction T.
  • the wings 14 are fixed to the non-skin side T2 of the wearing article 100 in a state where the wings 14 are attached to the wearing article 100 (for example, underwear), so that excrement excreted from the skin side T1.
  • the wing 14 is fixed to the non-skin side T2 of the wearing article 100, when the wearer wears the absorbent article 1, at least a part of the display unit 64 and the wearer's in the thickness direction T. Wearing article 100 exists between the skin. For this reason, at the time of wearing the absorbent article 1, at least a part of the display unit 64 becomes difficult to touch the skin of the wearer. Even if the indicator contained in the display unit 64 can damage the skin, the safety of the wearer can be improved.
  • the inspection member 60 may be fixed (joined) to at least one of the absorbent core 20, the top sheet 30, the back sheet 40, and the side sheet 50.
  • the inspection member 60 may be fixed by, for example, an adhesive (for example, a hot melt adhesive (HMA)) for joining the materials of the absorbent article 1 together.
  • HMA hot melt adhesive
  • at least one of the contact portion 62 and the display portion 64 may be fixed.
  • at least a part of the contact part 62 may be fixed, and at least a part of the display part 64 may be fixed.
  • the inspection member 60 may have a portion other than the contact portion 62 and the display portion 64 fixed.
  • the inspection member 60 may have a fixed part configured by at least a part of the part other than the contact part 62 and the display part 64. It may be fixed by an adhesive applied on the fixing part. By fixing the inspection member 60, it is possible to prevent the contact portion 62 from moving outside the reach.
  • the adhesive portion 70 is a region provided with an adhesive for fixing the absorbent article 1 to the wearing article 100.
  • the adhesive section 70 is disposed on the non-skin side T2 of the back sheet 40 and is for fixing the absorbent article 1 to a worn article (for example, underwear) 100.
  • the adhesive portion 70 may have a central adhesive portion 72 and a side adhesive portion 74. As shown in FIG. 2A, the central adhesive portion 72 is disposed on the non-skin side T2 of the back sheet 40 in the main body 12. The central adhesive portion 72 has an adhesive for fixing the main body 12 to the wearing article 100. The side adhesive portion 74 is arranged on the non-skin side T2 of the back sheet 40 on the wing 14. The side adhesive portion 74 has an adhesive for fixing the wing 14 to the wearing article 100.
  • the wearer may be able to visually recognize the display unit 64 with the wearing article 100 put on his / her leg by removing the wing 14 from the wearing article 100. Thereby, the wearer can easily check the health condition.
  • the adhesive strength of the side adhesive portion 74 may be smaller than the adhesive strength of the adhesive for fixing the inspection member 60. Thereby, the wearer may remove the back sheet 40 from the wearing article 100 by holding the exposed portion 644 of the display unit 64 and pulling the exposed portion 644 as shown in FIG. 3A. The wearer can easily remove the wing 14 from the wearing article 100.
  • the adhesive strength of the side adhesive portion 74 may be larger than the adhesive strength of the adhesive for fixing the side sheet 50. Accordingly, even if the wearer grasps the exposed portion 644 of the display unit 64 and pulls the exposed portion 644 as shown in FIG. 3B, the top sheet 30 and the inspection member 60 can be removed from the back sheet 40. Good. This allows the wearer to directly check not only the exposed portion 644 but also the non-exposed portion 642, so that the wearer can easily check the health condition.
  • FIG. 4 is a diagram for describing each modification example according to the first embodiment.
  • FIG. 4A is a cross-sectional view for explaining a modification (part 1) according to the first embodiment.
  • FIG. 4B is a diagram for describing a modified example (part 2) according to the first embodiment.
  • FIG. 4C is a diagram for describing a modified example (part 3) according to the first embodiment.
  • FIG. 5 is a cross-sectional view for explaining each modification example according to the first embodiment.
  • FIG. 5A is a cross-sectional view for explaining a modification (part 4) according to the first embodiment.
  • FIG. 5 is a cross-sectional view for explaining a modification (part 4) according to the first embodiment.
  • FIG. 5B is a cross-sectional view for explaining a modification (part 5) according to the first embodiment.
  • FIG. 6 is a diagram for explaining a modification example according to the first embodiment.
  • FIG. 6A is a cross-sectional view illustrating a modified example (No. 6) according to the first embodiment.
  • FIG. 6B is an enlarged sectional view taken along line BB shown in FIG. 6A.
  • FIG. 7 is a diagram for describing each modification example according to the first embodiment.
  • FIG. 7A is a plan view of the absorbent article 1 in a modification (part 7) according to the first embodiment as viewed from the skin surface side.
  • FIG. 7B is a plan view of the absorbent article 1 according to a modification (No.
  • FIG. 7C is a plan view of the absorbent article 1 in the modification (No. 9) according to the first embodiment as viewed from the skin side.
  • FIG. 7D is a plan view of the absorbent article 1 in a modification (10) according to the first embodiment as viewed from the skin surface side.
  • FIG. 8 is a diagram for describing each modification example according to the first embodiment. Specifically, FIG. 8A is a plan view of the absorbent article 1 in a modification (No. 11) according to the embodiment as viewed from the skin surface side.
  • FIG. 8B is a plan view of the absorbent article 1 as viewed from the skin surface side in a modification (twelfth) according to the first embodiment. The description of the same parts as those in the first embodiment will be omitted.
  • the contact portion 62 may be arranged on the skin surface side T1 with respect to the absorbent core 20. Therefore, the contact portion 62 may contact the surface of the absorbent core 20 on the skin side T1.
  • the contact portion 62 may be disposed between the absorbent core 20 and the topsheet 30. Thereby, the excrement easily comes into contact with the contact portion 62 without being blocked by the absorbent core 20.
  • the contact portions 62 may be arranged between the absorbent cores 20 in the thickness direction T.
  • the contact portion 62 may be arranged between the absorbent cores 20 by being inserted from the side surface of the absorbent core 20 in the width direction W.
  • the absorbent core 20 may be provided with an opening on a side surface of the absorbent core 20 for inserting the contact portion 62 (the inspection member 60).
  • the contact portion 62 may be disposed between the absorbent cores 20 by being sandwiched between two absorbent cores 20 stacked in the thickness direction T. The excrement absorbed by the absorbent core 20 diffuses in the absorbent core 20, so that the excrement easily comes into contact with the contact portion 62.
  • the contact portion 62 may contact the side surface of the absorbent core 20.
  • the contact portion 62 may be in contact with the excrement diffused to the side surface of the absorbent core 20 in the width direction W. Thereby, the excrement easily comes into contact with the contact portion 62 easily.
  • the contact portion 62 may not overlap the absorbent core 20 in the thickness direction T as long as the contact portion 62 is arranged in the range of the excrement.
  • the absorbent article 1 may have a guiding portion 22 for guiding excrement to at least a part of the contact portion 62.
  • the guide portion 22 may be an area that is easier to draw in liquid (excretion) than its surroundings. Since the excrement is guided to at least a part of the contact portion 62 by the guide portion 22, more excrement can be brought into contact with the contact portion 62.
  • the indicator can be colored based on many detection targets, and the inspection accuracy can be improved.
  • the absorbent core 20 may have a low-weight portion 221 as the guide portion 22.
  • the basis weight of the absorbent material in the low basis weight portion 221 is lower than the basis weight of the surrounding absorbent material. Therefore, excrement is more easily diffused in the low weight portion 221 than in the surrounding area.
  • the low weight portion 221 may extend from the skin surface of the absorbent core 20 to the non-skin surface side in the thickness direction.
  • the basis weight of the low basis weight portion 221 may be a value larger than 0.
  • the basis weight of the low basis weight portion 221 may be zero. That is, the low-weight portion 221 may be an opening penetrating the absorbent core 20 in the thickness direction T.
  • the absorbent core 20 may have an opening penetrating the absorbent core 20 in the thickness direction.
  • the contact portion 62 arranged on the non-skin side T2 with respect to the absorbent core 20 may overlap the low-weight portion 221 (for example, an opening) in the thickness direction T. .
  • the indicator can be colored based on many detection targets, and the inspection accuracy can be improved.
  • the contact portion 62 disposed on the non-skin side T2 with respect to the absorbent core 20 does not have to overlap the low-weight portion 221 (for example, an opening) in the thickness direction T. Therefore, in a plan view in the thickness direction T, the contact portion 62 may be arranged at a position away from the opening.
  • the excrement is more likely to reach the non-skin side T2 of the absorbent core 20 where the contact portion 62 is arranged by passing through the opening than through the gap of the fiber constituting the absorbent member of the absorbent core 20. .
  • the excrement reaching the non-skin side T2 can reach the contact portion 62 by diffusion.
  • the time required to reach the contact portion 62 can be reduced, and a large amount of excrement can reach the contact portion 62. Thereby, the inspection accuracy can be improved.
  • the contact portion 62 contains the indicator
  • the indicator may be dissolved in the excrement that has reached the contact portion 62.
  • the contact portion 62 does not overlap the opening in the thickness direction T, it is difficult for excrement to reach the non-skin side T2 of the absorbent core 20 through the opening. For this reason, even if the indicator can stimulate the skin, it is difficult for excrement containing the indicator to reach the non-skin side T2 of the top sheet 30, and the safety of the wearer can be enhanced.
  • the top sheet 30 has a plurality of protrusions 32 arranged in parallel, which are formed by being bent to have a wavy cross section, and a plurality of protrusions 32 adjacent to each other. And a bottom portion (s) 34 disposed therebetween.
  • the bottom portion 34 may extend from a region overlapping the absorbent core 20 in the thickness direction T to a region overlapping the contact portion 62 in the thickness direction T.
  • the excrement E excreted in the absorption area AR flows down to the bottom 34 even when excreted in the projection 32. Therefore, the excrement E is easily collected on the bottom 34 and reaches the position overlapping the contact portion 62 in the thickness direction T using the bottom 34 as a path.
  • the contact portion 62 may be arranged away from the absorbent core 20.
  • the display unit 64 may extend from the outer edge of the absorbent core 20 in the front-rear direction L. Therefore, at least a part of the display unit 64 may be disposed on the flap unit 80.
  • the flap 80 is a portion from the outer edge of the absorbent core 20 to the outer edge of the absorbent article 1.
  • the flap 80 may include a front flap 81 that is a flap in the front area S1 and a rear flap 82 that is a flap in the rear area S2.
  • At least a part of the display unit 64 may extend from the outer edge of the absorbent core 20 in the front-rear direction L in the front side area S1. Therefore, at least a part of the display unit 64 may be disposed on the front flap unit 81.
  • the front flap portion 81 In a state where the absorbent article 1 is lowered to a position near the knee, the front flap portion 81 is at a position where it is easy to visually recognize. Therefore, the wearer can easily visually recognize the display section 64 without completely removing the absorbent article 1 from the body.
  • At least the front side area S1 includes the inspection member 60 that detects a target component contained in urine. And at least a part of the contact portion 62 can be arranged in the front side area S1. Thereby, more excrement can be brought into contact with the contact portion 62.
  • the indicator can be colored based on many detection targets, and the inspection accuracy can be improved.
  • the inspection member 60 which detects the target component contained in the stool is a target.
  • the indicator can be colored based on many detection targets, and the inspection accuracy can be improved.
  • the inspection member 60 may be arranged on the non-skin side T2 with respect to the top sheet 30. It is possible to prevent the inspection member 60 from directly touching the wearer's skin. Thereby, the discomfort at the time of wearing due to the inspection member 60 directly hitting the skin of the wearer can be suppressed. Furthermore, even if the indicator can give irritation to the skin, it becomes difficult for the indicator to touch the skin of the wearer, and the safety of the wearer can be enhanced.
  • the top sheet 30 may have transparency. Thereby, the wearer may be able to visually recognize the coloration of the inspection member 60 via the top sheet 30. Further, as described above, the wearer may be able to visually recognize the coloration of the inspection member 60 by peeling the top sheet 30 (and / or the side sheet 50) from the back sheet 40.
  • the transparency of the topsheet 30 can be specified by the opacity (OP). If the topsheet 30 has 0% opacity, it is completely transparent. On the other hand, when the topsheet 30 has 100% opacity, it does not have transparency, that is, the topsheet 30 does not transmit light. Therefore, the opacity of the topsheet 30 is less than 100%.
  • the opacity of the top sheet 30 may be 50% or less so that the color of the display unit 64 can be visually recognized more accurately.
  • the opacity of the top sheet 30 may be 8.5% or less in order to more accurately recognize the color of the display unit 64.
  • a dispersion colorimeter may be used.
  • a dispersion colorimeter is available from BYK-Gardner GmbH (Geretsried, Germany) under the trade name “BYK-Gardner Color-Guide 45/0” (Geretsried). Catalog No. 6800). The measurement can be performed at a viewing angle of 2 ° (degrees) using the light source “A”.
  • the dispersion colorimeter comprises a light source for illuminant A (ie, something similar to an incandescent lamp having a correlated color temperature of about 3000 K), a flat table, a white standard plate, a standard black plate, a multi-cell light.
  • a photodetector comprising a detector diode array; and a computer.
  • White and black standard plates are available from the company under catalog numbers 6811 and 6810, respectively.
  • Opacity (OP) can be obtained by the following equation.
  • OP (%) (Yb / Yw) ⁇ 100 This process is repeated at least five times for one sample sheet material, and the average value of the measured opacity (OP) is calculated and recorded with a colorimeter. The average value of the measured opacity is called the opacity of the sheet material.
  • the topsheet 30 is a heat source that compresses the topsheet 30 in the thickness direction T while heating over a predetermined region of a part of the surface of a nonwoven fabric (for example, SMS (spunbond / meltblown / spunbond)).
  • a compression process may be performed.
  • a high-density part may be formed in the top sheet 30.
  • the compression process for forming the high-density portion is performed by subjecting the top sheet 30 (nonwoven fabric) to a known pressure process such as a calendering process or an embossing process.
  • the fibers on the surface of the nonwoven fabric are compacted, whereby fine irregularities on the surface are reduced and the surface is in a smooth state as compared with a region where the high-density portion is not formed.
  • the top sheet 30 may have transparency.
  • the top sheet 30 has been described as an example, when the display unit 64 overlaps the side sheet 50 in the thickness direction T, the side sheet 50 has transparency similarly to the top sheet 30. Good.
  • At least a part of the display unit 64 may extend from the outer edge 10 e of the absorbent article main body 10.
  • a portion extending from the outer edge 10e of the absorbent article main body 10 corresponds to the exposed portion 644. Since at least a part of the display unit 64 extends from the outer edge 10e of the absorbent article main body 10, at least a part of the display unit 64 is arranged at a position where excrement cannot be diffused. Accordingly, it is possible to prevent at least a part of the display unit 64 from being covered with excrement.
  • the wearer since at least a part of the display unit 64 extends from the outer edge 10e of the absorbent article main body 10, the wearer can directly view the display unit 64. Therefore, it is possible for the wearer to easily grasp the correct health condition.
  • At least a part of the display unit 64 may extend from the outer edge 10 e of the absorbent article main body 10.
  • the wearer can visually recognize the display portion 64 (the exposed portion 644).
  • the wearer can easily confirm the presence or absence of coloration.
  • At least a part of the display section 64 may extend from the outer edge 10e of the absorbent article main body 10. At least a portion of the display 64 may extend from an outer edge of the wing 14. Since the wings 14 are fixed to the non-skin side T2 of the wearing article 100, the excrement excreted from the skin side hardly adheres to the wings 14. This makes it difficult for at least a part of the display unit 64 to be covered with the excrement, and makes it easier for the wearer to visually recognize the display unit without being affected by the excrement.
  • the wing 14 is fixed to the non-skin surface side T2 of the wearing article 100, even if the exposed portion 644 exists, the exposed portion 644 is less likely to touch the wearer's skin. Even if the indicator contained in the exposed portion 644 can damage the skin, the safety of the wearer can be improved.
  • At least a part of the display part 64 may extend from the outer edge 10e of the absorbent article main body 10 in the rear area S2 as well as in the front area S1 or the central area S3.
  • the absorbent article 1 may have a plurality of inspection members 60 whose detection targets are different from each other.
  • the display units 64 included in each of the plurality of inspection members 60 may be arranged at different positions in the thickness direction T. Since a plurality of inspection members 60 whose detection targets are different from each other are provided, a plurality of items indicating a health condition can be confirmed with one absorbent article 1. Since the display portions 64 included in each of the plurality of inspection members 60 are arranged at positions different from each other in the thickness direction T, the wearer can easily recognize each of the display portions 64 and overlook some of the display portions 64. Can be suppressed.
  • the plurality of inspection members 60 may include a first inspection member 60A and a second inspection member 60B.
  • the display part 64A of the first inspection member 60A may be arranged on one wing 14A, and the display part 64B of the second inspection member 60B may be arranged on the other wing 14B.
  • the display section 64A of the first inspection member 60A may be disposed in the front side area S1. Therefore, at least a part of the display unit 64 ⁇ / b> A may be disposed on the front flap unit 81. Further, the display section 64B of the second inspection member 60B may be arranged in the rear area S2. Therefore, at least a part of the display unit 64 ⁇ / b> B may be disposed on the rear flap unit 82.
  • the first inspection member 60A may be the inspection member 60 that detects a target component contained in urine as a detection target.
  • the second inspection member 60B may be the inspection member 60 that detects a target component contained in the stool.
  • FIG. 9 is a plan view of the absorbent article according to the second embodiment as viewed from the skin side.
  • FIG. 10 is a plan view of the absorbent article according to the second embodiment as viewed from the non-skin side.
  • FIG. 11 is a cross-sectional view of the absorbent article according to the second embodiment. Specifically, FIG. 11 is a cross-sectional view along the line AA shown in FIG.
  • the absorbent article 1 includes the absorbent core 20, the back sheet 40, and the inspection member 60. Further, the absorbent article 1 may include the top sheet 30, the side sheet 50, and the adhesive section 70.
  • the back sheet 40 is arranged on the non-skin side with respect to the absorbent core 20.
  • the back sheet 40 may have liquid impermeability.
  • the back sheet 40 has transparency. Thereby, as shown in FIG. 11, even if the inspection member 60 is arranged on the skin surface side T1 with respect to the back sheet 40 in the thickness direction T, as shown in FIG. It is possible.
  • the term “visible” refers to a distance of about 30 to 50 cm in a room (approximately: 500 to 750 lx (lux)) brightly illuminated with a neutral white color (color temperature reference: 4600 to 5400 K (Kelvin)). This means that a subject having good visual acuity (1.0 or more) with both eyes can visually recognize the subject when viewing it.
  • the transparency of the back sheet 40 can be specified by the opacity (OP).
  • the backsheet 40 is completely transparent if it has 0% opacity.
  • the opacity of the back sheet 40 is less than 100%.
  • the opacity of the back sheet 40 may be 50% or less so that the inspection member 60 (the display unit 64) can be visually recognized more accurately.
  • the opacity of the back sheet 40 may be 8.5% or less in order to more accurately view the color of the display unit 64.
  • the backsheet 40 is subjected to a heat compression process of compressing the backsheet 40 in the thickness direction T while heating over the entire area of the surface of the nonwoven fabric (for example, SMS (spunbond / meltblown / spunbond)). May be. Thereby, a high-density portion may be formed on the back sheet 40.
  • the heat compression process for forming the high-density portion is performed by subjecting the back sheet 40 (nonwoven fabric) to a known pressure process such as a calendering process or an embossing process.
  • the fibers on the surface of the nonwoven fabric are compacted, whereby fine irregularities on the surface are reduced and the surface is in a smooth state as compared with a region where the high-density portion is not formed.
  • the back sheet 40 may have transparency.
  • a zipper sound is less likely to be generated when the absorbent article 1 is opened, and it is difficult for others to notice when using the absorbent article 1.
  • the adhesive section 70 may have transparency.
  • the central adhesive portion 72 overlaps (a part of) the display portion 64 in the thickness direction T. For this reason, the central adhesive portion 72 may have transparency.
  • the adhesive section 70 may have transparency by being made of, for example, HMA.
  • the absorbent article 1 has a hydrophobic portion 90 having hydrophobicity.
  • the hydrophobic portion 90 is disposed in an extension region ER extending in the thickness direction T and the horizontal direction from the display portion 64 on the skin surface side with respect to the back sheet 40.
  • the hydrophobic portion 90 When the hydrophobic portion 90 is disposed in the extension region ER extending from the display portion 64 in the thickness direction T, the excrement excreted on the skin surface side T1 of the absorbent article 1 is displayed in the thickness direction T on the display portion.
  • the hydrophobic portion 90 exists on a diffusion path that diffuses toward 64. Since the hydrophobic part 90 has hydrophobicity, it is easy to suppress the water-soluble excrement from diffusing to the display part 64 side.
  • the hydrophobic part 90 When the hydrophobic part 90 is arranged in the extension region ER extending in the horizontal direction from the display part 64, the excrement diffused inside the absorbent article 1 is diffused in the horizontal direction toward the display part 64.
  • the hydrophobic part 90 exists on the diffusion path.
  • the hydrophobic part 90 can easily suppress the water-soluble excrement from diffusing to the display part 64 side. As described above, it is easy to suppress the excrement from covering the display unit 64 or overlapping the display unit 64, and it is easy to ensure the visibility of the display unit 64. Accordingly, when the wearer visually recognizes the display unit 64 from the back sheet 40 side, the wearer can easily grasp the correct health condition.
  • the hydrophobic portion 90 arranged in the extension region ER may be arranged in the reach of the excretion excreted in the absorption region AR. This can suppress the excrement reaching the hydrophobic part 90 from being diffused to the display part 64 side, so that the visibility of the display part 64 can be easily secured. Thereby, when the wearer visually recognizes the display unit 64 from the back seat side, it becomes easier for the wearer to grasp an accurate health condition.
  • the hydrophobic part 90 may be in contact with the display part 64. It is possible to suppress the excrement from reaching the display unit 64. Thereby, the visibility of the display unit 64 can be ensured, and the wearer can easily grasp the correct health condition.
  • the hydrophobic portion 90 disposed in the extension region ER includes a skin-side hydrophobic portion 92 disposed on the skin surface side T1 with respect to the display portion 64 and a non-skinned portion disposed on the non-skin surface side T2 with respect to the display portion 64. It may include a skin-side hydrophobic portion 94 and a side-surface-side hydrophobic portion 96 disposed outside the display portion 64 in the horizontal direction (the width direction W in FIG. 11).
  • the skin-side hydrophobic portion 92 that is the hydrophobic portion 90 may be in contact with the skin-side surface of the display unit 64. Thereby, it is possible to suppress the excrement that diffuses from the skin surface side T1 to the non-skin surface side T2 from reaching the display unit 64. The visibility of the display unit 64 can be ensured, and the wearer can easily grasp the correct health condition.
  • the non-skin side hydrophobic portion 94 which is the hydrophobic portion 90 may be in contact with the skin side surface of the display portion 64. Thereby, it is possible to suppress the excrement from reaching the surface of the display section 64 visually recognized from the back sheet side. The visibility of the display unit 64 can be ensured, and the wearer can easily grasp the correct health condition.
  • the side surface side hydrophobic portion 96 which is the hydrophobic portion 90 may be in contact with the side surface of the display portion 64. Thereby, it is possible to suppress the excrement diffused in the horizontal direction from reaching the display unit 64. The visibility of the display unit 64 can be ensured, and the wearer can easily grasp the correct health condition.
  • the hydrophobic portion 90 may cover the periphery of the display portion 64. Therefore, the hydrophobic portion 90 may be arranged in a region different from the extension region ER.
  • the hydrophobic part 90 may cover the entire surface of the display part 64.
  • the hydrophobic part 90 may cover a part of the display part 64.
  • the hydrophobic part 90 may cover a part of the contact part 62.
  • the hydrophobic part 90 does not cover the entire surface of the contact part 62 so that the excrement reaches the contact part 62.
  • the hydrophobic portion 90 can be constituted by a layer or a member having hydrophobicity.
  • a water-repellent layer as the hydrophobic portion 90 may be provided by performing a water-repellent process of attaching (applying) a water-repellent agent to a part of the contact portion 62 by a water-repellent spray, a coating device, or the like.
  • the member constituting the display unit 64 may be impregnated with a water repellent.
  • a portion to which the water repellent is not to be attached (for example, (a part of) the contact portion 62) may be covered with a masking tape or the like.
  • the contact portion 62 may be exposed by peeling off a masking tape or the like.
  • the water repellent may be a silicone water repellent or a fluorine water repellent. It is preferable that the water repellent (hydrophobic portion 90) does not easily discolor.
  • the hydrophobic portion 90 may be made of the same material as the back sheet 40.
  • the hydrophobic part 90 may be formed of a bonding layer (for example, a hot melt adhesive (HMA)) for bonding the members constituting the absorbent article 1. Thereby, the inspection member 60 can be fixed and the hydrophobic portion 90 can be formed.
  • HMA hot melt adhesive
  • the hydrophobic portion 90 may have transparency.
  • the non-skin side hydrophobic portion 94 may have transparency in order to make the coloration easily visible.
  • the skin-side hydrophobic portion 92 since the skin-side hydrophobic portion 92 is disposed closer to the skin surface T1 than the display portion 64, the skin-side hydrophobic portion 92 does not need to have transparency, and may have transparency. Further, the side surface side hydrophobic portion 96 does not need to have transparency, and may have transparency.
  • FIG. 12 is a diagram for describing each modification (Nos. 1 to 4) according to the second embodiment.
  • FIG. 12 is a cross-sectional view of the absorbent article 1 for describing a modified example (part 1) of the second embodiment
  • FIG. 12B is a sectional view for describing a modified example (part 2) of the second embodiment.
  • FIG. 12C is a cross-sectional view of the absorbent article 1
  • FIG. 12C is a cross-sectional view of the absorbent article 1 for describing a modification (part 3) of the second embodiment
  • FIG. 12D is a modification of the second embodiment.
  • FIG. 13 is a diagram for describing each modification example (No. 5 to No. 6) according to the second embodiment.
  • FIG. 13A is a plan view of the absorbent article 1 for explaining a fifth modification of the second embodiment as viewed from the non-skin side
  • FIG. 13B is a second embodiment. It is the top view which looked at the absorbent article 1 for demonstrating the example of a change (the 6) from the non-skin side.
  • FIG. 14 is a diagram for describing each modification example (No. 7 to No. 8) according to the second embodiment.
  • FIG. 14A is a plan view of the absorbent article 1 for explaining a modification (No.
  • FIG. 14B is a second embodiment. It is the top view which looked at the absorptive article 1 for explaining the modification (the 8) of (a) from the non-skin side.
  • FIG. 15 is a cross-sectional view of the absorbent article 1 for describing a modified example (No. 9) according to the second embodiment. The description of the same parts as those in the first and second embodiments will be omitted.
  • the hydrophobic portion 90 may be arranged so as to contact the surface of the display surface 64 on the skin surface side T1, and may not be arranged on the non-skin surface side T2 than the display portion 64.
  • the hydrophobic portion 90 does not need to be arranged so as to be in contact with the horizontal outer surface of the display portion 64.
  • the hydrophobic portion 90 may be arranged so as to contact the surface of the non-skin surface side T2 of the display portion 64, and need not be arranged on the skin surface side T1 than the display portion 64.
  • the hydrophobic portion 90 does not need to be arranged so as to be in contact with the horizontal outer surface of the display portion 64.
  • the inspection member 60 may be arranged between the absorbent core 20 and the back sheet 40.
  • a sheet-shaped sheet member may be disposed as the hydrophobic portion 90 between the absorbent core 20 and the display portion 64. Since the sheet member is disposed between the absorbent core 20 and the display unit 64, it is possible to suppress the excrement diffused from the skin side T1 to the non-skin side T2 from reaching the display unit 64. Thereby, the visibility of the display unit 64 can be ensured, and the wearer can easily grasp the correct health condition.
  • the hydrophobic portion 90 may be a core wrap 25 wrapping the absorbent core 20.
  • the core wrap 25 may have a hydrophilic part 222 and a hydrophobic part 90 having hydrophilicity.
  • the hydrophilic part 222 may be located on the skin surface side T1 with respect to the hydrophobic part 90.
  • the hydrophobic portion 90 located on the non-skin side T2 with respect to the absorbent core 20 may overlap with a part of the absorbent core 20 in a plan view in the thickness direction T.
  • a portion that does not overlap with the absorbent core 20 in the thickness direction T may be a hydrophilic portion.
  • the hydrophobic portion 90 located on the non-skin side T2 with respect to the absorbent core 20 overlaps with the entire region of the absorbent core 20 in a plan view in the thickness direction T, the hydrophobic portion 90 causes excrement to reach the contact portion 62.
  • an aperture may be formed.
  • the absorbent article 1 may have an excretion port contact portion 35 that contacts the excretion port of the wearer.
  • the top sheet 30 may have the excretion opening contact part 35.
  • the hydrophobic portion 90 may be closer to the center 35 ⁇ / b> C of the excretion opening contact portion 35 than the display portion 64. Since the hydrophobic portion 90 is closer to the center 35C of the excretion port contact portion 35 than the display portion 64, the excrement discharged to the excretion port contact portion 35 is spread on the diffusion path for diffusing toward the display portion 64. There is a section 90.
  • the hydrophobic part 90 can suppress the excrement diffused from the excretion opening contact part 35 toward the display part 64 from reaching the display part 64. Thereby, the visibility of the display unit 64 can be ensured, and the wearer can easily grasp the correct health condition.
  • the hydrophobic portion 90 may be disposed so as to contact the inner surface of the display portion 64 in the front-rear direction L, and may not be disposed outside the display portion 64 in the front-rear direction L.
  • the hydrophobic part 90 may be arranged so as not to contact the display part 64. By disposing the hydrophobic part 90 apart from the display part 64, it is possible to suppress the excrement from being diffused to the vicinity of the display part 64. This makes it difficult for the excrement to reach the vicinity of the display section 64, and the wearer can be less likely to be confused by the color of the excrement.
  • the absorbent article 1 may include a skin-side member disposed on the skin-side T1 with respect to the display unit 64.
  • the skin-side member may have a background region BR that is a region that does not overlap with the display unit 64 in the thickness direction T and that is visible from the back sheet 40 side.
  • the skin-side member is the absorbent core 20
  • the skin-side member is the topsheet 30.
  • the color of the display unit 64 may be a color having a hue difference of 120 degrees or more in hue circle angle with respect to the color of the background region BR. Thereby, the display unit 64 is visually recognized by being emphasized by the color of the background region BR. Therefore, the wearer can easily visually recognize the display unit 64, and thus can easily grasp an accurate health condition.
  • the color of the display unit 64 may be a color having a hue difference of 165 degrees or more in the hue circle with respect to the color of the background region BR so that the display unit 64 can be visually emphasized.
  • the color of the display section 64 may be a color having a hue difference of 180 degrees in the hue circle with respect to the color of the background area BR, that is, a color complementary to the background area BR.
  • the color of the display section 64 may be a color having a hue difference of 120 degrees or more in the hue circle with respect to the color of the excrement. Thus, the display section is highlighted and visually recognized by the color of the excrement. This makes it easier for the wearer to visually recognize the display unit, so that the wearer can easily grasp the correct health condition.
  • the color of the display portion 64 may be a color having a hue difference of 165 degrees or more in the hue circle angle with respect to the color of the excrement, and may be 180 degrees so that the display portion 64 can be visually emphasized. Good.
  • the color of the display unit 64 may be a color before the indicator is colored. Thus, the wearer can easily visually recognize the display unit 64 when the indicator is not colored.
  • the display unit 64 may be at least a part of the color after the indicator is colored. Thereby, the wearer can easily visually recognize (at least a part of) the display unit 64 when the indicator is colored.
  • the hue difference is a color of 45 degrees or more in the angle of the hue circle
  • the color around the display unit 64 may be a color having a hue difference of 45 degrees or less as an angle of a hue circle with respect to the color of the background region BR.
  • the color of the inspection member 60 itself except for the display unit 64 may be a color having a hue difference of 45 degrees or less in hue circle angle with respect to the color of the background region BR.
  • the color of the background area BR may be a color having a hue difference of 45 degrees or less in terms of the hue circle with respect to the color of the excrement. Even if the excrement permeates the skin-side member, the color of the background area is a color having a hue difference of 3 or less with respect to the color of the excrement, so that the excrement is inconspicuous. This makes it easier for the wearer to visually recognize the display section 64 without being confused by the color of the excrement, and thus to easily grasp the correct health condition.
  • the color of the background area BR may be a color having a hue difference of 1 or less with respect to the color of the excrement, and the color of the background area BR is the same color as the excrement. It may be.
  • the color of the background area BR may be a color having a hue difference of 30 degrees or less and a color of 15 degrees or less with respect to the color of the excrement in a hue circle angle. May be.
  • the color of the background area BR may be the same color as the color of the excrement (that is, 0 degrees in the hue circle).
  • At least the color of the display member 64 around the inspection member may be a color having a hue difference of 120 degrees or more in hue circle angle with respect to the color of the background region BR. Accordingly, the color around the display unit 64 can be easily visually recognized, and the display unit 64 can be easily visually recognized. At least the color around the display unit 64 of the inspection member may be a color having a hue difference of 165 degrees or more in the hue circle angle with respect to the color of the background area BR, and may be 180 degrees. In addition, the color of the inspection member 60 itself may be a color having a hue difference of 120 degrees or more, a color of 165 degrees or more, or 180 degrees with respect to the color of the background area BR in a hue circle angle. May be.
  • the color of at least the periphery of the display unit 64 in the inspection member may be a color having a hue difference of 120 degrees or more in the hue circle with respect to the color of the excrement. Thereby, even if excrement permeates into the skin side member, the color around the display section 64 can be easily visually recognized, and the display section 64 can be easily visually recognized.
  • the color of at least the periphery of the display unit 64 in the inspection member may be a color having a hue difference of 165 degrees or more in the hue circle with respect to the color of the background region BR, and may be 180 degrees.
  • the color of the inspection member 60 itself may be a color having a hue difference of 120 degrees or more, a color of 165 degrees or more, or 180 degrees with respect to the color of the excrement in a hue circle angle. Good.
  • the color around the display unit 64 (or the color of the inspection member 60 itself other than the display unit 64) is white, the color of the display unit 64 (the color before or after the coloration) is red, and the background
  • the color of the region BR may be black. Since white has a high lightness and black has a low lightness, the white surrounding the display unit 64 is better illuminated against the black background, and the red color of the display unit 64 can be clearly recognized.
  • the lightness difference between the part to be visually recognized (the display unit 64, the periphery of the display unit 64, etc.) and the other region (the background region BR, excrement, etc.) It may be 125 or more.
  • the lightness (difference) can be calculated using “((R value X 299) + (G value X 587) + (B value X 114)) / 1000”.
  • the hue difference can be measured by a general measuring method.
  • a hue difference can be measured by using a hue circle such as “Munsell hue circle” or “PCCS hue circle”.
  • a hue circle such as “Munsell hue circle” or “PCCS hue circle”.
  • a color having a hue of 8 or more with the color of the display unit 64 has an angle of 120 degrees or more from the color of the display unit 64.
  • a color having a hue difference of 11 or more from the color of the display unit 64 has an angle of 165 degrees or more from the color of the display unit 64, and a color having a hue difference of 12 from the color of the display unit 64 is a color of the display unit 64.
  • the angle from the color is 180 degrees (that is, the complementary color).
  • At least a part of the display unit 64 may be arranged on one of the pair of wings 14 in the thickness direction T. Since the wing 14 is fixed to the non-skin side T2 of the wearing article 100 in a state where the wing 14 is attached to the wearing article 100 (for example, underwear), excrement excreted from the skin side T1 adheres to the wing 14. hard. This makes it difficult for at least a part of the display unit 64 to be covered with excrement, and makes it easier for the wearer to visually recognize the display unit 64 without being affected by the excrement.
  • the hydrophobic portion 90 is arranged on the surface of the display portion 64 on the skin surface side T1. Since at least a part of the display unit 64 is disposed on the wing 14, the display unit 64 and the hydrophobic unit 90 need not be disposed in the reach. In addition, even when the display unit 64 and the hydrophobic unit 90 are not arranged in a range where the excrement reaches in general use, the excrement is displayed on the display unit 64 due to unexpected movement of the wearer. May be reached. Even in such a case, it is easy to suppress the excrement from reaching the display part 64 by the hydrophobic part 90 arranged in the extension area.
  • the back sheet 40 may have transparency.
  • the back sheet 40 may have the same transparency as the above-described top sheet 30. Thereby, the wearer may be able to visually recognize the coloration of the inspection member 60 from the back sheet 40 side via the back sheet 40.
  • the display unit 64 is exposed and the contact unit 62 is not exposed.
  • the contact portion 62 may be exposed.
  • the contact part 62 and the display part 64 are different (for example, the inspection member 60 using the immunochromatography method)
  • at least a part of the contact part 62 is arranged on the skin side T1 with respect to the top sheet 30 in the absorption region AR. You may.
  • the contact portion 62 does not contain the indicator. For this reason, even if the contact portion 62 touches the skin of the wearer, there is no possibility of damaging the skin of the wearer.
  • the indicator can be colored based on many detection targets, and the inspection accuracy can be improved.
  • at least a part of the display unit 64 may be disposed on the non-skin side T2 with respect to the top sheet 30 (and / or the side sheet 50).
  • the inspection member 60 is closer to the non-skin side T2 than the top sheet 30. May be arranged. This makes it difficult for the indicator to touch the wearer's skin, even if the indicator can stimulate the skin, thereby improving the safety of the wearer.
  • the present invention is not limited to this.
  • a region overlapping with the display unit 64 may have transparency.
  • Other parts of the back sheet 40 may not have transparency.
  • the hydrophobic portion 90 is in contact with the surface of the display portion 64 in the thickness direction T, but is not limited to this.
  • the hydrophobic part 90 may be arranged at a position separated from the display part 64 in the thickness direction T.
  • the absorbent article 1 may have a guiding portion that makes it easy to draw in the excrement in order to make it difficult for the excrement to reach the display section 64.
  • the guide portion may be arranged near the contact portion 62 or may be arranged to contact the contact portion 62.
  • the inspection member 60 has a linear plate shape.
  • the inspection member 60 may have, for example, one or more folds. Therefore, the inspection member 60 may have, for example, a two-fold or three-fold shape.
  • the inspection member 60 may be configured by a member folded into a Z shape. Thereby, the inspection member 60 can be arranged inside the absorbent article 1 in a compact state. Since the area of the inspection member 60 is reduced, deterioration of the touch of the wearer by the inspection member 60 can be easily suppressed.
  • the inspection member 60 is folded so that at least a part of the contact portion 62 contacts another member other than the inspection member 60 (that is, at least a part of the contact portion 62 faces another member). And may be arranged. Thereby, even if the inspection member 60 is folded, the excrement can easily reach the contact portion 62.
  • the inspection member 60 is folded so that at least a part of the display unit 64 abuts on another member other than the inspection member 60 (that is, at least a part of the display unit 64 faces another member). And may be arranged. Thereby, even if the inspection member 60 is folded, the wearer can easily visually recognize the display unit 64.
  • the wearer may acquire the test information by sending color information (image information and / or video information) indicating the color of the display unit 64 to a network (management server).
  • the wearer may acquire the color information by photographing the exposed display unit 64 with a camera built in a communication device owned by the wearer (user), for example.
  • the wearer can send the color information to the management server via the communication device.
  • the wearer may send user information indicating the wearer's information together with the coloration information.
  • the user information is, for example, at least one of a user identifier, a communication device identifier, information indicating the type of excrement, information indicating the type of the absorbent article 1 (inspection member 60), information specifying a detection target, and the like. is there.
  • the wearer may house the absorbent article 1 including the inspection member 60 or the inspection member 60 itself in an accommodation device capable of detecting a color reaction by the indicator.
  • the storage device may irradiate the display unit 64 with visible light to detect a color reaction.
  • the storage device irradiates special light having a special wavelength different from visible light (for example, ultraviolet light having a shorter wavelength than visible light) to the inspection member 60 capable of confirming coloration by the indicator, and Light having a wavelength may be applied to the display unit 64.
  • the accommodation device may acquire the color information by photographing while irradiating visible light or special light in the accommodation device. As described above, by photographing the display unit 64 while irradiating light in the housing device, it is possible to accurately confirm the coloration without being affected by the surrounding environment.
  • the accommodation device may send the color information acquired by photographing the display unit 64 to a network (management server).
  • the accommodation device may include the identifier of the accommodation device as the user information.
  • the housing device may send the acquired color information to the communication device owned by the wearer.
  • the wearer may determine the presence or absence of coloration by displaying the display unit 64 on the communication device. Thereby, the wearer can check the health condition more accurately.
  • the wearer may send the color information acquired from the housing device to the network via the communication device, as described above.
  • the management server can determine the health condition of the wearer (user) based on the coloration information (and the user information).
  • the management server may transmit the information indicating the determination result to the communication device that is the transmission source of the color information.
  • the management server may transmit, to the communication device, advice information indicating advice based on the determination result, together with the determination information indicating the determination result.
  • the management server determines the associated communication device (that is, the identifier of the user) based on the identifier of the communication device (user identifier) associated with the identifier of the accommodation device.
  • the determination information (and the advice information) may be transmitted to the communication device owned by the user.
  • the communication device may display the determination result based on the determination information received by the communication device. Thereby, the wearer can grasp the health condition based on the displayed determination result. The wearer can obtain an objective determination result, not based on the wearer's own determination. Further, when receiving the advice information, the communication device may display the advice. Thereby, the wearer can grasp the advice.
  • the communication device has a program for executing the above-described various processes.
  • the communication device has a memory for storing a program and a processor for executing the program stored in the memory.
  • the program may be obtainable from a network (for example, a management server).
  • the absorbent article 1 is a sanitary napkin, but is not limited thereto.
  • the absorbent article 1 may be, for example, a tape-type or pants-type disposable diaper.
  • the central region S3 may be a region provided with a leg-hole opening disposed around the wearer's leg.
  • the leg opening is a portion that is recessed inward in the width direction from the outer edge of the absorbent article toward the inside in the width direction.
  • the central region S3 may be a region in which a portion that is recessed inward in the width direction from the outer edge of the absorbent core is provided toward the inside in the width direction.
  • the central region S3 may be a region where the middle and high portions, which are regions thicker than the surrounding absorbent cores, are arranged.
  • the absorbent article 1 may have, for example, a front side area S1, a rear side area S2, and a central area S3 so that the absorbent article 1 is divided into three equal parts in the front-rear direction L.

Abstract

An absorbent article 1 according to the present invention comprises: an absorbent core 20 containing an absorbent material; a top sheet 30 that is disposed closer to a skin surface side T1 than the absorbent core 20 and has an absorbent region AR that overlaps the absorbent core 20 in a through-thickness direction T; and an inspection member 60 for inspecting the state of health of the wearer. The inspection element 60 comprises a contact part 62 that contacts the excreta of the wearer, and a display part 64 that displays the state of health of the wearer. The display part 64 contains an indicator that changes color on the basis of a detection target contained in the excreta contacting the contact part 62. At least part of the contact part 62 is disposed within a range reached by excreta excreted into the absorbent region AR. At least part of the display part 64 does not overlap the absorbent core 20 in the through-thickness direction T.

Description

吸収性物品Absorbent articles
 本発明は、吸収性物品に関する。 The present invention relates to an absorbent article.
 特許文献1の図1には、着用者の健康状態を検査するための検査部材を備える吸収性物品が開示されている。検査部材は、着用者の健康状態を表示する表示部を有する。表示部は、排泄物に含まれる検出対象に基づいて呈色する指示薬(インジケータ)を含んでいる。このため、排泄物に検出対象が含まれる場合、指示薬の呈色反応により表示部の色が変化する。着用者は、表示部を視認することで、健康状態を確認することができる。 図 FIG. 1 of Patent Document 1 discloses an absorbent article provided with an inspection member for inspecting a wearer's health condition. The inspection member has a display unit that displays the health condition of the wearer. The display unit includes a color indicator based on a detection target contained in the excrement. For this reason, when the excrement includes the detection target, the color of the display unit changes due to the color reaction of the indicator. The wearer can confirm the health condition by visually recognizing the display unit.
 吸収性物品は、検査部材を備えているため、着用者は、健康状態を手軽に検査することができる。 Since the absorbent article is provided with the inspection member, the wearer can easily inspect the health condition.
特表2003-517584号公報JP-T-2003-517584
 特許文献1に開示された吸収性物品では、前後方向及び幅方向の中央に検査部材が配置されている。これにより、着用者の排泄物が、検査部材へ向けて排泄され易くなり、着用者の排泄物によって検査部材の少なくとも一部が覆われることがある。検査部材を覆う排泄物により表示部が隠された場合には、着用者は、表示部を視認できず、健康状態を確認できない。また、着用者が、排泄物を介して表示部を視認できたとしても、排泄物の色によって表示部の色を誤認する可能性がある。このように、着用者が正確な健康状態を排泄物により把握できないおそれがある。 で は In the absorbent article disclosed in Patent Document 1, the inspection member is disposed at the center in the front-rear direction and the width direction. Accordingly, the excrement of the wearer is easily excreted toward the inspection member, and at least a part of the inspection member may be covered by the excrement of the wearer. When the display unit is hidden by the excrement covering the inspection member, the wearer cannot visually recognize the display unit and cannot check the health condition. Further, even if the wearer can visually recognize the display unit via the excrement, there is a possibility that the color of the display unit is erroneously recognized based on the color of the excrement. Thus, there is a possibility that the wearer may not be able to grasp the exact health condition based on the excrement.
 そこで、着用者の健康状態を検査するための検査部材を備えつつも、着用者が正確な健康状態を把握し易い吸収性物品が望まれる。 Therefore, there is a demand for an absorbent article that is provided with an inspection member for inspecting the health condition of the wearer and that allows the wearer to easily grasp the exact health condition.
 本開示に係る吸収性物品は、前後方向と、前記前後方向に直交する幅方向と、前記前後方向及び前記幅方向に直交する厚さ方向と、吸収材料を含む吸収コアと、前記吸収コアよりも肌面側に配置され、かつ前記厚さ方向において前記吸収コアと重なる吸収領域を有するトップシートと、着用者の健康状態を検査するための検査部材と、を備える。前記検査部材は、前記着用者の排泄物を接触させる接触部と、前記着用者の健康状態を表示する表示部と、を有する。前記表示部は、前記接触部に接触した前記排泄物に含まれる検出対象に基づいて呈色する指示薬を含む。前記接触部の少なくとも一部は、前記吸収領域に排泄された排泄物が到達する範囲に配置されている。前記表示部の少なくとも一部は、前記吸収コアと前記厚さ方向において重ならない。 The absorbent article according to the present disclosure includes a front-rear direction, a width direction orthogonal to the front-rear direction, a thickness direction orthogonal to the front-rear direction and the width direction, an absorbent core including an absorbent material, and an absorbent core. A top sheet having an absorption region that is arranged on the skin surface side and overlaps the absorption core in the thickness direction, and an inspection member for inspecting a health condition of a wearer. The inspection member has a contact portion for contacting the excrement of the wearer and a display portion for displaying a health condition of the wearer. The display unit includes an indicator that changes color based on a detection target included in the excrement contacted with the contact unit. At least a part of the contact portion is arranged in a range where the excrement excreted in the absorption region reaches. At least a part of the display unit does not overlap with the absorbing core in the thickness direction.
 本開示に係る吸収性物品は、前後方向と、前記前後方向に直交する幅方向と、前記前後方向及び前記幅方向に直交する厚さ方向と、前記前後方向及び前記幅方向に平行である水平方向と、吸収材料を含む吸収コアと、前記吸収コアよりも非肌面側に配置されているバックシートと、着用者の健康状態を検査するための検査部材と、を備える。前記検査部材は、前記厚さ方向において前記バックシートよりも肌面側に配置されている。前記検査部材は、排泄物に含まれる検出対象に基づいて呈色する指示薬を含む表示部を有する。前記表示部は、前記バックシート側から視認可能である。前記バックシートよりも肌面側において、前記表示部から前記厚さ方向及び前記水平方向へ延びる延長領域に、疎水性を有する疎水部が配置されている。 The absorbent article according to the present disclosure has a front-rear direction, a width direction orthogonal to the front-rear direction, a thickness direction orthogonal to the front-rear direction and the width direction, and a horizontal direction parallel to the front-rear direction and the width direction. A direction, an absorbent core containing an absorbent material, a backsheet arranged on a non-skin side than the absorbent core, and an inspection member for inspecting a health condition of a wearer. The inspection member is arranged on the skin surface side of the back sheet in the thickness direction. The inspection member has a display unit including an indicator that changes color based on a detection target included in the excrement. The display unit is visible from the back sheet side. A hydrophobic portion having hydrophobicity is arranged in an extension region extending from the display portion in the thickness direction and the horizontal direction on the skin surface side of the back sheet.
第1実施形態に係る吸収性物品を肌面側から見た平面図である。It is the top view which looked at the absorbent article concerning a 1st embodiment from the skin side. 第1実施形態に係る吸収性物品の断面図である。It is a sectional view of an absorptive article concerning a 1st embodiment. 第1実施形態に係る吸収性物品を説明するための図である。It is a figure for explaining the absorptive article concerning a 1st embodiment. 第1実施形態に係る各変更例(その1からその3)を説明するための図である。It is a figure for explaining each modification example (the 1 to 3) concerning a 1st embodiment. 第1実施形態に係る各変更例(その4からその5)を説明するための図である。It is a figure for explaining each modification example (the 4 to 5) concerning a 1st embodiment. 第1実施形態に係る各変更例(その6)を説明するための図である。It is a figure for explaining each modification example (the 6) concerning a 1st embodiment. 第1実施形態に係る各変更例(その7からその10)を説明するための図である。It is a figure for explaining each modification example (the 7 to 10) concerning a 1st embodiment. 第1実施形態に係る各変更例(その11からその12)を説明するための図である。It is a figure for explaining each modification example (the 11th to the 12th) concerning a 1st embodiment. 第2実施形態に係る吸収性物品を肌面側から見た平面図である。It is the top view which looked at the absorbent article concerning a 2nd embodiment from the skin side. 第2実施形態に係る吸収性物品を非肌面側から見た平面図である。It is the top view which looked at the absorbent article concerning a 2nd embodiment from the non-skin side. 第2実施形態に係る吸収性物品の断面図である。It is sectional drawing of the absorbent article which concerns on 2nd Embodiment. 第2実施形態に係る各変更例(その1からその4)を説明するための図である。It is a figure for explaining each modification example (the 1 to 4) concerning a 2nd embodiment. 第2実施形態に係る各変更例(その5からその6)を説明するための図である。It is a figure for explaining each modification example (the 5 to 6) concerning a 2nd embodiment. 第2実施形態に係る各変更例(その7からその8)を説明するための図である。It is a figure for explaining each modification example (the 7 to 8) concerning a 2nd embodiment. 第2実施形態に係る変更例(その9)を説明するための図である。It is a figure for explaining the example of a change (the 9) concerning a 2nd embodiment.
 (1)実施形態の概要
 本明細書及び添付図面の記載により、少なくとも以下の事項が明らかとなる。
(1) Outline of Embodiment At least the following matters will be apparent from the description of the present specification and the accompanying drawings.
 一態様に係る吸収性物品は、前後方向と、前記前後方向に直交する幅方向と、前記前後方向及び前記幅方向に直交する厚さ方向と、吸収材料を含む吸収コアと、前記吸収コアよりも肌面側に配置され、かつ前記厚さ方向において前記吸収コアと重なる吸収領域を有するトップシートと、着用者の健康状態を検査するための検査部材と、を備える。前記検査部材は、前記着用者の排泄物を接触させる接触部と、前記着用者の健康状態を表示する表示部と、を有する。前記表示部は、前記接触部に接触した前記排泄物に含まれる検出対象に基づいて呈色する指示薬を含む。前記接触部の少なくとも一部は、前記吸収領域に排泄された排泄物が到達する範囲に配置されている。前記表示部の少なくとも一部は、前記吸収コアと前記厚さ方向において重ならない。 The absorbent article according to one aspect includes a front-rear direction, a width direction perpendicular to the front-rear direction, a thickness direction perpendicular to the front-rear direction and the width direction, an absorbent core including an absorbent material, and A top sheet having an absorption region that is arranged on the skin surface side and overlaps the absorption core in the thickness direction, and an inspection member for inspecting a health condition of a wearer. The inspection member has a contact portion for contacting the excrement of the wearer and a display portion for displaying a health condition of the wearer. The display unit includes an indicator that changes color based on a detection target included in the excrement contacted with the contact unit. At least a part of the contact portion is arranged in a range where the excrement excreted in the absorption region reaches. At least a part of the display unit does not overlap with the absorbing core in the thickness direction.
 本態様によれば、接触部の少なくとも一部は、排泄物が到達する範囲に配置されているため、排泄物を接触部に接触させることができる。これにより、表示部に含まれる指示薬が呈色可能となり、表示部が健康状態を表示することができる。また、表示部の少なくとも一部を吸収コアと重ならないことで、着用者は、表示部の少なくとも一部を吸収コアに遮られずに、表示部を視認し易くなる。さらに、大部分の排泄物は吸収コアに吸収されるため、表示部の少なくとも一部を吸収コアと重ならないことで、表示部の少なくとも一部が排泄物に接触し難くなる。これにより、表示部の少なくとも一部が排泄物に覆われ難くなり、着用者は、排泄物の影響を受けずに表示部を視認し易くなる。以上により、着用者が表示部を視認し易くなるため、着用者が正確な健康状態を把握し易くすることができる。 According to this aspect, since at least a part of the contact portion is arranged in a range where the excrement reaches, the excrement can be brought into contact with the contact portion. Thereby, the indicator contained in the display unit can be colored, and the display unit can display the health condition. In addition, since at least part of the display unit does not overlap with the absorbent core, the wearer can easily view the display unit without blocking at least part of the display unit with the absorbent core. Furthermore, since most excrement is absorbed by the absorbent core, at least a part of the display does not overlap with the absorbent core, so that at least a part of the display does not easily come into contact with excrement. This makes it difficult for at least a part of the display unit to be covered with the excrement, and makes it easier for the wearer to visually recognize the display unit without being affected by the excrement. As described above, since the wearer can easily visually recognize the display unit, it is easy for the wearer to grasp the correct health condition.
 好ましい一態様によれば、前記接触部の少なくとも一部は、前記吸収コアと接触する。排泄物は、吸収コアに排泄されるため、接触部の少なくとも一部が吸収コアと接触することで、より多くの排泄物を接触部に接触させることができる。これにより、指示薬が多くの検出対象に基づいて呈色可能となり、検査精度を向上できる。 According to a preferred embodiment, at least a part of the contact portion contacts the absorbent core. Since the excrement is excreted in the absorbent core, more excretion can be brought into contact with the contact portion by contacting at least a part of the contact portion with the absorbent core. Thus, the indicator can be colored based on many detection targets, and the inspection accuracy can be improved.
 好ましい一態様によれば、前記接触部の少なくとも一部は、前記厚さ方向において前記吸収コアと重なる。排泄物は、吸収コアに排泄されるため、接触部の少なくとも一部が吸収コアと重なることで、より多くの排泄物を接触部に接触させることができる。これにより、指示薬が多くの検出対象に基づいて呈色可能となり、検査精度を向上できる。 According to a preferred embodiment, at least a part of the contact portion overlaps the absorbent core in the thickness direction. Since the excrement is excreted in the absorbent core, at least a part of the contact portion overlaps with the absorbent core, so that more excrement can be brought into contact with the contact portion. Thus, the indicator can be colored based on many detection targets, and the inspection accuracy can be improved.
 好ましい一態様によれば、前記吸収性物品は、前記排泄物を前記接触部の少なくとも一部へ誘導する誘導部を有する。排泄物は、誘導部により、接触部の少なくとも一部へ誘導されるため、より多くの排泄物を接触部に接触させることができる。これにより、指示薬が多くの検出対象に基づいて呈色可能となり、検査精度を向上できる。 According to a preferred embodiment, the absorbent article has a guiding portion for guiding the excrement to at least a part of the contact portion. Since the excrement is guided to at least a part of the contact portion by the guide portion, more excrement can be brought into contact with the contact portion. Thus, the indicator can be colored based on many detection targets, and the inspection accuracy can be improved.
 好ましい一態様によれば、前記吸収性物品は、前記吸収コアを有する本体部と、前記本体部から前記幅方向の外側に延出し、着用物品に装着された状態において前記着用物品の非肌面側に固定される一対のウイングと、を有する。前記表示部の少なくとも一部は、前記厚さ方向において前記一対のウイングの一方に配置されている。ウイングは、着用物品(例えば、下着)に装着された状態において着用物品の非肌面側に固定されるため、肌面側から排泄される排泄物は、ウイングに付着し難い。これにより、表示部の少なくとも一部が排泄物に覆われ難くなり、着用者は、排泄物の影響を受けずに表示部を視認し易くなる。また、ウイングは、着用物品の非肌面側に固定されるため、着用者が吸収性物品を着用した際に、厚さ方向において表示部の少なくとも一部と着用者の肌との間には着用物品が存在する。このため、吸収性物品の着用時において、表示部の少なくとも一部が、着用者の肌に触れ難くなる。表示部に含まれる指示薬が肌にダメージを与え得るものであっても、着用者の安全性を高めることができる。 According to a preferred aspect, the absorbent article has a main body having the absorbent core and a non-skin surface of the wearing article that extends from the main body to the outside in the width direction and is attached to the wearing article. And a pair of wings fixed to the side. At least a part of the display unit is disposed on one of the pair of wings in the thickness direction. Since the wing is fixed to the non-skin side of the wearing article when attached to the wearing article (for example, underwear), the excrement excreted from the skin side hardly adheres to the wing. This makes it difficult for at least a part of the display unit to be covered with the excrement, and makes it easier for the wearer to visually recognize the display unit without being affected by the excrement. In addition, since the wing is fixed to the non-skin side of the wearing article, when the wearer wears the absorbent article, at least a part of the display section and the wearer's skin are in the thickness direction. There is a wearing article. For this reason, at the time of wearing the absorbent article, it is difficult for at least a part of the display unit to touch the wearer's skin. Even if the indicator contained in the display unit can damage the skin, the safety of the wearer can be improved.
 好ましい一態様によれば、前記厚さ方向の平面視において、前記表示部の少なくとも一部は、前記吸収コアの前記前後方向の外端縁から延出している。排泄物は、吸収性物品の前後方向の端部側よりも中央側に排泄され易いため、吸収コアの前後方向の外端縁を超えて拡散し難い。表示部の少なくとも一部は、吸収コアの前後方向の外端縁から延出しているため、排泄物に覆われ難く、着用者は、排泄物の影響を受けずに表示部を視認し易くなる。 According to a preferred aspect, in the plan view in the thickness direction, at least a portion of the display unit extends from an outer edge of the absorbent core in the front-rear direction. The excrement is more likely to be excreted toward the center than the end in the front-rear direction of the absorbent article, so that it is difficult for the excrement to spread beyond the outer edge of the absorbent core in the front-rear direction. At least a portion of the display unit extends from the outer edge of the absorbent core in the front-rear direction, so that the display unit is not easily covered with excrement, and the wearer can easily view the display unit without being affected by the excrement. .
 好ましい一態様によれば、前記吸収性物品は、前記検査部材以外の部材により構成される吸収性物品本体を有する。前記厚さ方向の平面視において、前記表示部の少なくとも一部は、前記吸収性物品本体の外端縁から延出している。吸収性物品本体の外端縁から表示部の少なくとも一部が延出しているため、表示部の少なくとも一部は、排泄物が拡散できない位置に配置されている。これにより、表示部の少なくとも一部が排泄物に覆われることを抑制できる。また、吸収性物品本体の外端縁から表示部の少なくとも一部が延出しているため、着用者は、表示部を直接視認することができる。従って、着用者が正確な健康状態を把握し易くすることができる。 According to a preferred embodiment, the absorbent article has an absorbent article main body composed of members other than the inspection member. In a plan view in the thickness direction, at least a part of the display unit extends from an outer edge of the absorbent article main body. Since at least a part of the display unit extends from the outer edge of the absorbent article main body, at least a part of the display unit is arranged at a position where excrement cannot be diffused. Thereby, it can suppress that at least one copy of a display part is covered with excrement. In addition, since at least a part of the display unit extends from the outer edge of the absorbent article main body, the wearer can directly visually recognize the display unit. Therefore, it is possible for the wearer to easily grasp the correct health condition.
 好ましい一態様によれば、前記吸収性物品は、前記検出対象が互いに異なる複数の検査部材を有する。前記複数の検査部材それぞれが有する前記表示部は、前記厚さ方向において互いに異なる位置に配置されている。検出対象が互いに異なる複数の検査部材を備えるため、1つの吸収性物品で健康状態を示す複数の項目を確認することができる。複数の検査部材それぞれが有する表示部が厚さ方向において互いに異なる位置に配置されているため、着用者が、各表示部を視認し易くなり、一部の表示部を見落とすことを抑制できる。 According to a preferred embodiment, the absorbent article has a plurality of inspection members whose detection targets are different from each other. The display units of each of the plurality of inspection members are arranged at different positions in the thickness direction. Since the detection target is provided with a plurality of inspection members different from each other, a plurality of items indicating the health condition can be confirmed with one absorbent article. Since the display units included in each of the plurality of inspection members are arranged at positions different from each other in the thickness direction, the wearer can easily recognize each of the display units, and it is possible to suppress oversight of some of the display units.
 好ましい一態様によれば、前記検査部材は、前記トップシートよりも非肌面側に配置されている。検査部材がトップシートよりも非肌面側に配置されているため、検査部材が着用者の肌に直接触れることを抑制できる。これにより、着用者の肌に検査部材が直接当たることによる着用時の違和感を抑制できる。さらに、指示薬が肌へ刺激を与え得るものであっても、着用者の肌に指示薬が触れ難くなり、着用者の安全性を高めることができる。 According to a preferred embodiment, the inspection member is arranged on a non-skin side than the top sheet. Since the inspection member is arranged on the non-skin side than the top sheet, it is possible to suppress the inspection member from directly touching the wearer's skin. Thereby, the discomfort at the time of wearing due to the inspection member directly hitting the skin of the wearer can be suppressed. Furthermore, even if the indicator can give irritation to the skin, it becomes difficult for the indicator to touch the skin of the wearer, and the safety of the wearer can be enhanced.
 好ましい一態様によれば、前記接触部は、前記吸収コアよりも非肌面側に配置されている。前記吸収コアは、前記厚さ方向において前記吸収コアを貫通する開孔を有する。前記接触部は、前記厚さ方向において前記開孔と重ならない。排泄物は、吸収コアの吸収部材を構成する繊維の隙間を通り抜けるよりも、開孔を通ることで、接触部が配置されている吸収コアの非肌面側へ到達し易くなる。このため、接触部へ到達するまでの時間を短縮でき、多くの排泄物が接触部へ到達可能となる。これにより、検査精度を向上できる。また、接触部が指示薬を含んでいる場合、接触部に到達した排泄物に指示薬が溶解することがある。しかしながら、接触部が厚さ方向において開孔と重ならないため、排泄物が開孔を通じて吸収コアの非肌面側へ到達し難くなる。このため、指示薬が肌へ刺激を与え得るものであっても、指示薬を含む排泄物がトップシートの非肌面側にまで到達し難くなり、着用者の安全性を高めることができる。 According to a preferred embodiment, the contact portion is arranged on a non-skin side with respect to the absorbent core. The absorption core has an opening penetrating the absorption core in the thickness direction. The contact portion does not overlap with the opening in the thickness direction. The excrement is more likely to reach the non-skin side of the absorbent core where the contact portion is arranged by passing through the opening than through the gap between the fibers constituting the absorbent member of the absorbent core. Therefore, the time required to reach the contact portion can be reduced, and a large amount of excrement can reach the contact portion. Thereby, the inspection accuracy can be improved. Further, when the contact portion contains the indicator, the indicator may be dissolved in the excrement reaching the contact portion. However, since the contact portion does not overlap the opening in the thickness direction, it is difficult for the excrement to reach the non-skin surface side of the absorbent core through the opening. For this reason, even if the indicator can stimulate the skin, it is difficult for the excrement containing the indicator to reach the non-skin side of the top sheet, and the safety of the wearer can be improved.
 一態様に係る吸収性物品は、前後方向と、前記前後方向に直交する幅方向と、前記前後方向及び前記幅方向に直交する厚さ方向と、前記前後方向及び前記幅方向に平行である水平方向と、吸収材料を含む吸収コアと、前記吸収コアよりも非肌面側に配置されているバックシートと、着用者の健康状態を検査するための検査部材と、を備える。前記検査部材は、前記厚さ方向において前記バックシートよりも肌面側に配置されている。前記検査部材は、排泄物に含まれる検出対象に基づいて呈色する指示薬を含む表示部を有する。前記表示部は、前記バックシート側から視認可能である。前記バックシートよりも肌面側において、前記表示部から前記厚さ方向及び前記水平方向へ延びる延長領域に、疎水性を有する疎水部が配置されている。 The absorbent article according to one aspect has a front-rear direction, a width direction perpendicular to the front-rear direction, a thickness direction perpendicular to the front-rear direction and the width direction, and a horizontal direction parallel to the front-rear direction and the width direction. A direction, an absorbent core containing an absorbent material, a backsheet arranged on a non-skin side than the absorbent core, and an inspection member for inspecting a health condition of a wearer. The inspection member is arranged on the skin surface side of the back sheet in the thickness direction. The inspection member has a display unit including an indicator that changes color based on a detection target included in the excrement. The display unit is visible from the back sheet side. A hydrophobic portion having hydrophobicity is arranged in an extension region extending from the display portion in the thickness direction and the horizontal direction on the skin surface side of the back sheet.
 ここで、特表2002-539890号公報には、着用者の健康状態を検査するための検査部材を備える吸収性物品が開示されている。検査部材は、着用者の健康状態を表示する表示部を有する。表示部は、排泄物に含まれる検出対象に基づいて呈色する指示薬(インジケータ)を含んでいる。着用差の排泄物が検査部材にまで到達した後、当該排泄物に検出対象が含まれる場合、指示薬の呈色反応により表示部の色が変化する。 Here, Japanese Patent Application Publication No. 2002-538890 discloses an absorbent article provided with an inspection member for inspecting a wearer's health condition. The inspection member has a display unit that displays the health condition of the wearer. The display unit includes a color indicator based on a detection target contained in the excrement. After the excrement of the difference in wearing reaches the inspection member, if the excrement includes the detection target, the color of the display unit changes due to the color reaction of the indicator.
 検査部材は、液不透過性のフィルムの内面に接触配置されている。フィルムには、のぞき窓を形成する透明な範囲から、表示部を視認することができる。着用者は、表示部を視認することで、健康状態を確認することができる。 The inspection member is placed in contact with the inner surface of the liquid impermeable film. In the film, the display portion can be visually recognized from a transparent area forming a viewing window. The wearer can confirm the health condition by visually recognizing the display unit.
 しかしながら、特表2002-539890号公報に開示された吸収性物品では、着用者の排泄物が検査部材に到達することにより、着用者の排泄物が検査部材の少なくとも一部を覆ったり、検査部材と重なったりすることがある。検査部材を覆う排泄物により表示部が隠された場合には、着用者は、表示部を視認できず、健康状態を確認できない。また、着用者が、表示部と重なった排泄物を介して表示部を視認できたとしても、排泄物の色によって表示部の色を誤認する可能性がある。このように、着用者が正確な健康状態を排泄物により把握できないおそれがある。 However, in the absorbent article disclosed in JP-T-2002-538890, the excrement of the wearer reaches at least one of the inspection members when the excrement of the wearer reaches the inspection member. And may overlap. When the display unit is hidden by the excrement covering the inspection member, the wearer cannot visually recognize the display unit and cannot check the health condition. Further, even if the wearer can visually recognize the display unit via the excrement that overlaps the display unit, there is a possibility that the color of the display unit is erroneously recognized based on the color of the excrement. Thus, there is a possibility that the wearer may not be able to grasp the exact health condition based on the excrement.
 そこで、着用者の健康状態を検査するための検査部材を備えつつも、着用者が正確な健康状態を把握し易い吸収性物品が望まれる。 Therefore, there is a demand for an absorbent article that is provided with an inspection member for inspecting the health condition of the wearer and that allows the wearer to easily grasp the exact health condition.
 上述の本態様に係る吸収性物品では、疎水部が、表示部から厚さ方向へ延びる延長領域に配置されている場合には、吸収性物品の肌面側に排泄された排泄物が厚さ方向において表示部の方へ拡散する拡散経路上に、疎水部が存在する。疎水部は、疎水性を有するため、水溶性の排泄物が表示部側へ拡散することを抑制し易い。また、疎水部が、表示部から水平方向へ延びる延長領域に配置されている場合には、吸収性物品の内部に拡散した排泄物が水平方向において表示部の方へ拡散する拡散経路上に、疎水部が存在する。疎水部は、水溶性の排泄物が表示部側へ拡散することを抑制し易い。また、表示部が、吸収性物品の着用中に排泄物が到達する範囲に配置されていない場合であっても、想定外の着用者の動きによって、排泄物が表示部にまで到達することがある。このような場合であっても、排泄物が延長領域に配置されている疎水部によって表示部に到達することを抑制し易い。以上より、排泄物が、表示部を覆ったり、表示部と重なったりすることを抑制し易く、表示部の視認性を確保し易くなる。これにより、着用者は、表示部をバックシート側から視認した場合に、着用者が正確な健康状態を把握し易くなる。 In the above-described absorbent article according to the present aspect, when the hydrophobic part is disposed in the extension area extending in the thickness direction from the display part, the excrement excreted on the skin side of the absorbent article has a thickness. The hydrophobic part exists on the diffusion path that diffuses toward the display part in the direction. Since the hydrophobic part has hydrophobicity, it is easy to suppress the water-soluble excrement from diffusing to the display part side. Further, when the hydrophobic portion is disposed in an extension region extending in the horizontal direction from the display portion, on the diffusion path in which the excrement diffused inside the absorbent article is diffused in the horizontal direction toward the display portion, There is a hydrophobic part. The hydrophobic part can easily prevent the water-soluble excrement from diffusing to the display part side. Further, even when the display unit is not arranged in a range where the excrement reaches while the absorbent article is worn, the excrement may reach the display unit due to unexpected movement of the wearer. is there. Even in such a case, it is easy to suppress the excrement from reaching the display unit by the hydrophobic part arranged in the extension area. As described above, it is easy to suppress the excrement from covering or overlapping the display unit, and it is easy to ensure the visibility of the display unit. Accordingly, when the wearer visually recognizes the display unit from the back seat side, the wearer can easily grasp the correct health condition.
 好ましい一態様によれば、吸収性物品は、前記吸収コアよりも肌面側に配置され、かつ前記厚さ方向において前記吸収コアと重なる吸収領域を有するトップシートを有する。前記延長領域に配置されている前記疎水部は、前記吸収領域に排泄された排泄物が到達する範囲に配置されている。これにより、疎水部にまで到達した排泄物が表示部側へ拡散することを抑制できるため、表示部の視認性を確保し易くなる。これにより、着用者は、表示部をバックシート側から視認した場合に、着用者が正確な健康状態を把握し易くなる。 According to a preferred embodiment, the absorbent article has a top sheet that is arranged on the skin surface side of the absorbent core and has an absorbent region overlapping the absorbent core in the thickness direction. The hydrophobic part disposed in the extension region is disposed in a range where the excrement discharged in the absorption region reaches. This can prevent the excrement reaching the hydrophobic part from being diffused to the display part side, so that the visibility of the display part can be easily secured. Accordingly, when the wearer visually recognizes the display unit from the back seat side, the wearer can easily grasp the correct health condition.
 好ましい一態様によれば、前記疎水部は、前記表示部と接触している。これにより、排泄物が表示部に到達することを抑制できる。これにより、表示部の視認性を確保することができ、着用者が正確な健康状態を把握し易くなる。 According to a preferred embodiment, the hydrophobic part is in contact with the display part. Thereby, it is possible to suppress the excrement from reaching the display unit. Thereby, the visibility of the display unit can be secured, and the wearer can easily grasp the correct health condition.
 本態様によれば、前記疎水部は、前記表示部の肌面側の表面と接触している。これにより、肌面側から非肌面側へ拡散する排泄物が表示部に到達することを抑制できる。これにより、表示部の視認性を確保することができ、着用者が正確な健康状態を把握し易くなる。 According to this aspect, the hydrophobic portion is in contact with the surface on the skin surface side of the display unit. Thereby, it is possible to suppress the excrement diffusing from the skin surface side to the non-skin surface side from reaching the display unit. Thereby, the visibility of the display unit can be secured, and the wearer can easily grasp the correct health condition.
 好ましい一態様によれば、前記疎水部は、前記表示部の非肌面側の表面と接触している。これにより、バックシート側から視認される表示部の表面に排泄物が到達することを抑制できる。これにより、表示部の視認性を確保することができ、着用者が正確な健康状態を把握し易くなる。 According to a preferred embodiment, the hydrophobic portion is in contact with a surface on the non-skin side of the display unit. Thereby, it is possible to suppress the excrement from reaching the surface of the display section visually recognized from the back sheet side. Thereby, the visibility of the display unit can be secured, and the wearer can easily grasp the correct health condition.
 好ましい一態様によれば、前記厚さ方向において、前記吸収コアと前記バックシートとの間に前記検査部材が配置されている。前記厚さ方向において、前記吸収コアと前記表示部との間にシート状のシート部材が、前記疎水部として配置されている。シート部材は、吸収コアと表示部との間に配置されているため、肌面側から非肌面側へ拡散する排泄物が表示部に到達することを抑制できる。これにより、表示部の視認性を確保することができ、着用者が正確な健康状態を把握し易くなる。 According to a preferred aspect, the inspection member is arranged between the absorbent core and the back sheet in the thickness direction. In the thickness direction, a sheet-like sheet member is arranged as the hydrophobic portion between the absorbing core and the display unit. Since the sheet member is disposed between the absorbent core and the display unit, it is possible to suppress the excrement diffused from the skin surface side to the non-skin surface side from reaching the display unit. Thereby, the visibility of the display unit can be secured, and the wearer can easily grasp the correct health condition.
 好ましい一態様によれば、吸収性物品1は、前記着用者の排泄口に当接する排泄口当接部を有する。前記厚さ方向の平面視において、前記疎水部は、前記表示部よりも前記排泄口当接部の中心に近い。疎水部は、表示部よりも排泄口当接部の中心に近いため、排泄口当接部に排泄された排泄物が表示部の方へ拡散する拡散経路上に、疎水部が存在する。疎水部は、排泄口当接部から表示部の方へ拡散する排泄物が表示部に到達することを抑制できる。これにより、表示部の視認性を確保することができ、着用者が正確な健康状態を把握し易くなる。 According to a preferred embodiment, the absorbent article 1 has an excretion port contact portion that contacts the excretion port of the wearer. In a plan view in the thickness direction, the hydrophobic portion is closer to the center of the excretion opening contact portion than the display portion. Since the hydrophobic part is closer to the center of the excretion port contact part than the display part, the hydrophobic part exists on the diffusion path in which the excrement excreted in the excretion port contact part diffuses toward the display part. The hydrophobic part can suppress the excrement diffused from the excretion opening contact part toward the display part from reaching the display part. Thereby, the visibility of the display unit can be secured, and the wearer can easily grasp the correct health condition.
 好ましい一態様によれば、吸収性物品1は、前記表示部よりも肌面側に配置されている肌面側部材を有する。前記肌面側部材は、前記厚さ方向において前記表示部と重ならない領域であり、かつ前記バックシート側から視認可能である背景領域を有する。前記表示部の色は、前記背景領域の色に対して色相差が色相環の角度で120度以上の色である。これにより、背景領域の色によって表示部が強調されて視認される。これにより、着用者は、表示部を視認し易くなるため、正確な健康状態を把握し易くなる。 According to a preferred embodiment, the absorbent article 1 has a skin-side member disposed closer to the skin than the display unit. The skin surface side member is a region that does not overlap with the display unit in the thickness direction, and has a background region that is visible from the back sheet side. The color of the display unit is a color having a hue difference of 120 degrees or more in a hue circle with respect to the color of the background area. Thus, the display portion is visually recognized by being emphasized by the color of the background region. This makes it easier for the wearer to visually recognize the display unit, so that the wearer can easily grasp the correct health condition.
 好ましい一態様によれば、前記表示部の色は、前記排泄物の色に対して色相差が色相環の角度で120度以上の色である。これにより、排泄物の色によって表示部が強調されて視認される。これにより、着用者は、表示部を視認し易くなるため、正確な健康状態を把握し易くなる。 According to a preferred embodiment, the color of the display unit is a color having a hue difference of 120 degrees or more in terms of a hue circle with respect to the color of the excrement. Thereby, the display portion is visually recognized with the display portion highlighted by the color of the excrement. This makes it easier for the wearer to visually recognize the display unit, so that the wearer can easily grasp the correct health condition.
 好ましい一態様によれば、吸収性物品1は、前記表示部よりも肌面側に配置されている肌面側部材を有する。前記肌面側部材は、前記厚さ方向において前記表示部と重ならない領域であり、かつ前記バックシート側から視認可能である背景領域を有する。前記背景領域の色は、前記排泄物の色に対して色相差が色相環の角度で45度以下の色である。排泄物が肌面側部材に浸透したとしても、背景領域の色は、排泄物の色に対して色相差が色相環の角度で45度以下の色であるため、排泄物が目立たなくなる。これにより、着用者は、排泄物の色に惑わされずに、表示部を視認し易くなるため、正確な健康状態を把握し易くなる。 According to a preferred embodiment, the absorbent article 1 has a skin-side member disposed closer to the skin than the display unit. The skin surface side member is a region that does not overlap with the display unit in the thickness direction, and has a background region that is visible from the back sheet side. The color of the background area is a color having a hue difference of 45 degrees or less in the hue circle with respect to the color of the excrement. Even if the excrement permeates the skin-side member, the color of the background area is a color whose hue difference is not more than 45 degrees in the hue circle angle with respect to the color of the excrement, so that the excrement is inconspicuous. This makes it easier for the wearer to visually recognize the display unit without being distracted by the color of the excrement, thereby making it easier to grasp an accurate health condition.
 (2)吸収性物品の概略構成
 以下、図面を参照して、第1実施形態に係る吸収性物品の概略ついて説明する。吸収性物品は、生理用ナプキン、パンティライナー、失禁パッド、糞便パッドのような吸収性物品であってよい。吸収性物品は、下着のような着用物品の内側に取り付けられて使用される物品であってよい。本実施の形態の吸収性物品1は、生理用ナプキンである。
(2) Schematic Configuration of Absorbent Article Hereinafter, an outline of the absorbent article according to the first embodiment will be described with reference to the drawings. The absorbent article may be an absorbent article such as a sanitary napkin, panty liner, incontinence pad, stool pad. The absorbent article may be an article used by being attached to the inside of a wearing article such as underwear. The absorbent article 1 of the present embodiment is a sanitary napkin.
 なお、以下の図面の記載において、同一又は類似の部分には、同一又は類似の符号を付している。ただし、図面は模式的なものであり、各寸法の比率等は現実のものとは異なる場合があることに留意すべきである。したがって、具体的な寸法等は、以下の説明を参酌して判断すべきである。また、図面相互間においても互いの寸法の関係や比率が異なる部分が含まれる場合がある。 In the following description of the drawings, the same or similar parts are denoted by the same or similar reference numerals. However, it should be noted that the drawings are schematic and ratios of dimensions may be different from actual ones. Therefore, specific dimensions and the like should be determined in consideration of the following description. In addition, there may be a case where parts having different dimensional relationships and ratios between drawings are included.
 図1は、第1実施形態に係る吸収性物品を肌面側から見た平面図である。図2は、第1実施形態に係る吸収性物品の断面図である。具体的には、図2Aは、図1に示すA-A線に沿った断面図である。図2Bは、着用物品(下着)に装着された状態における吸収性物品の断面図である。図3は、第1実施形態に係る吸収性物品を説明するための図である。具体的には、図3Aは、吸収性物品を着用物品から取り外す一例(その1)を示す断面図である。図3Bは、吸収性物品を着用物品から取り外す一例(その2)を示す断面図である。 FIG. 1 is a plan view of the absorbent article according to the first embodiment viewed from the skin side. FIG. 2 is a cross-sectional view of the absorbent article according to the first embodiment. Specifically, FIG. 2A is a cross-sectional view along the line AA shown in FIG. Drawing 2B is a sectional view of an absorptive article in the state where it was attached to a wearing article (underwear). FIG. 3 is a diagram for explaining the absorbent article according to the first embodiment. Specifically, FIG. 3A is a cross-sectional view illustrating an example (part 1) of removing the absorbent article from the wearing article. FIG. 3B is a cross-sectional view illustrating an example (part 2) of removing the absorbent article from the wearing article.
 なお、「肌面側」は、着用中(使用中)に着用者の肌に面する側に相当する。「非肌面側」は、着用中(使用中)に着用者の肌とは反対に向けられる側に相当する。 The “skin side” corresponds to the side facing the wearer's skin during wearing (during use). “Non-skin side” corresponds to the side that is turned away from the wearer's skin during wearing (during use).
 図1及び図2に示すように、吸収性物品1は、前後方向L及び幅方向Wを有する。前後方向Lは、着用者の前側(腹側)から後側(背側)に延びる方向、又は着用者の後側から前側に延びる方向である。幅方向Wは、前後方向Lと直交する方向である。吸収性物品は、肌面側T1と非肌面側T2に延びる厚さ方向Tを有する。なお、吸収性物品は、前後方向L及び幅方向Wに平行である水平方向を有してよい。 As shown in FIGS. 1 and 2, the absorbent article 1 has a front-rear direction L and a width direction W. The front-rear direction L is a direction extending from the front side (abdominal side) to the rear side (back side) of the wearer, or a direction extending from the rear side of the wearer to the front side. The width direction W is a direction orthogonal to the front-rear direction L. The absorbent article has a thickness direction T extending to the skin side T1 and the non-skin side T2. Note that the absorbent article may have a horizontal direction that is parallel to the front-rear direction L and the width direction W.
 なお、本明細書において、外側縁は、幅方向における外側端であり、内側縁は、幅方向における内側端である。 In the present specification, the outer edge is an outer edge in the width direction, and the inner edge is an inner edge in the width direction.
 吸収性物品1は、中央域S3、前側域S1及び後側域S2を有する。中央域S3は、着用者の排泄口(例えば膣口)に当接する排泄口当接部を有する領域である。吸収性物品が着用物品(例えば、下着)に装着されたときに、中央域S3は、着用物品の股下部に位置する。つまり、中央域は、着用者の股下、すなわち着用者の両足の間に配置される領域である。図1における実施の形態では、中央域S3は、吸収性物品1を着用物品へ留めるウイング14が設けられる領域である。前側域S1は、中央域S3よりも前側に位置する。後側域S2は、中央域S3よりも後側に位置する。 The absorbent article 1 has a central area S3, a front area S1 and a rear area S2. The central area S3 is an area having an excretion port contact portion that contacts an excretion port (for example, a vaginal opening) of the wearer. When the absorbent article is worn on the wearing article (for example, underwear), the central region S3 is located at the crotch of the wearing article. That is, the central region is a region located between the wearer's crotch, that is, between the wearer's feet. In the embodiment in FIG. 1, the central region S3 is a region where the wings 14 for fastening the absorbent article 1 to the wearing article are provided. The front side area S1 is located on the front side of the central area S3. The rear area S2 is located behind the central area S3.
 図1及び図2に示すように、吸収性物品1は、検査部材60以外の部材により構成される吸収性物品本体10と、検査部材60と、を備えてよい。吸収性物品本体10は、検査部材60を備えていない生理用ナプキンなどの一般的な吸収性物品に対応してよい。すなわち、吸収性物品本体10は、検査部材60を備えていない吸収性物品1に対応してよい。 As shown in FIGS. 1 and 2, the absorbent article 1 may include an absorbent article main body 10 formed of members other than the inspection member 60, and the inspection member 60. The absorbent article main body 10 may correspond to a general absorbent article such as a sanitary napkin that does not include the inspection member 60. That is, the absorbent article main body 10 may correspond to the absorbent article 1 having no inspection member 60.
 吸収性物品本体10は、本体部12と一対のウイング14とにより構成されてよい。本体部12は、吸収コア20を有する。本体部12は、ウイング14よりも幅方向Wにおいて内側の部分である。一対のウイング14は、本体部12から幅方向Wの外側に延出し、着用物品に装着された状態において着用物品の非肌面側T2に固定される。本体部12とウイング14との境界は、前後方向Lに延びる折り目FLである。 The absorbent article main body 10 may be constituted by the main body 12 and a pair of wings 14. The main body 12 has an absorbent core 20. The main body portion 12 is a portion inside the wing 14 in the width direction W. The pair of wings 14 extend from the main body 12 to the outside in the width direction W, and are fixed to the non-skin side T2 of the wearing article when attached to the wearing article. The boundary between the main body 12 and the wing 14 is a fold FL extending in the front-rear direction L.
 吸収性物品1は、吸収コア20、トップシート30、検査部材60を備える。また、吸収性物品1は、バックシート40、サイドシート50、粘着部70を備えてよい。 The absorbent article 1 includes the absorbent core 20, the top sheet 30, and the inspection member 60. Further, the absorbent article 1 may include a back sheet 40, a side sheet 50, and an adhesive section 70.
 吸収コア20は、液体を吸収する吸収材料を含む。吸収材料は、例えば、親水性繊維、パルプ及び高吸水性高分子(SAP)から形成できる。吸収コア20は、コアラップ(図示せず)によって包まれていてよい。コアラップは、少なくとも吸収コア20よりも肌対向面側で吸収コア20を覆っていればよい。具体的一例として、コアラップは、吸収コア20よりも肌面側に配置されるシートと、吸収コア20よりも非肌面側に配置されるシートと、を有していてよい。吸収コア20は、コアラップによって覆われていなくてもよい。 The absorbent core 20 includes an absorbent material that absorbs liquid. Absorbent materials can be formed, for example, from hydrophilic fibers, pulp and superabsorbent polymers (SAP). The absorbent core 20 may be wrapped by a core wrap (not shown). The core wrap only needs to cover the absorbent core 20 at least on the skin-facing surface side of the absorbent core 20. As a specific example, the core wrap may include a sheet disposed on the skin side of the absorbent core 20 and a sheet disposed on the non-skin side of the absorbent core 20. The absorbent core 20 may not be covered by the core wrap.
 吸収コア20は、少なくとも中央域S3に配置されている。吸収体コアは、中央域S3から前側域S1まで延びていてもよい。吸収体コアは、中央域S3から後側域S2まで延びていてもよい。 The absorbent core 20 is arranged at least in the central area S3. The absorber core may extend from the central area S3 to the front area S1. The absorber core may extend from the central area S3 to the rear area S2.
 トップシート30は、吸収コア20よりも肌面側に配置される。トップシート30は、厚さ方向Tにおいて吸収コアと重なる吸収領域ARを有する。 The top sheet 30 is arranged on the skin side with respect to the absorbent core 20. The top sheet 30 has an absorption region AR overlapping the absorption core in the thickness direction T.
 トップシート30は、液透過性を有する。トップシート30は、不織布、織布、有孔プラスチックシート、メッシュシート等、液体を透過する構造を有する任意のシート状の材料から構成されてよい。織布や不織布の素材としては、天然繊維、化学繊維のいずれも使用できる。 The top sheet 30 has liquid permeability. The topsheet 30 may be made of any sheet-like material having a structure that allows liquid to pass through, such as a nonwoven fabric, a woven fabric, a perforated plastic sheet, or a mesh sheet. As the material of the woven or nonwoven fabric, any of natural fibers and chemical fibers can be used.
 バックシート40は、液不透過性を有する。バックシート40は、ポリエチレンシート、ポリプロピレン等を主体としたラミネート不織布、通気性の樹脂フィルム、スパンボンド、又はスパンレース等の不織布に通気性の樹脂フィルムが接合されたシートなどの材料から構成されてよい。 The back sheet 40 has liquid impermeability. The back sheet 40 is made of a material such as a sheet in which a breathable resin film is joined to a nonwoven fabric such as a laminated nonwoven fabric mainly composed of polyethylene sheet or polypropylene, a breathable resin film, spunbond, or spunlace. Good.
 サイドシート50は、トップシート30の外側縁を覆ってよい。サイドシート50は、幅方向Wにおけるトップシート30の外側縁を覆い、トップシート30よりも幅方向Wの外側へ延びてよい。なお、吸収性物品1はサイドシート50を有さなくてもよい。 The side sheet 50 may cover the outer edge of the top sheet 30. The side sheet 50 may cover the outer edge of the top sheet 30 in the width direction W, and may extend outside the top sheet 30 in the width direction W. Note that the absorbent article 1 may not have the side sheet 50.
 サイドシート50は、トップシート30と同様の材料から構成することができる。ただし、トップシート30に付着した体液が、サイドシート50を乗り越えて、幅方向Wにおいて吸収性物品1の外側へ漏れ出すことを防止するためには、サイドシート50は、疎水性又は撥水性を有してよい。サイドシート50は、幅方向Wにおける吸収コア20の外側縁、後述するウイング14及び後述するフラップ部80に配置されてよい。 The side sheet 50 can be made of the same material as the top sheet 30. However, in order to prevent the bodily fluid attached to the top sheet 30 from crossing the side sheet 50 and leaking out of the absorbent article 1 in the width direction W, the side sheet 50 has hydrophobicity or water repellency. May have. The side sheet 50 may be disposed on the outer edge of the absorbent core 20 in the width direction W, the wing 14 described later, and the flap portion 80 described later.
 検査部材60は、着用者の健康状態を検査するための部材である。検査部材60は、着用者の健康状態(を示す色)を指示薬により表示する。本実施の形態では、健康状態を検査するために、例えば、イムノクロマト法、又は試験紙法を用いることができる。 The inspection member 60 is a member for inspecting a wearer's health condition. The inspection member 60 displays the health condition (color indicating) of the wearer with an indicator. In the present embodiment, for examining a health condition, for example, an immunochromatography method or a test paper method can be used.
 イムノクロマト法は、抗体を含む標識粒子が敷き詰められた部材(例えば、セルロース膜)上に、排泄物(例えば、血液など)を滴下することで行われる。排泄物中に、検出対象(具体的には、検出対象となる対象成分(例えば、抗原))が含まれている場合、当該検出対象と抗体とが抗原抗体反応を起こして複合体を形成する。形成された複合体は、毛細管現象によって膜上を移動する。複合体の移動先には、別種の抗体(指示薬)が線状に配置されている。複合体が、別種の抗体と結合して呈色する。呈色(色の変化)の有無により着用者の健康状態が示される。着用者は、呈色の有無を目視により判定することで健康状態を確認することができる。 The immunochromatography method is performed by dropping excrement (eg, blood) on a member (eg, a cellulose membrane) on which labeled particles containing antibodies are spread. When the excrement contains a detection target (specifically, a target component (eg, an antigen) to be detected), the detection target and the antibody cause an antigen-antibody reaction to form a complex. . The formed complex moves on the membrane by capillary action. A different type of antibody (indicator) is linearly arranged at the destination of the complex. The complex is colored by binding to another type of antibody. The presence or absence of coloration (color change) indicates the health condition of the wearer. The wearer can confirm the health condition by visually determining the presence or absence of coloration.
 試験紙法は、検査部材60に含まれる指示薬が、排泄物に含まれる検出対象と反応することにより呈色する。呈色(指示薬の色の変化)の有無により着用者の健康状態が示される。着用者は、指示薬による呈色(指示薬の色の変化)を目視により判定することで健康状態を確認することができる。 In the test paper method, the indicator is included in the inspection member 60 and color is generated when the indicator reacts with the detection target included in the excrement. The presence or absence of coloration (change in the color of the indicator) indicates the health condition of the wearer. The wearer can visually confirm the coloration (change in the color of the indicator) by the indicator to confirm the health condition.
 排泄物は、例えば、血液、尿、大便、汗、おりものなどが挙げられる。健康状態を示す項目は、例えば、体調関連(pH、鉄欠乏性貧血、腎機能、心筋梗塞、炎症・感染症、栄養状態評価など)、妊娠関連(生理周期予測、排卵予測など)、精神関連(鬱傾向、薬物など)が挙げられる。検出対象は、例えば、尿中老廃物(尿比重)、白血球、水素イオン(pH)、蛋白質、ブドウ糖、ケトン体、ウロビリノーゲン、ビリルビン、尿潜血、亜硝酸塩、ステロイド、ペプチド、芳香族化合物、FSH(卵胞刺激ホルモン)、BUN(Urea nitorogen)、AlB(Albumin)、LPS(リポ多糖)、hCG(ヒト絨毛性ゴナドトロピン)、LH(黄体刺激ホルモン)、U-ALB、CRP(C-リアクディブ・プロテイン)、ミオグロビン、CK-MB、トロポニンI、トロポニンT、ヘモグロビン、ストレップA、HBs抗体、HIV抗体、TP抗体、ロタウイルス、インフルエンザウイルス、アデノウイルス、DNA、O-157、コカイン、マリファナ、モルヒネなどが一例として挙げられる。 Excretions include, for example, blood, urine, stool, sweat, vaginal discharge, and the like. Items indicating health status include, for example, physical condition-related (pH, iron deficiency anemia, renal function, myocardial infarction, inflammation / infection, nutritional status evaluation, etc.), pregnancy-related (physiological cycle prediction, ovulation prediction, etc.), mental-related (Depression, drugs, etc.). The detection target is, for example, urine waste (urine specific gravity), leukocyte, hydrogen ion (pH), protein, glucose, ketone body, urobilinogen, bilirubin, urinary occult blood, nitrite, steroid, peptide, aromatic compound, FSH ( Follicle stimulating hormone), BUN (Urea @ nitorogen), AlB (Albumin), LPS (lipopolysaccharide), hCG (human chorionic gonadotropin), LH (luteinizing hormone), U-ALB, CRP (C-reactiv protein), Examples include myoglobin, CK-MB, troponin I, troponin T, hemoglobin, strep A, HBs antibody, HIV antibody, TP antibody, rotavirus, influenza virus, adenovirus, DNA, O-157, cocaine, marijuana, morphine and the like. No.
 検査部材60は、接触部62と表示部64とを有する。接触部62は、排泄物を接触させる部分である。表示部64は、着用者の健康状態(を示す色)を表示する部分である。表示部64は、接触部62に接触した排泄物に含まれる検出対象に基づいて呈色する指示薬を含む。指示薬は、検出対象又は検出対象を由来とするもの(例えば、複合体)と反応することにより呈色する化学物質(無機物、有機物)である。 The inspection member 60 has a contact part 62 and a display part 64. The contact part 62 is a part for making excretion contact. The display unit 64 is a part that displays the health state (color indicating) of the wearer. The display unit 64 includes an indicator that changes color based on the detection target contained in the excrement that has come into contact with the contact unit 62. The indicator is a chemical substance (inorganic substance, organic substance) that is colored by reacting with a detection target or a substance derived from the detection target (for example, a complex).
 例えば、イムノクロマト法では、接触部62は、抗体を含む標識粒子が配置されている領域へ排泄物(検査対象)を誘導する部分である。接触部62は、標識粒子が配置されている領域を含んでよい。排泄物が接触部62に触れることで、排泄物に含まれる検出対象(抗原)と抗体とが抗原抗体反応を起こして複合体を形成する。表示部64は、複合体と結合して呈色する指示薬(別種の抗体)が配置されている領域(検出ライン)を含む。従って、イムノクロマト法が用いられる場合、接触部62と表示部64とは異なる位置に配置されている。従って、この場合、接触部62と表示部64とは異なるものである。 For example, in the immunochromatography, the contact portion 62 is a portion for guiding excrement (test target) to a region where the labeled particles including the antibody are arranged. The contact portion 62 may include a region where the label particles are arranged. When the excrement touches the contact portion 62, the detection target (antigen) and the antibody contained in the excretion cause an antigen-antibody reaction to form a complex. The display unit 64 includes a region (detection line) in which an indicator (another type of antibody) that is colored by binding to the complex is arranged. Therefore, when the immunochromatography method is used, the contact section 62 and the display section 64 are arranged at different positions. Therefore, in this case, the contact section 62 and the display section 64 are different.
 なお、検査部材60は、検査が適切である場合に、検出対象となる目的の抗原の有無にかかわらず呈色する領域であるコントロールラインを含んでよい。コントロールラインは、検出ライン(表示部64)よりも接触部62から離れて配置されている。 Note that the test member 60 may include a control line that is a color region regardless of the presence or absence of the target antigen to be detected when the test is appropriate. The control line is located farther from the contact section 62 than the detection line (display section 64).
 一方、試験紙法では、接触部62は、指示薬が配置されている領域を少なくとも含む。接触部62に含まれる指示薬が検出対象と反応して呈色するため、接触部62と表示部64とが同じ位置に配置されている。従って、この場合、接触部62と表示部64とは、同一のものである。 On the other hand, in the test paper method, the contact portion 62 includes at least a region where the indicator is arranged. Since the indicator contained in the contact part 62 reacts with the detection target to give a color, the contact part 62 and the display part 64 are arranged at the same position. Therefore, in this case, the contact portion 62 and the display portion 64 are the same.
 以上のように、イムノクロマト法が用いられる場合、接触部62は、標識粒子を含み、表示部64は、着用者の健康状態を表示するための指示薬を含む。試験紙法が用いられる場合、接触部62、すなわち、表示部64は、着用者の健康状態を表示するための指示薬を含む。 As described above, when the immunochromatography method is used, the contact portion 62 includes a label particle, and the display portion 64 includes an indicator for displaying a wearer's health condition. When the test strip method is used, the contact part 62, that is, the display part 64, includes an indicator for displaying the health condition of the wearer.
 なお、接触部62は、排泄物(検出対象)を表示部64へ誘導させるためにのみ設けられている場合、指示薬を含まなくてよい。 In the case where the contact portion 62 is provided only for guiding the excrement (a detection target) to the display portion 64, the contact portion 62 may not include the indicator.
 検査部材60は、指示薬を保持又は含有できる部材であればよい。検査部材60は、例えば、紙、不織布、織布などのいずれかの材料により構成できる。検査部材60の剛性は、吸収性物品1に使用される部材の剛性以下であってよい。これにより、吸収性物品1が検査部材60を備えていても、着用者の肌触りの悪化を抑制し易くなる。図1等に示すように、検査部材60は、例えば、直線状の板状であってよい。 The inspection member 60 may be any member that can hold or contain the indicator. The inspection member 60 can be made of any material such as paper, nonwoven fabric, and woven fabric. The rigidity of the inspection member 60 may be equal to or less than the rigidity of the member used for the absorbent article 1. Thereby, even if the absorbent article 1 is provided with the inspection member 60, it becomes easy to suppress deterioration of the touch of the wearer. As shown in FIG. 1 and the like, the inspection member 60 may be, for example, a linear plate shape.
 図2Aに示すように、接触部62の少なくとも一部は、吸収領域ARに排泄された排泄物が到達する範囲である到達範囲に配置されている。これにより、着用者から排泄された排泄物を接触部62に接触させることができる。従って、表示部64に含まれる指示薬が呈色可能となり、表示部64が健康状態を表示することができる。 AAs shown in FIG. 2A, at least a part of the contact portion 62 is arranged in a reach range where the excrement excreted in the absorption area AR reaches. Thereby, the excrement excreted from the wearer can be brought into contact with the contact portion 62. Therefore, the indicator contained in the display unit 64 can be colored, and the display unit 64 can display the health condition.
 接触部62の少なくとも一部は、吸収コアと接触してよい。排泄物は、吸収コア20に排泄されるため、より多くの排泄物を接触部62に接触させることができる。これにより、指示薬が多くの検出対象に基づいて呈色可能となり、検査精度を向上できる。図2Aでは、接触部62の一部が吸収コア20に接触している。 少 な く と も At least a part of the contact portion 62 may be in contact with the absorbent core. Since the excrement is excreted in the absorbent core 20, more excretion can be brought into contact with the contact portion 62. Thus, the indicator can be colored based on many detection targets, and the inspection accuracy can be improved. In FIG. 2A, a part of the contact portion 62 is in contact with the absorbent core 20.
 また、接触部62の少なくとも一部は、厚さ方向Tにおいて吸収コア20と重なってよい。排泄物は、吸収コア20に排泄されるため、より多くの排泄物を接触部に接触させることができる。これにより、指示薬が多くの検出対象に基づいて呈色可能となり、検査精度を向上できる。図2Aでは、接触部62の一部が厚さ方向Tにおいて吸収コア20と重なっている。接触部62の残りは、厚さ方向において吸収コア20と重なっていない。 少 な く と も At least a part of the contact portion 62 may overlap the absorbent core 20 in the thickness direction T. Since the excrement is excreted in the absorbent core 20, more excretion can be brought into contact with the contact portion. Thus, the indicator can be colored based on many detection targets, and the inspection accuracy can be improved. In FIG. 2A, a part of the contact portion 62 overlaps the absorbent core 20 in the thickness direction T. The rest of the contact portion 62 does not overlap with the absorbent core 20 in the thickness direction.
 到達範囲は、排泄物が液体である場合、排泄物の拡散範囲であってよい。到達範囲は、排泄物が固体/半固体である場合、着用中に排泄物が広がる範囲であってよい。前後方向L及び幅方向Wに沿った方向である水平方向(すなわち、厚さ方向Tの平面視)において、到達範囲の最大範囲は、一般的な使用の場合には、吸収領域ARに排泄された排泄物が拡散可能であるトップシート30に直接的又は間接的に接触する各液透過性シートの少なくともいずれかと重なる領域である。なお、トップシート30に「間接的に」接触する液透過性シートは、他の液透過性シートを介してトップシート30と接触していることを意味する。トップシート30に排泄された排泄物が他の液透過性シート介して、当該液透過性シートにまで拡散可能である。一方で、厚さ方向T(すなわち、吸収性物品1の断面)において、到達範囲の最大範囲は、トップシート30の肌面側T1の表面からバックシート40の肌面側T1の表面までの範囲である。 The reaching range may be a diffusion range of the excrement when the excrement is a liquid. The reach may be a range where the excrement spreads during wear when the excrement is solid / semi-solid. In a horizontal direction that is a direction along the front-rear direction L and the width direction W (that is, a plan view in the thickness direction T), in a general use, the maximum range of the reaching range is excreted in the absorption region AR. This is an area that overlaps with at least one of the liquid-permeable sheets that directly or indirectly comes into contact with the top sheet 30 through which excrement that can be diffused. Note that a liquid-permeable sheet that comes into “indirect” contact with the top sheet 30 means that it is in contact with the top sheet 30 via another liquid-permeable sheet. The excrement excreted in the top sheet 30 can be diffused to the liquid permeable sheet via another liquid permeable sheet. On the other hand, in the thickness direction T (that is, in the cross section of the absorbent article 1), the maximum range of the reaching range is a range from the surface of the top sheet 30 on the skin side T1 to the surface of the back sheet 40 on the skin side T1. It is.
 接触部62の少なくとも一部は、到達範囲の最大範囲内に配置されていればよい。接触部62の少なくとも一部は、排泄物を接触部62へ容易に到達するように、厚さ方向Tにおいて、トップシート30と重なる位置に配置されたり、吸収コア20に重なる位置に配置されたり、中央域S3に配置されたり、着用者の排泄口に当接する排泄口当接部の範囲に配置されてよい。これにより、着用者から排泄された排泄物を接触部62に接触させることができる。従って、表示部64に含まれる指示薬が呈色可能となり、表示部64が健康状態を表示することができる。 少 な く と も At least a part of the contact portion 62 only needs to be arranged within the maximum range of the reaching range. At least a part of the contact portion 62 is disposed at a position overlapping the top sheet 30 in the thickness direction T or at a position overlapping the absorbent core 20 so that the excrement easily reaches the contact portion 62. , May be arranged in the central area S3, or may be arranged in the range of the excretion opening contact portion that contacts the excretion opening of the wearer. Thereby, the excrement excreted from the wearer can be brought into contact with the contact portion 62. Therefore, the indicator contained in the display unit 64 can be colored, and the display unit 64 can display the health condition.
 表示部64の少なくとも一部は、吸収コア20と厚さ方向Tにおいて重ならない。これにより、着用者は、表示部64の少なくとも一部を吸収コア20に遮られずに、表示部64を視認し易くなる。さらに、大部分の排泄物は吸収コア20に吸収されるため、表示部64の少なくとも一部が吸収コア20と重ならないことで、表示部64の少なくとも一部が排泄物に接触し難くなる。これにより、表示部64の少なくとも一部が排泄物に覆われ難くなり、着用者は、排泄物の影響を受けずに表示部64を視認し易くなる。以上により、着用者が表示部64を視認し易くなるため、着用者が正確な健康状態を把握し易くすることができる。図2Aでは、表示部64の全てが吸収コア20と厚さ方向Tにおいて重なっていない。 少 な く と も At least a part of the display unit 64 does not overlap with the absorbing core 20 in the thickness direction T. This makes it easier for the wearer to visually recognize the display unit 64 without blocking at least a part of the display unit 64 with the absorbent core 20. Furthermore, since most of the excrement is absorbed by the absorbent core 20, at least a part of the display unit 64 does not overlap with the absorbent core 20, so that at least a part of the display unit 64 does not easily come into contact with the excrement. This makes it difficult for at least a part of the display unit 64 to be covered with excrement, and makes it easier for the wearer to visually recognize the display unit 64 without being affected by the excrement. As described above, since the wearer can easily visually recognize the display unit 64, the wearer can easily grasp the correct health condition. In FIG. 2A, not all of the display portions 64 overlap the absorbing core 20 in the thickness direction T.
 なお、試験紙法が用いられた検査部材60を吸収性物品1が備える場合には、検査部材60のうち指示薬を含む領域の一部が到達範囲に配置されている。指示薬を含む残りの領域である表示部64が吸収コア20と厚さ方向Tにおいて重ならない。到達範囲に配置されている領域から排泄物が浸透して、表示部64が呈色可能である。なお、到達範囲に配置されている領域は、接触部62であると同時に表示部64でもあるため、呈色可能である。従って、この場合には、表示部64の一部が厚さ方向において吸収コア20と重なっている。 In the case where the absorbent member 1 includes the inspection member 60 using the test paper method, a part of the region of the inspection member 60 containing the indicator is disposed in the reach. The display portion 64, which is the remaining region including the indicator, does not overlap with the absorbent core 20 in the thickness direction T. The excrement penetrates from the area arranged in the reaching range, and the display unit 64 can display color. In addition, since the area | region arrange | positioned in the reaching range is the display part 64 at the same time as the contact part 62, it can color. Therefore, in this case, a part of the display unit 64 overlaps the absorbing core 20 in the thickness direction.
 一方、イムノクロマト法が用いられた検査部材60を吸収性物品1が備える場合には、抗体を含む標識粒子が配置されている領域へ排泄物(検査対象)を誘導する部分(接触部62の少なくとも一部)が到達範囲に配置されている。検出対象由来の複合体と結合して呈色する別種の抗体(指示薬)が配置されている領域である検出ライン(表示部64)が吸収コア20と厚さ方向Tにおいて重ならない。 On the other hand, when the absorbent member 1 includes the test member 60 using the immunochromatography method, a portion (at least the contact portion 62) that guides the excrement (test target) to the region where the labeled particles including the antibody are arranged. Are located in reach. The detection line (display portion 64), which is the region where another type of antibody (indicator) that is colored by binding to the complex derived from the detection target, does not overlap with the absorption core 20 in the thickness direction T.
 図2Aに示すように、検査部材60は、サイドシート50に形成された露出開口52に挿入されていてもよい。これにより、表示部64の少なくとも一部が露出していてもよい。具体的には、表示部64は、サイドシート50よりも非肌面側T2に位置する非露出部642とサイドシート50よりも肌面側T1に位置する露出部644とを有してよい。非露出部642は、サイドシート50を介して間接的に視認できてよい。露出部644は、直接的に視認できる。 検 査 As shown in FIG. 2A, the inspection member 60 may be inserted into the exposure opening 52 formed in the side sheet 50. Thereby, at least a part of the display unit 64 may be exposed. Specifically, the display unit 64 may include a non-exposed portion 642 located on the non-skin side T2 than the side sheet 50 and an exposed portion 644 located on the skin side T1 than the side sheet 50. The non-exposed portion 642 may be indirectly visible through the side sheet 50. The exposed part 644 is directly visible.
 イムノクロマト法が用いられた検査部材60において、露出部644は、表示部64の少なくとも一部である検出ラインを有してよい。これにより、着用者は、表示部64を直接視認できるため、健康状態を手軽に確認することができる。また、露出部644は、検出ラインを含まずに、コントロールラインを有してよい。これにより、着用者は、露出部644を視認することで、検査が適切に行われたことを手軽に確認することができる。 In the inspection member 60 using the immunochromatography method, the exposed part 644 may have a detection line that is at least a part of the display part 64. This allows the wearer to directly check the display section 64, and thus can easily check the health condition. Further, the exposure section 644 may have a control line without including the detection line. Thereby, the wearer can easily confirm that the inspection has been properly performed by visually recognizing the exposed portion 644.
 なお、ウイング14にトップシート30が配置されていた場合、「サイドシート50」が「トップシート30」に置き換えられてもよい。 In the case where the top sheet 30 is arranged on the wing 14, the "side sheet 50" may be replaced with the "top sheet 30".
 表示部64の少なくとも一部は、厚さ方向Tにおいて一対のウイング14の一方に配置されてよい。図2Bに示すように、ウイング14は、着用物品100(例えば、下着)に装着された状態において着用物品100の非肌面側T2に固定されるため、肌面側T1から排泄される排泄物は、ウイング14に付着し難い。これにより、表示部64の少なくとも一部が排泄物に覆われ難くなり、着用者は、排泄物の影響を受けずに表示部64を視認し易くなる。 少 な く と も At least a part of the display unit 64 may be arranged on one of the pair of wings 14 in the thickness direction T. As shown in FIG. 2B, the wings 14 are fixed to the non-skin side T2 of the wearing article 100 in a state where the wings 14 are attached to the wearing article 100 (for example, underwear), so that excrement excreted from the skin side T1. Hardly adhere to the wing 14. This makes it difficult for at least a part of the display unit 64 to be covered with excrement, and makes it easier for the wearer to visually recognize the display unit 64 without being affected by the excrement.
 また、ウイング14は、着用物品100の非肌面側T2に固定されるため、着用者が吸収性物品1を着用した際に、厚さ方向Tにおいて表示部64の少なくとも一部と着用者の肌との間には着用物品100が存在する。このため、吸収性物品1の着用時において、表示部64の少なくとも一部が、着用者の肌に触れ難くなる。表示部64に含まれる指示薬が肌にダメージを与え得るものであっても、着用者の安全性を高めることができる。 In addition, since the wing 14 is fixed to the non-skin side T2 of the wearing article 100, when the wearer wears the absorbent article 1, at least a part of the display unit 64 and the wearer's in the thickness direction T. Wearing article 100 exists between the skin. For this reason, at the time of wearing the absorbent article 1, at least a part of the display unit 64 becomes difficult to touch the skin of the wearer. Even if the indicator contained in the display unit 64 can damage the skin, the safety of the wearer can be improved.
 検査部材60は、吸収コア20、トップシート30、バックシート40、サイドシート50の少なくともいずれかに固定(接合)されてよい。検査部材60は、例えば、吸収性物品1の資材どうしを接合するための接着剤(例えば、ホットメルト型接着剤(HMA))により固定されてよい。検査部材60は、接触部62及び表示部64の少なくとも一方が固定されてよい。検査部材60は、接触部62の少なくとも一部が固定されてよく、表示部64の少なくとも一部が固定されてよい。検査部材60は、接触部62と表示部64と以外の部分が固定されてよい。例えば、検査部材60は、接触部62及び表示部64以外の部分の少なくとも一部により構成される固定部を有してよい。固定部上に塗布された接着剤により、固定されてよい。検査部材60を固定することにより、接触部62が到達範囲の外側へ移動することを抑制できる。 The inspection member 60 may be fixed (joined) to at least one of the absorbent core 20, the top sheet 30, the back sheet 40, and the side sheet 50. The inspection member 60 may be fixed by, for example, an adhesive (for example, a hot melt adhesive (HMA)) for joining the materials of the absorbent article 1 together. In the inspection member 60, at least one of the contact portion 62 and the display portion 64 may be fixed. In the inspection member 60, at least a part of the contact part 62 may be fixed, and at least a part of the display part 64 may be fixed. The inspection member 60 may have a portion other than the contact portion 62 and the display portion 64 fixed. For example, the inspection member 60 may have a fixed part configured by at least a part of the part other than the contact part 62 and the display part 64. It may be fixed by an adhesive applied on the fixing part. By fixing the inspection member 60, it is possible to prevent the contact portion 62 from moving outside the reach.
 粘着部70は、吸収性物品1を着用物品100に止めるための粘着剤が設けられた領域である。粘着部70は、バックシート40の非肌面側T2上に配置され、かつ着用物品(例えば、下着)100に吸収性物品1を固定するためのものである。 The adhesive portion 70 is a region provided with an adhesive for fixing the absorbent article 1 to the wearing article 100. The adhesive section 70 is disposed on the non-skin side T2 of the back sheet 40 and is for fixing the absorbent article 1 to a worn article (for example, underwear) 100.
 粘着部70は、中央粘着部72とサイド粘着部74とを有してよい。図2Aに示すように、中央粘着部72は、本体部12におけるバックシート40の非肌面側T2上に配置される。中央粘着部72は、本体部12を着用物品100に止める粘着剤を有する。サイド粘着部74は、ウイング14におけるバックシート40の非肌面側T2上に配置される。サイド粘着部74は、ウイング14を着用物品100に止める粘着剤を有する。 The adhesive portion 70 may have a central adhesive portion 72 and a side adhesive portion 74. As shown in FIG. 2A, the central adhesive portion 72 is disposed on the non-skin side T2 of the back sheet 40 in the main body 12. The central adhesive portion 72 has an adhesive for fixing the main body 12 to the wearing article 100. The side adhesive portion 74 is arranged on the non-skin side T2 of the back sheet 40 on the wing 14. The side adhesive portion 74 has an adhesive for fixing the wing 14 to the wearing article 100.
 着用者は、図3A及び図3Bに示すように、ウイング14を着用物品100から外すことにより、着用物品100を脚にかけた状態で、表示部64を視認可能であってよい。これにより、着用者は、手軽に健康状態を確認することができる。 As shown in FIGS. 3A and 3B, the wearer may be able to visually recognize the display unit 64 with the wearing article 100 put on his / her leg by removing the wing 14 from the wearing article 100. Thereby, the wearer can easily check the health condition.
 サイド粘着部74の接着強度は、検査部材60を固定する接着剤の接合強度よりも小さくてよい。これにより、着用者が、表示部64の露出部644を把持して、図3Aに示すように、当該露出部644を引っ張ることにより、バックシート40を着用物品100から外せてもよい。着用者は、ウイング14を着用物品100から手軽に外すことができる。 (4) The adhesive strength of the side adhesive portion 74 may be smaller than the adhesive strength of the adhesive for fixing the inspection member 60. Thereby, the wearer may remove the back sheet 40 from the wearing article 100 by holding the exposed portion 644 of the display unit 64 and pulling the exposed portion 644 as shown in FIG. 3A. The wearer can easily remove the wing 14 from the wearing article 100.
 サイド粘着部74の接着強度は、サイドシート50を固定する接着剤の接合強度よりも大きくてよい。これにより、着用者が、表示部64の露出部644を把持して、図3Bに示すように、当該露出部644を引っ張ることにより、トップシート30及び検査部材60をバックシート40から外せてもよい。これにより、着用者は、露出部644だけでなく、非露出部642も直接視認可能となるため、健康状態を手軽に確認することができる。 (4) The adhesive strength of the side adhesive portion 74 may be larger than the adhesive strength of the adhesive for fixing the side sheet 50. Accordingly, even if the wearer grasps the exposed portion 644 of the display unit 64 and pulls the exposed portion 644 as shown in FIG. 3B, the top sheet 30 and the inspection member 60 can be removed from the back sheet 40. Good. This allows the wearer to directly check not only the exposed portion 644 but also the non-exposed portion 642, so that the wearer can easily check the health condition.
 (3)変更例
 次に、第1実施形態に係る吸収性物品1の各変更例について、図4から図8を用いて説明する。図4は、第1実施形態に係る各変更例を説明するための図である。具体的には、図4Aは、第1実施形態に係る変更例(その1)を説明するための断面図である。図4Bは、第1実施形態に係る変更例(その2)を説明するための図である。図4Cは、第1実施形態に係る変更例(その3)を説明するための図である。図5は、第1実施形態に係る各変更例を説明するための断面図である。具体的には、図5Aは、第1実施形態に係る変更例(その4)を説明するための断面図である。図5Bは、第1実施形態に係る変更例(その5)を説明するための断面図である。図6は、第1実施形態に係る変更例を説明するための図である。具体的には、図6Aは、第1実施形態に係る変更例(その6)を説明するための断面図である。図6Bは、図6Aに示すB-B線に沿った拡大断面図である。図7は、第1実施形態に係る各変更例を説明するための図である。具体的には、図7Aは、第1実施形態に係る変更例(その7)における吸収性物品1を肌面側から見た平面図である。図7Bは、第1実施形態に係る変更例(その8)における吸収性物品1を肌面側から見た平面図である。図7Cは、第1実施形態に係る変更例(その9)における吸収性物品1を肌面側から見た平面図である。図7Dは、第1実施形態に係る変更例(その10)における吸収性物品1を肌面側から見た平面図である。図8は、第1実施形態に係る各変更例を説明するための図である。具体的には、図8Aは、実施形態に係る変更例(その11)における吸収性物品1を肌面側から見た平面図である。図8Bは、第1実施形態に係る変更例(その12)における吸収性物品1を肌面側から見た平面図である。なお、上述の第1実施形態と同様の部分は説明を省略する。
(3) Modified Examples Next, modified examples of the absorbent article 1 according to the first embodiment will be described with reference to FIGS. FIG. 4 is a diagram for describing each modification example according to the first embodiment. Specifically, FIG. 4A is a cross-sectional view for explaining a modification (part 1) according to the first embodiment. FIG. 4B is a diagram for describing a modified example (part 2) according to the first embodiment. FIG. 4C is a diagram for describing a modified example (part 3) according to the first embodiment. FIG. 5 is a cross-sectional view for explaining each modification example according to the first embodiment. Specifically, FIG. 5A is a cross-sectional view for explaining a modification (part 4) according to the first embodiment. FIG. 5B is a cross-sectional view for explaining a modification (part 5) according to the first embodiment. FIG. 6 is a diagram for explaining a modification example according to the first embodiment. Specifically, FIG. 6A is a cross-sectional view illustrating a modified example (No. 6) according to the first embodiment. FIG. 6B is an enlarged sectional view taken along line BB shown in FIG. 6A. FIG. 7 is a diagram for describing each modification example according to the first embodiment. Specifically, FIG. 7A is a plan view of the absorbent article 1 in a modification (part 7) according to the first embodiment as viewed from the skin surface side. FIG. 7B is a plan view of the absorbent article 1 according to a modification (No. 8) according to the first embodiment as viewed from the skin side. FIG. 7C is a plan view of the absorbent article 1 in the modification (No. 9) according to the first embodiment as viewed from the skin side. FIG. 7D is a plan view of the absorbent article 1 in a modification (10) according to the first embodiment as viewed from the skin surface side. FIG. 8 is a diagram for describing each modification example according to the first embodiment. Specifically, FIG. 8A is a plan view of the absorbent article 1 in a modification (No. 11) according to the embodiment as viewed from the skin surface side. FIG. 8B is a plan view of the absorbent article 1 as viewed from the skin surface side in a modification (twelfth) according to the first embodiment. The description of the same parts as those in the first embodiment will be omitted.
 図4Aに示すように、接触部62は、吸収コア20よりも肌面側T1に配置されてもよい。従って、接触部62は、吸収コア20の肌面側T1の表面と接触してもよい。接触部62は、吸収コア20とトップシート30との間に配置されてよい。これにより、吸収コア20に遮られずに、排泄物が容易に接触部62へ接触し易くなる。 AAs shown in FIG. 4A, the contact portion 62 may be arranged on the skin surface side T1 with respect to the absorbent core 20. Therefore, the contact portion 62 may contact the surface of the absorbent core 20 on the skin side T1. The contact portion 62 may be disposed between the absorbent core 20 and the topsheet 30. Thereby, the excrement easily comes into contact with the contact portion 62 without being blocked by the absorbent core 20.
 図4Bに示すように、接触部62は、厚さ方向Tにおいて吸収コア20の間に配置されてよい。接触部62は、吸収コア20の幅方向Wの側面から挿入されることにより、吸収コア20の間に配置されてよい。吸収コア20は、吸収コア20の側面に接触部62(検査部材60)を挿入するための開口が設けられてよい。或いは、接触部62は、厚さ方向Tに重ねられている2つの吸収コア20の間に挟まれることにより、吸収コア20の間に配置されてよい。吸収コア20が吸収した排泄物が吸収コア20内を拡散することにより、排泄物が容易に接触部62へ接触し易くなる。 接触 As shown in FIG. 4B, the contact portions 62 may be arranged between the absorbent cores 20 in the thickness direction T. The contact portion 62 may be arranged between the absorbent cores 20 by being inserted from the side surface of the absorbent core 20 in the width direction W. The absorbent core 20 may be provided with an opening on a side surface of the absorbent core 20 for inserting the contact portion 62 (the inspection member 60). Alternatively, the contact portion 62 may be disposed between the absorbent cores 20 by being sandwiched between two absorbent cores 20 stacked in the thickness direction T. The excrement absorbed by the absorbent core 20 diffuses in the absorbent core 20, so that the excrement easily comes into contact with the contact portion 62.
 図4Cに示すように、接触部62は、吸収コア20の側面に接触してもよい。接触部62は、接触部62は、吸収コア20の幅方向Wの側面にまで拡散した排泄物と接触してもよい。これにより、排泄物が容易に接触部62へ接触し易くなる。なお、図4Cに示すように、接触部62は、排泄物の到達範囲に配置されていれば、接触部62は、厚さ方向Tにおいて吸収コア20と重ならなくもよい。 接触 As shown in FIG. 4C, the contact portion 62 may contact the side surface of the absorbent core 20. The contact portion 62 may be in contact with the excrement diffused to the side surface of the absorbent core 20 in the width direction W. Thereby, the excrement easily comes into contact with the contact portion 62 easily. In addition, as shown in FIG. 4C, the contact portion 62 may not overlap the absorbent core 20 in the thickness direction T as long as the contact portion 62 is arranged in the range of the excrement.
 図5Aに示すように、吸収性物品1は、排泄物を接触部62の少なくとも一部へ誘導する誘導部22を有してよい。誘導部22は、周囲よりも液体(排泄物)を引き込み易い領域であってよい。排泄物は、誘導部22により、接触部62の少なくとも一部へ誘導されるため、より多くの排泄物を接触部62に接触させることができる。これにより、指示薬が多くの検出対象に基づいて呈色可能となり、検査精度を向上できる。 AAs shown in FIG. 5A, the absorbent article 1 may have a guiding portion 22 for guiding excrement to at least a part of the contact portion 62. The guide portion 22 may be an area that is easier to draw in liquid (excretion) than its surroundings. Since the excrement is guided to at least a part of the contact portion 62 by the guide portion 22, more excrement can be brought into contact with the contact portion 62. Thus, the indicator can be colored based on many detection targets, and the inspection accuracy can be improved.
 具体的には、吸収コア20には、誘導部22として低目付部221を有してよい。低目付部221の吸収材料の目付は、周囲の吸収材料の目付よりも低い。従って、低目付部221では、周囲よりも排泄物が拡散しやすい。低目付部221は、厚さ方向において吸収コア20の肌面から非肌面側まで延びてよい。低目付部221の目付は、0より大きい値であってよい。或いは、低目付部221の目付は、0であってよい。すなわち、低目付部221は、厚さ方向Tにおいて吸収コア20を貫通する開孔であってよい。吸収コア20は、厚さ方向において吸収コア20を貫通する開孔を有してよい。 Specifically, the absorbent core 20 may have a low-weight portion 221 as the guide portion 22. The basis weight of the absorbent material in the low basis weight portion 221 is lower than the basis weight of the surrounding absorbent material. Therefore, excrement is more easily diffused in the low weight portion 221 than in the surrounding area. The low weight portion 221 may extend from the skin surface of the absorbent core 20 to the non-skin surface side in the thickness direction. The basis weight of the low basis weight portion 221 may be a value larger than 0. Alternatively, the basis weight of the low basis weight portion 221 may be zero. That is, the low-weight portion 221 may be an opening penetrating the absorbent core 20 in the thickness direction T. The absorbent core 20 may have an opening penetrating the absorbent core 20 in the thickness direction.
 図5Aに示すように、吸収コア20よりも非肌面側T2に配置されている接触部62の少なくとも一部は、厚さ方向Tにおいて低目付部221(例えば、開孔)と重なってよい。これにより、開孔を通じて排泄物が接触部62へより到達し易くなる。指示薬が多くの検出対象に基づいて呈色可能となり、検査精度を向上できる。 As shown in FIG. 5A, at least a part of the contact portion 62 arranged on the non-skin side T2 with respect to the absorbent core 20 may overlap the low-weight portion 221 (for example, an opening) in the thickness direction T. . This makes it easier for the excrement to reach the contact portion 62 through the opening. The indicator can be colored based on many detection targets, and the inspection accuracy can be improved.
 図5Bに示すように、吸収コア20よりも非肌面側T2に配置されている接触部62は、厚さ方向Tにおいて低目付部221(例えば、開孔)と重ならなくてよい。従って、厚さ方向Tの平面視において、接触部62は、開孔から離れた位置に配置されてよい。排泄物は、吸収コア20の吸収部材を構成する繊維の隙間を通り抜けるよりも、開孔を通ることで、接触部62が配置されている吸収コア20の非肌面側T2へ到達し易くなる。非肌面側T2へ到達した排泄物は、拡散により接触部62にまで到達することができる。このため、接触部62へ到達するまでの時間を短縮でき、多くの排泄物が接触部62へ到達可能となる。これにより、検査精度を向上できる。また、接触部62が指示薬を含んでいる場合、接触部62に到達した排泄物に指示薬が溶解することがある。しかしながら、接触部62が厚さ方向Tにおいて開孔と重ならないため、排泄物が開孔を通じて吸収コア20の非肌面側T2へ到達し難くなる。このため、指示薬が肌へ刺激を与え得るものであっても、指示薬を含む排泄物がトップシート30の非肌面側T2にまで到達し難くなり、着用者の安全性を高めることができる。 5B, as shown in FIG. 5B, the contact portion 62 disposed on the non-skin side T2 with respect to the absorbent core 20 does not have to overlap the low-weight portion 221 (for example, an opening) in the thickness direction T. Therefore, in a plan view in the thickness direction T, the contact portion 62 may be arranged at a position away from the opening. The excrement is more likely to reach the non-skin side T2 of the absorbent core 20 where the contact portion 62 is arranged by passing through the opening than through the gap of the fiber constituting the absorbent member of the absorbent core 20. . The excrement reaching the non-skin side T2 can reach the contact portion 62 by diffusion. Therefore, the time required to reach the contact portion 62 can be reduced, and a large amount of excrement can reach the contact portion 62. Thereby, the inspection accuracy can be improved. When the contact portion 62 contains the indicator, the indicator may be dissolved in the excrement that has reached the contact portion 62. However, since the contact portion 62 does not overlap the opening in the thickness direction T, it is difficult for excrement to reach the non-skin side T2 of the absorbent core 20 through the opening. For this reason, even if the indicator can stimulate the skin, it is difficult for excrement containing the indicator to reach the non-skin side T2 of the top sheet 30, and the safety of the wearer can be enhanced.
 図6A及び図6Bに示すように、トップシート30は、断面が波状になるように曲げられることによって形成された、並列に配置されている複数の突状部32と、隣接する突状部の間に配置されている(複数の)底部34とを有してもよい。底部34は、厚さ方向Tにおいて吸収コア20と重なる領域から、厚さ方向Tにおいて接触部62と重なる領域まで延びてよい。吸収領域ARに排泄された排泄物Eは、突状部32に排泄された場合であっても、底部34へ流れ落ちる。このため、排泄物Eが、底部34に集まり、底部34を経路として、厚さ方向Tにおいて接触部62と重なる位置にまで到達し易くなる。このように、接触部62が、吸収コア20と接触していない場合であっても、誘導部22としての底部34により排泄物Eが接触部62へ誘導されることにより、接触部62の少なくとも一部が、排泄物Eの到達範囲へ配置されてよい。従って、図6Bに示すように、接触部62は、吸収コア20から離れて配置されていてもよい。 As shown in FIG. 6A and FIG. 6B, the top sheet 30 has a plurality of protrusions 32 arranged in parallel, which are formed by being bent to have a wavy cross section, and a plurality of protrusions 32 adjacent to each other. And a bottom portion (s) 34 disposed therebetween. The bottom portion 34 may extend from a region overlapping the absorbent core 20 in the thickness direction T to a region overlapping the contact portion 62 in the thickness direction T. The excrement E excreted in the absorption area AR flows down to the bottom 34 even when excreted in the projection 32. Therefore, the excrement E is easily collected on the bottom 34 and reaches the position overlapping the contact portion 62 in the thickness direction T using the bottom 34 as a path. As described above, even when the contact portion 62 is not in contact with the absorbent core 20, the excrement E is guided to the contact portion 62 by the bottom portion 34 as the guide portion 22, so that at least the contact portion 62 A part may be arranged in the reach of the excrement E. Therefore, as shown in FIG. 6B, the contact portion 62 may be arranged away from the absorbent core 20.
 図7Aに示すように、厚さ方向Tの平面視において、表示部64の少なくとも一部は、吸収コア20の前後方向Lの外端縁から延出してよい。従って、表示部64の少なくとも一部は、フラップ部80に配置されてよい。フラップ80部は、吸収コア20の外端縁から吸収性物品1の外側縁までの部分である。フラップ80部は、前側域S1におけるフラップ部である前側フラップ部81と、後側域S2におけるフラップ部である後側フラップ部82と、を有してよい。 As shown in FIG. 7A, in a plan view in the thickness direction T, at least a part of the display unit 64 may extend from the outer edge of the absorbent core 20 in the front-rear direction L. Therefore, at least a part of the display unit 64 may be disposed on the flap unit 80. The flap 80 is a portion from the outer edge of the absorbent core 20 to the outer edge of the absorbent article 1. The flap 80 may include a front flap 81 that is a flap in the front area S1 and a rear flap 82 that is a flap in the rear area S2.
 排泄物は、吸収性物品1の前後方向Lの端部側よりも中央側に排泄され易いため、吸収コア20の前後方向Lの外端縁を超えて拡散し難い。表示部64の少なくとも一部は、吸収コア20の前後方向Lの外端縁から延出しているため、排泄物に覆われ難く、着用者は、排泄物の影響を受けずに表示部64を視認し易くなる。 (4) Since excrement is more easily excreted toward the center than the end in the front-rear direction L of the absorbent article 1, it is difficult to diffuse beyond the outer edge of the absorbent core 20 in the front-rear direction L. Since at least a part of the display unit 64 extends from the outer edge of the absorbent core 20 in the front-rear direction L, it is difficult for the display unit 64 to be covered with the excrement, and the wearer can operate the display unit 64 without being affected by the excrement. It becomes easy to see.
 図7Aに示すように、表示部64の少なくとも一部は、前側域S1において、吸収コア20の前後方向Lの外端縁から延出してよい。従って、表示部64の少なくとも一部は、前側フラップ部81に配置されてよい。吸収性物品1を膝付近にまで下げた状態において、前側フラップ部81は、視認し易い位置にある。このため、着用者は、吸収性物品1を身体から完全に離さなくても、表示部64を簡単に視認することが可能である。 As shown in FIG. 7A, at least a part of the display unit 64 may extend from the outer edge of the absorbent core 20 in the front-rear direction L in the front side area S1. Therefore, at least a part of the display unit 64 may be disposed on the front flap unit 81. In a state where the absorbent article 1 is lowered to a position near the knee, the front flap portion 81 is at a position where it is easy to visually recognize. Therefore, the wearer can easily visually recognize the display section 64 without completely removing the absorbent article 1 from the body.
 また、前側域S1には、後側域S2と比較して、尿が到達し易いため、図7Aに示すように、尿に含まれる対象成分を検出対象とする検査部材60を少なくとも前側域S1に配置して、接触部62の少なくとも一部を前側域S1に配置することができる。これにより、より多くの排泄物を接触部62に接触させることができる。指示薬が多くの検出対象に基づいて呈色可能となり、検査精度を向上できる。 In addition, since urine easily reaches the front side area S1 as compared with the rear side area S2, as shown in FIG. 7A, at least the front side area S1 includes the inspection member 60 that detects a target component contained in urine. And at least a part of the contact portion 62 can be arranged in the front side area S1. Thereby, more excrement can be brought into contact with the contact portion 62. The indicator can be colored based on many detection targets, and the inspection accuracy can be improved.
 図7Bに示すように、後側域S2には、前側域S1と比較して、大便が到達し易いため、図7Bに示すように、大便に含まれる対象成分を検出対象とする検査部材60を少なくとも後側域S2に配置して、接触部62の少なくとも一部を後側域S2に配置することができる。これにより、より多くの排泄物を接触部62に接触させることができる。指示薬が多くの検出対象に基づいて呈色可能となり、検査精度を向上できる。 As shown in FIG. 7B, since the stool easily reaches the rear area S2 as compared with the front area S1, as shown in FIG. 7B, the inspection member 60 which detects the target component contained in the stool is a target. Can be arranged at least in the rear area S2, and at least a part of the contact portion 62 can be arranged in the rear area S2. Thereby, more excrement can be brought into contact with the contact portion 62. The indicator can be colored based on many detection targets, and the inspection accuracy can be improved.
 図7A及び図7Bに示すように、検査部材60は、トップシート30よりも非肌面側T2に配置されてよい。検査部材60が着用者の肌に直接触れることを抑制できる。これにより、着用者の肌に検査部材60が直接当たることによる着用時の違和感を抑制できる。さらに、指示薬が肌へ刺激を与え得るものであっても、着用者の肌に指示薬が触れ難くなり、着用者の安全性を高めることができる。 7A and 7B, the inspection member 60 may be arranged on the non-skin side T2 with respect to the top sheet 30. It is possible to prevent the inspection member 60 from directly touching the wearer's skin. Thereby, the discomfort at the time of wearing due to the inspection member 60 directly hitting the skin of the wearer can be suppressed. Furthermore, even if the indicator can give irritation to the skin, it becomes difficult for the indicator to touch the skin of the wearer, and the safety of the wearer can be enhanced.
 なお、トップシート30は、透明性を有してよい。これにより、着用者は、トップシート30を介して検査部材60の呈色を視認可能であってよい。また、着用者は、上述のように、トップシート30(及び/又はサイドシート50)をバックシート40から剥離することによって、検査部材60の呈色を視認可能であってよい。 In addition, the top sheet 30 may have transparency. Thereby, the wearer may be able to visually recognize the coloration of the inspection member 60 via the top sheet 30. Further, as described above, the wearer may be able to visually recognize the coloration of the inspection member 60 by peeling the top sheet 30 (and / or the side sheet 50) from the back sheet 40.
 トップシート30の透明性は、不透明度(OP)により特定できる。トップシート30は、0%の不透明度を有する場合、完全に透明である。一方、トップシート30は、100%の不透明度を有する場合、透明性を有さない、すなわち、トップシート30は、光を通さない。従って、トップシート30の不透明度は、100%未満である。表示部64の色をより正確に視認するために、トップシート30の不透明度は、50%以下であってよい。トップシート30の不透明度は、表示部64の色をさらに正確に視認するために、8.5%以下であってよい。 透明 The transparency of the topsheet 30 can be specified by the opacity (OP). If the topsheet 30 has 0% opacity, it is completely transparent. On the other hand, when the topsheet 30 has 100% opacity, it does not have transparency, that is, the topsheet 30 does not transmit light. Therefore, the opacity of the topsheet 30 is less than 100%. The opacity of the top sheet 30 may be 50% or less so that the color of the display unit 64 can be visually recognized more accurately. The opacity of the top sheet 30 may be 8.5% or less in order to more accurately recognize the color of the display unit 64.
 なお、不透明度を決定するためには、分光比色計(dispersion colorimeter)を使用してもよい。例えば、分光比色計(dispersion colorimeter)は、ビックガードナー社(BYK-Gardner  GmbH)(ドイツ、ゲレツリート(Geretsried))から商標名「ビックガードナーカラーガイド(BYK-Gardner  Color-Guide)45/0」(カタログ番号6800)の下で入手できる。光源「A」を用いて2°(度)の視角で測定を実施できる。この分光比色計(dispersion colorimeter)は、発光体A用の光源(即ち、約3000Kの相関色温度を有する白熱灯に近いもの)、平らなテーブル、白色標準プレート、標準黒色プレート、マルチセル型光検出器ダイオードアレイを備える光検出器、及びコンピュータを備える。白色及び黒色標準プレートは、同社からそれぞれカタログ番号6811及び6810の下で入手できる。 In order to determine the opacity, a dispersion colorimeter may be used. For example, a dispersion colorimeter is available from BYK-Gardner GmbH (Geretsried, Germany) under the trade name “BYK-Gardner Color-Guide 45/0” (Geretsried). Catalog No. 6800). The measurement can be performed at a viewing angle of 2 ° (degrees) using the light source “A”. The dispersion colorimeter comprises a light source for illuminant A (ie, something similar to an incandescent lamp having a correlated color temperature of about 3000 K), a flat table, a white standard plate, a standard black plate, a multi-cell light. A photodetector comprising a detector diode array; and a computer. White and black standard plates are available from the company under catalog numbers 6811 and 6810, respectively.
 測定する際、白色標準プレートを平らなテーブル上に配置する。サンプル材料を平らな状態で白色標準プレートに載せる。入射角が45°の光源でサンプル材料を照射する。サンプル材料から反射した反射光を光検出器により0°の受光角で受光する。反射光の反射率(Yw)を光検出器によって検出する。同様に、黒色標準プレートを平らなテーブル上に配置した後、サンプル材料を平らな状態で黒色標準プレート上に置く。入射角が45°の光源でサンプル材料を照射する。サンプル材料から反射した反射光を光検出器により0°の受光角で受光する。反射光の反射率(Yb)を光検出器によって検出する。 際 When measuring, place the white standard plate on a flat table. The sample material is placed flat on a white standard plate. The sample material is irradiated with a light source having an incident angle of 45 °. Light reflected from the sample material is received by a photodetector at a light receiving angle of 0 °. The reflectance (Yw) of the reflected light is detected by a photodetector. Similarly, after placing the black standard plate on a flat table, the sample material is placed flat on the black standard plate. The sample material is irradiated with a light source having an incident angle of 45 °. Light reflected from the sample material is received by a photodetector at a light receiving angle of 0 °. The reflectance (Yb) of the reflected light is detected by a photodetector.
 不透明度(OP)を次式により求めることができる。 Opacity (OP) can be obtained by the following equation.
  OP(%)=(Yb/Yw)×100
 このプロセスを1つのサンプルシート材料につき少なくとも5回繰り返し、測定した不透明度(OP)の平均値を計算し、比色計で記録する。測定した不透明度の平均値は、シート材料の不透明度と呼ばれる。
OP (%) = (Yb / Yw) × 100
This process is repeated at least five times for one sample sheet material, and the average value of the measured opacity (OP) is calculated and recorded with a colorimeter. The average value of the measured opacity is called the opacity of the sheet material.
 なお、トップシート30は、不織布(例えば、SMS(スパンボンド/メルトブローン/スパンボンド))の表面の一部の所定領域に亘って、加熱しながら、厚さ方向Tにトップシート30を圧縮する熱圧縮処理が施されてよい。これにより、トップシート30には、高密度部が形成されてよい。高密度部を形成する圧縮処理は、トップシート30(不織布)にカレンダー処理やエンボス処理等の公知の加圧加工を施すことによって行われる。高密度部では、不織布表面の繊維が押し固められることによって、高密度部が形成されていない領域と比較して、表面の微細な凹凸が減少し、平滑な状態となっている。このような熱圧縮処理により、トップシート30は、透明性を有してもよい。 Note that the topsheet 30 is a heat source that compresses the topsheet 30 in the thickness direction T while heating over a predetermined region of a part of the surface of a nonwoven fabric (for example, SMS (spunbond / meltblown / spunbond)). A compression process may be performed. Thereby, a high-density part may be formed in the top sheet 30. The compression process for forming the high-density portion is performed by subjecting the top sheet 30 (nonwoven fabric) to a known pressure process such as a calendering process or an embossing process. In the high-density portion, the fibers on the surface of the nonwoven fabric are compacted, whereby fine irregularities on the surface are reduced and the surface is in a smooth state as compared with a region where the high-density portion is not formed. By such a heat compression process, the top sheet 30 may have transparency.
 なお、トップシート30を例に挙げて説明したが、厚さ方向Tにおいて、表示部64がサイドシート50に重なる場合には、トップシート30と同様に、サイドシート50が透明性を有してよい。 Although the top sheet 30 has been described as an example, when the display unit 64 overlaps the side sheet 50 in the thickness direction T, the side sheet 50 has transparency similarly to the top sheet 30. Good.
 図7Cに示すように、厚さ方向Tの平面視において、表示部64の少なくとも一部は、吸収性物品本体10の外端縁10eから延出してもよい。この場合、吸収性物品本体10の外端縁10eから延出している部分が露出部644に対応する。吸収性物品本体10の外端縁10eから表示部64の少なくとも一部が延出しているため、表示部64の少なくとも一部は、排泄物が拡散できない位置に配置されている。これにより、表示部64の少なくとも一部が排泄物に覆われることを抑制できる。また、吸収性物品本体10の外端縁10eから表示部64の少なくとも一部が延出しているため、着用者は、表示部64を直接視認することができる。従って、着用者が正確な健康状態を把握し易くすることができる。 CAs shown in FIG. 7C, in a plan view in the thickness direction T, at least a part of the display unit 64 may extend from the outer edge 10 e of the absorbent article main body 10. In this case, a portion extending from the outer edge 10e of the absorbent article main body 10 corresponds to the exposed portion 644. Since at least a part of the display unit 64 extends from the outer edge 10e of the absorbent article main body 10, at least a part of the display unit 64 is arranged at a position where excrement cannot be diffused. Accordingly, it is possible to prevent at least a part of the display unit 64 from being covered with excrement. In addition, since at least a part of the display unit 64 extends from the outer edge 10e of the absorbent article main body 10, the wearer can directly view the display unit 64. Therefore, it is possible for the wearer to easily grasp the correct health condition.
 図7Cに示すように、前側域S1において、表示部64の少なくとも一部は、吸収性物品本体10の外端縁10eから延出してよい。吸収性物品1を膝付近にまで下げた状態において、着用者は、表示部64(露出部644)を視認することができる。着用者は、呈色の有無を容易に確認することができる。また、表示部64の少なくとも一部が吸収性物品本体10内に配置されていないため、排泄物に接触し難くなる。これにより、表示部の少なくとも一部が排泄物に覆われ難くなり、着用者は、排泄物の影響を受けずに表示部を視認し易くなる。 As shown in FIG. 7C, in the front side area S <b> 1, at least a part of the display unit 64 may extend from the outer edge 10 e of the absorbent article main body 10. In a state where the absorbent article 1 is lowered to near the knee, the wearer can visually recognize the display portion 64 (the exposed portion 644). The wearer can easily confirm the presence or absence of coloration. In addition, since at least a part of the display unit 64 is not arranged in the absorbent article main body 10, it is difficult to contact the excrement. This makes it difficult for at least a part of the display unit to be covered with the excrement, and makes it easier for the wearer to visually recognize the display unit without being affected by the excrement.
 図7Dに示すように、中央域S3において、表示部64の少なくとも一部は、吸収性物品本体10の外端縁10eから延出してよい。表示部64の少なくとも一部は、ウイング14の外側縁から延出してよい。ウイング14は、着用物品100の非肌面側T2に固定されるため、肌面側から排泄される排泄物は、ウイング14に付着し難い。これにより、表示部64の少なくとも一部が排泄物に覆われ難くなり、着用者は、排泄物の影響を受けずに表示部を視認し易くなる。さらに、ウイング14は、着用物品100の非肌面側T2に固定されるため、露出部644が存在しても、露出部644が着用者の肌に触れ難くなる。露出部644に含まれる指示薬が肌にダメージを与え得るものであっても、着用者の安全性を高めることができる。 DAs shown in FIG. 7D, in the central area S3, at least a part of the display section 64 may extend from the outer edge 10e of the absorbent article main body 10. At least a portion of the display 64 may extend from an outer edge of the wing 14. Since the wings 14 are fixed to the non-skin side T2 of the wearing article 100, the excrement excreted from the skin side hardly adheres to the wings 14. This makes it difficult for at least a part of the display unit 64 to be covered with the excrement, and makes it easier for the wearer to visually recognize the display unit without being affected by the excrement. Furthermore, since the wing 14 is fixed to the non-skin surface side T2 of the wearing article 100, even if the exposed portion 644 exists, the exposed portion 644 is less likely to touch the wearer's skin. Even if the indicator contained in the exposed portion 644 can damage the skin, the safety of the wearer can be improved.
 なお、前側域S1又は中央域S3だけでなく、後側域S2において、表示部64の少なくとも一部は、吸収性物品本体10の外端縁10eから延出してよい。 In addition, at least a part of the display part 64 may extend from the outer edge 10e of the absorbent article main body 10 in the rear area S2 as well as in the front area S1 or the central area S3.
 図8Aに示すように、吸収性物品1は、検出対象が互いに異なる複数の検査部材60有してよい。複数の検査部材60それぞれが有する表示部64は、厚さ方向Tにおいて互いに異なる位置に配置されてよい。検出対象が互いに異なる複数の検査部材60を備えるため、1つの吸収性物品1で健康状態を示す複数の項目を確認することができる。複数の検査部材60それぞれが有する表示部64が厚さ方向Tにおいて互いに異なる位置に配置されているため、着用者が、各表示部64を視認し易くなり、一部の表示部64を見落とすことを抑制できる。 AAs shown in FIG. 8A, the absorbent article 1 may have a plurality of inspection members 60 whose detection targets are different from each other. The display units 64 included in each of the plurality of inspection members 60 may be arranged at different positions in the thickness direction T. Since a plurality of inspection members 60 whose detection targets are different from each other are provided, a plurality of items indicating a health condition can be confirmed with one absorbent article 1. Since the display portions 64 included in each of the plurality of inspection members 60 are arranged at positions different from each other in the thickness direction T, the wearer can easily recognize each of the display portions 64 and overlook some of the display portions 64. Can be suppressed.
 例えば、複数の検査部材60は、第1検査部材60Aと、第2検査部材60Bとを有してよい。第1検査部材60Aの表示部64Aは、一方のウイング14Aに配置されてよく、第2検査部材60Bの表示部64Bは、他方のウイング14Bに配置されてよい。 For example, the plurality of inspection members 60 may include a first inspection member 60A and a second inspection member 60B. The display part 64A of the first inspection member 60A may be arranged on one wing 14A, and the display part 64B of the second inspection member 60B may be arranged on the other wing 14B.
 図8Bに示すように、第1検査部材60Aの表示部64Aは、前側域S1に配置されてよい。従って、表示部64Aの少なくとも一部は、前側フラップ部81に配置されてよい。また、第2検査部材60Bの表示部64Bは、後側域S2に配置されてよい。従って、表示部64Bの少なくとも一部は、後側フラップ部82に配置されてよい。第1検査部材60Aは、尿に含まれる対象成分を検出対象とする検査部材60であってよい。第2検査部材60Bは、大便に含まれる対象成分を検出対象とする検査部材60であってよい。このように、検出対象を含む排泄物が排泄されやすい領域へ、当該検出対象に基づいて呈色する指示薬を含む検出部材を配置することで、複数の健康状態が表示される場合であっても、着用者は、健康状態を把握し易くなる。 表示 As shown in FIG. 8B, the display section 64A of the first inspection member 60A may be disposed in the front side area S1. Therefore, at least a part of the display unit 64 </ b> A may be disposed on the front flap unit 81. Further, the display section 64B of the second inspection member 60B may be arranged in the rear area S2. Therefore, at least a part of the display unit 64 </ b> B may be disposed on the rear flap unit 82. The first inspection member 60A may be the inspection member 60 that detects a target component contained in urine as a detection target. The second inspection member 60B may be the inspection member 60 that detects a target component contained in the stool. In this way, even if a plurality of health conditions are displayed by arranging the detection member including the indicator that changes color based on the detection target in an area where the excrement including the detection target is easily excreted, Therefore, the wearer can easily grasp the health condition.
 (4)第2実施形態
 次に、第2実施形態に係る吸収性物品1について説明する。なお、上述の実施形態と同様の部分は、説明を省略する。
(4) Second Embodiment Next, an absorbent article 1 according to a second embodiment will be described. The description of the same parts as in the above-described embodiment will be omitted.
 図9は、第2実施形態に係る吸収性物品を肌面側から見た平面図である。図10は、第2実施形態に係る吸収性物品を非肌面側から見た平面図である。図11は、第2実施形態に係る吸収性物品の断面図である。具体的には、図11は、図9に示すA-A線に沿った断面図である。 FIG. 9 is a plan view of the absorbent article according to the second embodiment as viewed from the skin side. FIG. 10 is a plan view of the absorbent article according to the second embodiment as viewed from the non-skin side. FIG. 11 is a cross-sectional view of the absorbent article according to the second embodiment. Specifically, FIG. 11 is a cross-sectional view along the line AA shown in FIG.
 吸収性物品1は、吸収コア20、バックシート40、検査部材60を備える。また、吸収性物品1は、トップシート30、サイドシート50、粘着部70を備えてよい。 The absorbent article 1 includes the absorbent core 20, the back sheet 40, and the inspection member 60. Further, the absorbent article 1 may include the top sheet 30, the side sheet 50, and the adhesive section 70.
 バックシート40は、吸収コア20よりも非肌面側に配置されている。バックシート40は、液不透過性を有してよい。バックシート40は、透明性を有する。これにより、図11に示すように、検査部材60は、厚さ方向Tにおいてバックシート40よりも肌面側T1に配置されていても、図10に示すように、後述する表示部64を視認可能である。 The back sheet 40 is arranged on the non-skin side with respect to the absorbent core 20. The back sheet 40 may have liquid impermeability. The back sheet 40 has transparency. Thereby, as shown in FIG. 11, even if the inspection member 60 is arranged on the skin surface side T1 with respect to the back sheet 40 in the thickness direction T, as shown in FIG. It is possible.
 なお、本発明における「視認可能」とは、昼白色(色温度目安 4600~5400 K(ケルビン))で明るく照明された室内(目安:500~750 lx(ルクス))で約30~50cmの距離で、良好な視力(1.0以上)を両眼に有する被験者が対象物を見たときに視認できる事を意味している。 In the present invention, the term “visible” refers to a distance of about 30 to 50 cm in a room (approximately: 500 to 750 lx (lux)) brightly illuminated with a neutral white color (color temperature reference: 4600 to 5400 K (Kelvin)). This means that a subject having good visual acuity (1.0 or more) with both eyes can visually recognize the subject when viewing it.
 バックシート40の透明性は、不透明度(OP)により特定できる。バックシート40は、0%の不透明度を有する場合、完全に透明である。一方、バックシート40は、100%の不透明度を有する場合、透明性を有さない、すなわち、バックシート40は、光を通さない。従って、バックシート40の不透明度は、100%未満である。検査部材60(表示部64)をより正確に視認するために、バックシート40の不透明度は、50%以下であってよい。バックシート40の不透明度は、表示部64の色をさらに正確に視認するために、8.5%以下であってよい。 透明 The transparency of the back sheet 40 can be specified by the opacity (OP). The backsheet 40 is completely transparent if it has 0% opacity. On the other hand, when the back sheet 40 has 100% opacity, it does not have transparency, that is, the back sheet 40 does not transmit light. Therefore, the opacity of the back sheet 40 is less than 100%. The opacity of the back sheet 40 may be 50% or less so that the inspection member 60 (the display unit 64) can be visually recognized more accurately. The opacity of the back sheet 40 may be 8.5% or less in order to more accurately view the color of the display unit 64.
 バックシート40は、不織布(例えば、SMS(スパンボンド/メルトブローン/スパンボンド))の表面の全領域に亘って、加熱しながら、厚さ方向Tにバックシート40を圧縮する熱圧縮処理が施されてよい。これにより、バックシート40には、高密度部が形成されてよい。高密度部を形成する熱圧縮処理は、バックシート40(不織布)にカレンダー処理やエンボス処理等の公知の加圧加工を施すことによって行われる。高密度部では、不織布表面の繊維が押し固められることによって、高密度部が形成されていない領域と比較して、表面の微細な凹凸が減少し、平滑な状態となっている。当該熱圧縮処理により、バックシート40は、透明性を有してもよい。なお、当該処理が施された不織布製のバックシート40を用いることにより、開封時にガサガサというジッピング音が発生し難く、吸収性物品1を使用する際に他者に気付かれ難くなる。 The backsheet 40 is subjected to a heat compression process of compressing the backsheet 40 in the thickness direction T while heating over the entire area of the surface of the nonwoven fabric (for example, SMS (spunbond / meltblown / spunbond)). May be. Thereby, a high-density portion may be formed on the back sheet 40. The heat compression process for forming the high-density portion is performed by subjecting the back sheet 40 (nonwoven fabric) to a known pressure process such as a calendering process or an embossing process. In the high-density portion, the fibers on the surface of the nonwoven fabric are compacted, whereby fine irregularities on the surface are reduced and the surface is in a smooth state as compared with a region where the high-density portion is not formed. By the heat compression process, the back sheet 40 may have transparency. In addition, by using the backsheet 40 made of the nonwoven fabric that has been subjected to the treatment, a zipper sound is less likely to be generated when the absorbent article 1 is opened, and it is difficult for others to notice when using the absorbent article 1.
 粘着部70は、透明性を有してよい。図10において、中央粘着部72は、厚さ方向Tにおいて、表示部64(の一部)と重なっている。このため、中央粘着部72は、透明性を有してよい。粘着部70は、例えば、HMAにより構成されることで透明性を有してよい。 The adhesive section 70 may have transparency. In FIG. 10, the central adhesive portion 72 overlaps (a part of) the display portion 64 in the thickness direction T. For this reason, the central adhesive portion 72 may have transparency. The adhesive section 70 may have transparency by being made of, for example, HMA.
 図9から図11に示すように、吸収性物品1は、疎水性を有する疎水部90を備えている。疎水部90は、バックシート40よりも肌面側において、表示部64から厚さ方向T及び水平方向へ延びる延長領域ERに配置されている。 吸収 As shown in FIGS. 9 to 11, the absorbent article 1 has a hydrophobic portion 90 having hydrophobicity. The hydrophobic portion 90 is disposed in an extension region ER extending in the thickness direction T and the horizontal direction from the display portion 64 on the skin surface side with respect to the back sheet 40.
 疎水部90が、表示部64から厚さ方向Tへ延びる延長領域ERに配置されている場合には、吸収性物品1の肌面側T1に排泄された排泄物が厚さ方向Tにおいて表示部64の方へ拡散する拡散経路上に、当該疎水部90が存在する。疎水部90は、疎水性を有するため、水溶性の排泄物が表示部64側へ拡散することを抑制し易い。また、疎水部90が、表示部64から水平方向へ延びる延長領域ERに配置されている場合には、吸収性物品1の内部に拡散した排泄物が水平方向において表示部64の方へ拡散する拡散経路上に、当該疎水部90が存在する。疎水部90は、水溶性の排泄物が表示部64側へ拡散することを抑制し易い。以上より、排泄物が、表示部64を覆ったり、表示部64と重なったりすることを抑制し易く、表示部64の視認性を確保し易くなる。これにより、着用者は、表示部64をバックシート40側から視認した場合に、着用者が正確な健康状態を把握し易くなる。 When the hydrophobic portion 90 is disposed in the extension region ER extending from the display portion 64 in the thickness direction T, the excrement excreted on the skin surface side T1 of the absorbent article 1 is displayed in the thickness direction T on the display portion. The hydrophobic portion 90 exists on a diffusion path that diffuses toward 64. Since the hydrophobic part 90 has hydrophobicity, it is easy to suppress the water-soluble excrement from diffusing to the display part 64 side. When the hydrophobic part 90 is arranged in the extension region ER extending in the horizontal direction from the display part 64, the excrement diffused inside the absorbent article 1 is diffused in the horizontal direction toward the display part 64. The hydrophobic part 90 exists on the diffusion path. The hydrophobic part 90 can easily suppress the water-soluble excrement from diffusing to the display part 64 side. As described above, it is easy to suppress the excrement from covering the display unit 64 or overlapping the display unit 64, and it is easy to ensure the visibility of the display unit 64. Accordingly, when the wearer visually recognizes the display unit 64 from the back sheet 40 side, the wearer can easily grasp the correct health condition.
 本実施の形態のように、延長領域ERに配置されている疎水部90は、吸収領域ARに排泄された排泄物が到達する到達範囲に配置されてよい。これにより、疎水部90にまで到達した排泄物が表示部64側へ拡散することを抑制できるため、表示部64の視認性を確保し易くなる。これにより、着用者は、表示部64をバックシート側から視認した場合に、着用者が正確な健康状態を把握し易くなる。 疎 水 As in the present embodiment, the hydrophobic portion 90 arranged in the extension region ER may be arranged in the reach of the excretion excreted in the absorption region AR. This can suppress the excrement reaching the hydrophobic part 90 from being diffused to the display part 64 side, so that the visibility of the display part 64 can be easily secured. Thereby, when the wearer visually recognizes the display unit 64 from the back seat side, it becomes easier for the wearer to grasp an accurate health condition.
 図11に示すように、疎水部90は、表示部64と接触してよい。排泄物が表示部64に到達することを抑制できる。これにより、表示部64の視認性を確保することができ、着用者が正確な健康状態を把握し易くなる。 疎 水 As shown in FIG. 11, the hydrophobic part 90 may be in contact with the display part 64. It is possible to suppress the excrement from reaching the display unit 64. Thereby, the visibility of the display unit 64 can be ensured, and the wearer can easily grasp the correct health condition.
 延長領域ERに配置されている疎水部90は、表示部64よりも肌面側T1に配置されている肌側疎水部92と、表示部64よりも非肌面側T2に配置されている非肌側疎水部94と、表示部64よりも水平方向(図11では幅方向W)の外側に配置されている側面側疎水部96と、を有してよい。 The hydrophobic portion 90 disposed in the extension region ER includes a skin-side hydrophobic portion 92 disposed on the skin surface side T1 with respect to the display portion 64 and a non-skinned portion disposed on the non-skin surface side T2 with respect to the display portion 64. It may include a skin-side hydrophobic portion 94 and a side-surface-side hydrophobic portion 96 disposed outside the display portion 64 in the horizontal direction (the width direction W in FIG. 11).
 疎水部90である肌側疎水部92は、表示部64の肌面側の表面と接触してよい。これにより、肌面側T1から非肌面側T2へ拡散する排泄物が表示部64に到達することを抑制できる。表示部64の視認性を確保することができ、着用者が正確な健康状態を把握し易くなる。 The skin-side hydrophobic portion 92 that is the hydrophobic portion 90 may be in contact with the skin-side surface of the display unit 64. Thereby, it is possible to suppress the excrement that diffuses from the skin surface side T1 to the non-skin surface side T2 from reaching the display unit 64. The visibility of the display unit 64 can be ensured, and the wearer can easily grasp the correct health condition.
 疎水部90である非肌側疎水部94は、表示部64の肌面側の表面と接触してよい。これにより、バックシート側から視認される表示部64の表面に排泄物が到達することを抑制できる。表示部64の視認性を確保することができ、着用者が正確な健康状態を把握し易くなる。 非 The non-skin side hydrophobic portion 94 which is the hydrophobic portion 90 may be in contact with the skin side surface of the display portion 64. Thereby, it is possible to suppress the excrement from reaching the surface of the display section 64 visually recognized from the back sheet side. The visibility of the display unit 64 can be ensured, and the wearer can easily grasp the correct health condition.
 疎水部90である側面側疎水部96は、表示部64の側面と接触してよい。これにより、水平方向へ拡散する排泄物が表示部64に到達することを抑制できる。表示部64の視認性を確保することができ、着用者が正確な健康状態を把握し易くなる。 (4) The side surface side hydrophobic portion 96 which is the hydrophobic portion 90 may be in contact with the side surface of the display portion 64. Thereby, it is possible to suppress the excrement diffused in the horizontal direction from reaching the display unit 64. The visibility of the display unit 64 can be ensured, and the wearer can easily grasp the correct health condition.
 図11に示すように、疎水部90は、表示部64の周囲を覆ってよい。従って、疎水部90は、延長領域ERと異なる領域にも配置されてよい。疎水部90は、表示部64の全面を覆ってよい。疎水部90は、表示部64の一部を覆ってもよい。疎水部90は、接触部62の一部を覆ってよい。接触部62へ排泄物を到達させるために、疎水部90は、接触部62の全面を覆わない。 疎 水 As shown in FIG. 11, the hydrophobic portion 90 may cover the periphery of the display portion 64. Therefore, the hydrophobic portion 90 may be arranged in a region different from the extension region ER. The hydrophobic part 90 may cover the entire surface of the display part 64. The hydrophobic part 90 may cover a part of the display part 64. The hydrophobic part 90 may cover a part of the contact part 62. The hydrophobic part 90 does not cover the entire surface of the contact part 62 so that the excrement reaches the contact part 62.
 疎水部90は、疎水性を有する層又は部材により構成可能である。例えば、撥水スプレー、コーティング装置などにより、接触部62の一部に撥水剤を付着(塗布)する撥水加工することにより、疎水部90としての撥水層が設けられてよい。表示部64を構成する部材を、撥水剤に含浸してもよい。撥水剤を付着させたくない部分(例えば、接触部62(の一部))は、マスキングテープ等により覆っていてよい。接触部62を疎水部90により覆った後にマスキングテープ等を剥がすことにより、接触部62を露出させてよい。撥水剤は、シリコン系撥水剤でもよく、フッ素系撥水剤でもよい。撥水剤(疎水部90)は、変色し難いものであることが好ましい。 The hydrophobic portion 90 can be constituted by a layer or a member having hydrophobicity. For example, a water-repellent layer as the hydrophobic portion 90 may be provided by performing a water-repellent process of attaching (applying) a water-repellent agent to a part of the contact portion 62 by a water-repellent spray, a coating device, or the like. The member constituting the display unit 64 may be impregnated with a water repellent. A portion to which the water repellent is not to be attached (for example, (a part of) the contact portion 62) may be covered with a masking tape or the like. After covering the contact portion 62 with the hydrophobic portion 90, the contact portion 62 may be exposed by peeling off a masking tape or the like. The water repellent may be a silicone water repellent or a fluorine water repellent. It is preferable that the water repellent (hydrophobic portion 90) does not easily discolor.
 疎水部90は、バックシート40と同様の材料から構成されてもよい。疎水部90は、吸収性物品1を構成する各部材を接合するための接合層(例えば、ホットメルト型接着剤(HMA))により構成されてよい。これにより、検査部材60を固定できると共に疎水部90を形成することができる。 The hydrophobic portion 90 may be made of the same material as the back sheet 40. The hydrophobic part 90 may be formed of a bonding layer (for example, a hot melt adhesive (HMA)) for bonding the members constituting the absorbent article 1. Thereby, the inspection member 60 can be fixed and the hydrophobic portion 90 can be formed.
 疎水部90は、透明性を有してよい。例えば、非肌側疎水部94は、呈色を視認し易くするために、透明性を有してよい。一方、肌側疎水部92は、表示部64よりも肌面側T1に配置されているため、透明性を有さなくてよいし、透明性を有してよい。また、側面側疎水部96は、透明性を有さなくてよいし、透明性を有してよい。 The hydrophobic portion 90 may have transparency. For example, the non-skin side hydrophobic portion 94 may have transparency in order to make the coloration easily visible. On the other hand, since the skin-side hydrophobic portion 92 is disposed closer to the skin surface T1 than the display portion 64, the skin-side hydrophobic portion 92 does not need to have transparency, and may have transparency. Further, the side surface side hydrophobic portion 96 does not need to have transparency, and may have transparency.
 (5)変更例
 次に、第2実施形態に係る吸収性物品1の各変更例について、図12から図15を用いて説明する。図12は、第2実施形態に係る各変更例(その1からその4)を説明するための図である。図12は、第2実施形態の変更例(その1)を説明するための吸収性物品1の断面図であり、図12Bは、第2実施形態の変更例(その2)を説明するための吸収性物品1の断面図であり、図12Cは、第2実施形態の変更例(その3)を説明するための吸収性物品1の断面図であり、図12Dは、第2実施形態の変更例(その4)を説明するための吸収性物品1の断面図である。図13は、第2実施形態に係る各変更例(その5からその6)を説明するための図である。具体的には、図13Aは、第2実施形態の変更例(その5)を説明するための吸収性物品1を非肌面側から見た平面図であり、図13Bは、第2実施形態の変更例(その6)を説明するための吸収性物品1を非肌面側から見た平面図である。図14は、第2実施形態に係る各変更例(その7からその8)を説明するための図である。具体的には、図14Aは、第2実施形態の変更例(その7)を説明するための吸収性物品1を非肌面側から見た平面図であり、図14Bは、第2実施形態の変更例(その8)を説明するための吸収性物品1を非肌面側から見た平面図である。図15は、第2実施形態に係る変更例(その9)を説明するための吸収性物品1の断面図である。なお、上述の第1及び第2実施形態と同様の部分は説明を省略する。
(5) Modification Examples Next, modification examples of the absorbent article 1 according to the second embodiment will be described with reference to FIGS. FIG. 12 is a diagram for describing each modification (Nos. 1 to 4) according to the second embodiment. FIG. 12 is a cross-sectional view of the absorbent article 1 for describing a modified example (part 1) of the second embodiment, and FIG. 12B is a sectional view for describing a modified example (part 2) of the second embodiment. FIG. 12C is a cross-sectional view of the absorbent article 1, and FIG. 12C is a cross-sectional view of the absorbent article 1 for describing a modification (part 3) of the second embodiment, and FIG. 12D is a modification of the second embodiment. It is sectional drawing of the absorbent article 1 for describing the example (the 4). FIG. 13 is a diagram for describing each modification example (No. 5 to No. 6) according to the second embodiment. Specifically, FIG. 13A is a plan view of the absorbent article 1 for explaining a fifth modification of the second embodiment as viewed from the non-skin side, and FIG. 13B is a second embodiment. It is the top view which looked at the absorbent article 1 for demonstrating the example of a change (the 6) from the non-skin side. FIG. 14 is a diagram for describing each modification example (No. 7 to No. 8) according to the second embodiment. Specifically, FIG. 14A is a plan view of the absorbent article 1 for explaining a modification (No. 7) of the second embodiment when viewed from the non-skin side, and FIG. 14B is a second embodiment. It is the top view which looked at the absorptive article 1 for explaining the modification (the 8) of (a) from the non-skin side. FIG. 15 is a cross-sectional view of the absorbent article 1 for describing a modified example (No. 9) according to the second embodiment. The description of the same parts as those in the first and second embodiments will be omitted.
 図12Aに示すように、疎水部90は、表示部64の肌面側T1の表面に接触するように配置されてよく、表示部64よりも非肌面側T2には配置されなくてよい。疎水部90は、表示部64の水平方向の外側の表面に接触するように配置されなくてよい。 AAs shown in FIG. 12A, the hydrophobic portion 90 may be arranged so as to contact the surface of the display surface 64 on the skin surface side T1, and may not be arranged on the non-skin surface side T2 than the display portion 64. The hydrophobic portion 90 does not need to be arranged so as to be in contact with the horizontal outer surface of the display portion 64.
 図12Bに示すように、疎水部90は、表示部64の非肌面側T2の表面に接触するように配置されてよく、表示部64よりも肌面側T1には配置されなくてよい。疎水部90は、表示部64の水平方向の外側の表面に接触するように配置されなくてよい。 疎 水 As shown in FIG. 12B, the hydrophobic portion 90 may be arranged so as to contact the surface of the non-skin surface side T2 of the display portion 64, and need not be arranged on the skin surface side T1 than the display portion 64. The hydrophobic portion 90 does not need to be arranged so as to be in contact with the horizontal outer surface of the display portion 64.
 図12Cに示すように、吸収コア20とバックシート40との間に検査部材60が配置されてよい。吸収性物品1は、吸収コア20と表示部64との間にシート状のシート部材が疎水部90として配置されてよい。シート部材は、吸収コア20と表示部64との間に配置されているため、肌面側T1から非肌面側T2へ拡散する排泄物が表示部64に到達することを抑制できる。これにより、表示部64の視認性を確保することができ、着用者が正確な健康状態を把握し易くなる。 検 査 As shown in FIG. 12C, the inspection member 60 may be arranged between the absorbent core 20 and the back sheet 40. In the absorbent article 1, a sheet-shaped sheet member may be disposed as the hydrophobic portion 90 between the absorbent core 20 and the display portion 64. Since the sheet member is disposed between the absorbent core 20 and the display unit 64, it is possible to suppress the excrement diffused from the skin side T1 to the non-skin side T2 from reaching the display unit 64. Thereby, the visibility of the display unit 64 can be ensured, and the wearer can easily grasp the correct health condition.
 図12Dに示すように、疎水部90は吸収コア20を包むコアラップ25であってよい。コアラップ25は、親水性を有する親水部222と疎水部90とを有してよい。親水部222は、疎水部90よりも肌面側T1に位置してよい。吸収コア20よりも非肌面側T2に位置する疎水部90は、厚さ方向Tの平面視において、吸収コア20の一部と重なってよい。厚さ方向Tにおいて吸収コア20と重ならない部分は、親水部であってよい。吸収コア20よりも非肌面側T2に位置する疎水部90は、厚さ方向Tの平面視において、吸収コア20の全領域と重なる場合、当該疎水部90は、排泄物が接触部62へ到達するために、開孔が形成されてよい。 疎 水 As shown in FIG. 12D, the hydrophobic portion 90 may be a core wrap 25 wrapping the absorbent core 20. The core wrap 25 may have a hydrophilic part 222 and a hydrophobic part 90 having hydrophilicity. The hydrophilic part 222 may be located on the skin surface side T1 with respect to the hydrophobic part 90. The hydrophobic portion 90 located on the non-skin side T2 with respect to the absorbent core 20 may overlap with a part of the absorbent core 20 in a plan view in the thickness direction T. A portion that does not overlap with the absorbent core 20 in the thickness direction T may be a hydrophilic portion. When the hydrophobic portion 90 located on the non-skin side T2 with respect to the absorbent core 20 overlaps with the entire region of the absorbent core 20 in a plan view in the thickness direction T, the hydrophobic portion 90 causes excrement to reach the contact portion 62. To reach, an aperture may be formed.
 図13Aに示すように、吸収性物品1は、着用者の排泄口に当接する排泄口当接部35を有してよい。トップシート30は、排泄口当接部35を有してよい。厚さ方向Tの平面視において、疎水部90は、表示部64よりも排泄口当接部35の中心35Cに近くてよい。疎水部90は、表示部64よりも排泄口当接部35の中心35Cに近いため、排泄口当接部35に排泄された排泄物が表示部64の方へ拡散する拡散経路上に、疎水部90が存在する。疎水部90は、排泄口当接部35から表示部64の方へ拡散する排泄物が表示部64に到達することを抑制できる。これにより、表示部64の視認性を確保することができ、着用者が正確な健康状態を把握し易くなる。 AAs shown in FIG. 13A, the absorbent article 1 may have an excretion port contact portion 35 that contacts the excretion port of the wearer. The top sheet 30 may have the excretion opening contact part 35. In a plan view in the thickness direction T, the hydrophobic portion 90 may be closer to the center 35 </ b> C of the excretion opening contact portion 35 than the display portion 64. Since the hydrophobic portion 90 is closer to the center 35C of the excretion port contact portion 35 than the display portion 64, the excrement discharged to the excretion port contact portion 35 is spread on the diffusion path for diffusing toward the display portion 64. There is a section 90. The hydrophobic part 90 can suppress the excrement diffused from the excretion opening contact part 35 toward the display part 64 from reaching the display part 64. Thereby, the visibility of the display unit 64 can be ensured, and the wearer can easily grasp the correct health condition.
 疎水部90は、表示部64の前後方向Lの内側表面に接触するように配置されてよく、表示部64よりも前後方向Lの外側には配置されてなくよい。 The hydrophobic portion 90 may be disposed so as to contact the inner surface of the display portion 64 in the front-rear direction L, and may not be disposed outside the display portion 64 in the front-rear direction L.
 図13Bに示すように、疎水部90は、表示部64に接触しないように配置されてよい。疎水部90は、表示部64から離して配置されることで、表示部64の近傍にまで排泄物が拡散することを抑制できる。これにより、表示部64の近傍に排泄物が到達し難くなり、着用者は、排泄物の色に惑わされ難くすることができる。 疎 水 As shown in FIG. 13B, the hydrophobic part 90 may be arranged so as not to contact the display part 64. By disposing the hydrophobic part 90 apart from the display part 64, it is possible to suppress the excrement from being diffused to the vicinity of the display part 64. This makes it difficult for the excrement to reach the vicinity of the display section 64, and the wearer can be less likely to be confused by the color of the excrement.
 図14A及び図14Bに示すように、吸収性物品1は、表示部64よりも肌面側T1に配置されている肌面側部材を有してよい。肌面側部材は、厚さ方向Tにおいて表示部64と重ならない領域であり、かつバックシート40側から視認可能である背景領域BRを有してよい。図14Aでは、肌面側部材は吸収コア20であり、図14Bでは、肌面側部材はトップシート30である。表示部64の色は、背景領域BRの色に対して色相差が色相環の角度で120度以上の色であってよい。これにより、背景領域BRの色によって、表示部64が強調されて視認される。従って、着用者は、表示部64を視認し易くなるため、正確な健康状態を把握し易くなる。 AAs shown in FIGS. 14A and 14B, the absorbent article 1 may include a skin-side member disposed on the skin-side T1 with respect to the display unit 64. The skin-side member may have a background region BR that is a region that does not overlap with the display unit 64 in the thickness direction T and that is visible from the back sheet 40 side. In FIG. 14A, the skin-side member is the absorbent core 20, and in FIG. 14B, the skin-side member is the topsheet 30. The color of the display unit 64 may be a color having a hue difference of 120 degrees or more in hue circle angle with respect to the color of the background region BR. Thereby, the display unit 64 is visually recognized by being emphasized by the color of the background region BR. Therefore, the wearer can easily visually recognize the display unit 64, and thus can easily grasp an accurate health condition.
 表示部64をより強調して視認できるように、表示部64の色は、背景領域BRの色に対して色相差が色相環の角度で165度以上の色であってよい。表示部64の色は、背景領域BRの色に対して色相差が色相環の角度で180度の色、すなわち、背景領域BRの補色であってよい。 The color of the display unit 64 may be a color having a hue difference of 165 degrees or more in the hue circle with respect to the color of the background region BR so that the display unit 64 can be visually emphasized. The color of the display section 64 may be a color having a hue difference of 180 degrees in the hue circle with respect to the color of the background area BR, that is, a color complementary to the background area BR.
 また、表示部64の色は、排泄物の色に対して色相差が色相環の角度で120度以上の色であってよい。これにより、排泄物の色によって、表示部が強調されて視認される。これにより、着用者は、表示部を視認し易くなるため、正確な健康状態を把握し易くなる。表示部64をより強調して視認できるように、表示部64の色は、排泄物の色に対して色相差が色相環の角度で165度以上の色であってよく、180度であってよい。 The color of the display section 64 may be a color having a hue difference of 120 degrees or more in the hue circle with respect to the color of the excrement. Thus, the display section is highlighted and visually recognized by the color of the excrement. This makes it easier for the wearer to visually recognize the display unit, so that the wearer can easily grasp the correct health condition. The color of the display portion 64 may be a color having a hue difference of 165 degrees or more in the hue circle angle with respect to the color of the excrement, and may be 180 degrees so that the display portion 64 can be visually emphasized. Good.
 なお、表示部64の色は、指示薬が呈色する前の色であってよい。これにより、着用者は、指示薬が呈色していない場合に、表示部64を容易に視認することができる。表示部64は、指示薬が呈色した後の少なくとも一部の色であってよい。これにより、着用者は、指示薬が呈色した場合に、表示部64(の少なくとも一部)を容易に視認することができる。 The color of the display unit 64 may be a color before the indicator is colored. Thus, the wearer can easily visually recognize the display unit 64 when the indicator is not colored. The display unit 64 may be at least a part of the color after the indicator is colored. Thereby, the wearer can easily visually recognize (at least a part of) the display unit 64 when the indicator is colored.
 また、表示部64の色と表示部64の周囲の色とが、同一色及び類似色でない(例えば、色相差が色相環の角度で45度以上の色である)場合、検査部材のうち少なくとも表示部64の周囲の色が、背景領域BRの色に対して色相差が色相環の角度で45度以下の色であってよい。これにより、表示部64の色を容易に視認することができ、当該表示部64を視認し易くなる。表示部64を除く検査部材60自体の色が、背景領域BRの色に対して色相差が色相環の角度で45度以下の色であってよい。 In addition, when the color of the display unit 64 and the color around the display unit 64 are not the same and similar colors (for example, the hue difference is a color of 45 degrees or more in the angle of the hue circle), at least one of the inspection members The color around the display unit 64 may be a color having a hue difference of 45 degrees or less as an angle of a hue circle with respect to the color of the background region BR. Thereby, the color of the display unit 64 can be easily visually recognized, and the display unit 64 can be easily visually recognized. The color of the inspection member 60 itself except for the display unit 64 may be a color having a hue difference of 45 degrees or less in hue circle angle with respect to the color of the background region BR.
 また、背景領域BRの色は、排泄物の色に対して色相差が色相環の角度で45度以下の色であってよい。排泄物が肌面側部材に浸透したとしても、背景領域の色は、排泄物の色に対して色相差が3以下の色であるため、排泄物が目立たなくなる。これにより、着用者は、排泄物の色に惑わされずに、表示部64を視認し易くなるため、正確な健康状態を把握し易くなる。表示部64をより視認し易くするために、背景領域BRの色は、排泄物の色に対して色相差が1以下の色であってよく、背景領域BRの色は、排泄物と同じ色であってよい。排泄物をより目立たせなくするために、背景領域BRの色は、排泄物の色に対して色相差が色相環の角度で30度以下の色であってよく、15度以下の色であってよい。背景領域BRの色は、排泄物の色と同一の色(すなわち、色相環の角度で0度)であってよい。 The color of the background area BR may be a color having a hue difference of 45 degrees or less in terms of the hue circle with respect to the color of the excrement. Even if the excrement permeates the skin-side member, the color of the background area is a color having a hue difference of 3 or less with respect to the color of the excrement, so that the excrement is inconspicuous. This makes it easier for the wearer to visually recognize the display section 64 without being confused by the color of the excrement, and thus to easily grasp the correct health condition. In order to make the display unit 64 more easily recognizable, the color of the background area BR may be a color having a hue difference of 1 or less with respect to the color of the excrement, and the color of the background area BR is the same color as the excrement. It may be. In order to make the excrement less noticeable, the color of the background area BR may be a color having a hue difference of 30 degrees or less and a color of 15 degrees or less with respect to the color of the excrement in a hue circle angle. May be. The color of the background area BR may be the same color as the color of the excrement (that is, 0 degrees in the hue circle).
 また、検査部材のうち少なくとも表示部64の周囲の色が、背景領域BRの色に対して色相差が色相環の角度で120度以上の色であってよい。これにより、表示部64の周囲の色を容易に視認することができ、当該表示部64を視認し易くなる。検査部材のうち少なくとも表示部64の周囲の色が、背景領域BRの色に対して色相差が色相環の角度で165度以上の色であってよく、180度であってよい。また、検査部材60自体の色が、背景領域BRの色に対して色相差が色相環の角度で120度以上の色であってよく、165度以上の色であってよく、180度であってよい。 (4) At least the color of the display member 64 around the inspection member may be a color having a hue difference of 120 degrees or more in hue circle angle with respect to the color of the background region BR. Accordingly, the color around the display unit 64 can be easily visually recognized, and the display unit 64 can be easily visually recognized. At least the color around the display unit 64 of the inspection member may be a color having a hue difference of 165 degrees or more in the hue circle angle with respect to the color of the background area BR, and may be 180 degrees. In addition, the color of the inspection member 60 itself may be a color having a hue difference of 120 degrees or more, a color of 165 degrees or more, or 180 degrees with respect to the color of the background area BR in a hue circle angle. May be.
 検査部材のうち少なくとも表示部64の周囲の色が、排泄物の色に対して色相差が色相環の角度で120度以上の色であってよい。これにより、肌面側部材に排泄物が浸透したとしても、表示部64の周囲の色を容易に視認することができ、当該表示部64を視認し易くなる。検査部材のうち少なくとも表示部64の周囲の色が、背景領域BRの色に対して色相差が色相環の角度で165度以上の色であってよく、180度であってよい。また、検査部材60自体の色が、排泄物の色に対して色相差が色相環の角度で120度以上の色であってよく、165度以上の色であってよく、180度であってよい。 (4) The color of at least the periphery of the display unit 64 in the inspection member may be a color having a hue difference of 120 degrees or more in the hue circle with respect to the color of the excrement. Thereby, even if excrement permeates into the skin side member, the color around the display section 64 can be easily visually recognized, and the display section 64 can be easily visually recognized. The color of at least the periphery of the display unit 64 in the inspection member may be a color having a hue difference of 165 degrees or more in the hue circle with respect to the color of the background region BR, and may be 180 degrees. In addition, the color of the inspection member 60 itself may be a color having a hue difference of 120 degrees or more, a color of 165 degrees or more, or 180 degrees with respect to the color of the excrement in a hue circle angle. Good.
 表示部64の周囲の色(又は表示部64以外の検査部材60自体の色)が白色であり、表示部64の色(呈色前の色又は呈色後の色)が赤色であり、背景領域BRの色が黒色であってよい。白色は明度が高く、黒色は明度が低いため、背景が黒色に対して、表示部64の周囲の白色が良く映え、表示部64の赤色が明瞭に視認することができる。このように、明度差により目立たせ易くするために、例えば、視認したい部分(表示部64、表示部64の周囲など)とそれ以外の領域(背景領域BR、排泄物など)との明度差が125以上であってよい。明度(差)は、「((Rの値 X  299)  + (Gの値X  587)  + (Bの値 X  114)) /  1000」を用いて算出できる。なお、色相差は、一般的な測定方法により測定できる。例えば、「マンセル色相環」「PCCS色相環」などの色相環を用いることにより、色相差を測定できる。例えば、PCCS色相環において、表示部64の色との色相が8以上の色は、表示部64の色からの角度が120度以上である。表示部64の色との色相差が11以上の色は、表示部64の色からの角度が165度以上であり、表示部64の色との色相差が12の色は、表示部64の色からの角度が180度(すなわち、補色)である。 The color around the display unit 64 (or the color of the inspection member 60 itself other than the display unit 64) is white, the color of the display unit 64 (the color before or after the coloration) is red, and the background The color of the region BR may be black. Since white has a high lightness and black has a low lightness, the white surrounding the display unit 64 is better illuminated against the black background, and the red color of the display unit 64 can be clearly recognized. As described above, in order to make the lightness difference more conspicuous, for example, the lightness difference between the part to be visually recognized (the display unit 64, the periphery of the display unit 64, etc.) and the other region (the background region BR, excrement, etc.) It may be 125 or more. The lightness (difference) can be calculated using “((R value X 299) + (G value X 587) + (B value X 114)) / 1000”. The hue difference can be measured by a general measuring method. For example, a hue difference can be measured by using a hue circle such as “Munsell hue circle” or “PCCS hue circle”. For example, in the PCCS hue circle, a color having a hue of 8 or more with the color of the display unit 64 has an angle of 120 degrees or more from the color of the display unit 64. A color having a hue difference of 11 or more from the color of the display unit 64 has an angle of 165 degrees or more from the color of the display unit 64, and a color having a hue difference of 12 from the color of the display unit 64 is a color of the display unit 64. The angle from the color is 180 degrees (that is, the complementary color).
 図15に示すように、表示部64の少なくとも一部は、厚さ方向Tにおいて一対のウイング14の一方に配置されてよい。ウイング14は、着用物品100(例えば、下着)に装着された状態において着用物品100の非肌面側T2に固定されるため、肌面側T1から排泄される排泄物は、ウイング14に付着し難い。これにより、表示部64の少なくとも一部が排泄物に覆われ難くなり、着用者は、排泄物の影響を受けずに表示部64を視認し易くなる。 As shown in FIG. 15, at least a part of the display unit 64 may be arranged on one of the pair of wings 14 in the thickness direction T. Since the wing 14 is fixed to the non-skin side T2 of the wearing article 100 in a state where the wing 14 is attached to the wearing article 100 (for example, underwear), excrement excreted from the skin side T1 adheres to the wing 14. hard. This makes it difficult for at least a part of the display unit 64 to be covered with excrement, and makes it easier for the wearer to visually recognize the display unit 64 without being affected by the excrement.
 図15において、疎水部90は、表示部64の肌面側T1の表面に配置されている。表示部64の少なくとも一部はウイング14に配置されているため、表示部64及び疎水部90は、到達範囲に配置されなくてもよい。また、表示部64及び疎水部90が、一般的な使用において、排泄物が到達する範囲に配置されていない場合であっても、想定外の着用者の動きによって、排泄物が表示部64にまで到達することがある。このような場合であっても、排泄物が延長領域に配置されている疎水部90によって表示部64に到達することを抑制し易い。 に お い て In FIG. 15, the hydrophobic portion 90 is arranged on the surface of the display portion 64 on the skin surface side T1. Since at least a part of the display unit 64 is disposed on the wing 14, the display unit 64 and the hydrophobic unit 90 need not be disposed in the reach. In addition, even when the display unit 64 and the hydrophobic unit 90 are not arranged in a range where the excrement reaches in general use, the excrement is displayed on the display unit 64 due to unexpected movement of the wearer. May be reached. Even in such a case, it is easy to suppress the excrement from reaching the display part 64 by the hydrophobic part 90 arranged in the extension area.
 (6)その他実施形態
 以上、上述の実施形態を用いて本発明について詳細に説明したが、当業者にとっては、本発明が本明細書中に説明した実施形態に限定されるものではないということは明らかである。本発明は、特許請求の範囲の記載により定まる本発明の趣旨及び範囲を逸脱することなく修正及び変更態様として実施することができる。したがって、本明細書の記載は、例示説明を目的とするものであり、本発明に対して何ら制限的な意味を有するものではない。
(6) Other Embodiments As described above, the present invention has been described in detail with reference to the above embodiments. However, for those skilled in the art, the present invention is not limited to the embodiments described in this specification. Is clear. The present invention can be implemented as modified and changed aspects without departing from the spirit and scope of the present invention defined by the description of the claims. Therefore, the description in this specification is for the purpose of illustrative explanation, and has no restrictive meaning to the present invention.
 上述の第1実施形態において、バックシート40は、透明性を有してもよい。バックシート40は、上述のトップシート30と同様の透明性を有してよい。これにより、着用者は、バックシート40側からバックシート40を介して検査部材60の呈色を視認可能であってよい。 In the first embodiment described above, the back sheet 40 may have transparency. The back sheet 40 may have the same transparency as the above-described top sheet 30. Thereby, the wearer may be able to visually recognize the coloration of the inspection member 60 from the back sheet 40 side via the back sheet 40.
 上述の第1実施形態において、表示部64が露出しており、接触部62が露出していなかったが、これに限られない。接触部62が露出してもよい。接触部62と表示部64とが異なる場合(例えば、イムノクロマト法を用いた検査部材60)において、吸収領域ARにおいて、接触部62の少なくとも一部がトップシート30よりも肌面側T1に配置されてもよい。イムノクロマト法を用いた検査部材60では、接触部62は、指示薬を含まない。このため、接触部62が着用者の肌に触れたとしても、着用者の肌にダメージを与える虞がない。さらに、接触部62へ排泄物Eを直接接触可能であるため、指示薬が多くの検出対象に基づいて呈色可能となり、検査精度を向上できる。また、表示部64の少なくとも一部は、トップシート30(及び/又はサイドシート50)よりも非肌面側T2に配置されてもよい。これにより、表示部64に含まれる指示薬が肌に直接触れることを抑制できるため、着用者の安全性を高めることができる。 表示 In the above-described first embodiment, the display unit 64 is exposed and the contact unit 62 is not exposed. However, the present invention is not limited to this. The contact portion 62 may be exposed. When the contact part 62 and the display part 64 are different (for example, the inspection member 60 using the immunochromatography method), at least a part of the contact part 62 is arranged on the skin side T1 with respect to the top sheet 30 in the absorption region AR. You may. In the inspection member 60 using the immunochromatography method, the contact portion 62 does not contain the indicator. For this reason, even if the contact portion 62 touches the skin of the wearer, there is no possibility of damaging the skin of the wearer. Furthermore, since the excrement E can be brought into direct contact with the contact portion 62, the indicator can be colored based on many detection targets, and the inspection accuracy can be improved. Further, at least a part of the display unit 64 may be disposed on the non-skin side T2 with respect to the top sheet 30 (and / or the side sheet 50). Thereby, since the indicator contained in the display unit 64 can be prevented from directly touching the skin, the safety of the wearer can be improved.
 一方、接触部62と表示部64とが同じである場合(例えば、試験紙法を用いた検査部材60)において、上述したように、検査部材60がトップシート30よりも非肌面側T2に配置されてよい。これにより、指示薬が肌へ刺激を与え得るものであっても、着用者の肌に指示薬が触れ難くなり、着用者の安全性を高めることができる。 On the other hand, when the contact portion 62 and the display portion 64 are the same (for example, the inspection member 60 using the test paper method), as described above, the inspection member 60 is closer to the non-skin side T2 than the top sheet 30. May be arranged. This makes it difficult for the indicator to touch the wearer's skin, even if the indicator can stimulate the skin, thereby improving the safety of the wearer.
 上述の第2実施形態において、バックシート40の全面が透明性を有する例を挙げて説明したが、これに限られない。バックシート40は、厚さ方向Tにおいて、表示部64と重なる領域が透明性を有してよい。バックシート40のその他の部分は、透明性を有さなくてよい。バックシート40としての不織布の一部の領域に上述したエンボス処理を施すことにより、バックシート40の一部のみが透明性を有するようにしてもよい。これにより、また、不織布独特の柔らかな肌触りにより、使用者(着用者)に安心感を与えることができる。 In the above-described second embodiment, an example in which the entire surface of the back sheet 40 is transparent has been described, but the present invention is not limited to this. In the back sheet 40, in the thickness direction T, a region overlapping with the display unit 64 may have transparency. Other parts of the back sheet 40 may not have transparency. By performing the above-described embossing process on a part of the nonwoven fabric as the backsheet 40, only a part of the backsheet 40 may have transparency. Thereby, the user (wearer) can be given a sense of security by the soft touch unique to the nonwoven fabric.
 上述において、厚さ方向Tにおける表示部64の表面に疎水部90が接触していたが、これに限られない。例えば、疎水部90は、表示部64から厚さ方向Tに離れた位置に配置されてもよい。 In the above description, the hydrophobic portion 90 is in contact with the surface of the display portion 64 in the thickness direction T, but is not limited to this. For example, the hydrophobic part 90 may be arranged at a position separated from the display part 64 in the thickness direction T.
 上述において、吸収性物品1は、排泄物を表示部64に到達させ難くするために、排泄物を引き込みやすい誘導部を有してよい。誘導部が、排泄物を引き込むことで、表示部64にまで排泄物が到達し難くなる。誘導部は、接触部62の近傍に配置されてよく、接触部62に接触するように配置されてよい。 In the above description, the absorbent article 1 may have a guiding portion that makes it easy to draw in the excrement in order to make it difficult for the excrement to reach the display section 64. When the guiding unit draws in the excrement, it is difficult for the excrement to reach the display unit 64. The guide portion may be arranged near the contact portion 62 or may be arranged to contact the contact portion 62.
 上述の第1及び第2実施形態では、検査部材60は、直線状の板状であった。本実施形態では、検査部材60は、例えば、1以上の折り目を有してよい。従って、検査部材60は、例えば、2つ折り又は3つ折りの形状であってよい。検査部材60は、Z型に折り畳まれた部材により構成されてよい。これにより、検査部材60をコンパクトな状態で、吸収性物品1の内部へ配置することができる。検査部材60の面積が小さくなるため、検査部材60による着用者の肌触りの悪化を抑制し易くすることができる。 In the above-described first and second embodiments, the inspection member 60 has a linear plate shape. In the present embodiment, the inspection member 60 may have, for example, one or more folds. Therefore, the inspection member 60 may have, for example, a two-fold or three-fold shape. The inspection member 60 may be configured by a member folded into a Z shape. Thereby, the inspection member 60 can be arranged inside the absorbent article 1 in a compact state. Since the area of the inspection member 60 is reduced, deterioration of the touch of the wearer by the inspection member 60 can be easily suppressed.
 また、検査部材60は、接触部62の少なくとも一部が検査部材60以外の他の部材に当接する(すなわち、接触部62の少なくとも一部が他の部材と対向する)ように折られた状態で、配置されてよい。これにより、検査部材60が折られていても、接触部62に排泄物を到達し易くすることができる。 In addition, the inspection member 60 is folded so that at least a part of the contact portion 62 contacts another member other than the inspection member 60 (that is, at least a part of the contact portion 62 faces another member). And may be arranged. Thereby, even if the inspection member 60 is folded, the excrement can easily reach the contact portion 62.
 また、検査部材60は、表示部64の少なくとも一部が検査部材60以外の他の部材に当接する(すなわち、表示部64の少なくとも一部が他の部材と対向する)ように折られた状態で、配置されてよい。これにより、検査部材60が折られていても、着用者は、表示部64を視認し易くすることができる。 The inspection member 60 is folded so that at least a part of the display unit 64 abuts on another member other than the inspection member 60 (that is, at least a part of the display unit 64 faces another member). And may be arranged. Thereby, even if the inspection member 60 is folded, the wearer can easily visually recognize the display unit 64.
 なお、着用者は、表示部64の呈色を示す呈色情報(画像情報及び/又は映像情報)をネットワーク(管理サーバ)へ送ることで、検査情報を取得してもよい。例えば、着用者は、露出した表示部64を、例えば、着用者(ユーザ)が所有する通信装置に内蔵されたカメラにより撮影することで呈色情報を取得してもよい。着用者は、呈色情報を通信装置を介して管理サーバへ送ることができる。着用者は、呈色情報と共に着用者の情報を示すユーザ情報を送ってもよい。ユーザ情報は、例えば、ユーザの識別子、通信装置の識別子、排泄物の種類を示す情報、吸収性物品1(検査部材60)の種類を示す情報、検出対象を特定する情報などの少なくともいずれかである。 Note that the wearer may acquire the test information by sending color information (image information and / or video information) indicating the color of the display unit 64 to a network (management server). For example, the wearer may acquire the color information by photographing the exposed display unit 64 with a camera built in a communication device owned by the wearer (user), for example. The wearer can send the color information to the management server via the communication device. The wearer may send user information indicating the wearer's information together with the coloration information. The user information is, for example, at least one of a user identifier, a communication device identifier, information indicating the type of excrement, information indicating the type of the absorbent article 1 (inspection member 60), information specifying a detection target, and the like. is there.
 また、着用者は、検査部材60を含む吸収性物品1又は検査部材60そのものを、指示薬による呈色反応を検知可能である収容装置へ収容してよい。収容装置は、呈色反応を検知するために、可視光を表示部64へ照射してよい。収容装置は、可視光と異なる特殊な波長を有する特殊光(例えば、可視光よりも短い波長を有する紫外線)を照射することで指示薬による呈色を確認できる検査部材60に対して、当該特殊な波長を有する光を表示部64へ照射してよい。収容装置は、収容装置内において、可視光又は特殊光を照射しながら撮影することで呈色情報を取得してもよい。このように、収容装置内で、光を照射しながら表示部64を撮影することで、周囲の環境の影響を受けずに、正確に呈色を確認することができる。 着 用 Moreover, the wearer may house the absorbent article 1 including the inspection member 60 or the inspection member 60 itself in an accommodation device capable of detecting a color reaction by the indicator. The storage device may irradiate the display unit 64 with visible light to detect a color reaction. The storage device irradiates special light having a special wavelength different from visible light (for example, ultraviolet light having a shorter wavelength than visible light) to the inspection member 60 capable of confirming coloration by the indicator, and Light having a wavelength may be applied to the display unit 64. The accommodation device may acquire the color information by photographing while irradiating visible light or special light in the accommodation device. As described above, by photographing the display unit 64 while irradiating light in the housing device, it is possible to accurately confirm the coloration without being affected by the surrounding environment.
 収容装置は、表示部64を撮影することにより取得した呈色情報をネットワーク(管理サーバ)へ送ってもよい。この場合、収容装置は、ユーザ情報として、収容装置の識別子を含めてもよい。また、収容装置は、取得した呈色情報を着用者が所有する通信装置へ送ってもよい。着用者は、表示部64を通信装置へ表示することによって、呈色の有無を判定してもよい。これにより、着用者は、より正確に健康状態を確認できる。なお、着用者は、上述と同様に、収容装置から取得した呈色情報を通信装置を介してネットワークへ送ってもよい。 The accommodation device may send the color information acquired by photographing the display unit 64 to a network (management server). In this case, the accommodation device may include the identifier of the accommodation device as the user information. Further, the housing device may send the acquired color information to the communication device owned by the wearer. The wearer may determine the presence or absence of coloration by displaying the display unit 64 on the communication device. Thereby, the wearer can check the health condition more accurately. The wearer may send the color information acquired from the housing device to the network via the communication device, as described above.
 管理サーバは、呈色情報(及びユーザ情報)に基づいて、着用者(ユーザ)の健康状態を判定することができる。管理サーバは、判定結果を示す情報を呈色情報の送信元である通信装置へ送信してもよい。管理サーバは、判定結果を示す判定情報と共に、判定結果に基づくアドバイスを示すアドバイス情報を当該通信装置へ送信してもよい。管理サーバは、収容装置から呈色情報を受け取った場合であっても、収容装置の識別子と関連付けられている通信装置の識別子(ユーザの識別子)に基づいて、関連付けられている通信装置(すなわち、ユーザが所有する通信装置)へ判定情報(及びアドバイス情報)を送信してもよい。 The management server can determine the health condition of the wearer (user) based on the coloration information (and the user information). The management server may transmit the information indicating the determination result to the communication device that is the transmission source of the color information. The management server may transmit, to the communication device, advice information indicating advice based on the determination result, together with the determination information indicating the determination result. Even when the management server receives the color information from the accommodation device, the management server determines the associated communication device (that is, the identifier of the user) based on the identifier of the communication device (user identifier) associated with the identifier of the accommodation device. The determination information (and the advice information) may be transmitted to the communication device owned by the user.
 通信装置は、通信装置により受信した判定情報に基づいて、判定結果を表示してよい。これにより、着用者は、表示された判定結果によって健康状態を把握することができる。着用者は、着用者自身の判定によるものではなく、客観的な判定結果を取得できる。また、通信装置は、アドバイス情報を受信した場合には、アドバイスを表示してよい。これにより、着用者は、アドバイスを把握することができる。 The communication device may display the determination result based on the determination information received by the communication device. Thereby, the wearer can grasp the health condition based on the displayed determination result. The wearer can obtain an objective determination result, not based on the wearer's own determination. Further, when receiving the advice information, the communication device may display the advice. Thereby, the wearer can grasp the advice.
 通信装置は、上述した各種の処理を実行するためのプログラムを有する。通信装置は、プログラムを記憶するメモリ及びメモリに記憶されたプログラムを実行するプロセッサを有する。プログラムは、ネットワーク(例えば、管理サーバ)から取得可能であってよい。 The communication device has a program for executing the above-described various processes. The communication device has a memory for storing a program and a processor for executing the program stored in the memory. The program may be obtainable from a network (for example, a management server).
 上述の実施の形態では、吸収性物品1は、生理用ナプキンであったが、これに限られない。吸収性物品1は、例えば、テープ型又はパンツ型の使い捨ておむつであってよい。 で は In the above-described embodiment, the absorbent article 1 is a sanitary napkin, but is not limited thereto. The absorbent article 1 may be, for example, a tape-type or pants-type disposable diaper.
 上述の各実施形態において、中央域S3は、着用者の脚回りに配置される脚回り開口部が設けられた領域であってよい。脚回り開口部は、幅方向の内側に向かうにつれ、吸収性物品の外側縁から幅方向の内側に凹む部分である。或いは、吸収性物品1が、吸収コアを含む場合、中央域S3は、幅方向の内側に向かうにつれ、吸収コアの外側縁から幅方向の内側に凹む部分が設けられる領域であってよい。或いは、中央域S3は、周囲の吸収コアよりも厚い領域である中高部が配置されている領域であってよい。或いは、吸収性物品1は、例えば、吸収性物品1を前後方向Lに3等分に分けるように、前側域S1、後側域S2、中央域S3を有してよい。 In each of the above-described embodiments, the central region S3 may be a region provided with a leg-hole opening disposed around the wearer's leg. The leg opening is a portion that is recessed inward in the width direction from the outer edge of the absorbent article toward the inside in the width direction. Alternatively, when the absorbent article 1 includes an absorbent core, the central region S3 may be a region in which a portion that is recessed inward in the width direction from the outer edge of the absorbent core is provided toward the inside in the width direction. Alternatively, the central region S3 may be a region where the middle and high portions, which are regions thicker than the surrounding absorbent cores, are arranged. Alternatively, the absorbent article 1 may have, for example, a front side area S1, a rear side area S2, and a central area S3 so that the absorbent article 1 is divided into three equal parts in the front-rear direction L.
 上述において説明した各実施形態及び各変更例は、適宜組み合わされてよいことは勿論である。 各 Of course, each embodiment and each modified example described above may be appropriately combined.
 なお、日本国特許出願第2018-148035号(2018年8月6日出願)及び日本国特許出願第2018-148036号(2018年8月6日出願)の全内容が、参照により、本願明細書に組み込まれている。 The entire contents of Japanese Patent Application No. 2018-148035 (filed on August 6, 2018) and Japanese Patent Application No. 2018-148036 (filed on August 6, 2018) are incorporated herein by reference. Built in.

Claims (20)

  1.  吸収性物品であって、
     前後方向と、前記前後方向に直交する幅方向と、前記前後方向及び前記幅方向に直交する厚さ方向と、
     吸収材料を含む吸収コアと、
     前記吸収コアよりも肌面側に配置され、かつ前記厚さ方向において前記吸収コアと重なる吸収領域を有するトップシートと、
     着用者の健康状態を検査するための検査部材と、を備え、
     前記検査部材は、
      前記着用者の排泄物を接触させる接触部と、
      前記着用者の健康状態を表示する表示部と、を有し、
     前記表示部は、前記接触部に接触した前記排泄物に含まれる検出対象に基づいて呈色する指示薬を含み、
     前記接触部の少なくとも一部は、前記吸収領域に排泄された排泄物が到達する範囲に配置されており、
     前記表示部の少なくとも一部は、前記吸収コアと前記厚さ方向において重ならない、吸収性物品。
    An absorbent article,
    The front-rear direction, a width direction orthogonal to the front-rear direction, and a thickness direction orthogonal to the front-rear direction and the width direction,
    An absorbent core comprising an absorbent material;
    A top sheet having an absorption region that is arranged on the skin surface side of the absorbent core and overlaps with the absorbent core in the thickness direction,
    And an inspection member for inspecting a wearer's health condition,
    The inspection member,
    A contact portion for contacting the wearer's excrement,
    A display unit that displays the health condition of the wearer,
    The display unit includes an indicator that changes color based on a detection target included in the excrement contacted with the contact unit,
    At least a part of the contact portion is arranged in a range where the excreta excreted in the absorption region reaches,
    An absorbent article, wherein at least a part of the display unit does not overlap with the absorbent core in the thickness direction.
  2.  前記接触部の少なくとも一部は、前記吸収コアと接触する請求項1に記載の吸収性物品。 吸収 The absorbent article according to claim 1, wherein at least a part of the contact portion contacts the absorbent core.
  3.  前記接触部の少なくとも一部は、前記厚さ方向において前記吸収コアと重なる請求項2に記載の吸収性物品。 The absorbent article according to claim 2, wherein at least a part of the contact portion overlaps the absorbent core in the thickness direction.
  4.  前記排泄物を前記接触部の少なくとも一部へ誘導する誘導部を有する請求項1から3のいずれか1項に記載の吸収性物品。 The absorbent article according to any one of claims 1 to 3, further comprising a guide portion for guiding the excrement to at least a part of the contact portion.
  5.  前記吸収コアを有する本体部と、
     前記本体部から前記幅方向の外側に延出し、着用物品に装着された状態において前記着用物品の非肌面側に固定される一対のウイングと、を有し、
     前記表示部の少なくとも一部は、前記厚さ方向において前記一対のウイングの一方に配置されている請求項1から4のいずれか1項に記載の吸収性物品。
    A main body having the absorbent core,
    A pair of wings extending from the main body portion to the outside in the width direction and fixed to a non-skin side of the wearing article in a state of being attached to the wearing article,
    The absorbent article according to any one of claims 1 to 4, wherein at least a part of the display unit is arranged on one of the pair of wings in the thickness direction.
  6.  前記厚さ方向の平面視において、前記表示部の少なくとも一部は、前記吸収コアの前記前後方向の外端縁から延出している請求項1から4のいずれか1項に記載の吸収性物品。 The absorptive article according to any one of claims 1 to 4, wherein at least a part of the display unit extends from an outer edge of the absorbent core in the front-rear direction in a plan view in the thickness direction. .
  7.  前記検査部材以外の部材により構成される吸収性物品本体を有し、
     前記厚さ方向の平面視において、前記表示部の少なくとも一部は、前記吸収性物品本体の外端縁から延出している請求項1から6のいずれか1項に記載の吸収性物品。
    Having an absorbent article body constituted by members other than the inspection member,
    The absorbent article according to any one of claims 1 to 6, wherein in a plan view in the thickness direction, at least a part of the display section extends from an outer edge of the absorbent article body.
  8.  前記検出対象が互いに異なる複数の検査部材を有し、
     前記複数の検査部材それぞれが有する前記表示部は、前記厚さ方向において互いに異なる位置に配置されている請求項1から7のいずれか1項に記載の吸収性物品。
    The detection target has a plurality of inspection members different from each other,
    The absorbent article according to any one of claims 1 to 7, wherein the display units included in the plurality of inspection members are arranged at positions different from each other in the thickness direction.
  9.  前記検査部材は、前記トップシートよりも非肌面側に配置されている請求項1から8のいずれか1項に記載の吸収性物品。 吸収 The absorbent article according to any one of claims 1 to 8, wherein the inspection member is arranged on a non-skin side than the top sheet.
  10.  前記接触部は、前記吸収コアよりも非肌面側に配置されており、
     前記吸収コアは、前記厚さ方向において前記吸収コアを貫通する開孔を有し、
     前記接触部は、前記厚さ方向において前記開孔と重ならない請求項1から9のいずれか1項に記載の吸収性物品。
    The contact portion is arranged on the non-skin side than the absorbent core,
    The absorbent core has an opening penetrating the absorbent core in the thickness direction,
    The absorbent article according to any one of claims 1 to 9, wherein the contact portion does not overlap with the opening in the thickness direction.
  11.  吸収性物品であって、
     前後方向と、前記前後方向に直交する幅方向と、前記前後方向及び前記幅方向に直交する厚さ方向と、前記前後方向及び前記幅方向に平行である水平方向と、
     吸収材料を含む吸収コアと、
     前記吸収コアよりも非肌面側に配置されているバックシートと、
     着用者の健康状態を検査するための検査部材と、を備え、
     前記検査部材は、前記厚さ方向において前記バックシートよりも肌面側に配置されており、
     前記検査部材は、排泄物に含まれる検出対象に基づいて呈色する指示薬を含む表示部を有し、
     前記表示部は、前記バックシート側から視認可能であり、
     前記バックシートよりも肌面側において、前記表示部から前記厚さ方向及び前記水平方向へ延びる延長領域に、疎水性を有する疎水部が配置されている、吸収性物品。
    An absorbent article,
    The front-rear direction, a width direction orthogonal to the front-rear direction, a thickness direction orthogonal to the front-rear direction and the width direction, and a horizontal direction parallel to the front-rear direction and the width direction,
    An absorbent core comprising an absorbent material;
    A back sheet that is arranged on the non-skin side than the absorbent core,
    And an inspection member for inspecting a wearer's health condition,
    The inspection member is disposed closer to the skin surface than the back sheet in the thickness direction,
    The inspection member has a display unit including an indicator that changes color based on a detection target included in excrement,
    The display unit is visible from the back sheet side,
    An absorbent article, wherein a hydrophobic portion having hydrophobicity is arranged in an extension region extending from the display portion in the thickness direction and the horizontal direction on the skin surface side of the back sheet.
  12.  前記吸収コアよりも肌面側に配置され、かつ前記厚さ方向において前記吸収コアと重なる吸収領域を有するトップシートを有し、
     前記延長領域に配置されている前記疎水部は、前記吸収領域に排泄された排泄物が到達する範囲に配置されている請求項11に記載の吸収性物品。
    A top sheet having an absorption region that is arranged on the skin surface side of the absorbent core and overlaps the absorbent core in the thickness direction,
    The absorbent article according to claim 11, wherein the hydrophobic part disposed in the extension region is disposed in a range where excretion discharged in the absorption region reaches.
  13.  前記疎水部は、前記表示部と接触している請求項11又は12に記載の吸収性物品。 The absorbent article according to claim 11, wherein the hydrophobic part is in contact with the display part.
  14.  前記疎水部は、前記表示部の肌面側の表面と接触している請求項13に記載の吸収性物品。 The absorbent article according to claim 13, wherein the hydrophobic portion is in contact with the surface of the display portion on the skin side.
  15.  前記疎水部は、前記表示部の非肌面側の表面と接触している請求項13又は14に記載の吸収性物品。 The absorbent article according to claim 13 or 14, wherein the hydrophobic portion is in contact with a surface on the non-skin side of the display portion.
  16.  前記厚さ方向において、前記吸収コアと前記バックシートとの間に前記検査部材が配置されており、
     前記厚さ方向において、前記吸収コアと前記表示部との間にシート状のシート部材が、前記疎水部として配置されている請求項11から15のいずれか1項に記載の吸収性物品。
    In the thickness direction, the inspection member is disposed between the absorbent core and the back sheet,
    The absorbent article according to any one of claims 11 to 15, wherein a sheet-like sheet member is disposed as the hydrophobic part between the absorbent core and the display part in the thickness direction.
  17.  前記着用者の排泄口に当接する排泄口当接部を有し、
     前記厚さ方向の平面視において、前記疎水部は、前記表示部よりも前記排泄口当接部の中心に近い請求項11から16のいずれか1項に記載の吸収性物品。
    Having an excretion port abutting portion that contacts the excretion port of the wearer,
    The absorbent article according to any one of claims 11 to 16, wherein in a plan view in the thickness direction, the hydrophobic portion is closer to the center of the excretion opening contact portion than the display portion.
  18.  前記表示部よりも肌面側に配置されている肌面側部材を有し、
     前記肌面側部材は、前記厚さ方向において前記表示部と重ならない領域であり、かつ前記バックシート側から視認可能である背景領域を有し、
     前記表示部の色は、前記背景領域の色に対して色相差が色相環の角度で120度以上の色である請求項11から17のいずれか1項に記載の吸収性物品。
    Having a skin-side member disposed on the skin side relative to the display unit,
    The skin-side member is a region that does not overlap with the display unit in the thickness direction, and has a background region that is visible from the back sheet side.
    The absorptive article according to any one of claims 11 to 17, wherein the color of the display section is a color having a hue difference of 120 degrees or more in hue circle angle with respect to the color of the background area.
  19.  前記表示部の色は、前記排泄物の色に対して色相差が色相環の角度で120度以上の色である請求項11から18のいずれか1項に記載の吸収性物品。 19. The absorbent article according to any one of claims 11 to 18, wherein the color of the display unit is a color having a hue difference of 120 degrees or more in hue circle angle with respect to the color of the excrement.
  20.  前記表示部よりも肌面側に配置されている肌面側部材を有し、
     前記肌面側部材は、前記厚さ方向において前記表示部と重ならない領域であり、かつ前記バックシート側から視認可能である背景領域を有し、
     前記背景領域の色は、前記排泄物の色に対して色相差が色相環の角度で45度以下の色である請求項11から19のいずれか1項に記載の吸収性物品。
    Having a skin-side member disposed on the skin side relative to the display unit,
    The skin-side member is a region that does not overlap with the display unit in the thickness direction, and has a background region that is visible from the back sheet side.
    The absorbent article according to any one of claims 11 to 19, wherein the color of the background region is a color having a hue difference of 45 degrees or less in hue circle angle with respect to the color of the excrement.
PCT/JP2019/030997 2018-08-06 2019-08-06 Absorbent article WO2020032069A1 (en)

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JP7353528B1 (en) 2022-07-28 2023-09-29 ユニ・チャーム株式会社 absorbent articles

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