WO2018010668A1 - 吸湿用品 - Google Patents

吸湿用品 Download PDF

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Publication number
WO2018010668A1
WO2018010668A1 PCT/CN2017/092699 CN2017092699W WO2018010668A1 WO 2018010668 A1 WO2018010668 A1 WO 2018010668A1 CN 2017092699 W CN2017092699 W CN 2017092699W WO 2018010668 A1 WO2018010668 A1 WO 2018010668A1
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WIPO (PCT)
Prior art keywords
layer
detecting
detect
detection reagent
reagent
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PCT/CN2017/092699
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English (en)
French (fr)
Inventor
谢锡佳
杨国溜
利莉
蔡光合
陈宗哲
Original Assignee
广东茵茵股份有限公司
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Publication of WO2018010668A1 publication Critical patent/WO2018010668A1/zh

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    • 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
    • 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
    • A61F13/45Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the shape
    • A61F13/47Sanitary towels, incontinence pads or napkins
    • 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
    • A61F13/45Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the shape
    • A61F13/49Absorbent articles specially adapted to be worn around the waist, e.g. diapers
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/75Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated
    • G01N21/77Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator
    • G01N21/78Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator producing a change of colour
    • G01N21/80Indicating pH value
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing

Definitions

  • the present disclosure relates to the technical field of disposable absorbent articles, for example, to an absorbent article.
  • Disposable absorbent articles such as diapers, are primarily used to receive and contain excrement such as urine and feces to protect the garment from dirt. Most of the construction of disposable absorbent articles includes a permeable layer, a barrier layer, and an absorbent layer. With the continuous development of the industry, the comfort of use of disposable absorbent articles has gradually improved, and there has been great progress in antibacterial and odor removal, but the functions are relatively simple.
  • the present disclosure provides an absorbent article which is capable of detecting human body parameters in daily life by providing a detecting reagent on the absorbent article, and initially identifying whether the human body parameter is abnormal or whether the human body is damaged.
  • An absorbent article comprising a permeable layer, a barrier layer and an absorbing layer, the absorbing layer being disposed between the permeable layer and the barrier layer, at least at least one of the absorbing layer, the permeable layer and the barrier layer
  • a detection reagent for detecting at least one of urine, stool, menstrual blood, vaginal discharge, and sweat is provided on one.
  • the setting location of the detection reagent includes at least one of the following:
  • the permeation layer is away from one side of the absorbent layer, between the permeation layer and the absorbent layer, between the absorbent layer and the barrier layer, the interior of the permeation layer, and the interior of the absorbent layer .
  • the detecting reagent is a test strip, and the side of the detecting reagent away from the human body is provided with an adhesive, and the adhesive is set to fix the detecting reagent.
  • the detection reagent is in a liquid state, and the detection reagent is adsorbed on the absorption layer, the permeation layer or the barrier layer.
  • the detection reagent is in the form of a powder, and the detection reagent is embedded in the absorption layer, the permeation layer or the barrier layer.
  • the detection reagent is a paste, and the detection reagent is adhered to the absorption layer, the permeation layer or the barrier layer.
  • the type of the detection reagent for detecting urine is at least one type
  • the type of the detection reagent for detecting stool is at least one type
  • the type of the detection reagent for detecting menstrual blood is at least one type
  • the type of the detection reagent for detecting the leucorrhea is at least one;
  • the type of the detection reagent for detecting sweat is at least one kind.
  • a front waist portion disposed at a first end of the permeation layer, the barrier layer and the absorption layer, and a rear waist portion disposed at the permeation layer, the barrier layer and the absorption layer
  • the second end of the front waist portion is selectively affixed to the rear waist portion.
  • the distance between the detecting reagent and the rear waist portion is more than one time of the distance between the detecting reagent and the front waist portion. Less than the following.
  • the distance between the detecting reagent and the front waist portion is less than or twice 2.5 times the distance between the detecting reagent and the rear waist portion.
  • the detecting reagent when used for detecting sweat, is disposed on at least one of the absorbing layer, the permeable layer and the barrier layer and is located on a side close to the front waistline and close to the back At least one of the sides of the waist.
  • the detecting reagent when used for detecting urine, the detecting reagent comprises at least one of the following:
  • Tetrabromophenol blue set to detect protein
  • a pyrrole amino acid ester derivative configured to detect white blood cells
  • Diazonium salt set to detect white blood cells
  • Diisopropylbenzene dihydrogen peroxide set to detect occult blood, occult blood, urinary red blood cells and urinary hemoglobin;
  • Tetramethylbenzidine set to detect occult blood, occult blood, urinary red blood cells, and urinary hemoglobin;
  • P-aminobenzoic acid set to detect nitrite
  • N-naphthylethylenediamine configured to detect nitrite
  • Methyl red set to detect hydrogen ion concentration index PH
  • Bromophenol blue set to detect the specific gravity of PH or solid matter
  • a maleic anhydride polymer configured to detect the specific gravity of the solid matter
  • P-diethylaminobenzaldehyde set to detect urobilinogen
  • Colloidal gold-labeled pathogen monoclonal antibody set to detect pathogen antibodies in urine Colloidal gold-labeled pathogen monoclonal antibody set to detect pathogen antibodies in urine
  • Colloidal gold standard gold melamine monoclonal antibody set to detect melamine Colloidal gold standard gold melamine monoclonal antibody set to detect melamine.
  • the detecting reagent when used for detecting stool, the detecting reagent comprises at least one of the following:
  • a pyrrole amino acid ester derivative configured to detect white blood cells
  • Diazonium salt set to detect white blood cells
  • Diisopropylbenzene dihydrogen peroxide set to detect red blood cells and occult blood;
  • Tetramethylbenzidine set to detect red blood cells and occult blood
  • P-diethylaminobenzaldehyde set to detect fecal gallbladder
  • Dichloroaniline diazonium salt set to detect fecal bilirubin.
  • the detecting reagent when used to detect menstrual blood, the detecting reagent comprises at least one of the following:
  • a pyrrole amino acid ester derivative configured to detect white blood cells
  • Diazonium salt set to detect white blood cells
  • N-naphthylethylenediamine set to detect nitrite
  • the colloidal gold-labeled HCG mAb was set to detect HCG.
  • the detection reagent when used to detect leucorrhea, the detection reagent comprises at least one of the following:
  • a pyrrole amino acid ester derivative configured to detect white blood cells
  • Diazonium salt set to detect white blood cells
  • Tetramethylbenzidine set to detect hydrogen peroxide
  • Horseradish peroxidase set to detect hydrogen peroxide
  • Methyl red set to detect PH
  • Bromophenol blue set to detect PH
  • Potassium hydroxide set to detect amines.
  • the detecting reagent when used to detect sweat, the detecting reagent comprises at least one of the following Kind:
  • Bromophenol blue set to detect electrolyte specific gravity or PH
  • Methyl red set to detect PH
  • P-aminobenzoic acid set to detect nitrite
  • N-naphthylethylenediamine set to detect nitrite.
  • the present disclosure provides an absorbent article which is capable of detecting human body parameters in daily life by providing a detecting reagent on the absorbent article, and initially identifying whether the human body parameter is abnormal or whether the human body is damaged.
  • FIG. 1 is a schematic structural view of an absorbent article having a urine parameter detecting function according to Embodiment 1;
  • FIG. 2 is a plan view of the absorbent article having the urine parameter detecting function according to the first embodiment
  • FIG. 3 is a schematic structural view of an absorbent article having a urine parameter detecting function according to Embodiment 2;
  • Figure 4 is a plan view of the absorbent article having the urine parameter detecting function according to the second embodiment
  • FIG. 5 is a schematic structural view of an absorbent article having a urine parameter detecting function according to Embodiment 3;
  • Figure 6 is a plan view of the absorbent article having the urine parameter detecting function according to the third embodiment
  • FIG. 7 is a schematic structural view of an absorbent article having a stool parameter detecting function according to Embodiment 7;
  • Figure 8 is a plan view showing an absorbent article having a stool parameter detecting function according to the seventh embodiment
  • Embodiment 9 is a schematic structural view of an absorbent article having a stool parameter detecting function according to Embodiment 9;
  • Figure 10 is a plan view showing an absorbent article having a stool parameter detecting function according to a ninth embodiment
  • Figure 11 is a schematic view showing the structure of an absorbent article having a blood transfusion parameter detecting function according to the twelfth embodiment
  • Figure 12 is a plan view showing an absorbent article having a blood transfusion parameter detecting function according to the twelfth embodiment
  • Figure 13 is a schematic structural view of an absorbent article having a leucorrhea parameter detecting function according to the seventeenth embodiment
  • Figure 14 is a plan view of the absorbent article having the leucorrhea parameter detecting function according to the seventeenth embodiment
  • FIG. 15 is a schematic structural view of an absorbent article having a sweat parameter detecting function according to Embodiment 23;
  • Figure 16 is a plan view of the absorbent article having the sweat parameter detecting function according to the twenty-third embodiment
  • Figure 17 is a schematic structural view of an absorbent article according to Example 28;
  • Figure 18 is a plan view of the absorbent article of the twenty-eighth embodiment.
  • the present embodiment provides an absorbent article comprising a permeation layer, a barrier layer and an absorbent layer, the absorbent layer being disposed between the permeation layer and the barrier layer, the absorbent layer, the permeation layer and the At least one of the barrier layers is provided with a detection reagent for detecting at least one of urine, stool, menstrual blood, vaginal discharge, and sweat.
  • the absorbent article is exemplified in the following examples.
  • Embodiment 1 is a diagrammatic representation of Embodiment 1:
  • an absorbent article having a urine parameter detecting function includes a permeating layer 3, a barrier layer 5 and an absorbent layer 4, and the absorbent layer 4 is disposed in the permeate. Between the layer 3 and the barrier layer 5, a detection reagent 6 for detecting urine is provided on the absorption layer 4.
  • the absorption layer 4 is provided with a detection reagent 6 for detecting urine.
  • the detection reagent 6 is: a pyrrole amino acid ester derivative, used for detecting white blood cells, detecting urine by using a drying method and a leukocyte esterase method, and when the detection reagent 6 is positive, it will represent a human body. The urinary tract is infected.
  • the state of the detecting reagent 6 is a test strip, and the side of the detecting reagent 6 away from the human body is provided with an adhesive for fixing the detecting reagent 6.
  • the detection reagent 6 is disposed between the permeable layer 3 and the absorbing layer 4.
  • the detection reagent 6 is adhered to one side of the absorbing layer 4 close to the permeable layer 3.
  • a front waist portion 2 disposed at a first end of the permeable layer 3, the barrier layer 5 and the absorbing layer 4, and a rear waist portion 1 disposed at the permeable layer 3.
  • the second end of the barrier layer 5 and the absorbent layer 4, the front waistline portion 2 being selectively affixed to the back waistline portion 1.
  • the front waist portion 2 and the rear waist portion 1 are disposed at the same position as the present embodiment, and the front waist portion 2 is provided in a portion composed of the permeation layer 3, the barrier layer 5, and the absorbing layer 4.
  • the rear waist portion 1 is disposed at a second end of a portion of the permeation layer 3, the barrier layer 5, and the absorbing layer 4.
  • the distance between the detection reagent 6 and the rear waistline 1 is 1.5 times the distance between the detection reagent 3 and the front waistline 2.
  • the permeation layer 3, the barrier layer 5, and the absorbent layer 4 of the absorbent article of the present embodiment and other embodiments described below may be disposed between any two layers regardless of whether or not a test strip is provided. Fit each other.
  • Embodiment 2 is a diagrammatic representation of Embodiment 1:
  • an absorbent article having a urine parameter detecting function includes a permeating layer 3, an absorbing layer 4 and a barrier layer 5, and the absorbing layer 4 is disposed on the permeable layer 3. Between the barrier layer 5 and the barrier layer 5, the absorbent article further comprises a detection reagent 6, which is a liquid, adsorbed inside the permeation layer 3.
  • the detecting reagent 6 is: a diazonium salt for detecting white blood cells, detecting urine by using a drying method and a leukocyte esterase method, and when the detecting reagent 6 is positive, representing a human urinary tract Infected.
  • the front waist portion 2 and the rear waist portion 1 are further selectively attached to the rear waist portion 1 .
  • the distance between the detection reagent 6 and the rear waistline 1 is twice the distance between the detection reagent 6 and the front waistline 2 .
  • Embodiment 3 is a diagrammatic representation of Embodiment 3
  • Fig. 5 is a schematic view showing the structure of an absorbent article having a urine parameter detecting function according to a third embodiment
  • Fig. 6 is a plan view showing the absorbent article having a urine parameter detecting function according to the third embodiment.
  • an absorbent article having a urine parameter detecting function includes a permeating layer 3, an absorbing layer 4 and a barrier layer 5, and the absorbing layer 4 is disposed in the osmosis. Between the layer 3 and the barrier layer 5.
  • the first detecting reagent 6 for detecting urine is disposed between the absorbing layer 4 and the separator 5.
  • the state of the first detection reagent is a paste.
  • the first detection reagent is diisopropylbenzene dihydrogen peroxide for detecting occult blood, occult blood, urinary red blood cells and urinary hemoglobin.
  • the urine is detected by the dry method and the hemoglobin peroxidase method. If the first test reagent shows positive, red blood cells and hemoglobin are present in the urine, and may have urinary, kidney or bleeding diseases.
  • the permeation layer 3 is provided with a second detection reagent for detecting urine.
  • the second detection reagent 7 is disposed between the permeation layer 3 and the absorption layer 4.
  • the second detection reagent is in the form of a paste, and the second detection reagent is N-naphthylethylenediamine for detecting nitrite.
  • the urine is detected by the drying method and the nitrite reduction method, and if the second detection reagent is positive, it represents the human body. In the process of urinary urinary tract infection, the concentration of nitrite increases due to retention in the bladder.
  • the front waist portion 2 and the rear waist portion 1 are further selectively attached to the rear waist portion 1 .
  • the distance between the first detection reagent and the second detection reagent and the rear waistline 1 is 2.5 times the distance between the first detection reagent and the second detection reagent and the front waistline 2.
  • a gap is provided between the permeation layer 3, the absorbent layer 4, and the barrier layer 5.
  • the gap in fact, since the paste is thin, the absorbent layer 3, the absorbent layer 4 and the barrier layer 5 are bonded to each other after the absorbent article is finished. As shown in Figure 6, the shape of the paste can be irregular.
  • Embodiment 4 is a diagrammatic representation of Embodiment 4:
  • an absorbent article having a urine parameter detecting function includes a permeation layer, a barrier layer and an absorption layer, the absorption layer being disposed between the permeation layer and the barrier layer, the permeation layer A detection reagent for detecting urine is provided thereon.
  • the permeation layer is provided with a detection reagent for detecting urine.
  • the detection reagent is: dichloroaniline diazonium salt for detecting bilirubin.
  • the urine is detected by a drying method and an azo reaction method, and if the detection reagent is positive, it means that the bilirubin is increased due to liver disease, or the newborn has jaundice.
  • the state of the detection reagent is a liquid, and the detection reagent is adsorbed on the permeation layer.
  • the detection reagent is disposed inside the permeation layer.
  • the front waist portion and the rear waist portion are further selectively attached to the rear waist portion.
  • the distance between the detection reagent and the rear waistline is 1 times the distance between the detection reagent and the front waistline.
  • Embodiment 5 is a diagrammatic representation of Embodiment 5:
  • an absorbent article having a urine parameter detecting function includes a permeation layer, a barrier layer and an absorption layer, the absorption layer being disposed between the permeation layer and the barrier layer, the permeation layer A detection reagent for detecting urine is provided thereon.
  • the permeation layer is provided with a detection reagent for detecting urine.
  • the detection reagent is: a colloidal gold-labeled pathogen monoclonal antibody for detecting a urine pathogen antibody, and the urine is detected by a colloidal gold method and an immunochemical method, and when the detection reagent is positive, Represents a human body that may be infected with the pathogen.
  • the state of the detection reagent is a liquid, and the detection reagent is adsorbed on the permeation layer.
  • the detection reagent is disposed inside the permeation layer.
  • the front waist portion and the rear waist portion are further selectively attached to the rear waist portion.
  • the distance between the detecting reagent and the rear waist portion is 2.2 times the distance between the detecting reagent and the front waist portion.
  • an absorbent article having a urine parameter detecting function includes a permeation layer, a barrier layer and an absorption layer, the absorption layer being disposed between the permeation layer and the barrier layer, the absorption layer A detection reagent for detecting urine is provided on the permeation layer.
  • the front waist portion and the rear waist portion are further selectively attached to the rear waist portion.
  • the absorption layer is provided with a detection reagent for detecting urine.
  • the detection reagent is disposed between the absorption layer and the isolation layer.
  • the state of the detection reagent is a paste, and the detection reagent is attached to the absorption layer.
  • the detection reagent is attached to one side of the absorbing layer adjacent to the isolation layer.
  • the detection reagent is: dichloroaniline diazonium salt for detecting bilirubin.
  • the urine is detected by a drying method and an azo reaction method, and if the detection reagent is positive, it means that the bilirubin is increased due to liver disease, or the newborn has jaundice.
  • the distance between the detection reagent and the rear waistline is 2.5 times the distance between the detection reagent and the front waistline.
  • the osmotic layer is provided with a detection reagent for detecting urine.
  • the detection reagent is disposed between the permeation layer and the absorption layer.
  • the state of the detection reagent is a paste, and the detection reagent is attached to the permeation layer.
  • the detection reagent is attached to one side of the permeation layer adjacent to the absorption layer.
  • the detection reagent is: N-naphthylethylenediamine for detecting nitrite.
  • the urine is detected by the dry method and the nitrite reduction method. If the test reagent is positive, it means that the urine is in the bladder during the urinary urinary tract infection, and the concentration of nitrite is increased due to retention in the bladder.
  • the distance between the detection reagent and the rear waist portion is 1.8 times the distance between the detection reagent and the front waist portion.
  • an absorbent article having a stool parameter detecting function includes a permeating layer 3, a barrier layer 5 and an absorbent layer 4, and the absorbent layer 4 is disposed on the permeation layer. Between the barrier layer 5 and the barrier layer 5, a detection reagent 6 for detecting stool is disposed on the absorption layer 4.
  • the absorption layer 4 is provided with a detection reagent 6 for detecting stool.
  • the detection reagent 6 is: a pyrrole amino acid ester derivative, used for detecting white blood cells, detecting stool by using a drying method and a leukocyte esterase method, and when the detection reagent 6 is positive, it will represent a human body. Suffering from enteritis or bacterial dysentery.
  • the state of the detecting reagent 6 is a test strip, and the side of the detecting reagent 6 away from the human body is provided with an adhesive for fixing the detecting reagent 6.
  • the detection reagent 6 is disposed between the permeation layer 3 and the absorption layer 4.
  • the detection reagent 6 is adhered to one side of the absorbing layer 4 close to the permeable layer 3.
  • a front waist portion 2 disposed at a first end of the permeable layer 3, the barrier layer 5 and the absorbing layer 4, and a rear waist portion 1 disposed at the permeable layer 3.
  • the second end of the barrier layer 5 and the absorbent layer 4, the front waistline portion 2 being selectively affixed to the back waistline portion 1.
  • the distance between the detection reagent 6 and the front waistline 2 is 1.5 times the distance between the detection reagent 6 and the rear waistline 1 .
  • an absorbent article having a stool parameter detecting function includes a permeation layer, a barrier layer and an absorption layer, the absorption layer being disposed between the permeation layer and the barrier layer, on the absorption layer A detection reagent for detecting stool is provided.
  • a detection reagent for detecting stool is disposed on the absorption layer.
  • the detection reagent is: a pyrrole amino acid ester derivative, used for detecting white blood cells, detecting stool by using a drying method and a leukocyte esterase method, and when the detection reagent is positive, it will represent a human body. Enteritis or bacterial dysentery.
  • the state of the detecting reagent is a test strip, and the side of the detecting reagent away from the human body is provided with an adhesive, and the adhesive is used for fixing the detecting reagent.
  • the detection reagent is disposed between the permeation layer and the absorption layer.
  • the detection reagent is attached to one side of the absorbing layer adjacent to the permeable layer.
  • the front waist portion and the rear waist portion are further selectively attached to the rear waist portion.
  • the distance between the detection reagent and the front waist portion is twice the distance between the detection reagent and the rear waist portion.
  • Fig. 9 is a schematic view showing the structure of an absorbent article having a stool parameter detecting function according to a ninth embodiment
  • Fig. 10 is a plan view showing the absorbent article having a stool parameter detecting function according to the ninth embodiment.
  • an absorbent article having a stool parameter detecting function in the embodiment includes a permeation layer 3, an absorbing layer 4, a barrier layer 5, and a detecting reagent 6, and the absorbing layer 4 is disposed on the permeable layer. Between the barrier layer 5 and the barrier layer 5, a powdery detection reagent 6 for detecting stool is provided inside the absorption layer 4.
  • the detection reagent is: a pyrrole amino acid ester derivative, used for detecting white blood cells, detecting stool by using a drying method and a leukocyte esterase method, and when the detection reagent is positive, it will represent a human body. Suffering from enteritis or bacterial dysentery.
  • the front waist portion 2 and the rear waist portion 1 are further selectively attached to the rear waist portion 1 .
  • the distance between the detection reagent 6 and the front waistline 2 is 2.5 times the distance between the detection reagent 6 and the rear waistline 1.
  • an absorbent article having a stool parameter detecting function includes a permeation layer, a barrier layer and an absorbent layer, the absorption layer being disposed between the permeation layer and the barrier layer, the absorption layer and A detection reagent for detecting stool is disposed on the permeation layer.
  • a detection reagent for detecting stool is disposed on the absorption layer.
  • the detection reagent is: p-diethylaminobenzaldehyde, used for detecting fecal gallbladder, using a dry method and an aldehyde reaction method to detect stool, and if the test reagent is positive, the human body has hemolytic jaundice or liver sexual jaundice.
  • the state of the detection reagent is a powder, and the detection reagent is embedded in the absorption layer.
  • the detection reagent is disposed inside the absorption layer.
  • a Detecting Agent for detecting stool is disposed on the permeable layer.
  • the detection reagent is: dichloroaniline diazonium salt, used for detecting fecal bilirubin, using a dry method and an azo reaction method to detect stool, and if the detection reagent is positive, the human body has hemolytic jaundice or Obstructive jaundice.
  • the state of the detection reagent is a liquid, and the detection reagent is adsorbed on the permeation layer.
  • the detection reagent is disposed inside the permeation layer.
  • the front waist portion and the rear waist portion are further selectively attached to the rear waist portion.
  • the distance between the detection reagent and the front waist portion is 1 times the distance between the detection reagent and the rear waist portion.
  • an absorbent article having a stool parameter detecting function includes a permeation layer, a barrier layer and an absorption layer, the absorption layer being disposed between the permeation layer and the barrier layer, the absorption layer A detection reagent for detecting stool is provided on the permeation layer.
  • the front waist portion and the rear waist portion are further selectively attached to the rear waist portion.
  • a detection reagent for detecting stool is disposed on the absorption layer.
  • the detection reagent is: tetramethylbenzidine for detecting red blood cells and occult blood, detecting the stool by using a drying method and hemoglobin peroxidase method, and if the detection reagent is positive, it means that red blood cells and hemoglobin are present in the stool.
  • the human body may have bleeding from dysentery, enteritis, colon cancer or hemorrhoids.
  • the state of the detection reagent is a powder, and the detection reagent is embedded in the absorption layer.
  • the detection reagent is disposed inside the absorption layer. The distance between the detection reagent and the front waist portion is 2.2 times the distance between the detection reagent and the rear waist portion.
  • a Detecting Agent for detecting stool is disposed on the permeable layer.
  • the detection reagent is: dichloroaniline diazonium salt, used for detecting fecal bilirubin, using a dry method and an azo reaction method to detect stool, and if the detection reagent is positive, the human body has hemolytic jaundice or Obstructive jaundice.
  • the state of the detection reagent is a liquid, and the detection reagent is adsorbed on the permeation layer.
  • the detection reagent is disposed inside the permeation layer. The distance between the detection reagent and the front waistline portion is 2.0 times the distance between the detection reagent and the rear waistline portion.
  • an absorbent article having a blood transfusion parameter detecting function includes a permeation layer 3, a barrier layer 5 and an absorption layer 4, and the absorption layer 4 is disposed on the permeation layer. Between the barrier layer 5 and the barrier layer 5, a detection reagent 6 for detecting menstrual blood is disposed on the absorption layer 4.
  • the absorption layer 4 is provided with a detection reagent 6 for detecting menstrual blood.
  • the detection reagent 6 is: a pyrrole amino acid ester derivative, which is used for detecting white blood cells, and is used for detecting menstrual blood by using a drying method and a leukocyte esterase method, and when the detection reagent 6 is positive, it will represent a human body. The reproductive system has been disturbed.
  • the state of the detecting reagent 6 is a test strip, and the side of the detecting reagent 6 away from the human body is provided with an adhesive for fixing the detecting reagent 6.
  • the detection reagent 6 is disposed between the permeation layer 3 and the absorption layer 4.
  • the detection reagent 6 is adhered to one side of the absorbing layer 4 close to the permeable layer 3.
  • a front waist portion 2 disposed at a first end of the permeable layer 3, the barrier layer 5 and the absorbing layer 4, and a rear waist portion 1 disposed at the permeable layer 3.
  • the second end of the barrier layer 5 and the absorbent layer 4, the front waistline portion 2 being selectively affixed to the back waistline portion 1.
  • the distance between the detection reagent 6 and the rear waistline 1 is 1.5 times the distance between the detection reagent 6 and the front waistline 2.
  • an absorbent article having a blood transfusion parameter detecting function includes a permeation layer, a barrier layer and an absorption layer, the absorption layer being disposed between the permeation layer and the barrier layer, the absorption layer A detection reagent for detecting menstrual blood is provided.
  • a detection reagent for detecting menstrual blood is disposed on the absorption layer.
  • the detection reagent is: a diazonium salt for detecting leukocytes, and the menstrual blood is detected by using a drying method and a leukocyte esterase method, and when the detection reagent is positive, it represents a reproductive system of the human body.
  • the interference is: a diazonium salt for detecting leukocytes, and the menstrual blood is detected by using a drying method and a leukocyte esterase method, and when the detection reagent is positive, it represents a reproductive system of the human body. The interference.
  • the state of the detecting reagent is a test strip, and the side of the detecting reagent away from the human body is provided with an adhesive, and the adhesive is used for fixing the detecting reagent.
  • the detection reagent is disposed between the permeation layer and the absorption layer.
  • the detection reagent is attached to one side of the absorbing layer adjacent to the permeable layer.
  • the front waist portion and the rear waist portion are further selectively attached to the rear waist portion.
  • the distance between the detecting reagent and the rear waist portion is 2.5 times the distance between the detecting reagent and the front waist portion.
  • Embodiment 14 is a diagrammatic representation of Embodiment 14:
  • an absorbent article having a blood transfusion parameter detecting function includes a permeation layer, a barrier layer and an absorption layer, the absorption layer being disposed between the permeation layer and the barrier layer, the absorption layer A detection reagent for detecting menstrual blood is provided.
  • a detection reagent for detecting menstrual blood is disposed on the absorption layer.
  • the detection reagent is: a diazonium salt for detecting leukocytes, and the menstrual blood is detected by using a drying method and a leukocyte esterase method, and when the detection reagent is positive, it represents a reproductive system of the human body.
  • the interference is: a diazonium salt for detecting leukocytes, and the menstrual blood is detected by using a drying method and a leukocyte esterase method, and when the detection reagent is positive, it represents a reproductive system of the human body. The interference.
  • the state of the detection reagent is a powder, and the detection reagent is embedded on the absorption layer.
  • the detection reagent is disposed inside the absorption layer.
  • the front waist portion and the rear waist portion are further selectively attached to the rear waist portion.
  • the distance between the detecting reagent and the rear waist portion is the detecting reagent and the front waist
  • the distance of the circumference is twice.
  • an absorbent article having a blood transfusion parameter detecting function includes a permeation layer, a barrier layer and an absorption layer, the absorption layer being disposed between the permeation layer and the barrier layer, the absorption layer and A detection reagent for detecting menstrual blood is disposed on the permeation layer.
  • a detection reagent for detecting menstrual blood is disposed on the absorption layer.
  • the detection reagent is: p-aminophenyl arsenic acid, which is used for detecting nitrite, and the menstrual blood is detected by using a drying method and a nitrite reduction method, and the detection reagent is observed whether the reproductive system is infected.
  • the state of the detection reagent is a powder, and the detection reagent is embedded in the absorption layer.
  • the detection reagent is disposed inside the absorption layer.
  • a Detecting Agent for detecting menstrual blood is disposed on the permeable layer.
  • the detection reagent is: colloidal gold-labeled HCG (human chorionic gonadotropin, Human Chorionic Gonadotropin) monoclonal antibody, used for detecting HCG, using colloidal gold method and immunochemical method to detect menstrual blood, observing the detection reagent to know whether There may be abnormal menstruation or accidental abortion.
  • the state of the detection reagent is a liquid, and the detection reagent is adsorbed on the permeation layer.
  • the detection reagent is disposed inside the permeation layer.
  • the front waist portion and the rear waist portion are further selectively attached to the rear waist portion.
  • the distance between the detection reagent and the rear waistline is 1 times the distance between the detection reagent and the front waistline.
  • an absorbent article having a blood transfusion parameter detecting function comprising a permeation layer, a barrier layer and an absorption layer, the absorption layer being disposed between the permeation layer and the barrier layer, the absorption layer and the A detection reagent for detecting menstrual blood is provided on the permeation layer.
  • the front waist portion and the rear waist portion are further selectively attached to the rear waist portion.
  • the absorption layer is provided with a detection reagent for detecting menstrual blood.
  • the detection reagent is: a diazonium salt for detecting leukocytes, and the menstrual blood is detected by a drying method and a leukocyte esterase method, and when the detection reagent is positive, the reproductive system representing the human body is disturbed.
  • the state of the detection reagent is a powder, and the detection reagent is embedded in the absorption layer.
  • the detection reagent is disposed inside the absorption layer. The distance between the detection reagent and the rear waistline is 2.2 times the distance between the detection reagent and the front waistline.
  • a Detecting Agent for detecting menstrual blood is disposed on the permeable layer.
  • the detection reagent is: colloidal gold-labeled HCG monoclonal antibody, used for detecting HCG, using colloidal gold method and immunochemical method to detect menstrual blood, and observing the detection reagent to know whether there is abnormal menstruation or accidental abortion.
  • the state of the detection reagent is a liquid, and the detection reagent is adsorbed on the permeation layer.
  • the detection reagent is disposed inside the permeation layer. The distance between the detection reagent and the rear waist portion is 1.8 times the distance between the detection reagent and the front waist portion.
  • an absorbent article having a leucorrhea parameter detecting function includes a permeable layer 3, a barrier layer 5 and an absorbing layer 4, and the absorbing layer 4 is disposed on the permeable layer. Between the barrier layer 5 and the barrier layer 5, a detection reagent 6 for detecting a leucorrhea is disposed on the absorption layer 4.
  • the absorption layer 4 is provided with a detection reagent 6 for detecting the leucorrhea.
  • the detection reagent 6 is: 5-bromo-4-chloro-3-purine neuraminic acid, used for detecting sialidase, and detecting vaginal discharge by using a drying method and an enzymatic coloring method.
  • the detection reagent 6 is positive, it will represent infectious vaginitis in the human body.
  • the state of the detecting reagent 6 is a test strip, and the side of the detecting reagent 6 away from the human body is provided with an adhesive for fixing the detecting reagent 6.
  • the detection reagent 6 is disposed between the permeation layer 3 and the absorption layer 4.
  • the detection reagent 6 is adhered to one side of the absorbing layer 4 close to the permeable layer 3.
  • a front waist portion 2 disposed at a first end of the permeable layer 3, the barrier layer 5 and the absorbing layer 4, and a rear waist portion 1 disposed at the permeable layer 3.
  • the second end of the barrier layer 5 and the absorbent layer 4, the front waistline portion 2 being selectively affixed to the back waistline portion 1.
  • the distance between the detection reagent 6 and the rear waistline 1 is 1.5 times the distance between the detection reagent 6 and the front waistline 2.
  • an absorbent article having a leucorrhea parameter detecting function comprising a permeable layer, a barrier layer and an absorbing layer, wherein the absorbing layer is disposed between the permeable layer and the barrier layer, and the permeable layer is provided with useful For the detection of leucorrhea detection reagents.
  • a Detecting Reagent for detecting leucorrhea is disposed on the permeable layer.
  • the detection reagent is: potassium hydroxide for detecting an amine.
  • the test reagent has a fishy smell, it means that the human body has bacterial vaginosis.
  • the state of the detection reagent is a liquid, and the detection reagent is adsorbed on the permeation layer.
  • the detection reagent is disposed inside the permeation layer.
  • the front waist portion and the rear waist portion are further selectively attached to the rear waist portion.
  • the distance between the detection reagent and the rear waistline is twice the distance between the detection reagent and the front waistline.
  • an absorbent article having a leucorrhea parameter detecting function includes a permeable layer, a barrier layer and an absorbing layer, the absorbing layer being disposed between the permeable layer and the barrier layer, the absorbing layer and A detection reagent for detecting the leucorrhea is disposed on the permeation layer.
  • a detection reagent for detecting the leucorrhea is disposed on the absorption layer.
  • the detection reagent is disposed between the absorption layer and the isolation layer.
  • the state of the detection reagent is a paste, and the detection reagent is attached to the absorption layer.
  • the detection reagent is attached to one side of the absorbing layer adjacent to the isolation layer.
  • the detection reagent is: bromophenol blue for detecting PH (Hydrogen ion concentration) index. If the test reagent shows green color, it means that the human body has Candida vaginitis.
  • a Detecting Reagent for detecting leucorrhea is disposed on the permeable layer.
  • the detection reagent is disposed between the permeation layer and the absorption layer.
  • the state of the detection reagent is a paste, and the detection reagent is attached to the permeation layer.
  • the detection reagent is attached to one side of the permeation layer adjacent to the absorption layer.
  • the detection reagent is: methyl red for detecting PH. If the test reagent shows blue color, it means that the human body has trichomonas vaginitis.
  • the front waist portion and the rear waist portion are further selectively attached to the rear waist portion.
  • the distance between the detecting reagent and the rear waist portion is 2.5 times the distance between the detecting reagent and the front waist portion.
  • Embodiment 20 is a diagrammatic representation of Embodiment 20.
  • an absorbent article having a leucorrhea parameter detecting function includes a permeable layer, a barrier layer and an absorbing layer, the absorbing layer being disposed between the permeable layer and the barrier layer, the permeable layer A detection reagent for detecting the leucorrhea is provided.
  • a Detecting Reagent for detecting leucorrhea is disposed on the permeable layer.
  • the detection reagent is: a diazonium salt for detecting white blood cells.
  • the test reagent is positive, it means that the vagina of the human body is infected.
  • the state of the detection reagent is a liquid, and the detection reagent is adsorbed on the permeation layer.
  • the detection reagent is disposed inside the permeation layer.
  • the front waist portion and the rear waist portion are further selectively attached to the rear waist portion.
  • the distance between the detection reagent and the rear waistline is 1 times the distance between the detection reagent and the front waistline.
  • an absorbent article having a leucorrhea parameter detecting function includes a permeable layer, a barrier layer and an absorbing layer, the absorbing layer being disposed between the permeable layer and the barrier layer, the permeable layer A detection reagent for detecting the leucorrhea is provided.
  • a Detecting Reagent for detecting leucorrhea is disposed on the permeable layer.
  • the detection reagent is: horseradish peroxidase for detecting hydrogen peroxide.
  • the color of the detection reagent is changed, it means that the vaginal flora of the human body is normal, and if there is no discoloration, it means that the vaginal environment is morbid or in a sub-health state.
  • the state of the detection reagent is a liquid, and the detection reagent is adsorbed on the permeation layer.
  • the detection reagent is disposed inside the permeation layer.
  • the front waist portion and the rear waist portion are further selectively attached to the rear waist portion.
  • the distance between the detecting reagent and the rear waist portion is 2.2 times the distance between the detecting reagent and the front waist portion.
  • an absorbent article having a leucorrhea parameter detecting function includes a permeable layer, a barrier layer and an absorbing layer, the absorbing layer being disposed between the permeable layer and the barrier layer, the absorbing layer and A detection reagent for detecting the leucorrhea is disposed on the permeation layer.
  • the front waist portion and the rear waist portion are further selectively attached to the rear waist portion.
  • a detection reagent for detecting the leucorrhea is disposed on the absorption layer.
  • the detection reagent is disposed between the absorption layer and the isolation layer.
  • the state of the detection reagent is a paste, and the detection reagent is attached to the absorption layer.
  • the detection reagent is attached to one side of the absorbing layer adjacent to the isolation layer.
  • the detection reagent is: 5-bromo-4-chloro-3-indolyl salt for detecting sialidase.
  • the leucorrhea is detected by a drying method and an enzymatic chromogenic method, when the detection reagent is positive, Will represent the human body with infectious vaginitis.
  • the distance between the detection reagent and the rear waistline is 2.5 times the distance between the detection reagent and the front waistline.
  • a Detecting Reagent for detecting leucorrhea is disposed on the permeable layer.
  • the detection reagent is disposed between the permeation layer and the absorption layer.
  • the state of the detection reagent is a paste, and the detection reagent is attached to the permeation layer.
  • the detection reagent is attached to one side of the permeation layer adjacent to the absorption layer.
  • the detection reagent is: methyl red for detecting PH. If the test reagent shows blue color, it means that the human body has trichomonas vaginitis.
  • the distance between the detection reagent and the rear waistline is 2.2 times the distance between the detection reagent and the front waistline.
  • an absorbent article having a sweat parameter detecting function includes a permeating layer 3, a barrier layer 5 and an absorbent layer 4, and the absorbent layer 4 is disposed on the permeation layer. Between the barrier layer 5 and the barrier layer 5, a detection reagent 6 for detecting sweat is disposed on the absorption layer 4.
  • the absorption layer 4 is provided with a detection reagent 6 for detecting sweat.
  • the detection reagent 6 is: methyl red, used for detecting PH, and the sweat is detected by using a drying method and an indicator method.
  • the detection reagent 6 exhibits a pH value of 4.2-7.5, The electrolytes on behalf of the human body are normal, otherwise they are not normal.
  • the state of the detecting reagent 6 is a test strip, and the side of the detecting reagent 6 away from the human body is provided with an adhesive for fixing the detecting reagent 6.
  • the detection reagent 6 is disposed between the permeation layer 3 and the absorption layer 4.
  • the detection reagent 6 is adhered to one side of the absorbing layer 4 close to the permeable layer 3.
  • a front waist portion 2 disposed at a first end of the permeable layer 3, the barrier layer 5 and the absorbing layer 4, and a rear waist portion 1 disposed at the permeable layer 3.
  • the second end of the barrier layer 5 and the absorbent layer 4, the front waistline portion 2 being selectively affixed to the back waistline portion 1.
  • the detecting reagent 6 is disposed on a side of the absorbing layer 4 adjacent to the front waistline portion 2 and a side close to the rear waistline portion 1.
  • an absorbent article having a sweat parameter detecting function includes a permeating layer, a barrier layer and an absorbing layer, the absorbing layer being disposed between the permeable layer and the barrier layer, the absorbing layer A detection reagent for detecting sweat is provided.
  • a detection reagent for detecting sweat is disposed on the absorption layer.
  • the detection reagent is: methyl red, used for detecting PH, using a drying method and an indicator method
  • the pH of the test reagent is 4.2-7.5, the electrolyte intake of the human body is normal, otherwise it is not normal.
  • the state of the detection reagent is a liquid, and the detection reagent is adsorbed on the absorption layer.
  • the detection reagent is disposed inside the absorption layer.
  • the front waist portion and the rear waist portion are further selectively attached to the rear waist portion.
  • the distance between the detection reagent and the rear waistline is 2.3 times the distance between the detection reagent and the front waistline.
  • an absorbent article having a sweat parameter detecting function includes a permeating layer, a barrier layer and an absorbing layer, the absorbing layer being disposed between the permeable layer and the barrier layer, the absorbing layer A detection reagent for detecting sweat is provided.
  • a detection reagent for detecting sweat is disposed on the absorption layer.
  • the detecting reagent is: sodium hydroxide, which is used for detecting the specific gravity of the electrolyte.
  • the detection reagent exhibits a specific gravity, and if the specific gravity is 1.002 to 1.003, it is normal, otherwise, the human electrolyte is not normally taken up.
  • the state of the detecting reagent is a test strip, and the side of the detecting reagent away from the human body is provided with an adhesive, and the adhesive is used for fixing the detecting reagent.
  • the detection reagent is disposed between the permeation layer and the absorption layer.
  • the detection reagent is attached to one side of the absorbing layer adjacent to the permeable layer.
  • the front waist portion and the rear waist portion are further selectively attached to the rear waist portion.
  • the detecting reagent is disposed on a side of the absorbing layer near the front waistline and a side close to the back waistline.
  • an absorbent article having a sweat parameter detecting function includes a permeation layer, a barrier layer and an absorption layer, the absorption layer being disposed between the permeation layer and the barrier layer, the absorption layer and A detection reagent for detecting sweat is disposed on the permeation layer.
  • a detection reagent for detecting sweat is disposed on the absorption layer.
  • the state of the detection reagent is a liquid, and the detection reagent is adsorbed on the absorption layer.
  • the detection reagent is disposed inside the absorption layer.
  • the detection reagent is: p-aminobenzoic acid for detecting nitrite.
  • the osmotic layer is provided with a detection reagent for detecting sweat.
  • the state of the detection reagent is a paste, and the detection reagent is attached to the permeation layer.
  • the detection reagent is disposed inside the permeation layer.
  • the detection reagent is: vinyl methyl ether for detecting the specific gravity of the electrolyte.
  • the front waist portion and the rear waist portion are further selectively attached to the rear waist portion.
  • the distance between the detection reagent and the rear waistline is 1.5 times the distance between the detection reagent and the front waistline.
  • an absorbent article having a sweat parameter detecting function includes a permeation layer, a barrier layer and an absorption layer, the absorption layer being disposed between the permeation layer and the barrier layer, the absorption layer and A detection reagent for detecting sweat is disposed on the permeation layer.
  • the front waist portion and the rear waist portion are further selectively attached to the rear waist portion.
  • the absorption layer is provided with a detection reagent for detecting sweat.
  • the state of the detection reagent is a liquid, and the detection reagent is adsorbed on the absorption layer.
  • the detection reagent is disposed inside the absorption layer.
  • the detection reagent is: p-aminobenzoic acid for detecting nitrite.
  • the detection reagent reacts to bacteria in the sweat, suggesting whether the "sweat smell" is serious, or even causing skin diseases, which is commonly referred to as sweat rash and hair follicles. Inflammation, eczema, lice or lice.
  • the distance between the detection reagent and the rear waist portion is 1.8 times the distance between the detection reagent and the front waist portion.
  • the osmotic layer is provided with a detection reagent for detecting sweat.
  • the state of the detection reagent is a paste, and the detection reagent is attached to the permeation layer.
  • the detection reagent is disposed inside the permeation layer.
  • the detection reagent is: methyl red, used for detecting PH, and the sweat is detected by using a drying method and an indicator method.
  • the pH of the detection reagent is 4.2-7.5, the electrolyte intake of the human body is normal. Otherwise it is not normal.
  • the distance between the detection reagent and the rear waistline is twice the distance between the detection reagent and the front waistline.
  • the present embodiment provides an absorbent article comprising a permeation layer, a barrier layer and an absorbent layer, the absorbent layer being disposed between the permeation layer and the barrier layer, the absorbent layer, the permeation layer and the At least one of the barrier layers is provided with a detection reagent for detecting at least one of urine, stool, menstrual blood, vaginal discharge, and sweat.
  • Figure 17 is a schematic view showing the structure of the absorbent article of the twenty-eighth embodiment
  • Figure 18 is a plan view of the absorbent article of the twenty-eighth embodiment.
  • the absorbent article can be used to detect leucorrhea and stool.
  • the state of the first detecting reagent 6 for detecting the leucorrhea is a test strip, and is attached to one side of the absorbing layer 4 close to the barrier layer 5, and a second detecting reagent 7 for detecting stool is a test strip.
  • the side of the second detecting reagent 7 away from the human body is provided with an adhesive, and the second detecting reagent 7 may be attached to one side of the absorbing layer 4 close to the permeable layer 3.
  • the distance between the first detecting reagent 6 and the rear waistline 1 is 1.5 times the distance between the first detecting reagent 6 and the front waistline 2, and the second detecting reagent 7 and the The distance of the front waist portion 2 is 1.5 times the distance between the first detecting reagent 6 and the rear waist portion 1.
  • the absorbent article further comprises a front waist portion 2 and a rear waist portion 1 disposed at a first end of the permeating layer 3, the barrier layer 5 and the absorbent layer 4, the rear waist portion 1
  • the second waist end 3, the barrier layer 5, and the second end of the absorbent layer 4 are disposed, and the front waistline portion 2 is selectively affixed to the back waistline portion 1.
  • the present disclosure provides an absorbent article which is capable of detecting human body parameters in daily life by providing a detecting reagent on the absorbent article, and initially identifying whether the human body parameter is abnormal or whether the human body is damaged.

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Abstract

一种吸湿用品,包括渗透层(3)、阻隔层(5)和吸收层(4),吸收层(4)设置在渗透层(3)与阻隔层(5)之间,吸收层(4)、渗透层(3)和阻隔层(5)中的至少一个上设置有用于检测尿液、大便、经血、白带和汗液中至少一项的检测试剂(6)。

Description

吸湿用品 技术领域
本公开涉及一次性吸湿用品的技术领域,例如涉及一种吸湿用品。
背景技术
一次性吸湿用品诸如纸尿裤,主要被人们用以接收和容纳尿液和粪便等排泄物,从而保护衣服免受脏污。一次性吸湿用品的构造大都包括渗透层、阻隔层和吸收层。随着该行业的不断发展,一次性吸湿用品的使用舒适性逐渐得到提高,且在抗菌除味等方面也有很大的进展,但是功能较单一。
发明内容
本公开提供一种吸湿用品,通过在吸湿用品上设置检测试剂,实现在日常生活中对人体参数的检测,初步识别人体参数是否异常或者人体是否病变。
本公开采用以下技术方案:
一种吸湿用品,包括渗透层、阻隔层和吸收层,所述吸收层设置在所述渗透层与所述阻隔层之间,所述吸收层、所述渗透层和所述阻隔层中的至少一个上设置有用于检测尿液、大便、经血、白带和汗液中至少一项的检测试剂。
可选的,所述检测试剂的设置位置包括下述至少一个:
所述渗透层远离所述吸收层的一面,所述渗透层与所述吸收层之间,所述吸收层与所述隔离层之间,所述渗透层的内部,以及所述吸收层的内部。
可选的,所述检测试剂为试带,所述检测试剂远离人体的一侧设置有粘贴胶,所述粘贴胶设置为固定所述检测试剂。
可选的,所述检测试剂为液体状态,所述检测试剂吸附在所述吸收层、渗透层或者阻隔层上。
可选的,所述检测试剂为粉末状,所述检测试剂嵌进在所述吸收层、渗透层或者阻隔层上。
可选的,所述检测试剂为糊状物,所述检测试剂粘贴在所述吸收层、渗透层或者阻隔层上。
可选的,所述用于检测尿液的检测试剂的种类为至少一种;
所述用于检测大便的检测试剂的种类为至少一种;
所述用于检测经血的检测试剂的种类为至少一种;
所述用于检测白带的检测试剂的种类为至少一种;以及
所述用于检测汗液的检测试剂的种类为至少一种。
可选的,还包括前腰围部和后腰围部,所述前腰围部设置在渗透层、阻隔层和吸收层的第一端,所述后腰围部设置在渗透层、阻隔层和吸收层的第二端,所述前腰围部与所述后腰围部选择性粘贴连接。
可选的,当所述检测试剂用于检测尿液、经血或白带时,所述检测试剂与所述后腰围部的距离是所述检测试剂与所述前腰围部的距离的1倍以上2.5倍以下。
可选的,当所述检测试剂用于检测大便时,所述检测试剂与所述前腰围部的距离是所述检测试剂与所述后腰围部的距离的1倍以上2.5倍以下。
可选的,当所述检测试剂用于检测汗液时,所述检测试剂设置在吸收层、所述渗透层和所述阻隔层中的至少一个上且位于靠近前腰围部的一侧和靠近后腰围部的一侧中的至少一处。
可选的,当所述检测试剂用于检测尿液时,所述检测试剂包括以下至少一种:
四溴酚蓝,设置为检测蛋白质;
吡咯氨基酸酯衍生物,设置为检测白细胞;
重氮盐,设置为检测白细胞;
二异丙苯过氧化二氢,设置为检测隐血、潜血、尿红细胞以及尿血红蛋白;
四甲基联苯胺,设置为检测隐血、潜血、尿红细胞以及尿血红蛋白;
对氨基苯胂酸,设置为检测亚硝酸盐;
N-萘基乙二胺,设置为检测亚硝酸盐;
亚硝基铁氰化钠,设置为检测酮体;
甲基红,设置为检测氢离子浓度指数PH;
溴酚蓝,设置为检测PH或者固体物质比重;
乙烯基甲醚,设置为检测固体物质比重;
顺丁烯二酸酐聚合物,设置为检测固体物质比重;
氢氧化钠,设置为检测固体物质比重;
二氯苯胺重氮盐,设置为检测胆红素;
对二乙基氨基苯甲醛,设置为检测尿胆原;
2,6-二氯酚靛酚,设置为检测维生素C;
胶体金标记的病原体单抗,设置为检测尿液中病原体抗体;
胶体金标记的人绒毛膜促性腺激素HCG单抗,设置为检测尿液中HCG;以及
胶体金标金的三聚氰胺单抗,设置为检测三聚氰胺。
可选的,当所述检测试剂用于检测大便时,所述检测试剂包括以下至少一种:
吡咯氨基酸酯衍生物,设置为检测白细胞;
重氮盐,设置为检测白细胞;
二异丙苯过氧化二氢,设置为检测红细胞以及潜血;
四甲基联苯胺,设置为检测红细胞以及潜血;
对二乙基氨基苯甲醛,设置为检测粪胆原;以及
二氯苯胺重氮盐,设置为检测粪便胆红素。
可选的,当所述检测试剂用于检测经血时,所述检测试剂包括以下至少一种:
吡咯氨基酸酯衍生物,设置为检测白细胞;
重氮盐,设置为检测白细胞;
对氨苯基砷酸,设置为检测亚硝酸盐;
N-萘基乙二胺,设置为检测亚硝酸盐;以及
胶体金标记的HCG单抗,设置为检测HCG。
可选的,当所述检测试剂用于检测白带时,所述检测试剂包括以下至少一种:
吡咯氨基酸酯衍生物,设置为检测白细胞;
重氮盐,设置为检测白细胞;
四甲基联苯胺,设置为检测过氧化氢;
辣根过氧化物酶,设置为检测过氧化氢;
5-溴-4-氯-3-吲哚神经氨酸盐,设置为检测唾液酸苷酶;
甲基红,设置为检测PH;
溴酚蓝,设置为检测PH;以及
氢氧化钾,设置为检测胺。
可选的,当所述检测试剂用于检测汗液时,所述检测试剂包括以下至少一 种:
溴酚蓝,设置为检测电解质比重或者PH;
乙烯基甲醚,设置为检测电解质比重;
顺丁烯二酸酐聚合物,设置为检测电解质比重;
氢氧化钠,设置为检测电解质比重;
甲基红,设置为检测PH;
对氨基苯胂酸,设置为检测亚硝酸盐;以及
N-萘基乙二胺,设置为检测亚硝酸盐。
本公开提供一种吸湿用品,通过在吸湿用品上设置检测试剂,实现在日常生活中对人体参数的检测,初步识别人体参数是否异常或者人体是否病变。
附图概述
图1为实施例一所述的具备尿液参数检测功能的吸湿用品的结构示意图;
图2为实施例一所述的具备尿液参数检测功能的吸湿用品的俯视图;
图3为实施例二所述的具备尿液参数检测功能的吸湿用品的结构示意图;
图4为实施例二所述的具备尿液参数检测功能的吸湿用品的俯视图;
图5为实施例三所述的具备尿液参数检测功能的吸湿用品的结构示意图;
图6为实施例三所述的具备尿液参数检测功能的吸湿用品的俯视图;
图7为实施例七所述的具备大便参数检测功能的吸湿用品的结构示意图;
图8为实施例七所述的具备大便参数检测功能的吸湿用品的俯视图;
图9为实施例九所述的具备大便参数检测功能的吸湿用品的结构示意图;
图10为实施例九所述的具备大便参数检测功能的吸湿用品的俯视图;
图11为实施例十二所述的具备经血参数检测功能的吸湿用品的结构示意图;
图12为实施例十二所述的具备经血参数检测功能的吸湿用品的俯视图;
图13为实施例十七所述的具备白带参数检测功能的吸湿用品的结构示意图;
图14为实施例十七所述的具备白带参数检测功能的吸湿用品的俯视图;
图15为实施例二十三所述的具备汗液参数检测功能的吸湿用品的结构示意图;
图16为实施例二十三所述的具备汗液参数检测功能的吸湿用品的俯视图;
图17为实施例二十八所述的吸湿用品的结构示意图;
图18为实施例二十八所述的吸湿用品的俯视图。
具体实施方式
下面结合附图并通过具体实施方式来说明本公开的技术方案。在不冲突的情况下,以下实施例和实施例中的特征可以相互组合。
相关技术中,人们由于生理上的因素,容易患有各种疾病并且不容易被发现,特别是婴儿容易患有肠炎或者黄疸等疾病,女性很容易得到诸如生殖系统干扰、白带异常或者阴道炎等妇科疾病,从人们日常排泄物中的成分参数得知是否患有疾病是很有必要的,因此,检测尿液、大便、经血、白带或者汗液中的成分参数是人们身体检查中重要的一部分。上述检测一般需要去医院,花费大时间长。
本实施例提供了一种吸湿用品,包括渗透层、阻隔层和吸收层,所述吸收层设置在所述渗透层与所述阻隔层之间,所述吸收层、所述渗透层和所述阻隔层中的至少一个上设置有用于检测尿液、大便、经血、白带和汗液中至少一项的检测试剂。下述实施例中对所述吸湿用品进行举例说明。
实施例一:
如图1和图2所示,于本实施例中,一种具备尿液参数检测功能的吸湿用品,包括渗透层3、阻隔层5和吸收层4,所述吸收层4设置在所述渗透层3与所述阻隔层5之间,所述吸收层4上设置有用于检测尿液的检测试剂6。
于本实施例中,所述吸收层4上设置有用于检测尿液的一种检测试剂6。
可选的,所述检测试剂6为:吡咯氨基酸酯衍生物,用于检测白细胞,使用干化法和白细胞酯酶法对尿液进行检测,当所述检测试剂6呈现阳性时,将代表人体尿路受到感染。
可选的,所述检测试剂6的状态为试带,所述检测试剂6远离人体的一侧设置有粘贴胶,所述粘贴胶用于固定所述检测试剂6。
示例的,所述检测试剂6设置在所述渗透层3与所述吸收层4之间。所述检测试剂6粘贴在所述吸收层4上靠近所述渗透层3的一面。
可选的,还包括前腰围部2和后腰围部1,所述前腰围部2设置在渗透层3、阻隔层5和吸收层4的第一端,所述后腰围部1设置在渗透层3、阻隔层5和吸收层4的第二端,所述前腰围部2与所述后腰围部1选择性粘贴连接。需要说明的是,下述实施例中前腰围部2和后腰围部1的设置位置与本实施例相同,所述前腰围部2设置在渗透层3、阻隔层5和吸收层4构成的部分的第一端,所述后腰围部1设置在渗透层3、阻隔层5和吸收层4构成的部分的第二端。
可选的,所述检测试剂6与所述后腰围部1的距离是所述检测试剂3与所述前腰围部2的距离的1.5倍。
可选的,由于试带较薄,所以本实施例以及下述其他实施例中的吸湿用品的渗透层3、阻隔层5和吸收层4任意两层之间无论是否设置试带,都可以是相互贴合的。
实施例二:
图3为实施例二所述的具备尿液参数检测功能的吸湿用品的结构示意图;图4为实施例二所述的具备尿液参数检测功能的吸湿用品的俯视图。参见图3和图4,于本实施例中,一种具备尿液参数检测功能的吸湿用品,包括渗透层3、吸收层4和阻隔层5,所述吸收层4设置在所述渗透层3与所述阻隔层5之间,该吸湿用品还包括检测试剂6,该检测试剂6为液体,吸附在所述渗透层3内部。
可选的,所述检测试剂6为:重氮盐,用于检测白细胞,使用干化法和白细胞酯酶法对尿液进行检测,当所述检测试剂6呈现阳性时,将代表人体尿路受到感染。
可选的,还包括前腰围部2和后腰围部1,所述前腰围部2与所述后腰围部1选择性粘贴连接。可选的,所述检测试剂6与所述后腰围部1的距离是所述检测试剂6与所述前腰围部2的距离的2倍。
实施例三:
图5为实施例三所述的具备尿液参数检测功能的吸湿用品的结构示意图,图6为实施例三所述的具备尿液参数检测功能的吸湿用品的俯视图。如图5和图6所示,于本实施例中,一种具备尿液参数检测功能的吸湿用品,包括渗透层3、吸收层4和阻隔层5,所述吸收层4设置在所述渗透层3与所述阻隔层5之间。
于本实施例中,用于检测尿液的第一检测试剂6设置在所述吸收层4与所述隔离层5之间。所述第一检测试剂的状态为糊状物。所述第一检测试剂为:二异丙苯过氧化二氢,用于检测隐血、潜血、尿红细胞以及尿血红蛋白。使用干化法和血红蛋白过氧化物酶法对尿液进行检测,若第一检测试剂显示为阳性,则尿中存在红细胞和血红蛋白,可能患有泌尿系、肾脏疾病或出血性疾病。
可选的,所述渗透层3上设置有用于检测尿液的第二检测试剂。所述第二检测试剂7设置在所述渗透层3与所述吸收层4之间。所述第二检测试剂的状态为糊状物,所述第二检测试剂为:N-萘基乙二胺,用于检测亚硝酸盐。使用干化法和亚硝酸盐还原法对尿液进行检测,若第二检测试剂显示为阳性,则代表人体 在泌尿系尿路感染过程中尿液由于在膀胱内滞留而导致亚硝酸盐的浓度增加。
可选的,还包括前腰围部2和后腰围部1,所述前腰围2与所述后腰围部1选择性粘贴连接。所述第一检测试剂以及所述第二检测试剂与所述后腰围部1的距离是所述第一检测试剂以及所述第二检测试剂与所述前腰围部2的距离的2.5倍。
图5中为了体现所述糊状的第一检测试剂6以及糊状的第二检测试剂7(下述统称糊状物),所以在渗透层3、吸收层4和阻隔层5之间设置了间隙,实际上,由于糊状物较薄,所以吸湿用品成品后,渗透层3、吸收层4和阻隔层5之间是相互贴合的。如图6所示,所述糊状物的形状可以是不规则的。
实施例四:
于本实施例中,一种具备尿液参数检测功能的吸湿用品,包括渗透层、阻隔层和吸收层,所述吸收层设置在所述渗透层与所述阻隔层之间,所述渗透层上设置有用于检测尿液的检测试剂。
于本实施例中,所述渗透层上设置有用于检测尿液的一种检测试剂。
可选的,所述检测试剂为:二氯苯胺重氮盐,用于检测胆红素。通过干化法和偶氮反应法对尿液进行检测,所述检测试剂若为阳性,则代表肝病等致胆红素增高,或者新生儿患有黄疸。
可选的,所述检测试剂的状态为液体,所述检测试剂吸附在所述渗透层上。
可选的,所述检测试剂设置在所述渗透层的内部。
可选的,还包括前腰围部和后腰围部,所述前腰围部与所述后腰围部选择性粘贴连接。
可选的,所述检测试剂与所述后腰围部的距离是所述检测试剂与所述前腰围部的距离的1倍。
实施例五:
于本实施例中,一种具备尿液参数检测功能的吸湿用品,包括渗透层、阻隔层和吸收层,所述吸收层设置在所述渗透层与所述阻隔层之间,所述渗透层上设置有用于检测尿液的检测试剂。
于本实施例中,所述渗透层上设置有用于检测尿液的一种检测试剂。
可选的,所述检测试剂为:胶体金标记的病原体单抗,用于检测尿病原体抗体,使用胶体金法和免疫化学法对尿液进行检测,当所述检测试剂呈现的阳性时,将代表人体可能受到该病原体的感染。
可选的,所述检测试剂的状态为液体,所述检测试剂吸附在所述渗透层上。
可选的,所述检测试剂设置在所述渗透层的内部。
可选的,还包括前腰围部和后腰围部,所述前腰围部与所述后腰围部选择性粘贴连接。
可选的,所述检测试剂与所述后腰围部的距离是所述检测试剂与所述前腰围部的距离的2.2倍。
实施例六:
于本实施例中,一种具备尿液参数检测功能的吸湿用品,包括渗透层、阻隔层和吸收层,所述吸收层设置在所述渗透层与所述阻隔层之间,所述吸收层和所述渗透层上设置有用于检测尿液的检测试剂。
可选的,还包括前腰围部和后腰围部,所述前腰围部与所述后腰围部选择性粘贴连接。
可选的,所述吸收层上设置有用于检测尿液的一种检测试剂。所述检测试剂设置在所述吸收层与所述隔离层之间。所述检测试剂的状态为糊状物,所述检测试剂粘贴在所述吸收层上。所述检测试剂粘贴在所述吸收层靠近所述隔离层的一面上。所述检测试剂为:二氯苯胺重氮盐,用于检测胆红素。通过干化法和偶氮反应法对尿液进行检测,所述检测试剂若为阳性,则代表肝病等致胆红素增高,或者新生儿患有黄疸。所述检测试剂与所述后腰围部的距离是所述检测试剂与所述前腰围部的距离的2.5倍。
可选的,所述渗透层上设置有用于检测尿液的一种检测试剂。所述检测试剂设置在所述渗透层与所述吸收层之间。所述检测试剂的状态为糊状物,所述检测试剂粘贴在所述渗透层上。所述检测试剂粘贴在所述渗透层靠近所述吸收层的一面上。所述检测试剂为:N-萘基乙二胺,用于检测亚硝酸盐。使用干化法和亚硝酸盐还原法对尿液进行检测,若检测试剂显示为阳性,则代表人体在泌尿系尿路感染过程中尿液由于在膀胱内滞留而导致亚硝酸盐的浓度增加。所述检测试剂与所述后腰围部的距离是所述检测试剂与所述前腰围部的距离的1.8倍。
实施例七:
如图7和图8所示,于本实施例中,一种具备大便参数检测功能的吸湿用品,包括渗透层3、阻隔层5和吸收层4,所述吸收层4设置在所述渗透层3与所述阻隔层5之间,所述吸收层4上设置有用于检测大便的检测试剂6。
于本实施例中,所述吸收层4上设置有用于检测大便的一种检测试剂6。
可选的,所述检测试剂6为:吡咯氨基酸酯衍生物,用于检测白细胞,使用干化法和白细胞酯酶法对大便进行检测,当所述检测试剂6呈现的阳性时,将代表人体患有肠炎或细菌性痢疾。
可选的,所述检测试剂6的状态为试带,所述检测试剂6远离人体的一侧设置有粘贴胶,所述粘贴胶用于固定所述检测试剂6。
可选的,所述检测试剂6设置在所述渗透层3与所述吸收层4之间。所述检测试剂6粘贴在所述吸收层4上靠近所述渗透层3的一面。
可选的,还包括前腰围部2和后腰围部1,所述前腰围部2设置在渗透层3、阻隔层5和吸收层4的第一端,所述后腰围部1设置在渗透层3、阻隔层5和吸收层4的第二端,所述前腰围部2与所述后腰围部1选择性粘贴连接。
可选的,所述检测试剂6与所述前腰围部2的距离是所述检测试剂6与所述后腰围部1的距离的1.5倍。
实施例八:
于本实施例中,一种具备大便参数检测功能的吸湿用品,包括渗透层、阻隔层和吸收层,所述吸收层设置在所述渗透层与所述阻隔层之间,所述吸收层上设置有用于检测大便的检测试剂。
可选的,所述吸收层上设置有用于检测大便的一种检测试剂。
可选的,所述检测试剂为:吡咯氨基酸酯衍生物,用于检测白细胞,使用干化法和白细胞酯酶法对大便进行检测,当所述检测试剂呈现的阳性时,将代表人体患有肠炎或细菌性痢疾。
可选的,所述检测试剂的状态为试带,所述检测试剂远离人体的一侧设置有粘贴胶,所述粘贴胶用于固定所述检测试剂。
可选的,所述检测试剂设置在所述渗透层与所述吸收层之间。所述检测试剂粘贴在所述吸收层上靠近所述渗透层的一面。
可选的,还包括前腰围部和后腰围部,所述前腰围部与所述后腰围部选择性粘贴连接。
可选的,所述检测试剂与所述前腰围部的距离是所述检测试剂与所述后腰围部的距离的2倍。
实施例九:
图9为实施例九所述的具备大便参数检测功能的吸湿用品的结构示意图,图10为实施例九所述的具备大便参数检测功能的吸湿用品的俯视图。
如图9和图10所示,本实施例中具备大便参数检测功能的吸湿用品,包括渗透层3、吸收层4、阻隔层5以及检测试剂6,所述吸收层4设置在所述渗透层3与所述阻隔层5之间,所述吸收层4内部设置有用于检测大便的粉末状的检测试剂6。
于本实施例中,所述检测试剂为:吡咯氨基酸酯衍生物,用于检测白细胞,使用干化法和白细胞酯酶法对大便进行检测,当所述检测试剂呈现的阳性时,将代表人体患有肠炎或细菌性痢疾。
可选的,还包括前腰围部2和后腰围部1,所述前腰围2与所述后腰围部1选择性粘贴连接。
可选的,参见图4,所述检测试剂6与所述前腰围部2的距离是所述检测试剂6与所述后腰围部1的距离的2.5倍。
实施例十:
于本实施例中,一种具备大便参数检测功能的吸湿用品,包括渗透层、阻隔层和吸收层,所述吸收层设置在所述渗透层与所述阻隔层之间,所述吸收层和所述渗透层上设置有用于检测大便的检测试剂。
可选的,所述吸收层上设置有用于检测大便的一种检测试剂。所述检测试剂为:对二乙基氨基苯甲醛,用于检测粪胆原,使用干化法和醛反应法对大便进行检测,若检测试剂显示为阳性,则人体患有溶血性黄疸或者肝性黄疸。所述检测试剂的状态为粉末,所述检测试剂嵌进在所述吸收层上。所述检测试剂设置在所述吸收层的内部。
可选的,所述渗透层上设置有用于检测大便的一种检测试剂。所述检测试剂为:二氯苯胺重氮盐,用于检测粪便胆红素,使用干化法和偶氮反应法对大便进行检测,若检测试剂显示为阳性,则人体患有溶血性黄疸或者阻塞性黄疸。所述检测试剂的状态为液体,所述检测试剂吸附在所述渗透层上。所述检测试剂设置在所述渗透层的内部。
可选的,还包括前腰围部和后腰围部,所述前腰围部与所述后腰围部选择性粘贴连接。
可选的,所述检测试剂与所述前腰围部的距离是所述检测试剂与所述后腰围部的距离的1倍。
实施例十一:
于本实施例中,一种具备大便参数检测功能的吸湿用品,包括渗透层、阻隔层和吸收层,所述吸收层设置在所述渗透层与所述阻隔层之间,所述吸收层 和所述渗透层上设置有用于检测大便的检测试剂。
可选的,还包括前腰围部和后腰围部,所述前腰围部与所述后腰围部选择性粘贴连接。
可选的,所述吸收层上设置有用于检测大便的一种检测试剂。所述检测试剂为:四甲基联苯胺,用于检测红细胞以及潜血,使用干化法和血红蛋白过氧化物酶法对大便进行检测,若检测试剂显示为阳性,则表示大便中存在红细胞和血红蛋白,人体可能患有痢疾、肠炎、结肠癌或痔疮出血。所述检测试剂的状态为粉末,所述检测试剂嵌进在所述吸收层上。所述检测试剂设置在所述吸收层的内部。所述检测试剂与所述前腰围部的距离是所述检测试剂与所述后腰围部的距离的2.2倍。
可选的,所述渗透层上设置有用于检测大便的一种检测试剂。所述检测试剂为:二氯苯胺重氮盐,用于检测粪便胆红素,使用干化法和偶氮反应法对大便进行检测,若检测试剂显示为阳性,则人体患有溶血性黄疸或者阻塞性黄疸。所述检测试剂的状态为液体,所述检测试剂吸附在所述渗透层上。所述检测试剂设置在所述渗透层的内部。所述检测试剂与所述前腰围部的距离是所述检测试剂与所述后腰围部的距离的2.0倍。
实施例十二:
如图11和图12所示,于本实施例中,一种具备经血参数检测功能的吸湿用品,包括渗透层3、阻隔层5和吸收层4,所述吸收层4设置在所述渗透层3与所述阻隔层5之间,所述吸收层4上设置有用于检测经血的检测试剂6。
可选的,所述吸收层4上设置有用于检测经血的一种检测试剂6。
可选的,所述检测试剂6为:吡咯氨基酸酯衍生物,用于检测白细胞,使用干化法和白细胞酯酶法对经血进行检测,当所述检测试剂6呈现的阳性时,将代表人体的生殖系统受到了干扰。
可选的,所述检测试剂6的状态为试带,所述检测试剂6远离人体的一侧设置有粘贴胶,所述粘贴胶用于固定所述检测试剂6。
可选的,所述检测试剂6设置在所述渗透层3与所述吸收层4之间。所述检测试剂6粘贴在所述吸收层4上靠近所述渗透层3的一面。
可选的,还包括前腰围部2和后腰围部1,所述前腰围部2设置在渗透层3、阻隔层5和吸收层4的第一端,所述后腰围部1设置在渗透层3、阻隔层5和吸收层4的第二端,所述前腰围部2与所述后腰围部1选择性粘贴连接。
可选的,所述检测试剂6与所述后腰围部1的距离是所述检测试剂6与所述前腰围部2的距离的1.5倍。
实施例十三:
于本实施例中,一种具备经血参数检测功能的吸湿用品,包括渗透层、阻隔层和吸收层,所述吸收层设置在所述渗透层与所述阻隔层之间,所述吸收层上设置有用于检测经血的检测试剂。
于本实施例中,所述吸收层上设置有用于检测经血的一种检测试剂。
可选的,所述检测试剂为:重氮盐,用于检测白细胞,使用干化法和白细胞酯酶法对经血进行检测,当所述检测试剂呈现的阳性时,将代表人体的生殖系统受到了干扰。
可选的,所述检测试剂的状态为试带,所述检测试剂远离人体的一侧设置有粘贴胶,所述粘贴胶用于固定所述检测试剂。
可选的,所述检测试剂设置在所述渗透层与所述吸收层之间。所述检测试剂粘贴在所述吸收层上靠近所述渗透层的一面。
可选的,还包括前腰围部和后腰围部,所述前腰围部与所述后腰围部选择性粘贴连接。
可选的,所述检测试剂与所述后腰围部的距离是所述检测试剂与所述前腰围部的距离的2.5倍。
实施例十四:
于本实施例中,一种具备经血参数检测功能的吸湿用品,包括渗透层、阻隔层和吸收层,所述吸收层设置在所述渗透层与所述阻隔层之间,所述吸收层上设置有用于检测经血的检测试剂。
于本实施例中,所述吸收层上设置有用于检测经血的一种检测试剂。
可选的,所述检测试剂为:重氮盐,用于检测白细胞,使用干化法和白细胞酯酶法对经血进行检测,当所述检测试剂呈现的阳性时,将代表人体的生殖系统受到了干扰。
可选的,所述检测试剂的状态为粉末,所述检测试剂嵌进在所述吸收层上。
可选的,所述检测试剂设置在所述吸收层的内部。
可选的,还包括前腰围部和后腰围部,所述前腰围部与所述后腰围部选择性粘贴连接。
可选的,所述检测试剂与所述后腰围部的距离是所述检测试剂与所述前腰 围部的距离的2倍。
实施例十五:
于本实施例中,一种具备经血参数检测功能的吸湿用品,包括渗透层、阻隔层和吸收层,所述吸收层设置在所述渗透层与所述阻隔层之间,所述吸收层和所述渗透层上设置有用于检测经血的检测试剂。
于本实施例中,所述吸收层上设置有用于检测经血的一种检测试剂。所述检测试剂为:对氨苯基砷酸,用于检测亚硝酸盐,使用干化法和亚硝酸盐还原法对经血进行检测,观察检测试剂得知生殖系统是否受到感染。所述检测试剂的状态为粉末,所述检测试剂嵌进在所述吸收层上。所述检测试剂设置在所述吸收层的内部。
可选的,所述渗透层上设置有用于检测经血的一种检测试剂。所述检测试剂为:胶体金标记的HCG(人绒毛膜促性腺激素,Human Chorionic Gonadotropin)单抗,用于检测HCG,使用胶体金法和免疫化学法对经血进行检测,观察检测试剂得知是否存在非正常月经或者意外流产可能。所述检测试剂的状态为液体,所述检测试剂吸附在所述渗透层上。所述检测试剂设置在所述渗透层的内部。
可选的,还包括前腰围部和后腰围部,所述前腰围部与所述后腰围部选择性粘贴连接。
可选的,所述检测试剂与所述后腰围部的距离是所述检测试剂与所述前腰围部的距离的1倍。
实施例十六:
可选的,一种具备经血参数检测功能的吸湿用品,包括渗透层、阻隔层和吸收层,所述吸收层设置在所述渗透层与所述阻隔层之间,所述吸收层和所述渗透层上设置有用于检测经血的检测试剂。
可选的,还包括前腰围部和后腰围部,所述前腰围部与所述后腰围部选择性粘贴连接。
可选的,所述吸收层上设置有用于检测经血的一种检测试剂。所述检测试剂为:重氮盐,用于检测白细胞,使用干化法和白细胞酯酶法对经血进行检测,当所述检测试剂呈现的阳性时,将代表人体的生殖系统受到了干扰。所述检测试剂的状态为粉末,所述检测试剂嵌进在所述吸收层上。所述检测试剂设置在所述吸收层的内部。所述检测试剂与所述后腰围部的距离是所述检测试剂与所述前腰围部的距离的2.2倍。
可选的,所述渗透层上设置有用于检测经血的一种检测试剂。所述检测试剂为:胶体金标记的HCG单抗,用于检测HCG,使用胶体金法和免疫化学法对经血进行检测,观察检测试剂得知是否存在非正常月经或者意外流产可能。所述检测试剂的状态为液体,所述检测试剂吸附在所述渗透层上。所述检测试剂设置在所述渗透层的内部。所述检测试剂与所述后腰围部的距离是所述检测试剂与所述前腰围部的距离的1.8倍。
实施例十七:
如图13和图14所示,于本实施例中,一种具备白带参数检测功能的吸湿用品,包括渗透层3、阻隔层5和吸收层4,所述吸收层4设置在所述渗透层3与所述阻隔层5之间,所述吸收层4上设置有用于检测白带的检测试剂6。
于本实施例中,所述吸收层4上设置有用于检测白带的一种检测试剂6。
可选的,所述检测试剂6为:5-溴-4-氯-3-吲哚神经氨酸盐,用于检测唾液酸苷酶,使用干化法和酶促显色法对白带进行检测,当所述检测试剂6呈现阳性时,将代表人体具有感染性阴道炎。
可选的,所述检测试剂6的状态为试带,所述检测试剂6远离人体的一侧设置有粘贴胶,所述粘贴胶用于固定所述检测试剂6。
可选的,所述检测试剂6设置在所述渗透层3与所述吸收层4之间。所述检测试剂6粘贴在所述吸收层4上靠近所述渗透层3的一面。
可选的,还包括前腰围部2和后腰围部1,所述前腰围部2设置在渗透层3、阻隔层5和吸收层4的第一端,所述后腰围部1设置在渗透层3、阻隔层5和吸收层4的第二端,所述前腰围部2与所述后腰围部1选择性粘贴连接。
可选的,所述检测试剂6与所述后腰围部1的距离是所述检测试剂6与所述前腰围部2的距离的1.5倍。
实施例十八:
可选的,一种具备白带参数检测功能的吸湿用品,包括渗透层、阻隔层和吸收层,所述吸收层设置在所述渗透层与所述阻隔层之间,所述渗透层上设置有用于检测白带的检测试剂。
可选的,所述渗透层上设置有用于检测白带的一种检测试剂。
可选的,所述检测试剂为:氢氧化钾,用于检测胺。当所述检测试剂出现鱼腥臭味时,就代表着人体患有细菌性阴道病。
可选的,所述检测试剂的状态为液体,所述检测试剂吸附在所述渗透层上。
可选的,所述检测试剂设置在所述渗透层的内部。
可选的,还包括前腰围部和后腰围部,所述前腰围部与所述后腰围部选择性粘贴连接。
可选的,所述检测试剂与所述后腰围部的距离是所述检测试剂与所述前腰围部的距离的2倍。
实施例十九:
于本实施例中,一种具备白带参数检测功能的吸湿用品,包括渗透层、阻隔层和吸收层,所述吸收层设置在所述渗透层与所述阻隔层之间,所述吸收层和所述渗透层上设置有用于检测白带的检测试剂。
于本实施例中,所述吸收层上设置有用于检测白带的一种检测试剂。所述检测试剂设置在所述吸收层与所述隔离层之间。所述检测试剂的状态为糊状物,所述检测试剂粘贴在所述吸收层上。所述检测试剂粘贴在所述吸收层靠近所述隔离层的一面上。所述检测试剂为:溴酚蓝,用于检测PH(Hydrogen ion concentration,氢离子浓度)指数。若所述检测试剂显示绿色,则代表人体患有念珠菌性阴道炎。
可选的,所述渗透层上设置有用于检测白带的一种检测试剂。所述检测试剂设置在所述渗透层与所述吸收层之间。所述检测试剂的状态为糊状物,所述检测试剂粘贴在所述渗透层上。所述检测试剂粘贴在所述渗透层靠近所述吸收层的一面上。所述检测试剂为:甲基红,用于检测PH。若所述检测试剂显示蓝色,则代表人体患有滴虫性阴道炎。
可选的,还包括前腰围部和后腰围部,所述前腰围部与所述后腰围部选择性粘贴连接。
可选的,所述检测试剂与所述后腰围部的距离是所述检测试剂与所述前腰围部的距离的2.5倍。
实施例二十:
于本实施例中,一种具备白带参数检测功能的吸湿用品,包括渗透层、阻隔层和吸收层,所述吸收层设置在所述渗透层与所述阻隔层之间,所述渗透层上设置有用于检测白带的检测试剂。
可选的,所述渗透层上设置有用于检测白带的一种检测试剂。
可选的,所述检测试剂为:重氮盐,用于检测白细胞。当所述检测试剂呈现阳性时,就代表着人体的阴道受到感染。
可选的,所述检测试剂的状态为液体,所述检测试剂吸附在所述渗透层上。
可选的,所述检测试剂设置在所述渗透层的内部。
可选的,还包括前腰围部和后腰围部,所述前腰围部与所述后腰围部选择性粘贴连接。
可选的,所述检测试剂与所述后腰围部的距离是所述检测试剂与所述前腰围部的距离的1倍。
实施例二十一:
于本实施例中,一种具备白带参数检测功能的吸湿用品,包括渗透层、阻隔层和吸收层,所述吸收层设置在所述渗透层与所述阻隔层之间,所述渗透层上设置有用于检测白带的检测试剂。
可选的,所述渗透层上设置有用于检测白带的一种检测试剂。
可选的,所述检测试剂为:辣根过氧化物酶,用于检测过氧化氢。当所述检测试剂的颜色改变时,就代表着人体的阴道菌群正常,若无变色,则代表阴道环境病态或处于亚健康状态。
可选的,所述检测试剂的状态为液体,所述检测试剂吸附在所述渗透层上。
可选的,所述检测试剂设置在所述渗透层的内部。
可选的,还包括前腰围部和后腰围部,所述前腰围部与所述后腰围部选择性粘贴连接。
可选的,所述检测试剂与所述后腰围部的距离是所述检测试剂与所述前腰围部的距离的2.2倍。
实施例二十二:
于本实施例中,一种具备白带参数检测功能的吸湿用品,包括渗透层、阻隔层和吸收层,所述吸收层设置在所述渗透层与所述阻隔层之间,所述吸收层和所述渗透层上设置有用于检测白带的检测试剂。
可选的,还包括前腰围部和后腰围部,所述前腰围部与所述后腰围部选择性粘贴连接。
可选的,所述吸收层上设置有用于检测白带的一种检测试剂。所述检测试剂设置在所述吸收层与所述隔离层之间。所述检测试剂的状态为糊状物,所述检测试剂粘贴在所述吸收层上。所述检测试剂粘贴在所述吸收层靠近所述隔离层的一面上。所述检测试剂为:5-溴-4-氯-3-吲哚神经氨酸盐,用于检测唾液酸苷酶。使用干化法和酶促显色法对白带进行检测,当所述检测试剂呈现阳性时, 将代表人体具有感染性阴道炎。所述检测试剂与所述后腰围部的距离是所述检测试剂与所述前腰围部的距离的2.5倍。
可选的,所述渗透层上设置有用于检测白带的一种检测试剂。所述检测试剂设置在所述渗透层与所述吸收层之间。所述检测试剂的状态为糊状物,所述检测试剂粘贴在所述渗透层上。所述检测试剂粘贴在所述渗透层靠近所述吸收层的一面上。所述检测试剂为:甲基红,用于检测PH。若所述检测试剂显示蓝色,则代表人体患有滴虫性阴道炎。所述检测试剂与所述后腰围部的距离是所述检测试剂与所述前腰围部的距离的2.2倍。
实施例二十三:
如图15和图16所示,于本实施例中,一种具备汗液参数检测功能的吸湿用品,包括渗透层3、阻隔层5和吸收层4,所述吸收层4设置在所述渗透层3与所述阻隔层5之间,所述吸收层4上设置有用于检测汗液的检测试剂6。
于本实施例中,所述吸收层4上设置有用于检测汗液的一种检测试剂6。
可选的,所述检测试剂6为:甲基红,用于检测PH,使用干化法和指示剂法对汗液进行检测,当所述检测试剂6呈现的PH值为4.2-7.5时,将代表人体的电解质摄取正常,否则不正常。
可选的,所述检测试剂6的状态为试带,所述检测试剂6远离人体的一侧设置有粘贴胶,所述粘贴胶用于固定所述检测试剂6。
可选的,所述检测试剂6设置在所述渗透层3与所述吸收层4之间。所述检测试剂6粘贴在所述吸收层4上靠近所述渗透层3的一面。
可选的,还包括前腰围部2和后腰围部1,所述前腰围部2设置在渗透层3、阻隔层5和吸收层4的第一端,所述后腰围部1设置在渗透层3、阻隔层5和吸收层4的第二端,所述前腰围部2与所述后腰围部1选择性粘贴连接。
可选的,所述检测试剂6设置在所述吸收层4上靠近前腰围部2的一侧和靠近后腰围部1的一侧。
实施例二十四:
于本实施例中,一种具备汗液参数检测功能的吸湿用品,包括渗透层、阻隔层和吸收层,所述吸收层设置在所述渗透层与所述阻隔层之间,所述吸收层上设置有用于检测汗液的检测试剂。
于本实施例中,所述吸收层上设置有用于检测汗液的一种检测试剂。
可选的,所述检测试剂为:甲基红,用于检测PH,使用干化法和指示剂法 对汗液进行检测,当所述检测试剂呈现的PH值为4.2-7.5时,将代表人体的电解质摄取正常,否则不正常。
可选的,所述检测试剂的状态为液体,所述检测试剂吸附在所述吸收层上。
可选的,所述检测试剂设置在所述吸收层的内部。
可选的,还包括前腰围部和后腰围部,所述前腰围部与所述后腰围部选择性粘贴连接。
可选的,所述检测试剂与所述后腰围部的距离是所述检测试剂与所述前腰围部的距离的2.3倍。
实施例二十五:
于本实施例中,一种具备汗液参数检测功能的吸湿用品,包括渗透层、阻隔层和吸收层,所述吸收层设置在所述渗透层与所述阻隔层之间,所述吸收层上设置有用于检测汗液的检测试剂。
于本实施例中,所述吸收层上设置有用于检测汗液的一种检测试剂。
可选的,所述检测试剂为:氢氧化钠,用于检测电解质比重。通过干化法和多聚电解质离子解离法,使所述检测试剂显示比重,若比重为1.002~1.003,为正常,否则,则为人体电解质摄取不正常。
可选的,所述检测试剂的状态为试带,所述检测试剂远离人体的一侧设置有粘贴胶,所述粘贴胶用于固定所述检测试剂。
可选的,所述检测试剂设置在所述渗透层与所述吸收层之间。所述检测试剂粘贴在所述吸收层上靠近所述渗透层的一面。
可选的,还包括前腰围部和后腰围部,所述前腰围部与所述后腰围部选择性粘贴连接。
可选的,所述检测试剂设置在所述吸收层上靠近前腰围部的一侧和靠近后腰围部的一侧。
实施例二十六:
于本实施例中,一种具备汗液参数检测功能的吸湿用品,包括渗透层、阻隔层和吸收层,所述吸收层设置在所述渗透层与所述阻隔层之间,所述吸收层和所述渗透层上设置有用于检测汗液的检测试剂。
于本实施例中,所述吸收层上设置有用于检测汗液的一种检测试剂。所述检测试剂的状态为液体,所述检测试剂吸附在所述吸收层上。所述检测试剂设置在所述吸收层的内部。所述检测试剂为:对氨基苯胂酸,用于检测亚硝酸盐。 通过干化法和亚硝酸盐还原法,使所述检测试剂对汗液内的细菌起反应,提示是否“汗味”严重的,甚至是已经引起了皮肤疾病,就是人们通常所说的汗疹、毛囊炎、湿疹、疖子或痱子等。
可选的,所述渗透层上设置有用于检测汗液的一种检测试剂。所述检测试剂的状态为糊状物,所述检测试剂粘贴在所述渗透层上。所述检测试剂设置在所述渗透层的内部。所述检测试剂为:乙烯基甲醚,用于检测电解质比重。通过干化法和多聚电解质离子解离法,使所述检测试剂显示比重,若比重为1.002~1.003,为正常,否则,则为人体电解质摄取不正常。
可选的,还包括前腰围部和后腰围部,所述前腰围部与所述后腰围部选择性粘贴连接。
可选的,所述检测试剂与所述后腰围部的距离是所述检测试剂与所述前腰围部的距离的1.5倍。
实施例二十七:
于本实施例中,一种具备汗液参数检测功能的吸湿用品,包括渗透层、阻隔层和吸收层,所述吸收层设置在所述渗透层与所述阻隔层之间,所述吸收层和所述渗透层上设置有用于检测汗液的检测试剂。
可选的,还包括前腰围部和后腰围部,所述前腰围部与所述后腰围部选择性粘贴连接。
可选的,所述吸收层上设置有用于检测汗液的一种检测试剂。所述检测试剂的状态为液体,所述检测试剂吸附在所述吸收层上。所述检测试剂设置在所述吸收层的内部。所述检测试剂为:对氨基苯胂酸,用于检测亚硝酸盐。通过干化法和亚硝酸盐还原法,使所述检测试剂对汗液内的细菌起反应,提示是否“汗味”严重的,甚至是已经引起了皮肤疾病,就是人们通常所说的汗疹、毛囊炎、湿疹、疖子或痱子等。所述检测试剂与所述后腰围部的距离是所述检测试剂与所述前腰围部的距离的1.8倍。
可选的,所述渗透层上设置有用于检测汗液的一种检测试剂。所述检测试剂的状态为糊状物,所述检测试剂粘贴在所述渗透层上。所述检测试剂设置在所述渗透层的内部。所述检测试剂为:甲基红,用于检测PH,使用干化法和指示剂法对汗液进行检测,当所述检测试剂呈现的PH值为4.2-7.5时,将代表人体的电解质摄取正常,否则不正常。所述检测试剂与所述后腰围部的距离是所述检测试剂与所述前腰围部的距离的2倍。
实施例二十八:
本实施例提供了一种吸湿用品,包括渗透层、阻隔层和吸收层,所述吸收层设置在所述渗透层与所述阻隔层之间,所述吸收层、所述渗透层和所述阻隔层中的至少一个上设置有用于检测尿液、大便、经血、白带和汗液中至少一项的检测试剂。
图17为实施例二十八所述的吸湿用品的结构示意图,图18为实施例二十八所述的吸湿用品的俯视图。如图17和图18所示,示例性的,所述吸湿用品可以是用于检测白带和大便。
可选的,用于检测白带的第一检测试剂6的状态为试带,粘贴在所述吸收层4上靠近阻隔层5的一面,用于检测大便的一种第二检测试剂7为试带,所述第二检测试剂7远离人体的一侧设置有粘贴胶,所述第二检测试剂7可以是粘贴在所述吸收层4上靠近所述渗透层3的一面。
可选的,所述第一检测试剂6与所述后腰围部1的距离是所述第一检测试剂6与所述前腰围部2的距离的1.5倍,所述第二检测试剂7与所述前腰围部2的距离是所述第一检测试剂6与所述后腰围部1的距离的1.5倍。
可选的,所述吸湿用品还包括前腰围部2和后腰围部1,所述前腰围部2设置在渗透层3、阻隔层5和吸收层4的第一端,所述后腰围部1设置在渗透层3、阻隔层5和吸收层4的第二端,所述前腰围部2与所述后腰围部1选择性粘贴连接。
工业实用性
本公开提供一种吸湿用品,通过在吸湿用品上设置检测试剂,实现在日常生活中对人体参数的检测,初步识别人体参数是否异常或者人体是否病变。

Claims (16)

  1. 一种吸湿用品,包括渗透层、阻隔层和吸收层,所述吸收层设置在所述渗透层与所述阻隔层之间,所述吸收层、所述渗透层和所述阻隔层中的至少一个上设置有用于检测尿液、大便、经血、白带和汗液中至少一项的检测试剂。
  2. 根据权利要求1所述的吸湿用品,其中,所述检测试剂的设置位置包括下述至少一个:
    所述渗透层远离所述吸收层的一面,所述渗透层与所述吸收层之间,所述吸收层与所述隔离层之间,所述渗透层的内部,以及所述吸收层的内部。
  3. 根据权利要求1所述的吸湿用品,其中,所述检测试剂为试带,所述检测试剂远离人体的一侧设置有粘贴胶,所述粘贴胶设置为固定所述检测试剂。
  4. 根据权利要求1所述的吸湿用品,其中,所述检测试剂为液体状态,所述检测试剂吸附在所述吸收层、渗透层或者阻隔层上。
  5. 根据权利要求1所述的吸湿用品,其中,所述检测试剂为粉末状,所述检测试剂嵌进在所述吸收层、渗透层或者阻隔层上。
  6. 根据权利要求1所述的吸湿用品,其中,所述检测试剂为糊状物,所述检测试剂粘贴在所述吸收层、渗透层或者阻隔层上。
  7. 根据权利要求1所述的吸湿用品,其中,所述用于检测尿液的检测试剂的种类为至少一种;
    所述用于检测大便的检测试剂的种类为至少一种;
    所述用于检测经血的检测试剂的种类为至少一种;
    所述用于检测白带的检测试剂的种类为至少一种;以及
    所述用于检测汗液的检测试剂的种类为至少一种。
  8. 根据权利要求1所述的吸湿用品,还包括前腰围部和后腰围部,所述前腰围部设置在渗透层、阻隔层和吸收层的第一端,所述后腰围部设置在渗透层、阻隔层和吸收层的第二端,所述前腰围部与所述后腰围部选择性粘贴连接。
  9. 根据权利要求8所述的吸湿用品,其中,当所述检测试剂用于检测尿液、经血或白带时,所述检测试剂与所述后腰围部的距离是所述检测试剂与所述前腰围部的距离的1倍以上2.5倍以下。
  10. 根据权利要求8所述的吸湿用品,其中,当所述检测试剂用于检测大便时,所述检测试剂与所述前腰围部的距离是所述检测试剂与所述后腰围部的距离的1倍以上2.5倍以下。
  11. 根据权利要求8所述的吸湿用品,其中,当所述检测试剂用于检测汗液 时,所述检测试剂设置在吸收层、所述渗透层和所述阻隔层中的至少一个上且位于靠近前腰围部的一侧和靠近后腰围部的一侧中的至少一处。
  12. 根据权利要求1-6任意一项所述的吸湿用品,其中,当所述检测试剂用于检测尿液时,所述检测试剂包括以下至少一种:
    四溴酚蓝,设置为检测蛋白质;
    吡咯氨基酸酯衍生物,设置为检测白细胞;
    重氮盐,设置为检测白细胞;
    二异丙苯过氧化二氢,设置为检测隐血、潜血、尿红细胞以及尿血红蛋白;
    四甲基联苯胺,设置为检测隐血、潜血、尿红细胞以及尿血红蛋白;
    对氨基苯胂酸,设置为检测亚硝酸盐;
    N-萘基乙二胺,设置为检测亚硝酸盐;
    亚硝基铁氰化钠,设置为检测酮体;
    甲基红,设置为检测氢离子浓度指数PH;
    溴酚蓝,设置为检测PH或者固体物质比重;
    乙烯基甲醚,设置为检测固体物质比重;
    顺丁烯二酸酐聚合物,设置为检测固体物质比重;
    氢氧化钠,设置为检测固体物质比重;
    二氯苯胺重氮盐,设置为检测胆红素;
    对二乙基氨基苯甲醛,设置为检测尿胆原;
    2,6-二氯酚靛酚,设置为检测维生素C;
    胶体金标记的病原体单抗,设置为检测尿液中病原体抗体;
    胶体金标记的人绒毛膜促性腺激素HCG单抗,设置为检测尿液中HCG;以及
    胶体金标金的三聚氰胺单抗,设置为检测三聚氰胺。
  13. 根据权利要求1-6任意一项所述的吸湿用品,其中,当所述检测试剂用于检测大便时,所述检测试剂包括以下至少一种:
    吡咯氨基酸酯衍生物,设置为检测白细胞;
    重氮盐,设置为检测白细胞;
    二异丙苯过氧化二氢,设置为检测红细胞以及潜血;
    四甲基联苯胺,设置为检测红细胞以及潜血;
    对二乙基氨基苯甲醛,设置为检测粪胆原;以及
    二氯苯胺重氮盐,设置为检测粪便胆红素。
  14. 根据权利要求1-6任意一项所述的吸湿用品,其中,当所述检测试剂用于检测经血时,所述检测试剂包括以下至少一种:
    吡咯氨基酸酯衍生物,设置为检测白细胞;
    重氮盐,设置为检测白细胞;
    对氨苯基砷酸,设置为检测亚硝酸盐;
    N-萘基乙二胺,设置为检测亚硝酸盐;以及
    胶体金标记的HCG单抗,设置为检测HCG。
  15. 根据权利要求1-6任意一项所述的吸湿用品,其中,当所述检测试剂用于检测白带时,所述检测试剂包括以下至少一种:
    吡咯氨基酸酯衍生物,设置为检测白细胞;
    重氮盐,设置为检测白细胞;
    四甲基联苯胺,设置为检测过氧化氢;
    辣根过氧化物酶,设置为检测过氧化氢;
    5-溴-4-氯-3-吲哚神经氨酸盐,设置为检测唾液酸苷酶;
    甲基红,设置为检测PH;
    溴酚蓝,设置为检测PH;以及
    氢氧化钾,设置为检测胺。
  16. 根据权利要求1-6任意一项所述的吸湿用品,其中,当所述检测试剂用于检测汗液时,所述检测试剂包括以下至少一种:
    溴酚蓝,设置为检测电解质比重或者PH;
    乙烯基甲醚,设置为检测电解质比重;
    顺丁烯二酸酐聚合物,设置为检测电解质比重;
    氢氧化钠,设置为检测电解质比重;
    甲基红,设置为检测PH;
    对氨基苯胂酸,设置为检测亚硝酸盐;以及
    N-萘基乙二胺,设置为检测亚硝酸盐。
PCT/CN2017/092699 2016-07-13 2017-07-13 吸湿用品 WO2018010668A1 (zh)

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