JP7089413B2 - Wet wipes - Google Patents
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- JP7089413B2 JP7089413B2 JP2018114693A JP2018114693A JP7089413B2 JP 7089413 B2 JP7089413 B2 JP 7089413B2 JP 2018114693 A JP2018114693 A JP 2018114693A JP 2018114693 A JP2018114693 A JP 2018114693A JP 7089413 B2 JP7089413 B2 JP 7089413B2
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- A—HUMAN NECESSITIES
- A47—FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
- A47K—SANITARY EQUIPMENT NOT OTHERWISE PROVIDED FOR; TOILET ACCESSORIES
- A47K7/00—Body washing or cleaning implements
-
- A—HUMAN NECESSITIES
- A47—FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
- A47L—DOMESTIC WASHING OR CLEANING; SUCTION CLEANERS IN GENERAL
- A47L13/00—Implements for cleaning floors, carpets, furniture, walls, or wall coverings
- A47L13/10—Scrubbing; Scouring; Cleaning; Polishing
- A47L13/16—Cloths; Pads; Sponges
- A47L13/17—Cloths; Pads; Sponges containing cleaning agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/13—Amines
- A61K31/14—Quaternary ammonium compounds, e.g. edrophonium, choline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/75—Rutaceae (Rue family)
- A61K36/752—Citrus, e.g. lime, orange or lemon
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/12—Carboxylic acids; Salts or anhydrides thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/36—Carboxylic acids; Salts or anhydrides thereof
- A61K8/365—Hydroxycarboxylic acids; Ketocarboxylic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/43—Guanidines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
- A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
- A61K8/9783—Angiosperms [Magnoliophyta]
- A61K8/9789—Magnoliopsida [dicotyledons]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/70—Web, sheet or filament bases ; Films; Fibres of the matrix type containing drug
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/48—Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Chemical & Material Sciences (AREA)
- Birds (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Mycology (AREA)
- Biotechnology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Microbiology (AREA)
- Botany (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Alternative & Traditional Medicine (AREA)
- Medicinal Preparation (AREA)
- Medical Informatics (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
- Medicines Containing Plant Substances (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Detergent Compositions (AREA)
- Cleaning Implements For Floors, Carpets, Furniture, Walls, And The Like (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Description
本発明は、ウェットシートに関する。 The present invention relates to a wet sheet.
手の汚れの除去や清掃等に用いられる除菌効果を有するウェットシートとしては、大別して、含浸させる薬液にアルコールが含まれるものと、含まれないものとがあるが、従来、アルコールが含まれないものにおいては、除菌活性値を向上するために、プロピレングリコール及びパラベンを使用していた。しかし、プロピレングリコール及びパラベンを使用すると、薬液が使用者の肌に付着した際にべたつきを感じることがあった。
そこで、薬液にアルコールが含まれず、かつプロピレングリコール及びパラベンを使用しない、除菌効果を有するウェットシートが知られている(例えば、特許文献1参照)。
Wet wipes with a sterilizing effect used for removing stains on hands and cleaning are roughly classified into those containing alcohol and those not containing alcohol in the chemical solution to be impregnated, but conventionally, alcohol is contained. In those without, propylene glycol and paraben were used to improve the sterilization activity value. However, when propylene glycol and paraben were used, the drug solution sometimes felt sticky when it adhered to the user's skin.
Therefore, there is known a wet sheet having a sterilizing effect, which does not contain alcohol in the chemical solution and does not use propylene glycol and paraben (see, for example, Patent Document 1).
しかしながら、特許文献1に記載の発明においては、プロピレングリコール及びパラベンを含有しないものの、いまだ使用者が感じるべたつきの低減は十分ではなかった。 However, although the invention described in Patent Document 1 does not contain propylene glycol and paraben, the reduction in stickiness felt by the user is still insufficient.
本発明は、上記課題に鑑みてなされたものであって、十分な除菌力を有しつつ、使用者がべたつきを感じにくいウェットシートを提供することを目的とする。 The present invention has been made in view of the above problems, and an object of the present invention is to provide a wet sheet having sufficient sterilizing power and less sticky to the user.
上記課題を解決するため、請求項1に記載の発明は、
シート体に薬液を含浸させたウェットシートであって、
前記薬液は、
グレープフルーツ種子エキスと、アロエエキスと、グリセリンと、オレンジエキスと、を含有し、大腸菌及び黄色ブドウ球菌に対する除菌活性値が2.0以上であり、
接触角が35.75°以下であることを特徴とする。
本発明によれば、十分な除菌力を有しつつ、使用者がべたつきを感じにくいウェットシートを提供することができる。
請求項2に記載の発明は、請求項1に記載のウェットシートであって、
前記薬液は、
1.0×10
-2
質量%以上のグレープフルーツ種子エキスと、
1.0×10
-2
質量%以上のアロエエキスと、
1.0×10
-2
質量%以上のグリセリンと、
1.0×10
-2
質量%以上のオレンジエキスと、
を含有することを特徴とする
In order to solve the above problems, the invention according to claim 1 is
A wet sheet in which the sheet body is impregnated with a chemical solution.
The chemical solution is
It contains grapefruit seed extract , aloe extract, glycerin, and orange extract, and has a eradication activity value of 2.0 or more against Escherichia coli and Staphylococcus aureus.
It is characterized by having a contact angle of 35.75 ° or less.
According to the present invention, it is possible to provide a wet sheet that has sufficient sterilizing power and is less likely to be sticky to the user.
The invention according to claim 2 is the wet sheet according to claim 1.
The chemical solution is
1.0 × 10 -2 % by mass or more of grapefruit seed extract and
1.0 × 10 -2 mass% or more aloe extract and
1.0 × 10 -2 % by mass or more of glycerin,
1.0 x 10 -2 % by mass or more of orange extract and
It is characterized by containing
請求項3に記載の発明は、請求項1又は2に記載のウェットシートであって、
前記薬液は、
99.0質量%以上の水と、
1.0×10
-2
質量%以上、3.0×10
-2
質量%以下のグレープフルーツ種子エキスと、
5.0×10
-3
質量%のクエン酸と、
1.0×10
-3
質量%のクエン酸ナトリウムと、
5.0×10
-2
質量%の塩化ベンザルコニウムと、
3.0×10
-2
質量%の塩化セチルピリジニウムと、
2.0×10
-2
質量%のポリアミノプロピルビグアニドと、
を含有することを特徴とする。
本発明によれば、十分な除菌力を有しつつ、使用者がべたつきを感じにくいウェットシートを提供することができる。
The invention according to claim 3 is the wet sheet according to claim 1 or 2 .
The chemical solution is
With 99.0% by mass or more of water,
Grapefruit seed extract of 1.0 x 10 -2 % by mass or more and 3.0 x 10 -2 % by mass or less ,
5.0 × 10 -3 mass% citric acid and
1.0 × 10 -3 % by mass sodium citrate,
5.0 × 10 -2 % by mass of benzalkonium chloride,
3.0 × 10 -2 % by mass of cetylpyridinium chloride,
2.0 x 10 -2 % by weight polyaminopropyl biguanide,
It is characterized by containing.
According to the present invention, it is possible to provide a wet sheet that has sufficient sterilizing power and is less likely to be sticky to the user.
請求項4に記載の発明は、請求項1から3のいずれか一項に記載のウェットシートであって、
前記シート体は、引張強度が、MD方向に45N以上、CD方向に10N以上であることを特徴とする。
本発明によれば、ウェットシートを十分な強度とすることができる。
The invention according to claim 4 is the wet sheet according to any one of claims 1 to 3.
The sheet body is characterized in that the tensile strength is 45 N or more in the MD direction and 10 N or more in the CD direction.
According to the present invention, the wet sheet can have sufficient strength.
本発明によれば、十分な除菌力を有しつつ、使用者がべたつきを感じにくいウェットシートを提供することができる。 According to the present invention, it is possible to provide a wet sheet that has sufficient sterilizing power and is less likely to be sticky to the user.
以下、本発明の実施形態であるウェットシートについて詳細に説明する。ただし、本発明の技術的範囲は、これに限定されるものではない。 Hereinafter, the wet sheet according to the embodiment of the present invention will be described in detail. However, the technical scope of the present invention is not limited to this.
[実施形態の構成]
{全体構成}
本実施形態のウェットシートは、シート体に薬液が含浸されたものである。
[Structure of Embodiment]
{overall structure}
The wet sheet of the present embodiment is a sheet body impregnated with a chemical solution.
{シート体}
本発明において用いるシート体としては、後述の薬液を含浸させることができるものであれば、特に限定はないが、柄のない不織布であり、かつ引張強度(長辺100mm、短辺50mmの試験片を長辺方向に引っ張り、これが破断したときの最大点荷重によって測定した値(株式会社エー・アンド・ディー製のTENSILON RTG-1210を用いた。))が、抄紙機上の紙の進行方向(MD方向)に45N以上であり、抄紙機上の紙の進行方向と直角な方向(CD方向)に10N以上であることが望ましい。
{Sheet body}
The sheet body used in the present invention is not particularly limited as long as it can be impregnated with the chemical solution described later, but is a non-woven fabric without a handle and a test piece having a tensile strength (long side 100 mm, short side 50 mm). Is pulled in the long side direction, and the value measured by the maximum point load when it breaks (using TENSILON RTG-1210 manufactured by A & D Co., Ltd.) is the traveling direction of the paper on the paper making machine (. It is desirable that it is 45 N or more in the MD direction) and 10 N or more in the direction perpendicular to the traveling direction of the paper on the paper making machine (CD direction).
また、シート体を構成する原料繊維としては、レーヨン、PET(ポリエチレンテレフタレート)等を用いたものであることが望ましい。 Further, it is desirable that rayon, PET (polyethylene terephthalate) or the like is used as the raw material fiber constituting the sheet body.
また、シート体の目付は、20~80gsmであることが好ましい。なお、目付は、JIS P 8124:2011に従って測定した坪量をいう。 The basis weight of the sheet body is preferably 20 to 80 gsm. The basis weight refers to the basis weight measured according to JIS P 8124: 2011.
{薬液}
薬液としては、以下のものを用いる。
なお、薬液含浸率は50質量%以上、400質量%以下であることが好ましい。なお薬液含浸率とは、薬液含浸前のシート体の質量と、含浸させる薬液の質量とを測定し、薬液含浸前のシート体の質量に対する含浸させる薬液の質量の割合を算出したものをいう。
{Chemical solution}
The following chemicals are used.
The chemical impregnation rate is preferably 50% by mass or more and 400% by mass or less. The chemical impregnation rate is obtained by measuring the mass of the sheet body before the chemical solution impregnation and the mass of the chemical solution to be impregnated, and calculating the ratio of the mass of the chemical solution to be impregnated to the mass of the sheet body before the chemical solution impregnation.
薬液としては接触角が43°以下のものを用いる。接触角が36°以下のものを用いることがさらに好ましい。
なお、接触角は、固液界面解析システム(協和界面科学株式会社のDrop Master 300)を用いて液滴法にて測定を行った。具体的には、上記システムに付属のシリンジを用いて、液滴をアルミ製の台の表面に接触させて着滴させた後、自動的にパソコンに取得した画像の解析を行い、接触角を算出した。
As the chemical solution, one having a contact angle of 43 ° or less is used. It is more preferable to use one having a contact angle of 36 ° or less.
The contact angle was measured by the sessile drop method using a solid-liquid interface analysis system (Drop Master 300 of Kyowa Interface Science Co., Ltd.). Specifically, using the syringe attached to the above system, the droplets are brought into contact with the surface of an aluminum table to be deposited, and then the image acquired on the personal computer is automatically analyzed to determine the contact angle. Calculated.
また、清掃時の除菌効果を十分なものとするため、除菌力が99%以上である必要がある。
なお、ここで除菌力が99%以上とは、大腸菌及び黄色ブドウ球菌の両者に対して、除菌活性値が2.0以上であることをいう。なお、除菌活性値の測定は、一財社団法人 日本衛生材料工業連合会編、「ウエットワイパー類の除菌性能試験方法」(平成27年11月16日改定)に準じて行った。
具体的には、適当な汚れと共に細菌を試験担体(ステンレス板)に接種し、乾燥後拭取り装置に設置する。試験試料(ウエットワイプまたは対照液を塗布した綿布)を巻きつけたおもりで試験担体上を所定回数拭取り、5分間静置する。5分後、試験担体を不活性化剤に移し、試験試料の細菌の増殖を抑制したり死滅させる性質を不活性化させた後、試験担体上の生菌数を測定する。
試験試料の除菌活性値は、対照試料及び試験試料で拭取り後、それぞれの試験担体上に残存する生菌数の常用対数値の差で示す。
Further, in order to make the sterilizing effect at the time of cleaning sufficient, the sterilizing power needs to be 99% or more.
Here, the sterilizing power of 99% or more means that the sterilizing activity value is 2.0 or more with respect to both Escherichia coli and Staphylococcus aureus. The sterilization activity value was measured according to "Test method for sterilization performance of wet wipers" edited by Japan Sanitary Materials Industry Association (revised on November 16, 2015).
Specifically, the test carrier (stainless steel plate) is inoculated with bacteria together with appropriate stains, dried, and then installed in a wiping device. Wipe the test carrier a predetermined number of times with a weight wrapped with a test sample (wet wipe or cotton cloth coated with a control solution), and let stand for 5 minutes. After 5 minutes, the test carrier is transferred to an inactivating agent to inactivate the properties of the test sample that suppress or kill the growth of bacteria, and then the viable cell count on the test carrier is measured.
The sterilization activity value of the test sample is shown by the difference in the common logarithmic value of the viable cell count remaining on each test carrier after wiping with the control sample and the test sample.
このような薬液としては、具体的には、例えば以下の6成分を含有し、これら6成分の含有量の合計が1.0質量%以下であり、水の含有量が99.0質量%以上であるものを用いることができる。
1.0×10-2質量%以上、5.0×10-2質量%以下のグレープフルーツ種子エキス
1.0×10-3質量%以上、5.0×10-3質量%以下のクエン酸
1.0×10-3質量%以上、5.0×10-3質量%以下のクエン酸ナトリウム
1.0×10-2質量%以上、5.0×10-1質量%以下の塩化ベンザルコニウム
1.0×10-2質量%以上、5.0×10-2質量%以下の塩化セチルピリジニウム
1.0×10-3質量%以上、5.0×10-2質量%以下のポリアミノプロピルビグアニド
Specifically, such a chemical solution contains, for example, the following 6 components, the total content of these 6 components is 1.0% by mass or less, and the water content is 99.0% by mass or more. Can be used.
Grapefruit seed extract of 1.0 × 10 -2 % by mass or more and 5.0 × 10 -2 % by mass or less
Citric acid of 1.0 × 10 -3 % by mass or more and 5.0 × 10 -3 % by mass or less
1.0 × 10 -3 % by mass or more and 5.0 × 10 -3 % by mass or less of sodium citrate
Benzalkonium chloride of 1.0 × 10 -2 % by mass or more and 5.0 × 10 -1 % by mass or less
Cetylpyridinium chloride of 1.0 × 10 -2 % by mass or more and 5.0 × 10 -2 % by mass or less
Polyaminopropyl biguanide of 1.0 × 10 -3 % by mass or more and 5.0 × 10 -2 % by mass or less
グレープフルーツ種子エキスは、抗菌作用を有することから含有されているものである。
クエン酸は、pH調整及び緩衝作用を有することから含有されているものである。
クエン酸ナトリウムは、pH調整及び緩衝作用を有することから含有されているものである。
塩化ベンザルコニウムは、抗菌作用を有することから含有されているものである。
塩化セチルピリジニウムは、抗菌作用を有することから含有されているものである。
ポリアミノプロピルビグアニドは、抗菌作用を有することから含有されているものである。
Grapefruit seed extract is contained because it has an antibacterial effect.
Citric acid is contained because it has a pH adjusting and buffering action.
Sodium citrate is contained because it has a pH adjusting and buffering action.
Benzalkonium chloride is contained because it has an antibacterial effect.
Cetylpyridinium chloride is contained because it has an antibacterial effect.
Polyaminopropyl biguanide is contained because it has an antibacterial effect.
また、薬液はさらに、1.0×10-3質量%以上、5.0×10-2質量%以下のオレンジエキスを含有していてもよい。 Further, the chemical solution may further contain an orange extract of 1.0 × 10 -3 % by mass or more and 5.0 × 10 −2 % by mass or less.
{実施形態の効果}
十分な除菌効果を有するウェットシートを、アルコールを含有しない薬液を用いて製作した場合、従来のものにおいては、使用者が感じるべたつきを十分に低減できなかった。
これに対して、本実施形態によれば、薬液の接触角が上記の範囲であることによって、使用者の手肌等に付着した薬液が広がり易くなり、アルコールを含有せずとも、これが蒸発し易くなる。
したがって、アルコールを含有しない薬液を用いた場合においても、十分な除菌効果を有しつつ、使用者が感じるべたつきを低減することが可能となる。
{Effect of embodiment}
When a wet sheet having a sufficient sterilizing effect was produced using a chemical solution containing no alcohol, the conventional one could not sufficiently reduce the stickiness felt by the user.
On the other hand, according to the present embodiment, when the contact angle of the chemical solution is in the above range, the chemical solution adhering to the user's hand skin or the like is likely to spread, and the chemical solution evaporates even if it does not contain alcohol. It will be easier.
Therefore, even when a chemical solution containing no alcohol is used, it is possible to reduce the stickiness felt by the user while having a sufficient sterilizing effect.
次に、本発明の実施例及び比較例に係るウェットシートにつき、除菌力の評価、接触角測定及びべたつき等に関する評価を行った結果について説明する。 Next, the results of evaluation of the sterilizing power, measurement of the contact angle, stickiness, etc. of the wet sheets according to the examples and comparative examples of the present invention will be described.
[実施例及び比較例の構成]
以下の実施例及び比較例に係るウェットシートを用意した。
[Structure of Examples and Comparative Examples]
Wet wipes according to the following examples and comparative examples were prepared.
{実施例1}
(シート体)
大きさ:MD方向200mm、CD方向150mm
成分:レーヨン:40質量%、PET(ポリエチレンテレフタレート):40質量%、PE(ポリエチレン)及びPP(ポリプロピレン)の混合物:20質量%
構成:スパンレース不織布
目付:34g/m2
(薬液)
精製水:99.434%
塩化ベンザルコニウム50%水溶液:1.0×10-1%
(塩化ベンザルコニウム: 5.0×10-2%)
塩化セチルピリジニウム:3.0×10-2%
ポリアミノプロピルビグアニド20%水溶液:1.0×10-1%
(ポリアミノプロピルビグアニド: 2.0×10-2%)
グレープフルーツ種子エキス:1.0×10-2%
フェノキシエタノール:3.0×10-1%
クエン酸:5.0×10-3%
クエン酸ナトリウム:1.0×10-3%
アロエエキス:1.0×10-2%
グリセリン:1.0×10-2%
(薬液含浸率)
250%
{Example 1}
(Sheet body)
Size: MD direction 200mm, CD direction 150mm
Ingredients: Rayon: 40% by mass, PET (polyethylene terephthalate): 40% by mass, mixture of PE (polyethylene) and PP (polypropylene): 20% by mass
Composition: Spunlace non-woven fabric Metsuke: 34g / m 2
(Chemical solution)
Purified water: 99.434%
Benzalkonium chloride 50% aqueous solution: 1.0 × 10 -1 %
(Benzalkonium chloride: 5.0 × 10 -2 %)
Cetylpyridinium chloride: 3.0 x 10 -2 %
Polyaminopropyl biguanide 20% aqueous solution: 1.0 × 10 -1 %
(Polyaminopropyl biguanide: 2.0 x 10 -2 %)
Grapefruit seed extract: 1.0 x 10 -2 %
Phenoxyethanol: 3.0 x 10 -1 %
Citric acid: 5.0 x 10 -3 %
Sodium citrate: 1.0 x 10 -3 %
Aloe extract: 1.0 x 10 -2 %
Glycerin: 1.0 × 10 -2 %
(Chemical impregnation rate)
250%
{実施例2}
(シート体)
実施例1と同様。
(薬液)
精製水:99.424%
塩化ベンザルコニウム50%水溶液:1.0×10-1%
(塩化ベンザルコニウム: 5.0×10-2%)
塩化セチルピリジニウム:3.0×10-2%
ポリアミノプロピルビグアニド20%水溶液:1.0×10-1%
(ポリアミノプロピルビグアニド: 2.0×10-2%)
グレープフルーツ種子エキス:1.0×10-2%
フェノキシエタノール:3.0×10-1%
クエン酸:5.0×10-3%
クエン酸ナトリウム:1.0×10-3%
アロエエキス:1.0×10-2%
グリセリン:1.0×10-2%
オレンジエキス:1.0×10-2%
(薬液含浸率)
実施例1と同様。
{Example 2}
(Sheet body)
Same as Example 1.
(Chemical solution)
Purified water: 99.424%
Benzalkonium chloride 50% aqueous solution: 1.0 × 10 -1 %
(Benzalkonium chloride: 5.0 × 10 -2 %)
Cetylpyridinium chloride: 3.0 x 10 -2 %
Polyaminopropyl biguanide 20% aqueous solution: 1.0 × 10 -1 %
(Polyaminopropyl biguanide: 2.0 x 10 -2 %)
Grapefruit seed extract: 1.0 x 10 -2 %
Phenoxyethanol: 3.0 x 10 -1 %
Citric acid: 5.0 x 10 -3 %
Sodium citrate: 1.0 x 10 -3 %
Aloe extract: 1.0 x 10 -2 %
Glycerin: 1.0 × 10 -2 %
Orange extract: 1.0 × 10 -2 %
(Chemical impregnation rate)
Same as Example 1.
{実施例3}
(シート体)
実施例1と同様。
(薬液)
精製水:99.404%
塩化ベンザルコニウム50%水溶液:1.0×10-1%
(塩化ベンザルコニウム: 5.0×10-2%)
塩化セチルピリジニウム:3.0×10-2%
ポリアミノプロピルビグアニド20%水溶液:1.0×10-1%
(ポリアミノプロピルビグアニド: 2.0×10-2%)
グレープフルーツ種子エキス:3.0×10-2%
フェノキシエタノール:3.0×10-1%
クエン酸:5.0×10-3%
クエン酸ナトリウム:1.0×10-3%
アロエエキス:1.0×10-2%
グリセリン:1.0×10-2%
オレンジエキス:1.0×10-2%
(薬液含浸率)
実施例1と同様。
{Example 3}
(Sheet body)
Same as Example 1.
(Chemical solution)
Purified water: 99.404%
Benzalkonium chloride 50% aqueous solution: 1.0 × 10 -1 %
(Benzalkonium chloride: 5.0 × 10 -2 %)
Cetylpyridinium chloride: 3.0 x 10 -2 %
Polyaminopropyl biguanide 20% aqueous solution: 1.0 × 10 -1 %
(Polyaminopropyl biguanide: 2.0 x 10 -2 %)
Grapefruit seed extract: 3.0 x 10 -2 %
Phenoxyethanol: 3.0 x 10 -1 %
Citric acid: 5.0 x 10 -3 %
Sodium citrate: 1.0 x 10 -3 %
Aloe extract: 1.0 x 10 -2 %
Glycerin: 1.0 × 10 -2 %
Orange extract: 1.0 × 10 -2 %
(Chemical impregnation rate)
Same as Example 1.
{比較例1}
(シート体)
実施例1と同様。
(薬液)
精製水:96.184%
プロピレングリコール:3.0%
塩化ベンザルコニウム50%水溶液:1.0×10-1%
(塩化ベンザルコニウム: 5.0×10-2%)
塩化セチルピリジニウム:3.0×10-2%
ポリアミノプロピルビグアニド20%水溶液:1.0×10-1%
(ポリアミノプロピルビグアニド: 2.0×10-2%)
グレープフルーツ種子エキス:1.0×10-2%
パラオキシ安息香酸メチル:2.0×10-1%
パラオキシ安息香酸エチル:5.0×10-2%
パラオキシ安息香酸プロピル:2.0×10-2%
フェノキシエタノール:3.0×10-1%
クエン酸:5.0×10-3%
クエン酸ナトリウム:1.0×10-3%
(薬液含浸率)
実施例1と同様。
{Comparative Example 1}
(Sheet body)
Same as Example 1.
(Chemical solution)
Purified water: 96.184%
Propylene glycol: 3.0%
Benzalkonium chloride 50% aqueous solution: 1.0 × 10 -1 %
(Benzalkonium chloride: 5.0 × 10 -2 %)
Cetylpyridinium chloride: 3.0 x 10 -2 %
Polyaminopropyl biguanide 20% aqueous solution: 1.0 × 10 -1 %
(Polyaminopropyl biguanide: 2.0 x 10 -2 %)
Grapefruit seed extract: 1.0 x 10 -2 %
Methyl paraoxybenzoate: 2.0 x 10 -1 %
Ethyl paraoxybenzoate: 5.0 x 10 -2 %
Propyl paraoxybenzoate: 2.0 x 10 -2 %
Phenoxyethanol: 3.0 x 10 -1 %
Citric acid: 5.0 x 10 -3 %
Sodium citrate: 1.0 x 10 -3 %
(Chemical impregnation rate)
Same as Example 1.
[試験方法]
上記実施例及び比較例に係るウェットシートを用いて、以下の試験を行った。
[Test method]
The following tests were conducted using the wet sheets according to the above Examples and Comparative Examples.
{除菌力試験}
上記実施例及び比較例に用いられた薬液について、大腸菌及び黄色ブドウ球菌の2菌種に関する除菌活性値の測定を行った。
具体的には、段落0018に示した方法を用いた。
{Bactericidal power test}
The eradication activity values of the two species of Escherichia coli and Staphylococcus aureus were measured for the chemical solutions used in the above Examples and Comparative Examples.
Specifically, the method shown in paragraph 0018 was used.
{接触角測定}
上記実施例及び比較例に用いられた薬液について、接触角の測定を行った。
具体的には、段落0017に示した方法を用いた。
{Contact angle measurement}
The contact angles of the chemicals used in the above Examples and Comparative Examples were measured.
Specifically, the method shown in paragraph 0017 was used.
{べたつき等の評価}
上記実施例及び比較例に係るウェットシートについて、被験者8人に実際に手肌を拭かせ、べたつき難さ、乾き易さ、耐久性、拭き易さ、汚れ落ちにつき、1から7の7段階で評価させ、その平均値を算出した。なお、4を平均(一般的なウェットシート程度)として、極めて良好な場合に7、極めて不良な場合を1とし、平均よりやや良好な場合を5、平均よりやや不良な場合を3とし、平均より良好な場合を6、平均より不良な場合を2とした。
{Evaluation of stickiness etc.}
With respect to the wet sheets according to the above Examples and Comparative Examples, eight subjects were actually wiped on their hands, and the difficulty of stickiness, the ease of drying, the durability, the ease of wiping, and the removal of dirt were performed in 7 steps from 1 to 7. It was evaluated and the average value was calculated. In addition, 4 is an average (about a general wet sheet), 7 is an extremely good case, 1 is an extremely poor case, 5 is a little better than the average, and 3 is a slightly worse than the average. The better case was 6 and the worse than average was 2.
[試験結果]
試験の結果を表Iに示す。
[Test results]
The test results are shown in Table I.
[評価]
実施例と比較例との比較から、ウェットシートに含浸させる薬液の接触角を小さくすることによって、べたつき難さ、乾き易さ、拭き易さ、汚れ落ちを改善できることが分かる。
[evaluation]
From the comparison between the examples and the comparative examples, it can be seen that by reducing the contact angle of the chemical solution impregnated in the wet sheet, it is possible to improve the difficulty of stickiness, the ease of drying, the ease of wiping, and the removal of stains.
Claims (4)
前記薬液は、
グレープフルーツ種子エキスと、アロエエキスと、グリセリンと、オレンジエキスと、を含有し、大腸菌及び黄色ブドウ球菌に対する除菌活性値が2.0以上であり、
接触角が35.75°以下であることを特徴とするウェットシート。 A wet sheet in which the sheet body is impregnated with a chemical solution.
The chemical solution is
It contains grapefruit seed extract , aloe extract, glycerin, and orange extract, and has a eradication activity value of 2.0 or more against Escherichia coli and Staphylococcus aureus.
A wet sheet characterized by a contact angle of 35.75 ° or less.
1.0×101.0 × 10 -2-2 質量%以上のグレープフルーツ種子エキスと、Grapefruit seed extract by mass or more and
1.0×101.0 × 10 -2-2 質量%以上のアロエエキスと、With aloe extract of mass% or more,
1.0×101.0 × 10 -2-2 質量%以上のグリセリンと、With glycerin of mass% or more,
1.0×101.0 × 10 -2-2 質量%以上のオレンジエキスと、With more than% by mass of orange extract,
を含有することを特徴とする請求項1に記載のウェットシート。The wet sheet according to claim 1, wherein the wet sheet contains.
99.0質量%以上の水と、
1.0×10 -2 質量%以上、3.0×10 -2 質量%以下のグレープフルーツ種子エキスと、
5.0×10 -3 質量%のクエン酸と、
1.0×10 -3 質量%のクエン酸ナトリウムと、
5.0×10 -2 質量%の塩化ベンザルコニウムと、
3.0×10 -2 質量%の塩化セチルピリジニウムと、
2.0×10 -2 質量%のポリアミノプロピルビグアニドと、
を含有することを特徴とする請求項1又は2に記載のウェットシート。 The chemical solution is
With 99.0% by mass or more of water,
Grapefruit seed extract of 1.0 x 10 -2 % by mass or more and 3.0 x 10 -2 % by mass or less ,
5.0 × 10 -3 mass% citric acid and
1.0 × 10 -3 % by mass sodium citrate,
5.0 × 10 -2 % by mass of benzalkonium chloride,
3.0 × 10 -2 % by mass of cetylpyridinium chloride,
2.0 x 10 -2 % by weight polyaminopropyl biguanide,
The wet sheet according to claim 1 or 2 , wherein the wet sheet contains.
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JP2001206818A (en) | 1999-11-12 | 2001-07-31 | Pigeon Corp | Chemical solution for wet tissue, and packaged wet tissue |
JP2009131474A (en) | 2007-11-30 | 2009-06-18 | Daio Paper Corp | Wet tissue |
JP2015148023A (en) | 2014-02-06 | 2015-08-20 | ダイワボウホールディングス株式会社 | Nonwoven fabric for wet sheet, wet wiping sheet, and liquid impregnating skin covering sheet |
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