EP1229943A1 - Auto-adhesive composition - Google Patents

Auto-adhesive composition

Info

Publication number
EP1229943A1
EP1229943A1 EP00976181A EP00976181A EP1229943A1 EP 1229943 A1 EP1229943 A1 EP 1229943A1 EP 00976181 A EP00976181 A EP 00976181A EP 00976181 A EP00976181 A EP 00976181A EP 1229943 A1 EP1229943 A1 EP 1229943A1
Authority
EP
European Patent Office
Prior art keywords
natural rubber
weight
rubber latex
polymer
adhesive
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP00976181A
Other languages
German (de)
English (en)
French (fr)
Inventor
Florence Bonnet
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
National Starch and Chemical Investment Holding Corp
Original Assignee
National Starch and Chemical Investment Holding Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by National Starch and Chemical Investment Holding Corp filed Critical National Starch and Chemical Investment Holding Corp
Publication of EP1229943A1 publication Critical patent/EP1229943A1/en
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08CTREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
    • C08C1/00Treatment of rubber latex
    • C08C1/02Chemical or physical treatment of rubber latex before or during concentration
    • C08C1/04Purifying; Deproteinising
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/42Use of materials characterised by their function or physical properties
    • A61L15/58Adhesives
    • A61L15/585Mixtures of macromolecular compounds
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J107/00Adhesives based on natural rubber
    • C09J107/02Latex
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2666/00Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
    • C08L2666/02Organic macromolecular compounds, natural resins, waxes or and bituminous materials

Definitions

  • This invention relates to novel auto-adhesive compositions that are especially formulated for use on skin More particularly, the present invention relates to adhesive compositions that comprise low protein natural rubber latex and at least one polymer
  • the adhesive compositions of this invention are designed for cohesive elastic conforming bandages Such bandages adhere to themselves, but not to skin, hair or clothes Auto-adhesive bandages are used for dressing retention and are easy to apply especially on difficult parts of the body They are also used for fixation of padding material, cannulae and tubes, and for light compression and support bandages, and for application to the skin to protect wounds from contamination thereby reducing the danger of infection and guarding against further injury
  • Natural rubber latex provides adhesive compositions with excellent auto-adhesion and non-residue properties, but the problem of allergic reaction to proteins in these natural rubber latex persists
  • adhesives are made of specific blends of low protein natural rubber latex in combination with at least one polymer Proportions of these components may vary according to the requirements of the specific end products but in order to achieve the desired results of the present invention, at least 90 percent by weight of the low protein natural rubber latex and at least 1 percent by weight of the polymer are necessary in the adhesive
  • the low protein natural rubber latex is preferably present from 90 to 99 percent by weight, more preferably from 90 to 97 percent by weight, and the polymer is preferably present from 1 to 10 percent by weight, more preferably from 3 to 10 percent by weight
  • the adhesives of this invention are useful to prepare medical adhesive articles such as surgical bandages, athletic tapes, wound dressings and the like These adhesives may be coated onto any backing suitable for medical uses including occlusive (substantially non-breathable) and non-occlustve backings (breathable) Occlusive backings are also known as low porosity backings
  • occlusive backings include films, foams and laminates thereof
  • non limiting examples of non- occlusive backings include woven substrates, non woven substrates or melt blown webs, foams and thermally embossed non woven substrates
  • the present invention provides adhesive compositions comprising low-protein natural rubber latex and at least one polymer More particularly, the low-protein natural rubber latex content of the adhesive is at least 90 percent by weight, preferably from 90 to 99 percent by weight, more preferably from 90 to 97 percent by weight and the polymer is present in at least 1 percent by weight, preferably from 1 to 10 percent by weight, more preferably from 3 to 10 percent by weight
  • natural rubber latex as used in this invention is the naturally occurring form of rubber, i e , c ⁇ s-1 ,4-poly ⁇ soprene Amongst its natural sources is included the sap of the Havea brasiliensts rubber tree Natural rubber latex also comprises 1-2% proteins and it is known that some individuals are allergic to these proteins
  • Deproteinised natural rubber latex is known and used to lessen the allergic effects of e g surgical gloves and similar rubber products
  • latex could be used in combination with polymers of this invention to provide adhesives having desirable properties
  • the adhesive composition of this invention comprises deproteinised natural rubber latex and at least one polymer
  • the adhesive is applied to a bandage to provide good auto-adhesion, low or no residue skin adhesion after peeling, good viscosity during production and good peel coating weight
  • This invention provides the first adhesive product comprising deproteinised natural rubber latex having the above properties
  • polymer refers to a homopolymer, a copolymer or an adhesive polymer as well as any mixtures or blends of one or more homopolymers, and/or one or more copolymers, and/or one or more adhesive polymers
  • Copolymer refers to a polymeric material produced by the polymerisation of two or more dissimilar monomers, either with or without another functional group grafted thereto, as well as to a homopolymer with a functional group grafted thereto
  • copolymer includes, without limitation, random copolymers, block copolymers, sequential copolymers, and graft copolymers Typical monomers include, but are not limited to, hydroxyl substituted C1 to C12 esters of acrylic and methacry c acids, vinyl esters (vinyl acetate and vinyl propionate), vinyl ethers, fumarates, maleates, styrene, acrylonit ⁇ le
  • Adhesive polymer refers to a polymer that is inherently adhesive, or has been rendered adhesive by combining additives and/or modifiers with the polymer
  • Suitable additives and/or modifiers include, without limitation, tackifiers, plasticisers, stabilisers, cross-linking agents, and combinations thereof
  • Typical polymers include, without limitation, for example, polyolefins, non-elastome ⁇ c polyesters, non-elastome ⁇ c polyamides, cellulosic derived polymers, vinyl acetates, acrylates, vinyl chlorides and polyvmyl alcohols
  • trade name polymers suitable for use in the present invention include without limitation Vinamul 62118 a dextrine stabilised vinyl acetate-dibutyl maleate copolymer available from Vinamul, Vinamul 6152 a vinyl acetate-dibutyl maleate available from Vinamul, Airflex 920 a carboxylated Vinyl Acetate-Ethylene copolymer available from Air Product, Duroset 78-6964 E250 a ethylene / vinyl acetate copolymer available from National Starch and Chemical Company, Vinnapas LL8647
  • ingredients may be employed as desired and may include, for example, stabilisers, tackifiers, antioxidants, fibrous fillers, non-fibrous fillers, humectants, colorants, and deodorants or fragrances
  • a typical stabiliser that may be utilised in the mix to form the compositions of the present invention includes, for example the trade name product, Nopco S This is a highly sulphated fatty acid used in rubber industry to stabilise lattices during compounding, storage and application and is available from Henkel Other stabilisers may include Dapro DF 900 from
  • Typical antioxidants and/or metal transition ion scavengers that may be utilised in the mix to form the compositions of the present invention includes, for example hindered phenols, amines, and sulfur and phosphorous hydroxide decomposers A list of common antioxidants is given in McCutcheon's Functional Materials (1991 ), pp 13-18
  • a suitable antioxidant is available under the trade name product, Dispersion 2074M from Vita Liquid Polymers, this is an aqueous dispersion of Zinc Dibutyl Dithiocarbamate
  • the preparation according to the invention may also include a humectant Suitable humectants include glycerin, sorbitol, polyethylene glycol, propylene glycol, and other polyhyd ⁇ c alcohols
  • a suitable humectant is available under the trade name Polyethylene glycol 200 from ICI Surfactant - this is also called polyoxyethylene glycol
  • Defoaming agents may be used in the mix
  • the most common defoamers are given in McCutcheon's Functional Materials (1991), pgs 89-112
  • Typical defoamers include aluminium stearate, amyl alcohol, cap ⁇ llic alcohol, capryl alcohol, castor oil, corn oil, decyl alcohol, diethylene glycol monolaurate, glyceryl monostearate, mineral oil, pine oil, polyalkyl glycol, silicone oils, steanc acid, sulfonic acid salts, tributyl citrate and , tributyl phosphate
  • a suitable defoamer is available from Henkel under the trade name product Dehydran 1620 This is a blend of modified fatty alcohols and a polysiloxane
  • the above additives and other components such as the cure activators, pH control agents, and silicone oils employed in the latex formulations of the present invention may be present in the range of from 2 percent by weight to 9 percent by weight of the latex
  • the adhesive compositions of the invention may be prepared by mixing the latex and polymer, and any other desired ingredients, e g tackifiers, antioxidants, fillers etc in any convenient way (e g in a Sigma mixer)
  • the mixing can be carried out in a liquid medium which is a solvent for some or all of the ingredients, or which is an aqueous medium
  • Each of the ingredients can be added to the mixture as a solid, or as a molten liquid, or as a solution, emulsion or dispersion, as appropriate
  • the resulting liquid mixture, i e solution, emulsion or dispersion in a liquid carrier can be applied, if desired after further dilution, to the backing in conventional fashion, e g by spraying, painting, dipping or rolling
  • KDP 150 is an highly deproteinised Natural Rubber Latex available from Kao Corporation under this trade name
  • Revacryl 239 is a hard styr ene/acry c ester copolymer available from Harlow Chemical Company under this trade name
  • Dehydran 1620 is a blend of modified fatty alcohols and a polysiloxane available from Henkel under this trade name 4
  • Nopco S is a highly sulphated fatty and is available from Henkel under this trade name
  • Dispersion 2074M is an aqueous dispersion of Zinc Dibutyl Dithiocarbamate available from Vita Liquid Polymers under this trade name
  • This adhesive composition had a density of 0 95, a solids content of 59 to 62%, a pH of 9 5 to 10 5, and a viscosity in the range 80 to 130 cps
  • Tpeel (ASTM D1876-61 T) refers to the force required to separate the adhesive to adhesive bond using paper strips that are 1 inch wide, 12 inches long and 30 ⁇ m coated with the adhesive The specimens are bonded over 9 inches They are tested on an Instron tensometer 5 mm after bonding The paper strips are peeled apart and the force to do so recorded Higher Tpeel force means higher transfer from one side of the paper strip to the other Adhesives having Tpeel values between 2 and 4 N/25mm indicate acceptable tack levels and auto-adhesive properties
  • transfer means auto-adhesion is higher than the adhesion between the adhesive and the paper
  • Adhesion to skin was measured as follows tape samples 1 inch wide by 3 inches long were placed on the skin of a human subject using a predetermined constant pressure The tape was removed and a subjective evaluation of adhesion and residual tack was made and rated as no adhesion to skin. to 2 good adhesion; no tack. good adhesion; tack.
  • KDP 150 7 Duroset 78-6964
  • Examples 1 to 13 were formulated according to the teachings of the present invention All of these formulations show Tpeel values between 2 and 4 N/25mm and have good skin adhesion with no residual tack
  • KDP 150 highly deproteinised natural rubber latex
  • This formulation has a high Tpeel force and shows residual tack on skin
  • Comparative Example 15 contains polymer and highly derproteinised latex according to the invention, but the latex is present at level less than the claimed amount This formulation has very low Tpeel force and shows no adhesion on skin
  • Comparative Example 16 contains latex and polymer according to this invention, but both are present at levels outside their claimed amounts This formulation shows very high Tpeel force and shows residual tack on skin
  • the key amount of low-protein natural rubber latex is 90 to 97 percent by weight and the key amount by weight of polymer is

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Polymers & Plastics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Hematology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Adhesives Or Adhesive Processes (AREA)
EP00976181A 1999-11-17 2000-11-17 Auto-adhesive composition Withdrawn EP1229943A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB9927195.9A GB9927195D0 (en) 1999-11-17 1999-11-17 Auto-adhesive composition
GB9927195 1999-11-17
PCT/GB2000/004396 WO2001036011A1 (en) 1999-11-17 2000-11-17 Auto-adhesive composition

Publications (1)

Publication Number Publication Date
EP1229943A1 true EP1229943A1 (en) 2002-08-14

Family

ID=10864681

Family Applications (1)

Application Number Title Priority Date Filing Date
EP00976181A Withdrawn EP1229943A1 (en) 1999-11-17 2000-11-17 Auto-adhesive composition

Country Status (5)

Country Link
EP (1) EP1229943A1 (ja)
JP (1) JP2003514105A (ja)
AU (1) AU1406001A (ja)
GB (1) GB9927195D0 (ja)
WO (1) WO2001036011A1 (ja)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102020950A (zh) * 2011-01-14 2011-04-20 尚盟运动用品(惠阳)有限公司 高强力胶粘剂

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10137620A1 (de) * 2001-08-03 2003-09-11 Tesa Ag Klebeband insbesondere zu Verpackungszwecken
US20060194493A1 (en) * 2005-02-25 2006-08-31 Grant Cheney Pressure sensitive adhesive for surgical drapes
US8034430B2 (en) * 2005-10-27 2011-10-11 Kimberly-Clark Worldwide, Inc. Nonwoven fabric and fastening system that include an auto-adhesive material
US8518841B2 (en) 2006-08-04 2013-08-27 Kuraray Co., Ltd. Stretchable nonwoven fabric and tape
JPWO2017217194A1 (ja) * 2016-06-14 2019-04-04 株式会社トクヤマ 畜体保護材料、畜体保護膜形成用キット及び家畜の傷病部を保護する方法
CN111328354B (zh) 2017-11-10 2022-12-06 株式会社可乐丽 纤维构造体及其制造方法
CN109749662A (zh) * 2018-12-21 2019-05-14 南京斯瑞奇医疗用品有限公司 一种耐储存性能的天然乳胶胶粘剂及其制备方法
CN112704764B (zh) * 2020-12-28 2022-07-08 杭州高斯博医疗用品有限公司 适用于冷敷自粘压迫绷带的亲水型自粘胶、制备方法及应用
CN114288088B (zh) * 2021-12-27 2022-08-09 杭州高斯博医疗用品有限公司 一种自溶型强力自粘弹性绷带及其制备方法

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB853572A (en) * 1956-06-30 1960-11-09 Dunlop Rubber Co Rubber latex adhesive compositions
JPH0539222A (ja) * 1991-08-02 1993-02-19 Yoshitomi Pharmaceut Ind Ltd 鎮痛抗炎症貼付剤
JP3314094B2 (ja) * 1992-12-22 2002-08-12 日東電工株式会社 天然ゴム系粘着剤組成物及びその粘着テープ
JP3782834B2 (ja) * 1994-10-26 2006-06-07 株式会社トクホン 鎮痛抗炎症貼付剤
JPH0925468A (ja) * 1995-07-07 1997-01-28 Kao Corp グラフト天然ゴム系粘着剤及びその粘着テープ
JPH09217048A (ja) * 1996-02-08 1997-08-19 Kao Corp 感圧接着剤組成物及び情報担体用シート
JP3129651B2 (ja) * 1996-03-14 2001-01-31 住友ゴム工業株式会社 接着剤および粘着剤
US5962147A (en) * 1996-11-26 1999-10-05 General Latex And Chemical Corporation Method of bonding with a natural rubber latex and laminate produced

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO0136011A1 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102020950A (zh) * 2011-01-14 2011-04-20 尚盟运动用品(惠阳)有限公司 高强力胶粘剂

Also Published As

Publication number Publication date
AU1406001A (en) 2001-05-30
GB9927195D0 (en) 2000-01-12
WO2001036011A1 (en) 2001-05-25
JP2003514105A (ja) 2003-04-15

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