WO1996018422A1 - A lactic acid excreting polylactide sheet for use in absorbent articles - Google Patents

A lactic acid excreting polylactide sheet for use in absorbent articles Download PDF

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Publication number
WO1996018422A1
WO1996018422A1 PCT/SE1995/001455 SE9501455W WO9618422A1 WO 1996018422 A1 WO1996018422 A1 WO 1996018422A1 SE 9501455 W SE9501455 W SE 9501455W WO 9618422 A1 WO9618422 A1 WO 9618422A1
Authority
WO
WIPO (PCT)
Prior art keywords
lactic acid
polyester
surface material
monomer
material according
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.)
Ceased
Application number
PCT/SE1995/001455
Other languages
French (fr)
Inventor
Björn Larsson
Erik LAGERSTRÖM
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.)
Essity Hygiene and Health AB
Original Assignee
SCA Molnlycke AB
Molnlycke Vafveri AB
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to SK726-97A priority Critical patent/SK282638B6/en
Priority to PL95320668A priority patent/PL181613B1/en
Priority to EP19950941289 priority patent/EP0797457B1/en
Priority to DE69521910T priority patent/DE69521910T2/en
Priority to JP51868496A priority patent/JP3778565B2/en
Priority to AU42758/96A priority patent/AU698372B2/en
Application filed by SCA Molnlycke AB, Molnlycke Vafveri AB filed Critical SCA Molnlycke AB
Priority to CZ971802A priority patent/CZ180297A3/en
Priority to US08/849,768 priority patent/US6020453A/en
Publication of WO1996018422A1 publication Critical patent/WO1996018422A1/en
Priority to MXPA/A/1997/004251A priority patent/MXPA97004251A/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/04—Polyesters derived from hydroxycarboxylic acids, e.g. lactones
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS 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
    • A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/22—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
    • A61L15/26—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives thereof
    • 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
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31786—Of polyester [e.g., alkyd, etc.]

Definitions

  • the present invention relates to surface material for absorbent articles in the form of tampons, sanitary napkins, diapers or incontinence guards, for instance, preferably tampons and sani ⁇ tary napkins.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Materials Engineering (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Hematology (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Absorbent Articles And Supports Therefor (AREA)
  • Orthopedics, Nursing, And Contraception (AREA)
  • Laminated Bodies (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Polyesters Or Polycarbonates (AREA)

Abstract

Surface material for an absorbent article, wherein the material includes a surface layer which excretes lactic acid and/or an acid physiologically acceptable derivative thereof when the surface layer is immersed in a water volume, the weight ratio between surface layer and water volume being 1:100, in an amount such that the lactic acid and/or derivative excreted within a time period of at most 20 hours will impart a pH of at most 3.0 to the water volume.

Description

A LACTIC ACID EXCRETING POLYLACTIDE SHEET FOR USE IN
ABSORBENT ARTICLES
The present invention relates to surface material for absorbent articles in the form of tampons, sanitary napkins, diapers or incontinence guards, for instance, preferably tampons and sani¬ tary napkins.
It is known that a rich flora of primarily lactic acid-producing bacteria occur in the urogenital region of healthy women, both before and after the menopause. These bacteria have antagonistic properties against different occurring uropathogens, which is tought to be due to their ability to produce different anti- metabolites. A particularly important antimetabolite is, of course, lactic acid which has an inhibiting effect on different pathogenic microorganisms by lowering the pH in the urogenital environment.
It is also known that the production of lactic acid is disturbed in conjunction with menstruation, resulting in a decrease in the amount of lactic acid produced. This will, of course, result in a higher pH-value, which favours those microorganisms that generate bad-smelling substances, among other things. The growth of microorganisms is also liable to cause irritation of the skin and the mucous membrane in the urogenital region.
Those methods afforded by known techniques in counteracting these problems to a large extent involve the use of different tampons and sanitary napkins which have been impregnated with different substances that lower the pH-value in the present context. For instance, SE 9100364-0 and SE 8505491-4 describe tampons and napkins which have been impregnated with cultures of living lactic acid bacteria. Even though this type of technical solution would seem to be sympathetic at first sight, since there are used lactic acid bacteria which occur naturally in the urogenital region, a closer study of these specifications reve¬ als that the technique applied is both very complicated and highly sensitive. For instance, it is necessary to isolate the bacteria cultures and to determine their type before they can be finally incorporated in the tampon or the napkin with the aid o some form of adhesive. A further drawback with this technique, as pointed out in EP-Al 0,130,356, is that the pH-value in the vagina in conduction with menstruation already lies in the alkaline region when the tampon or the napkin is applied. This inhibits the growth of the lactic acid bacteria and therewith reduce their lactic acid production, or at least cause this production to fluctuate greatly.
The last-mentioned document, EP-Al 0,130,356, describes in turn a tampon whose absorbent body is impregnated with a citrate- containing buffer solution. Naturally, a buffer solution of this nature must be considered foreign to the body at least in the present context, although the most serious drawback with this technical solution resides, also in this case, in the additional and complicated working steps occasioned by the actual impregna¬ tion process in tampon manufacture.
Other technical solutions are described in US-A 3,794,034 and DE-Al 2,309,575. These solutions, however, are also encumbered with the same drawbacks.
A somewhat different technical solution is described in GB-A- 2,107,192, which relates to a tampon which may have a polylactic acid for instance incorporated in its absorbent body. It is proposed that this polymer is admixed in the fibre pulp of the absorbent body, in a powder, granule or fibre form. This tech¬ nical solution thus also necessitates the application of at least one additional stage in the manufacture of the tampon, namely the stage in which the polylactic acid is mixed in the fibre pulp. The object of the tampon is to lower the pH-value within the tampon, whereas, on the other hand, the pH-value externally of the tampon is permitted to adopt such high values as 4.5.
WO 91/08726 also describes the use of polylactic acid in absor¬ bent articles, more specifically in the top and bottom sheets of such articles. These sheets, however, are designed solely to fulfil a specific purpose, namely that the absorbent article shall be considered to represent an article which is biological¬ ly degradable after use. The document makes no mention of the possibility that the polylactic acid could be used to adjust the pH-value with the purpose of counteracting bad smells or irrita- tion of the skin/mucous membrane.
JP 61-149 160 also describes the use of polylactic acid in absorbent articles for medical purposes. In this case, the polylactic acid is present in the form of a sponge. The only reason given for the use of precisely polylactic acid is to render the sponge biologically degradable.
WO 90/01521 describes plastic films comprised of polylactic acid, among other things. However, these plastic films are intended solely for conventional packaging purposes. The docu¬ ment gives no indication that the film could be used in absor¬ bent articles.
There is an obvious need for biologically degradable tampons and sanitary napkins with which bad smells and the risk of irrita¬ tion of the skin and mucous membrane in the urogenital region of the user can be counteracted and controlled continuously when the article is in use, and which can also be produced in a simple fashion.
The object of the present invention is to provide an absorbent article which satisfies this need.
This object is achieved in accordance with the present invention with the aid of a surface material of the kind mentioned in the introduction that has the characteristic features set forth in the characterizing clause of the following Claim 1.
An inventive surface material is able to ensure that the con- centration of lactic acid and/or lactic acid derivative in the urogenital region of menstruating women using an absorbent ar¬ ticle provided with such surface material will be sufficient in use, and will remain sufficient in use, to establish a pH-value of at most 4.0 in this region. Different embodiments of the present invention will be apparent from the following subclaims.
The outer layer of the surface material will preferably be comprised essentially of at least a lactic acid-based polyester, or as this polymer is also called, a polylactide i.e. a polymer of the formula
CH? CH3 CH3 I I I
HO-CH-CO[-0-CH-CO-]n-0-CH-C00H
where n is the number of monomer units in the average polymer chain. The number-average molecular mass, l , is preferably at most 50,000, and more preferably at most 40,000.
It should be noted that the expression "lactic acid-based poly¬ ester" as used here will also include polymers of the aforesaid formula in which one or more hydrogen atoms are replaced with one or more suitable groups, for instance methyl or ethyl.
The aforesaid surface layer may be the outermost layer of the surface material, although it may also form a major part of the surface material or the whole of said material. The surface material may be comprised of an outer layer of the aforesaid kind that is deposited on a substrate consisting of high molecu¬ lar weight polylactide, i.e. a polylactide for which M„>50,000, although the substrate may also be comprised of some other suitable material, for instance a polymer, such as polyethylene, polypropylene, a polyester or the like; it is also conceivable for the substrate to include or to consist of mixtures of such polymers. The surface material, or in certain cases at least the substrate, will conveniently have those properties that are normally required of a surface material with regard to its liquid permeability, softness, mechanical strength, stretchabi- lity, and so on. The substrate may be imparted these properties, by introducing different additives, such as a softener, for instance. According to one preferred embodiment, the lactic acid-based polyester is modified to include relatively large areas of amorphous material as it has been found that amorphous material will hydrolyze more rapidly than crystalline material, probably because of its higher permeability to water and vapour respec¬ tively, which means that the amorphous material will be con¬ verted more rapidly to lactic acid and/or lactic acid derivati¬ ve. Examples of known methods of adjusting the crystallinity of lactic acid-based polyester, for instance so as to obtain a practically amorphous polyester, are described in WO 94/07941 (see Example 26 in said document, for instance).
The lactic acid-based polyester will naturally contain a given quantity of monomers and/or oligomers necessitated by the laws of nature, for instance lactide when the polyester is polylac¬ tide; the equilibrium concentration with regard to lactide is normally about 1-3 percent by weight, calculated on the polylac¬ tide. Since there is reason to assume that the monomer will decompose quickly to lactic acid and/or lactic acid derivative than the corresponding polyester, the polyester layer is prefe¬ rably modified to have a higher monomer and/or oligomer con¬ centration than the equilibrium concentration. This higher concentration is preferably 10%-units, more preferably 5%-units greater than the corresponding equilibrium concentration. When the polyester is polylactide, the monomer/-oligomer concentra¬ tion, i.e. the lactide concentration, will preferably be 5-30 percent by weight, more preferably 10-25 percent by weight, calculated on the polylactide. By "oligomer" is meant in this document a polymer which comprises at most 10 mers. Known met- hods of achieving the aforesaid increases in concentration are described, for instance, in WO 90/01521, see for instance page 11, lines 24-32, or page 18, lines 19-34.
In another preferred embodiment, the outer sheet or surface layer includes an agent which accelerates depolymerization of the polyester and/or conversion of the polyester and/or its monomer/oligomers to lactic acid and/or lactic acid derivative, at least when the absorbent article is worn. Examples of such agents are mentioned in JP-A 4,168,149 and include such enzymes as lipase, amylase cellulase and enzymes for dehydrogenating lactic acid.
By treating the polyester in the surface layer with water and/or water vapour, the polyester can be prehydrolyzed so that the polyester will be converted to lactic acid and/or lactic acid derivative to a greater extent than would otherwise be the case, at least when the article is in use.
Further embodiments of the present invention will be apparent from the Claims dependent on Claim 1.
In addition to the aforementioned methods of modifying a lactic acid-based polyester with the intention of producing more lactic acid in the use in question, there are a number of other methods known to the person skilled in this art for achieving such modification, as will be evident from page 9, lines 17-25 of WO 92/04412.
The present invention is described below in more detail with reference to an Example.
Example
Different surface layer materials which included polylactide were immersed in water at room temperature. The pH of the water was measured immediately after immersing the material and also after the material had remained immersed for about 20 hours. About 0.4 g material was immersed in about 40 ml of water in each test. It was then possible to calculate the amount of lactic acid released on the basis of these data.
There was used as reference material a polylactide film which consisted to about 95% of polymerized L-lactic acid; this film is referred to below as Film 1. In addition to this film, there were also used a carded, thermobonded nonwoven material, a spun- bonded nonwoven material, staple fibres, and a carded, thermo¬ bonded nonwoven material made from these staple fibres; all these polylactide materials were essentially of the same non- modified type as Film 1.
The surface layer was used as surface material according to the present invention in three tests. These surface layers comprised polylactide films which had been modified to include an elevated monomer/oligomer concentration. One film had a monomer/oligomer concentration of about 24 percent by weight and is referred to below as Film 2. The corresponding concentration in another film, referenced Film 3, was about 11 percent by weight. A third film had a concentration of about 14 percent by weight.
The following Table sets forth the pH-values and the calculated amount of lactic acid released in percent by weight based on the original weight of the material concerned in the tests carried out on the aforesaid materials.
Non-modified n/N^ x pH immediately Released lactic pH after Released lactic acid material 1000 after immersion acid in percent 20 hours in percent by weigh by weight immediately immersion after 20 hours after immersion immersion
Film 1 60/135 5. 9 0 3.2 0.6
Carded and thermobonded nonwoven 62/137 4. 5 0.03 3.5 0.3
Spunbonded nonwoven 85/180 5. ,8 0 4.3 0.05
Staple fibres 65/140 4. .5 0.03 3.4 0.3
Carded and thermobonded nonwoven made from staple fibres 68/139 4. .3 0.05 3.1 0.6
Modified material monomer in percent by weight within parenthesis
Film 2 (24%) 37/92 2, .8 1.3 2.6 2.5 Film 3 (11%) 35/107 4..0 0.1 3.0 0.9 Film 4 (14%) 33/94 3..7 0.2 2.9 1.2
Mn = the number-average molecular mass M„ = the weight-average molecular mass
It will be seen from the Table that the non-modified materials gave the water volume in question a pH-value of at the lowest 3.1 after 20 hours treatment, whereas all the modified materials gave a pH-value of 3.0 or lower over a corresponding time pe¬ riod. The difference in released lactic acid is still more dramatic: In the case of the non-modified materials, the highest value was 0.6%, whereas the lowest value for the modified mate¬ rials was 0.9%. It will also be seen from the Table that the pH- values obtained immediately with the non-modified materials were not lower than 4.3 (corresponding to 0.05% released lactic acid), while the highest pH-value of the modified materials did not exceed 4.0 (corresponding to 0.1% released lactic acid).
Naturally, the present invention shall not be considered to be restricted to the aforedescribed exemplifying embodiments there¬ of or to the Example, and it will be understood that the in- vention is solely restricted by the following Claims, within whose scope other embodiments will be conceivable to the person skilled in this art. For instance, the inventive surface materi¬ al may be used to counteract bad smells generated in the use of diapers or incontinence guards.

Claims

1. Surface material for an absorbent article, including a surfa¬ ce layer mainly consisting of at least one lactic acid-based polyester which excretes lactic acid and/or an acid physiologi¬ cally acceptable derivative thereof when the surface layer is immersed in a volume of water, wherein the weight ratio between the surface layer and the water volume is 1:100, in an amount such that lactic acid and/or derivative that is excreted within a time period of at most 20 hours will impart to the water volume a pH of at most 3.0, characterized in that prior to being immersed in the water volume, the surface layer has a monomer and/or oligomer concentration which is essentially greater than the equilibrium concentration of monomer and/or oligomer corre¬ sponding to the amount of polyester present, the monomer and/or oligomer concentration being 5-30 percent by weight calculated on the polyester.
2. Surface material according to Claim 1, characterized in that the monomer and/or oligomer concentration is 10-25 percent by weight calculated on the polylester.
3. Surface material according to Claim 1 or Claim 2, charac¬ terized in that the lactic acid-based polyester, when the sur¬ face layer is immersed in said water volume, is partly converted in and/or outside the surface material to lactic acid and/or the acid, physiologically acceptable derivative thereof, said acid and/or said derivative then being excreted.
4. Surface material according to Claim 3, characterized in that when the surface layer is immersed in the water volume, the polyester is partly depolymerized to a monomer and/or oligomer which is or are then converted to lactic acid.
5. Surface material according to Claim 3 or Claim 4, wherein at least a part of the total amount of polyester has the formula CH3 H CH3
I I I
HO-CH-CO[-O-CH-CO-]n-0-CH-COOH
characterized in that number-average molecular mass, M.-, of this polyester is at most 50,000.
6. Surface material according to Claim 5, characterized in that M,, is at most 40,000.
7. Surface material according to any of the preceding Claims, characterized in that the monomer and/or oligomer concentration exceeds the equilibrium concentration by up to 10%-points.
8. Surface material according to Claim 7, characterized in that the monomer and/or oligomer concentration exceeds the equilib¬ rium concentration by up to 5%-points.
9. Surface material according to any of the preceding Claims, characterized in the polyester being a polylactide and the monomer and/or the oligomer or the oligomers being lactides.
10. Surface material according to any of the preceding Claims, characterized in that the surface layer includes an agent which accelerates the conversion of the polyester to lactic acid and/or lactic acid derivative, at least when the surface layer is immersed in said water volume.
11. Surface material according to any of the preceding Claims, characterized in that the surface layer includes an agent which accelerates both the depolymerization of the polyester and con¬ version of the polyester and its monomer to lactic acid and/or lactic acid derivative, at least when the surface layer is immersed in said water volume.
PCT/SE1995/001455 1994-12-13 1995-12-05 A lactic acid excreting polylactide sheet for use in absorbent articles Ceased WO1996018422A1 (en)

Priority Applications (9)

Application Number Priority Date Filing Date Title
PL95320668A PL181613B1 (en) 1994-12-13 1995-12-05 Lactic acid educing polylactide film for use on absorptive materials
EP19950941289 EP0797457B1 (en) 1994-12-13 1995-12-05 A lactic acid excreting polylactide sheet for use in absorbent articles
DE69521910T DE69521910T2 (en) 1994-12-13 1995-12-05 A LACTIC ACID LEAVING POLYLACTIDE SHEET FOR USE IN ABSORBENT ARTICLES
JP51868496A JP3778565B2 (en) 1994-12-13 1995-12-05 Lactic acid discharging polylactide sheet for use in absorbent articles
AU42758/96A AU698372B2 (en) 1994-12-13 1995-12-05 A lactic acid excreting polylactide sheet for use in absorbent articles
SK726-97A SK282638B6 (en) 1994-12-13 1995-12-05 Surface material of an absorbent article
CZ971802A CZ180297A3 (en) 1994-12-13 1995-12-05 Surface material for absorption article
US08/849,768 US6020453A (en) 1994-12-13 1995-12-05 Lactic acid excreting polylactide sheet for use in absorbent articles
MXPA/A/1997/004251A MXPA97004251A (en) 1994-12-13 1997-06-09 Polycylate lamina excertaating lactic acid, to be used in absorbent articles

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE9404348.6 1994-12-13
SE9404348A SE503906C2 (en) 1994-12-13 1994-12-13 Lactic acid secreting polylactide layers for use in absorbent articles

Publications (1)

Publication Number Publication Date
WO1996018422A1 true WO1996018422A1 (en) 1996-06-20

Family

ID=20396331

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/SE1995/001455 Ceased WO1996018422A1 (en) 1994-12-13 1995-12-05 A lactic acid excreting polylactide sheet for use in absorbent articles

Country Status (18)

Country Link
US (1) US6020453A (en)
EP (1) EP0797457B1 (en)
JP (1) JP3778565B2 (en)
AU (1) AU698372B2 (en)
CO (1) CO4650192A1 (en)
CZ (1) CZ180297A3 (en)
DE (1) DE69521910T2 (en)
ES (1) ES2160724T3 (en)
GB (1) GB2296013B (en)
IL (1) IL116302A0 (en)
PE (1) PE1997A1 (en)
PL (1) PL181613B1 (en)
SE (1) SE503906C2 (en)
SK (1) SK282638B6 (en)
TN (1) TNSN95127A1 (en)
TR (1) TR199501513A1 (en)
WO (1) WO1996018422A1 (en)
ZA (1) ZA9510319B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2001259432B2 (en) * 2000-05-03 2005-04-21 Amgen Inc. Modified peptides, comprising an FC domain, as therapeutic agents
US8399012B2 (en) 2006-04-17 2013-03-19 Kimberly-Clark Worldwide, Inc. Degradable therapeutic delivery device

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19713908A1 (en) * 1997-04-04 1998-10-08 Symbio Herborn Group Gmbh & Co Vaginal tampon and process for its manufacture
US6235869B1 (en) * 1998-10-20 2001-05-22 United States Surgical Corporation Absorbable polymers and surgical articles fabricated therefrom
SE513261C2 (en) * 1998-12-16 2000-08-14 Sca Hygiene Prod Ab Absorbent articles comprising a synergistic combination of a pH-regulating substance and lactic acid bacteria
IL138183A0 (en) 2000-08-31 2001-10-31 Rostam Ltd Ph reducing formulation and delivery system for a tampon
SE518097C2 (en) * 2000-10-03 2002-08-27 Ellen Ab Process for the preparation of an absorbent sanitary article comprising lactic acid producing bacteria as well as such
US7037983B2 (en) 2002-06-14 2006-05-02 Kimberly-Clark Worldwide, Inc. Methods of making functional biodegradable polymers
US7994078B2 (en) * 2002-12-23 2011-08-09 Kimberly-Clark Worldwide, Inc. High strength nonwoven web from a biodegradable aliphatic polyester
US7892218B2 (en) * 2004-03-03 2011-02-22 Rostam Ltd. pH reducing formulation
US20080200890A1 (en) * 2006-12-11 2008-08-21 3M Innovative Properties Company Antimicrobial disposable absorbent articles
US20110224637A1 (en) * 2010-02-16 2011-09-15 Playtex Products, Llc LOW pH, OPTIMAL ORP, AND ODOR-REDUCING FIBERS, A PROCESS FOR MAKING THE FIBERS, AND ARTICLES MADE THEREFROM

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2107192A (en) * 1981-10-05 1983-04-27 Univ Delaware Tampon treated to inhibit pathogenic bacteria

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2309575A1 (en) * 1973-02-26 1974-09-05 J Matthias Dr Wenderlein Impregnated vaginal tampons - for protection against infection by acidity control
US3794034A (en) * 1973-02-27 1974-02-26 J Jones Odor reductant body waste pad
DE3320218A1 (en) * 1983-06-03 1984-12-06 Henkel KGaA, 4000 Düsseldorf TAMPONS WITH PROTECTIVE EFFECT FROM VAGINAL INFECT AND METHOD FOR THE PRODUCTION THEREOF
DE68928938T2 (en) * 1988-08-08 1999-09-30 Biopak Technology Ltd., Golden Process for the softening of lactide polymers
US5444113A (en) * 1988-08-08 1995-08-22 Ecopol, Llc End use applications of biodegradable polymers
DK0506775T3 (en) * 1989-12-19 1997-10-13 Procter & Gamble Disposable sanitary garments
AU8660191A (en) * 1990-09-06 1992-03-30 Biopak Technology, Ltd. Packaging thermoplastics from lactic acid
AU8616991A (en) * 1990-09-11 1992-03-30 E.I. Du Pont De Nemours And Company Films containing polyhydroxy acids
JP3077704B2 (en) * 1990-10-30 2000-08-14 株式会社島津製作所 Biodegradable plastic molding
BR9305660A (en) * 1992-10-02 1996-11-26 Cargill Inc Stable fusion lactide polymer films and processes for their manufacture
JPH06149169A (en) * 1992-11-10 1994-05-27 Toshiba Corp Crt display device
DE4412317A1 (en) * 1993-04-21 1994-10-27 Basf Ag Polylactide having a broadened molecular weight distribution
EP0654492B1 (en) * 1993-11-18 2002-04-03 Mitsui Chemicals, Inc. Degradable aliphatic polyester formed products

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2107192A (en) * 1981-10-05 1983-04-27 Univ Delaware Tampon treated to inhibit pathogenic bacteria

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2001259432B2 (en) * 2000-05-03 2005-04-21 Amgen Inc. Modified peptides, comprising an FC domain, as therapeutic agents
US8399012B2 (en) 2006-04-17 2013-03-19 Kimberly-Clark Worldwide, Inc. Degradable therapeutic delivery device
US8784868B2 (en) 2006-04-17 2014-07-22 Kimberly-Clark Worldwide, Inc. Degradable therapeutic delivery device

Also Published As

Publication number Publication date
JPH10510727A (en) 1998-10-20
TNSN95127A1 (en) 1996-02-06
GB2296013B (en) 1999-05-12
GB9524772D0 (en) 1996-02-07
GB2296013A (en) 1996-06-19
SK72697A3 (en) 1997-11-05
JP3778565B2 (en) 2006-05-24
MX9704251A (en) 1997-09-30
ES2160724T3 (en) 2001-11-16
SE9404348L (en) 1996-06-14
PE1997A1 (en) 1997-02-15
EP0797457B1 (en) 2001-07-25
DE69521910T2 (en) 2001-11-15
DE69521910D1 (en) 2001-08-30
TR199501513A1 (en) 1996-10-21
AU698372B2 (en) 1998-10-29
CZ180297A3 (en) 1997-11-12
IL116302A0 (en) 1996-03-31
PL320668A1 (en) 1997-10-13
SE9404348D0 (en) 1994-12-13
EP0797457A1 (en) 1997-10-01
AU4275896A (en) 1996-07-03
PL181613B1 (en) 2001-08-31
SE503906C2 (en) 1996-09-30
CO4650192A1 (en) 1998-09-03
SK282638B6 (en) 2002-10-08
US6020453A (en) 2000-02-01
ZA9510319B (en) 1996-06-19

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