AU2004243133A1 - New product - Google Patents

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AU2004243133A1
AU2004243133A1 AU2004243133A AU2004243133A AU2004243133A1 AU 2004243133 A1 AU2004243133 A1 AU 2004243133A1 AU 2004243133 A AU2004243133 A AU 2004243133A AU 2004243133 A AU2004243133 A AU 2004243133A AU 2004243133 A1 AU2004243133 A1 AU 2004243133A1
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polymer matrix
single layer
lactic acid
matrix film
layer polymer
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AU2004243133A
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AU2004243133B2 (en
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Ingrid Gustafson
Ulrika Husmark
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Essity Hygiene and Health AB
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SCA Hygiene Products AB
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    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N1/00Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
    • C12N1/20Bacteria; Culture media therefor
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K35/00Medicinal preparations containing materials or reaction products thereof with undetermined constitution
    • A61K35/66Microorganisms or materials therefrom
    • A61K35/74Bacteria
    • A61K35/741Probiotics
    • A61K35/744Lactic acid bacteria, e.g. enterococci, pediococci, lactococci, streptococci or leuconostocs
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K35/00Medicinal preparations containing materials or reaction products thereof with undetermined constitution
    • A61K35/66Microorganisms or materials therefrom
    • A61K35/74Bacteria
    • A61K35/741Probiotics
    • A61K35/744Lactic acid bacteria, e.g. enterococci, pediococci, lactococci, streptococci or leuconostocs
    • A61K35/747Lactobacilli, e.g. L. acidophilus or L. brevis
    • 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
    • A61L15/36Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing microorganisms
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18Manufacture of films or sheets
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N1/00Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
    • C12N1/04Preserving or maintaining viable microorganisms

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Microbiology (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Organic Chemistry (AREA)
  • Mycology (AREA)
  • Genetics & Genomics (AREA)
  • Wood Science & Technology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Zoology (AREA)
  • Biotechnology (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Manufacturing & Machinery (AREA)
  • Biochemistry (AREA)
  • General Engineering & Computer Science (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Virology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Biomedical Technology (AREA)
  • Molecular Biology (AREA)
  • Materials Engineering (AREA)
  • Hematology (AREA)
  • Polymers & Plastics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Absorbent Articles And Supports Therefor (AREA)
  • Laminated Bodies (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Orthopedics, Nursing, And Contraception (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

WO 2004/105822 PCT/SE2004/000806 New product Technical field The present invention refers to a film-shaped polymer matrix comprising lactic acid 5 producing bacteria in a film-shaped matrix consisting of (a) polymer(s) that is non toxic and non-irritant to a user's skin and mucous membranes. The invention also refers to a process for producing such a film-shaped polymer matrix and products containing it. 10 Background of the invention The urogenital area harbors a complex microbial ecosystem comprising more than 50 different bacterial species (Hill et al., Scand. J. Urol. Nephrol. 1984;86 (suppl.) 23-29). The dominating species for fertile women in this area are lactic acid pro 15 ducing bacteria belonging to the genus Lactobacillus. These lactic acid producing members are important for retaining a healthy microbial flora in these areas, and act as probiotic bacteria with an antagonistic effect against pathogenic microbial spe cies. Lactic acid producing bacteria inhibit growth and colonization by other micro organisms by occupying suitable niches for colonization, by forming biofilms and 20 competing for available nutrients, thereby excluding colonization by harmful micro organisms. Also, the production of hydrogen peroxide, specific inhibiting sub stances, such as bacteriocines, and organic acids (including lactic acid and acetic acid) that lower the pH, inhibit colonization by other microorganisms. 25 The microbial ecosystem of a healthy individual can be disturbed by the use of anti biotics, during hormonal changes, such as during pregnancy or use of contraceptives with estrogen, during menstruation, after menopause, in people suffering from dia betes etc. Also, microorganisms may spread from the anus to the urogenital area, thereby causing infections. This results in a disturbance of the normal microbial 30 flora and leaves the individual susceptible to microbial infections that cause vagini- WO 2004/105822 PCT/SE2004/000806 2 tis, urinary tract infections and ordinary skin infections. Microorganisms commonly associated with these kinds of infections belong to the genera Escherichia, Entero coccus, Psedomonas, Proteus, Klebsiella, Streptococcus, Staphylococcus, Gardner ella and Candida. Women are at particular risk due to their shorter distance between 5 the anus and the urogenital tract; specially at risk are young women, who not yet have a well developed microflora in the urogenital area and older women, who no longer have a protective flora. One way to reduce the problems with the kinds of infections described above is to 10 have a good personal hygiene. However, excessive use of cleaning agents not only decrease the amount of harmful microbes, but can harm the beneficial microbial flora, again render it susceptible for pathogenic species to colonize and cause infec tions. Alternatively, administration of lactic acid producing bacteria to the urogeni tal area and the skin in order to outcompete pathogenic species and facilitate rees 15 tablishment and maintenance of a beneficial microbial flora in these areas, have been found to be a successful means to treat and prevent microbial infections. It has been suggested that lactic acid producing bacteria can be delivered via ab sorbent products, such as diapers, sanitary napkins, panty liners and tampons, as de 20 scribed in, for example, in W092/13577, W097/02846, W099/17813, W099/45099 and WOOO/35502. A major problem with providing products intended to be used for transfer of lactic acid producing bacteria, is that the bacteria have to retain viability during transport 25 and storage of the products. Lactic acid producing bacteria rapidly lose viability un der moist conditions, and it is therefore important that the bacteria are not exposed to moisture. One way to partly overcome this problem in absorbent products pro vided with lactic acid producing bacteria has been to supply the products with the bacteria, drying said products to remove most of the moisture in them and providing 30 the product in moisture impervious packages (W099/17813).
WO 2004/105822 PCT/SE2004/000806 3 An alternative way to protect bacteria against moisture has been to disperse the bacteria in a hydrophobic substance (see e.g. US 4,518,696; WO 92/13577; WO 02/28446) which due to its hydrophobic character will prevent moisture to reach the embedded bacterial cells. 5 However, there is still a need to develop alternative ways of protecting lactic acid producing bacteria from moisture that are suitable for the intended administration of the bacteria to a subject and that can be stored for long time periods without loss of viability of the bacterial cells, and additionally allowing efficient transfer of the lac 10 tic acid producing bacteria to the user. In addition, there is still a need to develop manufacturing processes that are efficient and less expensive. Summary of the invention 15 The present inventors have surprisingly found an alternative way to protect lactic acid producing bacterial cells from moisture, thereby increasing bacterial survival during transport and storage. The presented solution also results in a high transfer of bacterial cells to the skin of a subject. According to the present invention the bacte rial cells are embedded in a film-shaped polymer matrix which protects the bacteria 20 from moisture thereby increasing their survival. The invention also relates to a proc ess for producing such a film-shaped polymer matrix comprising lactic acid pro ducing bacteria and products comprising such a film-shaped polymer matrix com prising lactic acid producing bacteria. 25 WO 2004/105822 PCT/SE2004/000806 4 Short description of the figures Fig. 1 depicts an illustrative example of an absorbent product, such as a sanitary napkin, diaper, panty liner, incontinence guard and the like comprising a film 5 shaped polymer matrix according to the present invention. Fig. 2 shows a cross-section of the absorbent product depicted in Fig. 1 along the line II-II in Fig. 1. 10 Fig. 3 depicts an schematic illustration of a tampon comprising a film-shaped poly mer matrix according to the present invention. Fig. 4 shows a cross-section of the absorbent product depicted in Fig. 3 along the line IV-IV in Fig. 3. 15 Fig. 5 shows the survival of lactic acid producing bacteria in film-shaped polymer matrixes according to the present invention during long term storage. Detailed description of the invention 20 The present invention is concerned with the problem with maintaining bacterial vi ability in products comprising lactic acid producing bacteria from the time for manufacturing until use of the product and obtaining a satisfactory transfer of the bacteria from the product to the user. A factor of major importance for increasing 25 bacterial survival during storage is that the bacteria have to be protected from moisture. The present inventors have surprisingly found that embedding the lactic acid producing bacteria in a film-shaped polymer matrix results in a greatly en hanced survival of the bacterial cells during storage. 30 WO 2004/105822 PCT/SE2004/000806 5 Polymers suitable for the film-shaped polymer matrix protect the bacterial cells from moisture during storage, but are dissolved in bodily fluids and therefore release the bacterial cells when exposed to wet or moist conditions. The film-shaped polymer matrix comprising the lactic acid producing bacteria according to the present inven 5 tion is composed of at least one polymer that is non-toxic and non-irritant to a user's skin and mucous membranes and at least one lactic acid producing bacterial strain. Polymers suitable for the present invention include natural hydrophilic polymers, such as polysaccharides and derivatives thereof, such as starch and cellulose (in cluding their derivatives), proteins, hydrophilic polymers, such as synthetic hydro 10 philic polymers, such as acrylate-based polymers, polyethers, such as polyethylene oxide, polyurethanes, polyamides, polyacrylnitrile, vinyl-based polymers, such as polyvinyl pyrrolidone and polyvinyl alcohol, etc.. Preferred polymers for the present invention include, but are not limited to, polyvinyl alcohol, polyethyleneoxide, poly vinyl pyrrolidone and starch. The polymer(s) form a film-shaped matrix that embed 15 the bacteria and thereby protect them from moisture. The polymers can be used alone or in different combinations. The film-shaped polymer matrix comprising lactic acid producing bacteria accord ing to the present invention may also include additional components. Examples of 20 such components include, but are not limited to, agents protecting the bacteria dur ing the manufacturing of the polymer film, like carbohydrates, such as maltose, su crose, trehalose, lactose, glucose and fructose, proteins, such as skim milk and al bumin, amino acids, such as Na-glutamate, polyols, such as xylitol, mannitol and sorbitol, and antioxidants, such as Na-ascorbate. The majority of these agents may 25 also act as nutrients for bacterial propagation once the polymer film is dissolved. Additional components are also exemplified by plasticizers that can be added to a polymer film comprising starch, like polyhydric alcohols, such as glycerol, polyols, sorbitol and polyvinyl alcohols, sucrose ester, such as sucrose stearate, fatty acids, such as palmitic acid, lipids based on esterified fatty acids, such as monoglycerides, 30 WO 2004/105822 PCT/SE2004/000806 6 diglycerides and triglycerides, waxes and amino alcohols, such as triethanolamine and N-methyl-diethanol amine, and enzymes, such as amylase. The concentration of the polymer solution is preferably between 0.1-10 (w/w) %, 5 more preferably 0.5-7 (w/w) %, most preferably 1-2 (w/w) %. The thickness of the film-shaped polymer matrix comprising lactic acid producing bacteria is preferably 50 [m-5 mm, more preferably 100 im-1 mm and most preferably 500 [m-1 mm. In order to increase bacterial survival the water activity of the film-shaped polymer 10 matrix comprising lactic acid producing bacteria is 0.30 or below, preferably 0.25 or below and most preferably 0.20 or below during at least 3 months storage at 23*C and 50% relative humidity. The number of lactic acid producing bacteria in the film-shaped polymer matrix ac 15 cording to the present invention is preferably 10 -10" CFU/g film, more preferably 109-1012 CFU /g film. In order for the film-shaped polymer matrix to allow sufficient transfer of bacteria the film-shaped polymer matrix preferably dissolves as rapidly as possible when ex 20 posed to moist or wet conditions and in either case within 6 hours, preferably within 4 hours. Lactic acid producing bacteria are chosen for the present invention due to their positive effect in preventing and treating microbial infection in the urogenital area 25 and on the skin. The bacteria are preferably isolated from the natural flora of a healthy person, preferably the bacteria are isolated from the skin or urogenital area. Preferred "lactic acid producing bacteria" for the object of the present invention in clude bacteria from the genera Lactobacillus, Lactococcus and Pediococcus. Pref erably the selected bacteria are from the species Lactococcus lactis, Lactobacillus 30 acidophilus, Lactobacillus curvatus or Lactobacillus plantarun. More preferably WO 2004/105822 PCT/SE2004/000806 7 the bacterial strain is selected from Lactobacillus plantarum. Even more preferably the lactic acid producing bacterium is Lactobacillusplantarum 931 (deposition No. (DSMZ): 11918). The lactic acid producing bacteria can be provided alone or in mixtures containing at least two bacterial strains. 5 To prevent water-vapor to permeate into the hydrophilic film-shaped polymer ma trix, thereby interfering with bacterial survival during storage, the film-shaped polymer matrix comprising lactic acid producing bacteria is preferably laminated with a water-vapor barrier-material. Thereby the survival of the bacterial cells is 10 further increased during storage. Lamination of a film-shaped polymer matrix com prising lactic acid producing bacteria according to the present invention also gives a mechanically stronger film, that can stand harsher treatment during transport and storage. The film-shaped polymer matrix comprising lactic acid producing bacteria can be laminated on one or both sides. In case the film-shaped polymer matrix is 15 laminated on both sides, the same laminate composition does not have to be used on both sides. Examples of materials suitable to use for a laminate include, but are not limited to, waxes, wax paper, aluminum foil, polyethylene films, ethylene copoly mer, and coextruded films, such as Suranex (Dow Chemical Company, Reinmuen ster, Germany). The lamination could be performed using coextrusion technique or 20 by running the film-shaped polymer matrices through rolling, slightly heated cylin ders. Optionally weak adhesives could be used to bond the film-shaped polymer matrix and laminate together. Ultrasonic techniques could also be used for bonding the film-shaped polymer matrix comprising lactic acid producing bacteria and lami nate together. Suitable laminate materials have a water vapor transmission rate of, 25 measured according to ASTME 398-83 at 37.8 "C (100"F) and 90% relative humid ity (RH), 10 g/m 2 /24 h or below, more preferably 5 g/m 2 /24 h or below, most pref erably 2 g/m 2 /24 h or below. The water-vapor barrier-material is to be removed be fore use of the product comprising the film-shaped polymer matrix.
WO 2004/105822 PCT/SE2004/000806 8 The manufacturing processes for preparing film-shaped polymer matrixes compris ing lactic acid producing bacteria according to the present invention involves pre paring an aqueous solution of (a) polymer(s) by dissolving the polymer(s) in water, dispersing the bacteria in the aqueous solution of (a) polymer(s) and subsequently 5 drying the dispersion of dissolved polymer and lactic acid producing bacteria on an inert surface at a temperature below 50"C. Optionally, additional components can be added to the polymer solution, either before or after dispersion of the bacteria in the aqueous solution of polymer(s). The aqueous solution of polymer can comprise one or more polymers. The polymer solution comprising the lactic acid producing bacte 10 ria is typically casted onto an inert surface, which can be a laminate material or other inert surface, such as the surface of a hygiene product, using a doctor's blade set to a predetermined width. The casted film-shaped polymer matrices are solidified as the solvent is rapidly evaporated. The evaporation could take place in ambient air, an oven, on a heated roll, by convective drying means or on a surface exposed to IR 15 radiation. Preferred temperature intervals during evaporation when heated roll or convective drying methods are used are 5-50"C, more preferably 20-40 0 C and most preferably 30-37 0 C. When IR-radiation is used for drying somewhat higher tem peratures can be reached without detrimental effects on bacterial survival, due to the short drying times that are required. Typically, drying times in the order of seconds 20 to minutes and drying temperatures up to 65C could be used for IR-drying. There after, optionally, the film-shaped polymer matrix comprising lactic acid producing bacteria can be laminated as described above. The specific growth conditions, harvest conditions and suitable additional compo 25 nents for the lactic acid producing bacteria has to be optimized for each specific strain in order to ensure a high survival of the bacteria during manufacturing and storage of the film-shaped polymer matrix. The skilled person is familiar with such optimizations. The lactic acid producing bacteria added to the polymer solution can either be freshly prepared or a frozen or dried preparation. Preferably freshly pre 30 pared bacterial preparations are used for the present invention.
WO 2004/105822 PCT/SE2004/000806 9 The dispersion of polymer and lactic acid producing bacteria which can be used for producing a film-shaped polymer matrix according to the present invention could also be directly casted or sprayed onto a material, or a material can be dipped in the dispersion of polymer and lactic acid producing bacteria, which after drying is a part 5 of a product, such as a hygiene product. There are other processes available for the formation of film-shaped polymer ma trixes comprising lactic acid producing bacteria, i.e. calendering and extrusions that can be used as long as they are operating at temperatures not harmful for the bacte 10 ria. When starch is used for manufacturing of the film-shaped polymer matrix the starch has to be gelatinized before use. One way this might be performed is by heating a suspension of the starch (grains or granules) in water at a temperature of approxi 15 mately 90-100"C for 30-60 min. Before addition of the bacteria to the gelatinized starch, the suspension is cooled to 37"C or less. The film-shaped polymer matrix comprising lactic acid producing bacteria accord ing to the present invention is preferably added to hygiene products, such as hygiene 20 tissues, incontinence guards, diaper, panty liners, tampons, sanitary napkins etc., in which the film-shaped polymer matrix comprising lactic acid producing bacteria, when exposed to moisture and wet conditions, result in dissolution of the film shaped polymer matrix and transfer of the lactic acid producing bacteria to the skin and/or the urogenital area. 25 By hygiene tissue" is meant any device for wiping skin, for instance, a washcloth, patch, towelette, napkin, wetwipe, and the like. The hygiene tissue provided can be composed of a matrix comprising any natural or synthetic fiber, such as rayon, cel lulose, regenerated cellulose, polyester, polyolefine fibers, textile and the like, or 30 foam, nonwoven, felt or batting, or combinations thereof. The film-shaped polymer WO 2004/105822 PCT/SE2004/000806 10 matrix comprising the lactic acid producing bacteria is applied to the hygiene tissue by dipping the tissue in a dispersion of polymer and lactic acid producing bacteria which can be used for producing a film-shaped polymer matrix before drying of the hygiene tissue. 5 The film-shaped polymer matrix comprising lactic acid producing bacteria accord ing to the present invention, is, as described above, particularly suitable for applica tion to absorbent products, such as sanitary napkins, panty-liners, diapers, tampons, incontinence guards etc, since these products provide a convenient means for deliv 10 ery of lactic acid producing bacteria to the urogenital area. The absorbent products according to the invention are preferably composed of a liquid permeable casing sheet, a liquid impermeable backing sheet, an absorbent layer, comprised of one or more layers, placed between said upper layer and said back sheet and optionally a device for adherence. The film-shaped polymer matrix according to the present in 15 vention is preferably placed on the permeable casing sheet, but can also be placed inside this. Alternatively, the film-shaped polymer matrix comprising lactic acid producing bacteria according to the present invention can be provided separately and placed on the absorbent product by the users before use. The number of probi otic bacteria in an absorbent product according to the present invention is 107-10"' 20 CFU, preferably 108-1011 CFU, most preferably10 9 -10 0 CFU. Below a more detailed description of an absorbent product, such as a sanitary nap kin, panty liner, diaper or incontinence guard is given. The absorbent product 1 shown in Fig. 1 and Fig. 2 (cross-section of the absorbent product depicted in Fig. 1 25 along the line II-II in Fig. 1) includes a liquid-permeable casing sheet or top sheet 2 disposed on that side of the absorbent product which is intended to lie proximal to the wearer in use. The liquid-permeable casing sheet 2 will conveniently consist in a somewhat soft, skin-friendly material. Different types of non-woven material are examples of suitable liquid-permeable materials. Other casing sheet materials that WO 2004/105822 PCT/SE2004/000806 11 can be used are perforated plastic films, net, knitted, crocheted or woven textiles, and combinations and laminates of the aforesaid types of material. The absorbent product 1 also includes a liquid-impermeable casing sheet or backing 5 sheet 3, disposed on that side of the napkin 1 distal from the wearer in use. The liq uid-impermeable casing sheet 3 is conventionally comprised of thin plastic film. Alternatively, there may be used a liquid-permeable material that has been rendered impermeable to liquid in some way or another. For instance, the liquid-permeable material may be coated with a glue that is impermeable to liquid, and the liquid 10 permeable layer laminated with a liquid-impermeable material, or hot-calendering a material that was initially liquid-permeable, such as to melt down the surface of the material and therewith obtain a liquid-impermeable layer. Alternatively, there may be used other textiles comprised of hydrophobic fibers and so impervious as to en able them to be used as a liquid barrier layer. The liquid-impermeable casing sheet 3 15 may beneficially be vapor permeable. The two casing sheets 2, 3 form a joining edge 4 that projects outwardly around the napkin contour line, and are mutually joined at this edge. The sheets may be joined together by means of any appropriate conventional technique, such as gluing, weld 20 ing or sewing. The absorption core 5 sandwiched between the casing sheets 2, 3 shall constitute the layer capable of receiving and storing essentially all liquid discharged by the wearer. The absorption core 5 may, for instance, be produced from cellulose pulp. This pulp 25 may exist in rolls, bales or sheets that are dry-defibred and converted in a fluffed state to a pulp mat, sometimes with an admixture of superabsorbents, which are polymers capable of absorbing several times their own weight of water or body liq uid (fluid). Examples of other usable materials are different types of foamed materi als known, for instance, from SE 9903070-2, natural fibers, such as cotton fibers, 30 peat, or the like. It is, of course, also possible to use absorbent synthetic fibers, or WO 2004/105822 PCT/SE2004/000806 12 mixtures of natural fibers and synthetic fibers. Patent Application SE 9903070-2 de scribes a compressed foam material of regenerated cellulose, e.g. viscose. Such foam material will preferably have a density of 0.1 to 2.0 g/cm 3 . The absorbent ma terial may also contain other components, such as foam-stabilizing means, liquid 5 dispersing means, or a binder, such as thermoplastic fibers, for instance, which have been heat-treated to hold short fibers and particles together so as to form a coherent unit. A fastener means 6 in the form of an elongate rectangular region of self-adhesive is 10 provided on the surface of the liquid-impermeable casing sheet 3 that lies distal from the wearer in use. The fastener means 6 extends over the major part of the liq uid-impermeable casing sheet 3. The invention is not restricted to the extension of the fastener means 6, and said means may have the form of elongate stripes, trans verse regions, dots, circles, or other patterns and configurations. Neither is the in 15 vention restricted to the use of solely adhesive fastener means, since friction fasten ers may be used and other types of mechanical fasteners, such as press studs, clips, girdles, pants or the like may be used when found suitable to do so. When an adhe sive fastener means is used this is commonly protected, by a protective layer 9, from adhering to other surfaces prior use, which would destroy the fastener means. 20 The film-shaped polymer matrix comprising lactic acid producing bacteria accord ing to the present invention, when used in an absorbent product, is arranged onto or directly beneath the liquid-permeable casing sheet 2. Preferably the film-shaped polymer matrix comprising lactic acid producing bacteria is placed in such a way 25 that the film-shaped polymer matrix does not cover the entire surface of the absorb ent product. In this way the film-shaped polymer matrix comprising lactic acid pro ducing bacteria does not interfere with absorption of bodily fluids (such as blood, urine, secretion etc.) by the absorbent product. Even if the film-shaped polymer ma trix comprising lactic acid producing bacteria solublizes by bodily fluids, initial ab 30 sorption by the absorbent product can be impaired before the film-shaped polymer WO 2004/105822 PCT/SE2004/000806 13 matrix is solubilized if the whole of an absorbent product is covered by the film shaped polymer matrix. On way to solve this is to supply the absorbent article with a film-shaped polymer matrix comprising lactic acid producing bacteria according to the present invention which has been punched, forming at least one opening through 5 which bodily fluids can be transported. More preferably, a carrier in the form of a net or loose non-woven sheet, dipped in a dispersion of polymer and lactic acid pro ducing bacteria which can be used for producing a film-shaped polymer matrix ac cording to the present invention, may also be arranged onto or directly beneath the liquid-permeable casing sheet. In Fig. 1 and 2 one way to place the film-shaped 10 polymer matrix comprising lactic acid producing bacteria is exemplified, wherein the film-shaped polymer matrix is placed in strings 8. In a similar manner to what is described above, a tampon comprising the film shaped polymer matrix can be prepared. Fig. 3 and 4 (cross-section of the tampon in 15 Fig. 3 along the line IV-IV) depict a schematic exemplary drawing of a tampon 10 comprising a film-shaped polymer matrix 13 according to the present invention, wherein the film-shaped polymer matrix 13 is arranged onto the casing sheet 11. Also depicted is the absorbent core 12. 20 The skilled person could easily use the above exemplary descriptions of hygiene products comprising a film-shaped polymer matrix according to the present inven tion to manufacture a hygiene product comprising a film-shaped polymer matrix ac cording to the invention. Therefore, alternative designs of a sanitary napkin, incon tinence guard, panty-liner, diaper, tampon, hygiene tissue etc are also included in the 25 present invention. The embedding of lactic acid producing bacteria in a film-shaped polymer matrix according to the present invention is also suitable for increasing the survival of the bacteria in pharmaceutical preparations and in the food industry. 30 WO 2004/105822 PCT/SE2004/000806 14 A film-shaped polymer matrix comprising lactic acid producing bacteria according to the present invention have several advantages. When freeze-dried bacteria or sus pensions of bacteria are added directly to a hygiene product, the product have to be dried in order for the inherent moisture content in the product not to affect bacterial 5 survival negatively. This is both a complicated process, since the whole product has to be dried, but drying of the hygiene product can also result in a lowered initial ab sorption of bodily fluids as some residual moisture facilitates initial absorption. In addition, further protection form moisture during transport and storage by water im pervious packaging is necessary for maintenance of bacterial survival in this case. 10 This necessity to provide the whole hygiene product in a moisture impervious packing unit results in higher production costs. In comparison, by embedding the bacteria in a film-shaped polymer matrix according to the present invention one avoids the need for drying the hygiene product and the use of moisture impervious packing units, still having a resulting high survival of the bacterial cells, even after 15 prolonged storage. The use of a film-shaped polymer matrix according to the present invention furthermore alleviates the use of freeze-dried bacterial preparations, which are the mostly common preparation form for bacteria for use in hygiene products, but which are costly and complicated to prepare. Instead suspensions of lactic acid producing bacteria can be used directly when preparing a film-shaped polymer ma 20 trix comprising lactic acid producing bacteria which is cheaper and more practical. A film-shaped polymer matrix comprising lactic acid producing bacteria can also be prefabricated and later placed on many different products, such as hygiene products etc. without any special adaptations for the different products. Also, the production 25 of products comprising bacteria requires special hygiene requirements at the manu facturing plant. Costs can therefore be reduced by producing the film-shaped poly mer matrix comprising lactic acid producing bacteria at another location. Using a film-shaped polymer matrix in order to protect lactic acid producing bacte 30 ria from moisture leads to high stability at common temperatures during transport WO 2004/105822 PCT/SE2004/000806 15 and storage, since the film structure in itself is very insensitive to temperature varia tions. Also, the dryness of the bacterial cells in the dry film-shaped polymer matrix renders the bacteria more heat tolerant. 5 Furthermore, the preparation of a film-shaped polymer matrix is more gentle to the lactic acid producing bacteria, compared to for example extrusion or spraying that is often used when the bacteria are mixed with hydrophobic substances. The use of a film-shaped polymer matrix comprising lactic acid producing bacteria 10 is also advantageous in terms of efficacy of transfer of the bacteria to the skin. When the film-shaped polymer matrix comprising lactic acid producing bacteria dis solves, fragments of the film-shaped polymer matrix may be transferred to the skin where they dissolve further. Thereby the film fragments act as a vehicle for transfer of the bacteria. Also, the use of a film-shaped polymer matrix ensures that the bacte 15 ria are kept in the outer layers of the hygiene product, thereby ensuring a high trans fer rate. When the film-shaped polymer matrix comprising lactic acid producing bacteria is applied to a hygiene product, transfer rates can also be optimized by the choice of commonly used surface materials. 20 The present invention therefore solves many of the problems associated with pro viding products comprising lactic acid producing bacteria. Below the present inven tion is further described by illustrative but non-limiting examples. Example 1 25 Production of a film-shaped polymer matrix comprising lactic acid producing bacte ria An aqueous polymer solution with a concentration of 0.1-10 % by weight is pre pared by dissolving polyethylene oxide, polyvinyl pyrrolidone, polyvinyl alcohol or 30 starch in water.
WO 2004/105822 PCT/SE2004/000806 16 One part of bacterial suspension (ca 1010 CFU/ml, BioNativ AB, Box 7979, 907 19 Umei, Sweden) comprising Lactobacillus plantarum 931 (deposition No. (DSMZ): 11918) is mixed with 9 parts of the polymer solution for 5 minutes. The mixture is poured into small petri-dishes in a quantity that ensures the right thickness and an 5 amount of bacteria of approximately 109 cfu/film-shaped polymer matrix. The re sulting film-shaped polymer matrix comprising lactic acid producing bacteria has a thickness of preferably 50 pm-5 mm, more preferably 100 gm-i mm and most pref erably 500 jim-1 mm. 10 The petri dish is placed in a climate chamber at a temperature of 37"C and with as low relative humidity as possible (10% or below), whereby the water evaporates and the film-shaped polymer matrix solidifies and the bacteria are immobilized in the film-shaped polymer matrix. 15 The water activity of the film-shaped polymer matrixes comprising lactic acid pro ducing bacteria is measured using an a,-instrument; DD401102 Aqualab Serie 3TE (ADAB Analytical Devices AB, Stockholm, Sweden). Within 1-2 weeks after production of the film-shaped polymer matrix transfer tests 20 from absorbent products comprising the film-shaped polymer matrix according to the present invention to skin are performed (see below). Example 2 Survival of L. plantarum 931 in film-shaped polymer matrices according to the pre 25 sent invention The film-shaped polymer matrix is placed in a climate chamber at 23 'C and 50% relative humidity. The survival of the bacteria is tested in a film-shaped polymer matrix according Example 1 furthermore coated with Caremelt (a mixture of waxes, 30 Cognis, Henkel KgaA, Dusseldorf, Germany). The survival of the bacteria in the WO 2004/105822 PCT/SE2004/000806 17 film-shaped polymer matrix is tested at predetermined intervals during several months (see below). To test the survival of the lactic acid producing bacteria in the film-shaped polymer 5 matrix, the film is placed in a petri-dish, immersed with 20 ml of NaCl (0,85%) and put on a shaking-device. After 40 minutes the film-shaped polymer matrix is dis solved and the survival of the bacteria is determined by counting the number of col ony forming units (CFU) by standard spread-plate techniques and cultivation on MRS agar (2 days of incubation at 37"C). The results are presented in Fig. 5, 10 wherein PVP is polyvinyl pyrrolidone. Example 3 Transfer of L. plantarurn 931 from a pantly-liner provided with a film-shaped poly mer matrix 15 Film-shaped polymer matrixes comprising lactic acid producing bacteria are pro duced as described in Example 1. About I cm 2 of film-shaped polymer matrix are cut out, weighted and placed on the nonwoven top-layer of a panty-liner specimen (a circle 2.5 cm in diameter, punched out of an absorbent product). 20 100 pl of NaCl are added to the absorbent product, comprising the film-shaped polymer matrix with bacteria, with a pipette, and the specimen is subsequently mounted, with constant pressure (elastic tape, and elastic bandage), on to the fore arm of volunteers. After 2 hours the product is removed and the number of trans 25 ferred Lactobacilli on the skin measured. A sterile stainless-steel cylinder (2.6 cm in diameter, height 2 cm) is held tight to the skin (that has been covered with the specimen), and 1 ml of phosphate buffer (0.1M, pH 7.2) is poured into the cylinder. With a smooth glass-stick the skin is gently "kneaded" for 1 minute. Afterwards, the buffer is collected with a pipette and CFU measured with spread- plate technique 30 and MRS agar.
WO 2004/105822 PCT/SE2004/000806 18 The percentage of transferred Lactobacilli is calculated by dividing the number of CFU collected from the skin area covered by the specimen with the total number of CFU in the film-shaped polymer matrix on the test specimen. The number of Lacto bacilli initially present on the skin at the sample site is very low, especially in re 5 spect of the number of L. plantarum 931 transferred to the skin. Therefore the num ber of Lactobacilli detected on the skin after the transfer test are considered to be a result of transfer from the specimen comprising L. plantarum 931. As a comparison, a panty liner with a dry bacterial preparation not embedded in a film-shaped poly mer matrix was used. As can be seen in Table 1 the percentage of bacteria trans 10 ferred to the skin from an absorbent product was enhanced using a film-shaped polymer matrix according to the present invention. Table 1 No. of CFU transferred Initial No. of Polymer Cone. (w/w) MW (kDa) to the skin CFU on product Transferred % PVOH 1 96 3.E+04 1.E+06 2.4 PVP 1 40 7.E+07 6.E+08 12.7 Comparison 2.E+05. 4.E+07 0,4 PVP = Polyvinyl pyrrolidone PVOH = Polyvinyl alcohol 15

Claims (15)

1. A single layer polymer matrix film comprising lactic acid producing bacteria in a pharmaceutically acceptable polymer(s), which pharmaceutically acceptable polymer(s) is able to protect bacterial cells from moisture during storage, but which can be dissolved in bodily fluids.
2. A single layer polymer matrix film according to claim 1, wherein the lactic acid producing bacterial strain(s) is isolated from the skin or urogenital area of a healthy person.
3. A single layer polymer matrix film according to claim 1 or 2 wherein the lactic acid producing bacterial strain is selected from the genera Pediococcus, Lactococcus, Lactobacillus or mixes thereof.
4. A single layer polymer matrix film according to claim 3 wherein the lactic acid producing bacterial strain is selected from at least Lactobacillus plantarum.
5. A single layer polymer matrix film according to claim 4 wherein the lactic acid producing bacterial strain is selected from at least Lactobacillus plantarum 931 (deposition No. (DSMZ): 11918).
6. A single layer polymer matrix film according to claims 1-5 wherein the polymer(s) is chosen from the group comprising polysaccharides and derivatives thereof and synthetic hydrophilic polymers and derivatives thereof.
7. A single layer polymer matrix film according to claims 1-6, wherein the polymer(s) is chosen from the group comprising polyvinyl alcohol, polyethyleneoxide, polyvinyl pyrrolidone, and starch.
8. A single layer polymer matrix film according to claims 1-7 further comprising additional components.
9. A single layer polymer matrix film according to claims 1-8 which single layer polymer matrix film has a thickness of preferably 50 pm-5 mm, more preferably 100 pm-I mm and most preferably 500 [Lm-1 mm.
10. A single layer polymer matrix film according to claims 1-9 wherein the water activity of the single layer polymer matrix film is 0.30 or below, preferably 0.25 or below and most preferably 0.20 or below.
11. A single layer polymer matrix film according to claims 1-10 wherein the bacterial concentration is 107 -10 14 CFU/g film, more preferably 101-1012 CFU /g film. WO 2004/105822 PCT/SE2004/000806 20
12. A single layer polymer matrix film according to claims 1-11 which single layer polymer matrix film further comprises a laminate layer placed on at least one side of the single layer polymer matrix film.
13. A hygiene product, such as a sanitary napkin, panty liner, diaper, incontinence guard, tampon, hygiene tissue, comprising a single layer polymer matrix film comprising lactic acid producing bacteria according to claims 1-12.
14. A process for producing a single layer polymer matrix film according to claims I 11 comprising lactic acid producing bacteria comprising the steps of: a) preparing an aqueous solution of (a) polymer(s) that is non-toxic and non-irritant to a user's skin and mucous membranes b) dispersing lactic acid producing bacteria in said solution of (a) polymer(s) c) optionally adding an additional component(s) to the dispersion d) drying said resulting dispersion comprising lactic acid producing bacteria on a inert surface, at a temperature below 50*C, thereby producing a single layer polymer matrix film c) optionally laminating the resulting single layer polymer matrix film; wherein steps b) and c) can be performed in any order.
15. A kit comprising a) a hygiene product, such as a sanitary napkin, panty liner, diaper, incontinence guard, tampon, hygiene tissue; and b) a single layer polymer matrix film according to claims 1-12.
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EP1651284A1 (en) 2006-05-03
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JP2007502900A (en) 2007-02-15
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SE0301552D0 (en) 2003-05-27
AU2004243133B2 (en) 2009-02-26
MXPA05011548A (en) 2005-12-15
SE526982C2 (en) 2005-11-29
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CA2523977A1 (en) 2004-12-09
CN100382851C (en) 2008-04-23

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