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US20020147432A1 - Absorbent articles with odor control - Google Patents

Absorbent articles with odor control Download PDF

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Publication number
US20020147432A1
US20020147432A1 US10/036,840 US3684001A US2002147432A1 US 20020147432 A1 US20020147432 A1 US 20020147432A1 US 3684001 A US3684001 A US 3684001A US 2002147432 A1 US2002147432 A1 US 2002147432A1
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Prior art keywords
odor control
absorbent article
control absorbent
odor
decomposition
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US10/036,840
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Lisa Baker
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Avintiv Specialty Materials LLC
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Individual
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Priority to US10/036,840 priority Critical patent/US20020147432A1/en
Assigned to POLYMER GROUP, INC. reassignment POLYMER GROUP, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: BAKER, LISA N.
Publication of US20020147432A1 publication Critical patent/US20020147432A1/en
Assigned to JPMORGAN CHASE BANK reassignment JPMORGAN CHASE BANK SECURITY AGREEMENT Assignors: POLYMER GROUP, INC.
Assigned to POLYMER GROUP, INC., FIBERTECH GROUP, INC. reassignment POLYMER GROUP, INC. RELEASE OF SECURITY INTEREST Assignors: JPMORGAN CHASE BANK, AS ADMINISTRATIVE AGENT
Assigned to CITICORP NORTH AMERICA, INC. AS FIRST LIEN COLLATERAL AGENT reassignment CITICORP NORTH AMERICA, INC. AS FIRST LIEN COLLATERAL AGENT SECURITY AGREEMENT Assignors: CHICOPEE, INC., FIBERTECH GROUP, INC, POLY-BOND, INC., POLYMER GROUP, INC.
Assigned to WILMINGTON TRUST COMPANY, AS SECOND LIEN COLLATERAL AGENT reassignment WILMINGTON TRUST COMPANY, AS SECOND LIEN COLLATERAL AGENT SECURITY AGREEMENT Assignors: CHICOPEE, INC., FIBERTECH GROUP, INC., POLY-BOND, INC., POLYMER GROUP, INC.
Assigned to PRISTINE BRANDS CORPORATION, PGI EUROPE, INC., FNA POLYMER CORP., BONLAM (S.C.), INC., TECHNETICS GROUP, INC., POLYMER GROUP, INC., DOMINION TEXTILE (USA) INC., FABRENE CORP., POLYLONIX SEPARATION TECHNOLOGIES, INC., FABRENE GROUP L.L.C., FIBERTECH GROUP, INC., LORETEX CORPORATION, PNA CORPORATION, FNA ACQUISITION, INC., PGI POLYMER, INC., POLY-BOND INC., FIBERGOL CORPORATION, CHICOPEE, INC., FABPRO ORIENTED POLYMERS, INC. reassignment PRISTINE BRANDS CORPORATION RELEASE OF SECURITY INTEREST IN PATENTS Assignors: CITICORP NORTH AMERICA, INC., AS FIRST LIEN COLLATERAL AGENT
Assigned to CITICORP NORTH AMERICA, INC., AS COLLATERAL AGENT reassignment CITICORP NORTH AMERICA, INC., AS COLLATERAL AGENT SECURITY AGREEMENT Assignors: CHICOPEE, INC., FIBERTECH GROUP, INC., PGI POLYMER, INC., POLY-BOND INC., POLYMER GROUP, INC.
Assigned to PRISTINE BRANDS CORPORATION, FABRENE GROUP L.L.C., FNA ACQUISITION, INC., PGI POLYMER, INC., FABRENE CORP., POLYMER GROUP, INC., LORETEX CORPORATION, FNA POLYMER CORP., BONLAM (S.C.), INC., TECHNETICS GROUP, INC., FABPRO ORIENTED POLYMERS, INC., PGI EUROPE, INC., FIBERGOL CORPORATION, DOMINION TEXTILE (USA) INC., FIBERTECH GROUP, INC., POLY-BOND INC., POLYLONIX SEPARATION TECHNOLOGIES, INC., CHICOPEE, INC., PNA CORPORATION reassignment PRISTINE BRANDS CORPORATION RELEASE OF SECURITY INTEREST IN PATENTS Assignors: WILMINGTON TRUST COMPANY, AS SECOND LIEN COLLATERAL AGENT
Abandoned legal-status Critical Current

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    • 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
    • A61L9/00Disinfection, sterilisation or deodorisation of air
    • A61L9/015Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone
    • A61L9/04Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone using substances evaporated in the air without heating
    • A61L9/042Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone using substances evaporated in the air without heating with the help of a macromolecular compound as a carrier or diluent
    • 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
    • A61L15/20Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing organic materials
    • 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
    • A61L15/46Deodorants or malodour counteractants, e.g. to inhibit the formation of ammonia or bacteria
    • 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
    • A61L9/00Disinfection, sterilisation or deodorisation of air
    • A61L9/01Deodorant compositions
    • 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
    • A61L2300/00Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
    • A61L2300/20Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices containing or releasing organic materials
    • A61L2300/21Acids
    • 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
    • A61L2300/00Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
    • A61L2300/40Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices characterised by a specific therapeutic activity or mode of action
    • A61L2300/404Biocides, antimicrobial agents, antiseptic agents

Definitions

  • the present invention is generally directed to the control of odors resulting from the decomposition of human efflux, and in particular, the effect of a hydroxydiphenyl ether in a modified acidic environment applied to a personal hygiene product to control odors resulting from autolytic and enzymatic decomposition of human exudates and excreta into volatile nitrogenous byproducts.
  • Disposable absorbent personal hygiene products are designed to capture and retain human excreta in a convenient and in-expensive article. Advances in performance have been made in disposable diapers, adult incontinence pads and feminine hygiene products to further improve waste acquisition and maintain skin wellness. Enhanced top-sheet layers have been introduced that reduce the contact abrasion due to friction of the personal hygiene against one's skin. Transfer intermediate layers are constantly in development whereby the waste, and in particular urine, is quickly wicked from the top-sheet to an absorbent core material. Improved core materials are available that can retain a liquid insult in spite of external compressive forces. While such advances have improved physical performance with regard to liquid and solid wastes, the decomposition of those wastes into volatile byproducts has been addressed with only limited effectiveness.
  • Disposable diapers and adult incontinence pads have improved in retention capability and can be worn for longer periods without loss of waste containment. While issues related to containment have improved, the development of odors remains a problem.
  • Urine a primary form of liquid waste encountered by diapers and incontinence pads, is comprised in significant part of urea.
  • the decomposition of urea results in the formation of volatile nitrogenous byproducts, most notably being ammonia, which are particularly malodorous.
  • ammonia odor may be controlled is to target the degradation pathways, which produce ammonia.
  • Enzymatic decomposition is an active process induced by specialized enzymes found in bacterial flora. Many genera of bacteria are ubiquitous to the human skin, the gastrointestinal tract, and the uro-genital tract as well as in the form of environmental contaminates found in the personal hygiene products itself. A general category of enzyme present in this flora allows for the breakdown of urea into ammonia. This enzyme is referred in general as a catalase, and specifically as a urease. When there is a liquid insult onto the hygiene product, bacteria are carried along with the liquid front and into the interstices of the fibrous construction. Ureases in the bacterial burden are active during this period, adding significantly to the production of ammonia. Certain bacteria are particularly receptive to this environment and will thrive, blooming the bacterial count and further increasing urea decomposition over time.
  • the present invention is directed to the control of noisome odors created by the decomposition of human waste in a personal hygiene product.
  • Control of the decomposition process is by the pre-application of an odor control compound comprising a hydroxydiphenyl ether in a modified acidic environment to one or more components of the personal hygiene product.
  • the odor control compound exhibits a multi-functional performance, affecting not only the odiferous decomposition byproducts, but also the biochemical decomposition and degradation pathways.
  • FIG. 1 and FIG. 2 shows typical hygiene product constructions, whereby the urine contacts 10 or 14 a proximal surface of the hygiene product, then wicks through that surface and one or more other dispersing layers, eventually being absorbed into the structure of a 12 lofty fibrous core.
  • Urea a compound comprising a significant amount of the urine chemistry, decomposes by autolytic and enzymatic mechanisms.
  • the urea is broken down into nitrogenous volatile byproducts, most notably being ammonia. As ammonia evolves out of the solid hygiene product, both malodorous and detrimental skin-wellness effects occur.
  • the production of ammonia is significantly curtailed.
  • the hydroxydiphenyl ether reduces the metabolic performance of bacteria present in the environment.
  • the presence of the hydroxydiphenyl ether in a modified acidic carrier further improves the bacteriostatic performance of the ether as well as introducing a pH shift that disfavors the further release of ammonia by inducing protonation of the ammonia into a nonvolatile ammonium ion.
  • the hydroxydiphenyl ether can be present in conjunction with the modified acidic carrier or located within immediate proximity.
  • a preferred embodiment involves the admixing of the hydroxydiphenyl ether with the modified acidic carrier in an aqueous solution. This aqueous solution can then be applied to one or more layers of the personal hygiene product prior to or during product fabrication.
  • the hydroxydiphenyl ether can be incorporated into the polymeric composition prior to the formation of that composition into a construct, such as a fiber, filament or film, with the modified acidic carrier being applied topically thereafter. As the hydroxydiphenyl ether blooms to the surface of the construct, interaction with the modified acidic carrier can readily occur.
  • FIG. 1 is a cross-sectional diagram of a typical personal hygiene product
  • FIG. 2 is a cross-sectional diagram of a modified personal hygiene product having a unified top sheet and transfer layer.
  • R′, R′′, and R′′′ are selected halogen substitutions.
  • a preferred hydroxydiphenyl ether is a trichloro- derivative as described and synthesized in U.S. Pat. Nos. 3,506,720 and 3,629,477, hereby incorporated by reference.
  • the trichlorodiphenyl ether exhibits bacteriostatic properties in the presence of the bacterial flora found in the personal hygiene product. It is postulated that the reduction of bacterial load reduces the number of viable and metabolically active bacteria, which results in a corresponding decrease in the concentration of catalases found in those bacteria.
  • a reduction in catalase activity primarily ureases, subsequently reduces the rate at which urea is decomposed into ammonia, and thereby reducing the noisome odors formed in the hygiene product.
  • modified acidic carriers include those acids that shift the pH of the trichlorodiphenyl ether environment to an approximate range of between 3.0 and 5.0. It is within the purview of the present invention that either inorganic or organic acids, alone or in combination, can be used in the capacity of a modified acidic carrier.
  • a presently preferred modified acid carrier is one selected from the aliphatic acids, with hexanedioic acid being most preferred.
  • the hydroxydiphenyl ether and modified acid carrier can be incorporated into a personal hygiene product, such as a sanitary napkin, diaper, training pant, incontinence pant, and the like, by a number of different routes, including as a topical treatment, a spin finish, and/or a melt additive.
  • Topical treatment is particularly efficacious in incorporating the odor control compound as a simple aqueous solution can be prepared and applied directly to a substrate material, which is then used as one or more component layers in the fabrication of a personal hygiene product.
  • Suitable substrate materials include nonwoven fabrics, woven fabrics, and films.
  • a 50 gram per square meter nonwoven fabric was fabricated from carded and thermally bonded staple fiber batt.
  • the staple fiber used was a Type T-187 blue pigmented polypropylene polymer with a 1.5′′ staple length and a diameter of 12 dpf, as supplied by Fibervisions of Athens, Ga.
  • the staple fiber was carded by conventional practice known to those skilled in the art and subsequently thermal bonded by use of a heated calender.
  • a calender temperature of about 340° F. and a nip pressure of 470 pounds per linear inch were employed.
  • Example 1 The nonwoven fabric of Example 1 was subsequently treated with an odor control compound comprising 3 mM trichlorodiphenyl ether, supplied as “MICROBAN” from the Microban Corporation, 68 mM hexanedioic acid, and deionized water.
  • a Weko Atomizer was used to uniformly distribute the odor control compound to the nonwoven fabric at an add-on level of 15% by weight.
  • Table 1 presents the effect of untreated and treated nonwoven fabric on bacterial growth.
  • Example 1 and Example 2 were placed on uniform bacterial lawns, then incubated overnight. Individually tested bacterial organisms where unable to live under the conditions imposed by the treated nonwoven material whereas the untreated material had no effect.
  • Table 2 is a variation of the zone of inhibition test performance given in Table 1. A test was performed whereby a bacterial broth receives a one inch sample of either Example 1 or Example 2, then allowed to incubate overnight. When compared to control bacterial broth of known viable organism count, the untreated material is seen to have no significant deleterious effect where as the odor control treated material has reduced viable cell count by at least 95 %.
  • Table 3 provides results on the effectiveness of the odor control compound on perceived odor production.
  • Ten inch by seven inch samples were taken from Example 1 and Example 2. These samples were then substituted for the transfer layer of a “SERENITY” brand adult incontinence pant, a registered trademark of Johnson & Johnson, and a five inch square sample of the entire construct excised from the central medial region of the pant. The construct samples were then transferred to the interior bottom surface of individual glass container. A 100 ml volume of mock urine seeded with bacteria was then applied to the samples and the glass containers closed. At time points throughout the testing period, the container was briefly opened and the odor compared against the control. As can be seen from the data provided, the perceived smell was significantly reduced.
  • the present invention is applicable to disposable absorbent articles such as incontinence briefs, incontinence undergarments, diapers, training pants, pull-on garments, feminine hygiene garments, sanitary napkins, and the like.
  • a diaper for example, preferably comprises a containment assembly comprising an odor control liquid pervious topsheet; a liquid impervious odor control backsheet joined to the odor control topsheet; and an odor control absorbent core positioned between the odor control topsheet and the odor control backsheet.
  • the odor control absorbent core has a pair of opposing longitudinal edges, an odor control inner surface and outer surface.
  • the diaper can further comprise elastic leg features, elastic waist features, and a landing member.

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  • Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Hematology (AREA)
  • Absorbent Articles And Supports Therefor (AREA)
  • Orthopedics, Nursing, And Contraception (AREA)
  • Disinfection, Sterilisation Or Deodorisation Of Air (AREA)

Abstract

The present invention is directed to the control of noisome odors created by the decomposition of human waste in a personal hygiene product. Control of the decomposition process is by the pre-application of an odor control compound comprising a hydroxydiphenyl ether in a modified acidic environment to one or more components of the personal hygiene product. The odor control compound exhibits a multi-functional performance, affecting not only the odiferous decomposition byproducts, but also the biochemical decomposition and degradation pathways.

Description

    TECHNICAL BACKGROUND
  • The present invention is generally directed to the control of odors resulting from the decomposition of human efflux, and in particular, the effect of a hydroxydiphenyl ether in a modified acidic environment applied to a personal hygiene product to control odors resulting from autolytic and enzymatic decomposition of human exudates and excreta into volatile nitrogenous byproducts. [0001]
  • BACKGROUND OF THE INVENTION
  • Disposable absorbent personal hygiene products are designed to capture and retain human excreta in a convenient and in-expensive article. Advances in performance have been made in disposable diapers, adult incontinence pads and feminine hygiene products to further improve waste acquisition and maintain skin wellness. Enhanced top-sheet layers have been introduced that reduce the contact abrasion due to friction of the personal hygiene against one's skin. Transfer intermediate layers are constantly in development whereby the waste, and in particular urine, is quickly wicked from the top-sheet to an absorbent core material. Improved core materials are available that can retain a liquid insult in spite of external compressive forces. While such advances have improved physical performance with regard to liquid and solid wastes, the decomposition of those wastes into volatile byproducts has been addressed with only limited effectiveness. [0002]
  • Disposable diapers and adult incontinence pads have improved in retention capability and can be worn for longer periods without loss of waste containment. While issues related to containment have improved, the development of odors remains a problem. [0003]
  • Urine, a primary form of liquid waste encountered by diapers and incontinence pads, is comprised in significant part of urea. The decomposition of urea results in the formation of volatile nitrogenous byproducts, most notably being ammonia, which are particularly malodorous. [0004]
  • Prior attempts to control ammonia odors have met with limited success. Sequesterants, such as cyclodextrins and zeolite clays are effective only in “capturing” the ammonia once formed. If the structure of the sequesterant becomes occluded or contaminated by the presence of the complex milieu of proteins and salts found in urine, functionality is significantly degraded. The use of acids to shift the pH of the urine insult, and thereby protonate the ammonia into a nonvolatile ammonium ion, has been tried with variable results due, once again, to the chemical complexity inherent to urine. The most practiced method for controlling malodorous decomposition byproducts has been the use of perfumes and fragrances. This practice, however, has generally been found unsatisfactory as ammonia odors are particularly pungent and difficult to mask. [0005]
  • An alternate method by which ammonia odor may be controlled is to target the degradation pathways, which produce ammonia. [0006]
  • Autolytic degradation of urea into ammonia occurs when urea is exposed to oxygen. In the environment of a personal hygiene product, and specifically in the fibrous component of a disposable diaper or incontinence pad, urine is wicked into interstices of the product's high loft structure. These interstices form micro-environments where urea autolysis then occurs. [0007]
  • Enzymatic decomposition is an active process induced by specialized enzymes found in bacterial flora. Many genera of bacteria are ubiquitous to the human skin, the gastrointestinal tract, and the uro-genital tract as well as in the form of environmental contaminates found in the personal hygiene products itself. A general category of enzyme present in this flora allows for the breakdown of urea into ammonia. This enzyme is referred in general as a catalase, and specifically as a urease. When there is a liquid insult onto the hygiene product, bacteria are carried along with the liquid front and into the interstices of the fibrous construction. Ureases in the bacterial burden are active during this period, adding significantly to the production of ammonia. Certain bacteria are particularly receptive to this environment and will thrive, blooming the bacterial count and further increasing urea decomposition over time. [0008]
  • Various attempts have been made to control bacterial metabolism and bacterial growth, and thereby reduce odors. As in ammonia protonation, the use of acids as a topical treatment is a relatively effective means for skewing the pH of the environment and imparting a deleterious effect on bacterial health. However, problems in attaining and maintaining a desired pH range against the broad range of urine chemistries encountered in the human population in not trivial. Further, producing a uniform distribution of the acid treatment so as to equally affect all microenvironments is complicated by the solubility of the acid. [0009]
  • There remains an unmet need for an effective treatment for controlling noisome decomposition byproducts, and specifically those byproducts, which are ammonia-based, from developing in soiled personal hygiene products. The odor control mechanism must exhibit sufficient robustness in the face of highly variable human waste chemistries while retaining stability during the hygiene product's shelf-life. The present invention addresses these issues through use of a hydroxydiphenyl ether in a modified acidic environment. [0010]
  • SUMMARY OF THE INVENTION
  • The present invention is directed to the control of noisome odors created by the decomposition of human waste in a personal hygiene product. Control of the decomposition process is by the pre-application of an odor control compound comprising a hydroxydiphenyl ether in a modified acidic environment to one or more components of the personal hygiene product. The odor control compound exhibits a multi-functional performance, affecting not only the odiferous decomposition byproducts, but also the biochemical decomposition and degradation pathways. [0011]
  • Human excreta and exudates are received and absorbed into the personal hygiene product. A particularly problematic human waste control issue involves a urine insult in a diaper or incontinence pad. FIG. 1 and FIG. 2 shows typical hygiene product constructions, whereby the urine contacts 10 or 14 a proximal surface of the hygiene product, then wicks through that surface and one or more other dispersing layers, eventually being absorbed into the structure of a 12 lofty fibrous core. Upon leaving the human body and being sequestered into the 12 absorbent core, the constituent chemistry of the urine begins to decompose. Urea, a compound comprising a significant amount of the urine chemistry, decomposes by autolytic and enzymatic mechanisms. The urea is broken down into nitrogenous volatile byproducts, most notably being ammonia. As ammonia evolves out of the solid hygiene product, both malodorous and detrimental skin-wellness effects occur. [0012]
  • By employing the compound of the present invention in one or more layers of the personal hygiene product, the production of ammonia is significantly curtailed. The hydroxydiphenyl ether reduces the metabolic performance of bacteria present in the environment. The presence of the hydroxydiphenyl ether in a modified acidic carrier further improves the bacteriostatic performance of the ether as well as introducing a pH shift that disfavors the further release of ammonia by inducing protonation of the ammonia into a nonvolatile ammonium ion. [0013]
  • The hydroxydiphenyl ether can be present in conjunction with the modified acidic carrier or located within immediate proximity. A preferred embodiment involves the admixing of the hydroxydiphenyl ether with the modified acidic carrier in an aqueous solution. This aqueous solution can then be applied to one or more layers of the personal hygiene product prior to or during product fabrication. Alternately, the hydroxydiphenyl ether can be incorporated into the polymeric composition prior to the formation of that composition into a construct, such as a fiber, filament or film, with the modified acidic carrier being applied topically thereafter. As the hydroxydiphenyl ether blooms to the surface of the construct, interaction with the modified acidic carrier can readily occur. [0014]
  • Other features and advantages of the present invention will become readily apparent from the following detailed description, the accompanying drawings, and the appended claims.[0015]
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • The invention will be more easily understood by a detailed explanation of the invention including drawings. Accordingly, drawings, which are particularly suited for explaining the invention, are attached herewith; however, it should be understood that such drawings are for explanation purposes only and are not necessarily to scale. The drawings are briefly described as follows: [0016]
  • FIG. 1 is a cross-sectional diagram of a typical personal hygiene product; and [0017]
  • FIG. 2 is a cross-sectional diagram of a modified personal hygiene product having a unified top sheet and transfer layer.[0018]
  • DETAILED DESCRIPTION
  • While the present invention is susceptible of embodiment in various forms, there is shown in the drawings and will hereinafter be described a presently preferred embodiment of the invention, with the understanding that the present disclosure is to be considered as an exemplification of the invention, and is not intended to limit the invention to the specific embodiment illustrated. [0019]
  • To control the production of volatile nitrogenous byproducts, most notably ammonia, produced from the decomposition of urine in a personal hygiene product, a hydroxydiphenyl ether of the following form is used: [0020]
    Figure US20020147432A1-20021010-C00001
  • Whereby R′, R″, and R′″, are selected halogen substitutions. A preferred hydroxydiphenyl ether is a trichloro- derivative as described and synthesized in U.S. Pat. Nos. 3,506,720 and 3,629,477, hereby incorporated by reference. [0021]
  • The trichlorodiphenyl ether exhibits bacteriostatic properties in the presence of the bacterial flora found in the personal hygiene product. It is postulated that the reduction of bacterial load reduces the number of viable and metabolically active bacteria, which results in a corresponding decrease in the concentration of catalases found in those bacteria. A reduction in catalase activity, primarily ureases, subsequently reduces the rate at which urea is decomposed into ammonia, and thereby reducing the noisome odors formed in the hygiene product. [0022]
  • By introducing the trichlorodiphenyl ether in a modified acidic carrier, performance of the mixture is significantly enhanced. Suitable modified acidic carriers include those acids that shift the pH of the trichlorodiphenyl ether environment to an approximate range of between 3.0 and 5.0. It is within the purview of the present invention that either inorganic or organic acids, alone or in combination, can be used in the capacity of a modified acidic carrier. A presently preferred modified acid carrier is one selected from the aliphatic acids, with hexanedioic acid being most preferred. [0023]
  • The hydroxydiphenyl ether and modified acid carrier can be incorporated into a personal hygiene product, such as a sanitary napkin, diaper, training pant, incontinence pant, and the like, by a number of different routes, including as a topical treatment, a spin finish, and/or a melt additive. Topical treatment is particularly efficacious in incorporating the odor control compound as a simple aqueous solution can be prepared and applied directly to a substrate material, which is then used as one or more component layers in the fabrication of a personal hygiene product. Suitable substrate materials include nonwoven fabrics, woven fabrics, and films. [0024]
  • EXAMPLES Example 1
  • A 50 gram per square meter nonwoven fabric was fabricated from carded and thermally bonded staple fiber batt. The staple fiber used was a Type T-187 blue pigmented polypropylene polymer with a 1.5″ staple length and a diameter of 12 dpf, as supplied by Fibervisions of Athens, Ga. The staple fiber was carded by conventional practice known to those skilled in the art and subsequently thermal bonded by use of a heated calender. A calender temperature of about 340° F. and a nip pressure of 470 pounds per linear inch were employed. [0025]
  • Example 2
  • The nonwoven fabric of Example 1 was subsequently treated with an odor control compound comprising 3 mM trichlorodiphenyl ether, supplied as “MICROBAN” from the Microban Corporation, 68 mM hexanedioic acid, and deionized water. A Weko Atomizer was used to uniformly distribute the odor control compound to the nonwoven fabric at an add-on level of 15% by weight. [0026]
  • Table 1 presents the effect of untreated and treated nonwoven fabric on bacterial growth. One inch square samples of Example 1 and Example 2 were placed on uniform bacterial lawns, then incubated overnight. Individually tested bacterial organisms where unable to live under the conditions imposed by the treated nonwoven material whereas the untreated material had no effect. [0027]
  • Table 2 is a variation of the zone of inhibition test performance given in Table 1. A test was performed whereby a bacterial broth receives a one inch sample of either Example 1 or Example 2, then allowed to incubate overnight. When compared to control bacterial broth of known viable organism count, the untreated material is seen to have no significant deleterious effect where as the odor control treated material has reduced viable cell count by at least 95 %. [0028]
  • Table 3 provides results on the effectiveness of the odor control compound on perceived odor production. Ten inch by seven inch samples were taken from Example 1 and Example 2. These samples were then substituted for the transfer layer of a “SERENITY” brand adult incontinence pant, a registered trademark of Johnson & Johnson, and a five inch square sample of the entire construct excised from the central medial region of the pant. The construct samples were then transferred to the interior bottom surface of individual glass container. A 100 ml volume of mock urine seeded with bacteria was then applied to the samples and the glass containers closed. At time points throughout the testing period, the container was briefly opened and the odor compared against the control. As can be seen from the data provided, the perceived smell was significantly reduced. [0029]
  • It should be understood that the present invention is applicable to disposable absorbent articles such as incontinence briefs, incontinence undergarments, diapers, training pants, pull-on garments, feminine hygiene garments, sanitary napkins, and the like. [0030]
  • A diaper, for example, preferably comprises a containment assembly comprising an odor control liquid pervious topsheet; a liquid impervious odor control backsheet joined to the odor control topsheet; and an odor control absorbent core positioned between the odor control topsheet and the odor control backsheet. The odor control absorbent core has a pair of opposing longitudinal edges, an odor control inner surface and outer surface. The diaper can further comprise elastic leg features, elastic waist features, and a landing member. [0031]
  • From the foregoing, it will be observed that numerous modifications and variations can be affected without departing from the true spirit and scope of the novel concept of the present invention. It is to be understood that no limitation with respect to the specific embodiments illustrated herein is intended or should be inferred. The disclosure is intended to cover, by the appended claims, all such modifications as fall within the scope of the claims. [0032]
    TABLE 1
    Zone of Inhibition (mm)
    Staphylococcus Escherichia Proteus
    Test Material epidermidis coli vulgaris
    Example 1 0 0 0
    Example 2 9 2 9
  • [0033]
    TABLE 2
    Viability Count
    Staphylococcus Escherichia Proteus
    Test Material epidermidis coli vulgaris
    Example 1  100%  100%  100%
    Example 2 0.36% 0.66% 4.58%
  • [0034]
    TABLE 3
    Perceived Odor (reduction in odor)
    Test Material 1 hr 2 hr 4 hr 6 hr 8 hr 12 hr
    Example 1  0%  0%  0%  0%  0%  0%
    Example 2 17% 41% 18% 30% 26% 42%

Claims (11)

What is claimed is:
1. An odor control absorbent article comprising;
a) providing a base substrate material,
b) providing a odor control compound,
c) the odor control compound comprising an admixture of a hydroxydiphenyl ether and a modified acid carrier,
d) applying the odor control compound topically to the base substrate material,
e) subsequently forming the treated base substrate material into a component material for a disposable absorbent article.
2. An odor control absorbent article as in claim 1, wherein the base material is selected from the group consisting of nonwoven fabrics, woven fabrics, polymeric films, and the combinations thereof.
3. An odor control absorbent article as in claim 1, wherein said hydroxydiphenyl ether is a trichlorodiphenyl ether.
4. An odor control absorbent article as in claim 1, wherein said modified acidic carrier is an organic acid.
5. An odor control absorbent article as in claim 4, wherein said organic acid is an aliphatic acid.
6. An odor control absorbent article as in claim 5, wherein the aliphatic acid is a hexanedioic acid.
7. An odor control absorbent article as in claim 1, wherein said odor control absorbent article is a diaper.
8. An odor control absorbent as in claim 1, wherein said odor control absorbent article is a sanitary napkin.
9. An odor control absorbent article as in claim 1, wherein said odor control absorbent article is a training pant.
10. An odor control absorbent article as in claim 1, wherein said odor control absorbent article is a pull-on garment.
11. An odor control absorbent article as in claim 1, wherein said odor control absorbent article is an incontinence garment.
US10/036,840 2000-12-21 2001-12-21 Absorbent articles with odor control Abandoned US20020147432A1 (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090203754A1 (en) * 2007-05-22 2009-08-13 Keck James L Anti-bacterial drug targeting of genome maintenance interfaces
WO2010015096A1 (en) * 2008-08-08 2010-02-11 Heiq Materials Ag Carrier system for subsequent application onto substrates and method therefor

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8138106B2 (en) 2005-09-30 2012-03-20 Rayonier Trs Holdings Inc. Cellulosic fibers with odor control characteristics
US8241747B2 (en) 2009-03-30 2012-08-14 Cellresin Technologies, Llc Malodor absorbent polymer and fiber

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3903007A (en) * 1963-02-22 1975-09-02 Ciba Geigy Corp Detergent composition containing halogenated 2-acyloxy-diphenylethers
US5178786A (en) * 1989-08-04 1993-01-12 The Lubrizol Corporation Corrosion-inhibiting compositions and functional fluids containing same

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3506720A (en) 1963-02-22 1970-04-14 Geigy Chem Corp Halogenated hydroxy-diphenyl ethers
US3629477A (en) 1966-08-08 1971-12-21 Geigy Chem Corp Halogenated diphenyether-containing compositions and control of pests therewith
GB1317156A (en) * 1969-06-05 1973-05-16 Boots Co Ltd Babies napkins
US3920020A (en) * 1974-06-12 1975-11-18 Personal Products Co Inhibiting production of undesirable products on body surfaces and environs
LU78554A1 (en) * 1977-11-21 1979-06-13 Ciba Geigy Ag PROCESS FOR PRODUCING NEW 3-HYDROXYDIPHENYL ETHERS
US4839080A (en) * 1987-04-30 1989-06-13 Neutrogena Corporation Antibacterial iodophor soap base composition and method of making same
WO1991012029A1 (en) * 1990-02-12 1991-08-22 The Procter & Gamble Company High capacity odor controlling compositions
USH1579H (en) * 1990-02-12 1996-08-06 Furio; Diane L. Odor-controlling compositions and articles
KR100322307B1 (en) * 1993-03-31 2002-07-27 더 프록터 앤드 갬블 캄파니 Absorption Absorption Products that Generate Scent Signals
CA2187820C (en) * 1994-04-13 2000-05-30 Chun-Tzer Chou Thermosetting powder coating compositions
US5734081A (en) * 1994-08-05 1998-03-31 Warner-Lambert Company Arylthio compounds
US6287634B1 (en) * 1995-12-22 2001-09-11 Amcol International Corporation Intercalates and exfoliates formed with monomeric ethers and esters; composite materials containing same methods of modifying rheology therewith
BR9709621A (en) * 1996-05-31 1999-08-10 Procter & Gamble Breathable perspiration pads with odor control
US5874067A (en) * 1996-10-24 1999-02-23 The Procter & Gamble Company Methods for controlling environmental odors on the body
US5935596A (en) * 1997-03-20 1999-08-10 Chesebrough-Pond's Usa Co. Delivery of skin benefit agents via adhesive strips
US6258368B1 (en) * 1997-06-04 2001-07-10 The Procter & Gamble Company Antimicrobial wipes
SG74666A1 (en) * 1997-10-21 2000-08-22 Givaudan Roure Int Beta-ketoester
ES2176951T3 (en) * 1998-01-28 2002-12-01 Procter & Gamble ANTIMICROBIAL ABSORBENT POLYMERS THAT FORM HYDROGEL.
CA2336178C (en) * 1998-06-26 2004-08-31 The Procter & Gamble Company A method for collecting and disposing of human waste

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3903007A (en) * 1963-02-22 1975-09-02 Ciba Geigy Corp Detergent composition containing halogenated 2-acyloxy-diphenylethers
US5178786A (en) * 1989-08-04 1993-01-12 The Lubrizol Corporation Corrosion-inhibiting compositions and functional fluids containing same

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090203754A1 (en) * 2007-05-22 2009-08-13 Keck James L Anti-bacterial drug targeting of genome maintenance interfaces
US8415393B2 (en) * 2007-05-22 2013-04-09 Wisconsin Alumni Research Foundation Anti-bacterial drug targeting of genome maintenance interfaces
WO2010015096A1 (en) * 2008-08-08 2010-02-11 Heiq Materials Ag Carrier system for subsequent application onto substrates and method therefor
CH699297A1 (en) * 2008-08-08 2010-02-15 Tex A Tec Ag Carrier system for subsequent application to substrates and method thereof.

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US6825392B2 (en) 2004-11-30
WO2002056819A2 (en) 2002-07-25
WO2002049679A2 (en) 2002-06-27
US20030023212A1 (en) 2003-01-30
WO2002056819A3 (en) 2003-05-30
EP1357948A2 (en) 2003-11-05
WO2002049679A3 (en) 2002-08-22
AU2002232751A1 (en) 2002-07-01
EP1343449A2 (en) 2003-09-17
AU2002246786A1 (en) 2002-07-30
EP1343449A4 (en) 2006-12-06

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