WO2011008441A1 - Light-activated antimicrobial article and method of use - Google Patents

Light-activated antimicrobial article and method of use Download PDF

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Publication number
WO2011008441A1
WO2011008441A1 PCT/US2010/039580 US2010039580W WO2011008441A1 WO 2011008441 A1 WO2011008441 A1 WO 2011008441A1 US 2010039580 W US2010039580 W US 2010039580W WO 2011008441 A1 WO2011008441 A1 WO 2011008441A1
Authority
WO
WIPO (PCT)
Prior art keywords
light
nylon material
light source
acridine dye
article
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/US2010/039580
Other languages
English (en)
French (fr)
Inventor
Maria A. Appeaning
Sonja K. Belgrade
Douglas E. Weiss
Narina Y. Stepanova
Caroline M. Ylitalo
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.)
3M Innovative Properties Co
Original Assignee
3M Innovative Properties Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 3M Innovative Properties Co filed Critical 3M Innovative Properties Co
Priority to US13/321,566 priority Critical patent/US8877125B2/en
Priority to BRPI1012154A priority patent/BRPI1012154A2/pt
Priority to CN201080037259.3A priority patent/CN102481385B/zh
Priority to JP2012517672A priority patent/JP2012532103A/ja
Priority to EP10740779A priority patent/EP2448603A1/en
Publication of WO2011008441A1 publication Critical patent/WO2011008441A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • 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
    • A61L9/16Disinfection, sterilisation or deodorisation of air using physical phenomena
    • A61L9/18Radiation
    • A61L9/20Ultraviolet radiation
    • A61L9/205Ultraviolet radiation using a photocatalyst or photosensitiser
    • 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
    • A61L2/00Disinfection or sterilisation of materials or objects, in general; Accessories therefor
    • A61L2/02Disinfection or sterilisation of materials or objects, in general; Accessories therefor using physical processes
    • A61L2/08Radiation
    • A61L2/088Radiation using photocatalysts or photosensitisers
    • 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
    • A61L2/00Disinfection or sterilisation of materials or objects, in general; Accessories therefor
    • A61L2/02Disinfection or sterilisation of materials or objects, in general; Accessories therefor using physical processes
    • A61L2/08Radiation
    • A61L2/10Ultraviolet [UV] radiation
    • 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
    • A61L2209/00Aspects relating to disinfection, sterilisation or deodorisation of air
    • A61L2209/10Apparatus features
    • A61L2209/12Lighting means
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/20Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
    • Y10T442/2525Coating or impregnation functions biologically [e.g., insect repellent, antiseptic, insecticide, bactericide, etc.]

Definitions

  • pathogenic microorganisms including bacteria, fungi and viruses.
  • many chemistries and methods have been developed to kill or inhibit the growth of pathogenic microorganisms including the development and use of antibiotics, antiviral agents and oxidizing agents.
  • Electromagnetic radiation in many wavelength ranges has also been used. It is known that pathogenic microorganisms may be killed or their growth inhibited by exposure of the microorganisms to light in the presence of oxygen and certain photosensitizers.
  • a useful method may comprise: providing a photosensitive nylon material consisting essentially of an acridine dye disposed on a nylon material, exposing the
  • kits may comprise a light source, and a photosensitive nylon article consisting essentially of an acridine dye disposed on a nylon material.
  • the kit may also comprise a light source, and a light-activated antimicrobial article consisting essentially of an acridine dye covalently bonded without a linking group to a nylon material.
  • Singlet oxygen is generated in neutrophils and macrophages for use in killing microorganisms.
  • Superoxide dismutases, catalases, and peroxidases are defenses against radical- and reduced-oxygen species, but are not effective against singlet oxygen.
  • a few microorganisms, such as Cercospora are inherently resistant to singlet oxygen, and Gram-positive bacteria are generally more easily killed by singlet oxygen than Gram-negative bacteria.
  • Enveloped viruses are inactivated by singlet oxygen more readily than nonenveloped viruses. It is notable that not a single documented case of acquired resistance by a bacterium, fungus, or virus to singlet oxygen is known.
  • Type I mechanism For photosensitizers that can pass through the lipid bilayer membrane into the interior of the cell where reducing agent concentrations, such as NADPH and glutathione, are high, the so-called Type I mechanism has been determined to be the predominant one leading to cell destruction. This mechanism involves, ultimately, the formation of a photosensitizer free radical and reactive oxygen species such as hydrogen peroxide, hydroxyl radical, and superoxide radical anion.
  • photosensitizers in free form (e.g., phthalocyanine, porphyrin, hypericin, and rose bengal) for killing bacteria and fungi and for inactivating viruses.
  • photosensitizers in free form (e.g., phthalocyanine, porphyrin, hypericin, and rose bengal) for killing bacteria and fungi and for inactivating viruses.
  • photosensitizers in free form (e.g., phthalocyanine, porphyrin, hypericin, and rose bengal) for killing bacteria and fungi and for inactivating viruses.
  • photosensitizers in free form (e.g., phthalocyanine, porphyrin, hypericin, and rose bengal) for killing bacteria and fungi and for inactivating viruses.
  • photosensitizers in free form (e.g., phthalocyanine, porphyrin, hypericin, and rose bengal) for killing bacteria and fungi and for in
  • Photosensitizers have been covalently or ionically bonded to beads, larger molecules, oligomers, macromolecules and polymers.
  • an ionic binder was used to bind dye to woven and nonwoven fabrics as disclosed in US 5,830,526 (Wilson et al.).
  • Positively charged polymer carrier was used to ionically bond rose bengal such that microbes were killed in the presence of oxygen and light.
  • Photodynamic inactivation of E. coli by rose bengal bonded to polystyrene beads was disclosed by Bezman et al. in Photochemistry and Photobiology, 28, 325-329, (1978).
  • Light-activated antimicrobial articles refers to the ability of an article or method to induce a photodynamic effect. In this sense, light-activated means that a photosensitizer is present and transfers energy from light to generate reactive species such as singlet oxygen, hydrogen peroxide, hydroxyl radical, superoxide radical anion,
  • the articles and methods disclosed herein are also "light-activated” in the sense that they can become antimicrobial when subjected to light.
  • Antimicrobial refers to the ability of an article or method to kill or inhibit the growth of microorganisms such as bacteria, fungi and viruses.
  • To "kill or inhibit the growth of includes limiting the presence of at least one virus, at least one bacterium, at least one fungus, or a combination thereof.
  • To “kill or inhibit the growth of also includes inactivation and prevention of the replication of or reducing the number of a microorganism. Different terms may be used for different microorganisms.
  • An article is considered to be "light-activated antimicrobial" if the article can be optically coupled to a light source such that when the light source is turned on to emit light, the article kills or inhibits the growth of some affected microorganism.
  • Various incubation and testing methods can be used to determine the number of colony forming units per sample of an affected microorganism.
  • the number of colony forming units killed or inhibited by the article can be determined by subjecting separate samples to light with and without the acticle, as long as the same or nearly the same incubation and testing methods are used.
  • "Light-activated antimicrobial" articles result in a decrease in colony forming units, for example, in an amount of from about 80 to 100%, or from about 90 to 99.99%.
  • a method is considered to be "light-activated antimicrobial” if the method involves some use of the light-activated antimicrobial article and/a light source to kill or inhibit the growth of some affected microorganism (as described above for the article).
  • Affected microorganisms include DNA viruses, RNA viruses, RNA
  • Affected microorganisms also include single- and double-stranded nucleic acid genomes.
  • Affected microorganisms include negative single-stranded RNA genomes such as
  • Orthomyxoviridae Rhabdoviridae, Paramyxoviridae, Bunyaviridae, and Filoviridae. These are enveloped viruses.
  • Orthomyxoviridae include the influenza viruses A, B, and C.
  • Rhabdoviridae include rabies virus and vesicular stomatitis virus.
  • Paramyxoviridae include parainfluenza virus of mammals (including mumps virus) and pneumovirus (such as respiratory syncytial viruses of man and cattle).
  • Bunyaviridae include hantavirus, which causes Korean hemorrhagic fever and hantavirus pulmonary syndrome.
  • Filoviridae include Marburg virus and Ebola virus.
  • Affected microorganisms include positive single-stranded RNA genomes such as Picornaviridae (non-enveloped), Retroviridae, and Togaviridae.
  • Picornaviridae include polioviruses, coxsackieviruses, hepatitis A virus, and rhinovirus.
  • Retroviridae include, for example, human immunodeficiency virus (HIV), simian
  • Togaviridae include Semliki Forest virus, yellow fever virus, Dengue virus, tick-borne virus, and rubella virus. Parvovirus (non-enveloped) is the only virus having a single- stranded negative-sense DNA genome. This virus primarily infects cats and dogs.
  • Affect microorganisms include double-stranded viruses such as Papovaviridae, Adenoviridae, Herpesviridae, Poxviridae, and Hepadnaviridae. With the exception Herpesviridae, these viruses are non-enveloped viruses.
  • Papovaviridae include papillomaviruses causing warts and tumors.
  • Adenoviridae include Mastadenovirus and a variety of viruses capable of infecting the respiratory tract.
  • Herpesviridae include herpes simplex 1 and 2, varicella zoster virus, cytomegalovirus, Epstein-Barr virus, human herpesvirus 6, antibodies to which are now known to be responsible for multiple sclerosis, and human herpesvirus 7.
  • Herpesviridae include variola and other pox-producing viruses.
  • Hepadnaviridae include human hepatitis B virus.
  • Affect microorganisms include bacteria such as Enter ococcus faecium, Staphylococcus aureus, Pseudomonas aeruginosa, and E. coli. Species may be Staphylococcus, Enterococcus, Streptococcus, Corynebacterium, Listeria, Neisseria, and Enter obacteriaceae (which includes the genera Escherichia, Salmonella, and Shigella). The coliforms are Gram-negative rods, generally in the family
  • Enterobacteriaceae Some coliforms colonize the intestinal tract of humans and other animals. Some coliforms are associated with disease. Surfaces and liquids can also be contaminated with these bacteria.
  • Affect microorganisms include fungi such as Candida albicans, which causes yeast infection of the oral cavity known as thrush and an infection of the female reproductive tract known as vulvovaginitis.
  • a light-activated antimicrobial article consisting essentially of a photosensitizer covalently bonded without a linking group to a nylon material.
  • the photosensitizer is preferably an acridine dye.
  • "consists essentially of means that the article consists mainly of the two components, but other components that do not especially contribute to the invention or the function of the invention may be present. Typically, these other components can be used in a total amount of from 0 to about 5 wt.% relative to the total dry weight of the acridine dye.
  • acridine dye is covalently bonded without a linking group to nylon material.
  • covalently bonded without a linking group means that the acridine dye is directly bonded to a polyamide chain or a former polyamide chain with 0 or 1 atoms in between the covalently bonded dye and the polyamide of the nylon material. If the acridine dye is covalently bonded with 0 atoms to the nylon material, then the dye is directly bonded, with no intervening atoms, to a main chain or former main chain of the nylon material.
  • the atom may comprise carbon, oxygen or nitrogen.
  • the article disclosed herein is distinguishable from grafted nylon polymers in which nylon is functionalized with a linking group such as acrylic acid, and then treated with a reactive species that ends up as a pendant group off the main chain polyamide of the nylon.
  • a linking group refers to a group having more than one atom.
  • the acridine dye can transfer energy of light emitted from a light source such that antimicrobial activity occurs.
  • Antimicrobial activity may result from the generation of one or more reactive species such as singlet oxygen, hydrogen peroxide, hydroxyl radical, superoxide radical anion, amine-functionalized photosensitizer radical and many other radicals that may be formed depending upon the particular environment of the acridine dye.
  • nylon material comprises any chemical structure referred to as nylon.
  • nylon comprises long polymer chains of repeating units linked by peptide bonds.
  • Nylons are often named on the basis of the number of carbon atoms separating adjacent peptide bonds.
  • Common nylon is known as nylon 6-6 which refers to hexamethylene groups between adjacent peptide bonds.
  • Nylon may also comprise homopolymer nylon 6 or ring-opened polycaprolactam that has been polymerized.
  • the nylon material may exist in the form of fibers, and the Federal Trade Commission has a definition for Nylon Fiber: A manufactured fiber in which the fiber forming substance is a long-chain synthetic polyamide in which less than 85% of the amide-linkages are attached directly (-CO-NH-) to two aliphatic groups.
  • the nylon material may be in the form of fibers.
  • the nylon material may be a nonwoven nylon material.
  • Electron beam processing or irradiating involves the production of electron beams by applying high voltage to tungsten wire filaments retained between a repeller plate and an extractor grid within a vacuum chamber maintained at about 10 "6 Torr.
  • the filaments are heated at a high current to produce electrons.
  • the electrons are guided and accelerated by a repeller plate and an extractor grid towards a thin window of metal foil.
  • the accelerated electrons traveling at speeds in excess of 10 7 meters/second (m/sec) and possessing about 10 to 300 kilo-electron volts (keV) pass out of the vacuum chamber through the foil window and penetrate whatever material is positioned immediately beyond the foil window.
  • Electron beam irradiating has been used for modifying various materials, including polymerizing, crosslinking, grafting and curing materials. For example, electron beam irradiating has been used to polymerize and/or crosslink various pressure-sensitive adhesives formulations coated on film substrates, and to cure various liquid coatings, such as printing inks. Electron beam irradiating can be used to modify a material without the need for coating solutions.
  • the amount of energy absorbed per unit mass, also known as the dose is measured in units of gray and conveniently expressed as kilograys (kGy), where 1 kGy is equal to 1,000 joules per kilogram.
  • the light-activated antimicrobial article may be made by subjecting the nylon material to a solution of the amine-functionalized photosensitizer.
  • the nylon material is removed from the bath and the wet sample subjected to electron beam irradiation.
  • the article may consist of additional components but only those that do not contribute to formation of the light-activated antimicrobial article. Additional components can be present in minor amounts, e.g., less than 5 wt% of the total weight of the dried coating materials on the nylon material.
  • the light-activated antimicrobial article is made by reaction between the photosensitizer and the nylon polyamide chains, wherein reaction is carried out by electron beam processing.
  • the amine-functionalized photosensitizer may be used in any amount, relative to the nylon material, that is needed to achieve a desired effect.
  • the amine-functionalized photosensitizer may be used in an amount effective in
  • the amine-functionalized photosensitizer may be used in an amount of from about 0.01 to about 10%, or from about 0.1 to about 5%, by weight, and relative to the weight of the layer or material in which the amine-functionalized photosensitizer is used.
  • Electron beam irradiation of a nylon nonwoven web coated with anti-microbial dyes creates a non-leaching, antimicrobial substrate that has a variety of uses in health care and also in consumer products.
  • the use of light activated antimicrobial dyes provides many useful properties. The antimicrobial activity could be turned on and off by controlling the amount of light on the web. The dye also provides a pleasing color, enhancing marketability.
  • the combination of nylon, the light-activated antimicrobial dye, and the optional electron beam irradiating treatment results in an enhanced non-leaching property so the dye doesn't bleed onto other surfaces when wetted and the nylon would maintain the same amount of antimicrobial dye even after extended use.
  • the light source may comprise any suitable light source.
  • the light source may comprise sunlight or ambient room lighting.
  • Exemplary light sources also include linear light sources such as cold cathode fluorescent lamps and point light sources such as light emitting diode (LEDs).
  • Exemplary light sources also include organic light-emitting devices (OLEDs), incandescent bulbs, fluorescent bulbs, halogen lamps,
  • UV bulbs infrared sources, near-infrared sources, lasers, or chemical light sources.
  • the light emitted by the light source may be visible or invisible.
  • At least one light source may be used. For example, from 1 to about 10,000 light sources may be used.
  • the light source may comprise a row of LEDs.
  • the light source may comprise LEDs arranged on a circuit such that light emitted from the LEDs lights up
  • the light source may be optically coupled to a viscoelastic material as described in U.S. Provisional Application No. 61/169973 filed on April 16, 2009 (64347US008, Sherman et al.), incorporated herein by reference.
  • the viscoelastic material may be positioned relative to the light-activated antimicrobial article so that light can be extracted from the viscoelastic material and absorbed by the acridine dye, as described in U.S. Provisional Application No. 61/220,505 filed on June 25, 2009 (65460US002, Appeaning et al), incorporated herein by reference.
  • the light-activated antimicrobial article may be disposed on a viscoelastic layer, and the light source may comprise an LED pressed into an edge of the viscoelastic layer.
  • the light source may be powered by any suitable means.
  • the light source may be powered using a battery, a DC power supply, an AC to DC power supply, an AC power supply, or a solar photovoltaic cell.
  • the light source may also be powered by motion such as walking.
  • the light-activated antimicrobial articles disclosed herein may be provided in any number of ways.
  • the light-activated antimicrobial articles may be provided as sheets or strips laid flat, or they can be rolled up to form a roll.
  • the light-activated antimicrobial articles may be packaged as single items, or in multiples, in sets, etc.
  • the light-activated antimicrobial articles may be provided in an assembled form, i.e., as part of some larger construction.
  • the light-activated antimicrobial articles may be provided in kits wherein a light source is provided in addition to the article.
  • the light source and article can be assembled together or separate from each other and assembled at some point by the user.
  • the light-activated antimicrobial articles may also be provided separately such that they can be mixed and matched according to the needs of the user.
  • the light-activated antimicrobial articles may be temporarily or permanently assembled.
  • a useful method may comprise: providing a photosensitive nylon material consisting essentially of an acridine dye disposed on a nylon material, exposing the
  • photosensitive nylon material to a microorganism, providing a light source, and activating the light source such that light emitted by the light source is absorbed by the acridine dye.
  • One half of the sample was subjected to electron beam irradiation as follows: An electron beam processor, CB-300 'Electrocurtain' (Energy Sciences, Inc.), was used. This processor uses a 12" wide PET web to convey samples through a 12" wide curtain beam of electrons. The sample construction was taped onto the web and conveyed through the processor at a speed of 20 fpm. The beam voltage was set at
  • Spectrophotometer to generate a standard curve.
  • the leaching liquid from the electron beam irradiated sample had a
  • concentration of 0.741 ppm and the leaching liquid from the non-electron beam irradiated sample had a concentration of 2.11 ppm.
  • the sample that was electron beam irradiated shows almost a 3 -fold concentration reduction. These concentrations are both very low compared to the initial 0.05 wt% (500 ppm) solution that was used to treat the nylon. This shows that the dye is strongly bound to the nylon.
  • Antimicrobial testing was carried out as described above. Growth in total colony forming units for each sample was recorded after 24 hour incubation with light.

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  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Apparatus For Disinfection Or Sterilisation (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)
PCT/US2010/039580 2009-06-30 2010-06-23 Light-activated antimicrobial article and method of use Ceased WO2011008441A1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
US13/321,566 US8877125B2 (en) 2009-06-30 2010-06-23 Light-activated antimicrobial articles and methods of use
BRPI1012154A BRPI1012154A2 (pt) 2009-06-30 2010-06-23 ativado por luz artigo microbicida e método de uso.
CN201080037259.3A CN102481385B (zh) 2009-06-30 2010-06-23 光活化抗微生物制品及其使用方法
JP2012517672A JP2012532103A (ja) 2009-06-30 2010-06-23 光活性化抗菌性物品及び使用方法
EP10740779A EP2448603A1 (en) 2009-06-30 2010-06-23 Light-activated antimicrobial article and method of use

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US22186509P 2009-06-30 2009-06-30
US61/221,865 2009-06-30

Publications (1)

Publication Number Publication Date
WO2011008441A1 true WO2011008441A1 (en) 2011-01-20

Family

ID=43221872

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2010/039580 Ceased WO2011008441A1 (en) 2009-06-30 2010-06-23 Light-activated antimicrobial article and method of use

Country Status (6)

Country Link
US (1) US8877125B2 (https=)
EP (1) EP2448603A1 (https=)
JP (1) JP2012532103A (https=)
CN (1) CN102481385B (https=)
BR (1) BRPI1012154A2 (https=)
WO (1) WO2011008441A1 (https=)

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US8864362B2 (en) 2009-10-30 2014-10-21 3M Innovative Properties Company Illumination device having remotely powered lightguide
US9285531B2 (en) 2008-08-08 2016-03-15 3M Innovative Properties Company Lightguide having a viscoelastic layer for managing light
US9480760B2 (en) 2009-06-25 2016-11-01 3M Innovative Properties Company Light-activated antimicrobial article and method of use
WO2018129006A1 (en) * 2017-01-06 2018-07-12 Dabney Paul System, retainer and method of preventing and treating nosocomial infections including methicillin-resistant staphylococcus aureus infections
US10228507B2 (en) 2008-07-10 2019-03-12 3M Innovative Properties Company Light source and optical article including viscoelastic lightguide disposed on a substrate
CN117684304A (zh) * 2023-11-21 2024-03-12 新疆大学 一种驼绒抗菌纱线制备方法及驼绒抗菌纱线

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US11859051B2 (en) * 2019-09-09 2024-01-02 Xerox Corporation Polyamides with in-backbone optical absorbers and related methods
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