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Smart, Self-Decontaminating Polymer and Method for Inhibiting The Growth Of A Bacteria and Fungus

a technology of antimicrobial system and polymer, which is applied in the direction of biocide, bandages, peptide/protein ingredients, etc., can solve the problems of argyria or silver toxicity, the risk of silver containing products for wound treatment, and the danger of silver toxicity,

Inactive Publication Date: 2015-06-25
FLIR DETECTION
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

This patent describes a material that can be applied to surfaces to prevent the growth of bacteria and fungus. The material contains a polymer, a protein that releases disinfectant and antioxidants when exposed to target analytes on the surface, and an excipient. The material can be photo-polymerized to form a gel or film. An initiator composition can be used to start the polymerization process. An inhibitor of catalase activity can also be applied to the surface. Additionally, a biocide composition can be added that is physically tethered to the protein or the crosslinked polymer, so that it is released when the protein is cleaved from the polymer.

Problems solved by technology

Most biocides are not specific in killing a particular type or class of organism and have negative effects on other (non-target) cells and tissues and can be harmful to the environment.
Furthermore, the use of silver containing products for wound treatment involves the risk of both argyria, or silver toxicity (Abraham T. Wan et. al., Determination of Silver in Blood, Urine, and Tissues of Volunteers and Burn Patients, 37 Clin. Chem. 1683, (1991); Alan B. G. Lansdown, A Pharmacological and Toxiological Profile of Silver as an Antimicrobial Agent in Medical Devices, 2010 Advances in Pharmacological Sciences, (2010).) and the emergence of resistant organisms (E J L Lowbury et. al., Topical chemoprophylaxis with silver sulphadiazine and silver nitrate chlorhexidine creams: emergence of sulphonamide-resistant Gram-negative bacilli, 1 British Medical Journal 493, (1976
However, biocides must be readily available as soon as conditions change and the hazard has exceeded a ‘threat’ concentration.
There are no materials currently which specifically produce antimicrobial compounds, such as oxidizers, only when the target organism is present.
One problem is that its rapid breakdown into water and oxygen make it difficult to use for prolong periods of time.
Also very high concentrations (>3%) of hydrogen peroxide are toxic to the host cells.
It does not proscribe a way to inhibit catalase from using the hydrogen peroxide that is produced from the oxidoreductase enzyme nor a way of being active longer than 2 days after application.
It does not disclose using enzymes that are can be activated by the environment that produce oxidizers when a target organism is present.
It does not disclose having the enzymes only activated by the environment.
It further does not teach that the polymers could be for anti-microbial purposes nor as a dressing.

Method used

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  • Smart, Self-Decontaminating Polymer and Method for Inhibiting The Growth Of A Bacteria and Fungus
  • Smart, Self-Decontaminating Polymer and Method for Inhibiting The Growth Of A Bacteria and Fungus
  • Smart, Self-Decontaminating Polymer and Method for Inhibiting The Growth Of A Bacteria and Fungus

Examples

Experimental program
Comparison scheme
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example 1

Synthesis of a Responsive Hydrogel

[0056]In this embodiment of the present invention, a film was selected as the application method of choice, and the formulation was optimized. The final formulation comprises five components: PEG (polyethylene glycol) diacrylate (22 wt %), PEG 10,000 g / mol (33 wt %), a UV (ultraviolet) initiator (10 wt %), a buffer (35 wt %), and modified chloroperoxidase and glucose oxidase enzymes (0.002%). Polyethylene glycol diacrylate (220 mg−molecular weight of 3,400 g / mol) and linear polyethylene glycol (330 mg−10,000 MW) are first added to 50 mM sodium phosphate solution (pH=8.0). Then, 100 μL of 15 wt % 2-hydroxy-1-[4-(2-hydrozyethoxy)phenyl]-2-methyl-1-propanone in ethanol is also added followed by the addition of glucose oxidase (40 units / mL final volume) and chloroperoxidase (20 units / mL final volume). A small volume (100 μL) of the solution was placed between two 25 mm diameter glass cover slips. The sample was then photopolymerized into a gel by exposi...

example 2

Synthesis of a Biogenic Amine Responsive Urethane

[0057]A predetermined unit activity of Monoamine Oxidase, Diamine Oxidase, and Peroxidase (1, 75, 108) is mixed together and dissolved in a sufficient amount of Potassium Phosphate Buffer pH 7.5 (50 mM) (See reactions in FIGS. 8 & 9). Unit activity of monoamine oxidase is defined herein as one unit of monoamine oxidase as the amount of enzyme that will oxidize one μmole of tyramine to p-hydroxyphenylacetaldehyde and hydrogen peroxide per minute at pH 7.5 at 37° C. under the specific assay conditions. Unit activity of diamine oxidase is defined as the amount of enzyme that will cause the formation of 1 μmole of hydrogen peroxide from putrescine per minute at pH 8.0 at 30° C. under the specific assay conditions. Unit activity of peroxidase is defined as the amount of enzyme that will form 1.0 mg purpurogallin from pyrogallol in 20 sec at pH 6.0 at 20° C. under the specific assay conditions. The resulting polymer produces chlorine in res...

example 3

Chlorination Response of Tailored Biopolymer to Glucose

[0063]The chlorinating activity of composite polymers was measured by following the chlorination of a colored substrate (thionin). The thionin is a blue-violet dye that absorbs at 598 nm and undergoes bleaching (to colorless) upon chlorination. A battery of tests were carried out in 100 mM phosphate citrate buffer at pH 4.0. The reactions employed the following reagents: 0.025 mM thionin and 20 mM NaCl (in citrate phosphate buffer), 0.3% v / v hydrogen peroxide (in deionized water), 18% w / v β-D-glucose (in deionized water), 20 Units / mL of chloroperoxidase in citrate phosphate buffer (where one unit of chloroperoxidase will catalyze the conversion of 1 umole monochlorodimedon to dichlorodimedone per minute at pH 2.75 and 25° C.) and 40 Units / mL of glucose oxidase (where one unit of glucose oxidase will oxidize 1.0 μmole of β-D-glucose to D-gluconolactone and hydrogen peroxide per minute at pH 5.1 at 35° C.). The reaction mixture co...

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Abstract

A smart antimicrobial material and dressing to inhibit microbial growth is provided. Endogenous chemicals, such as metabolites produced from bacteria are utilized as chemical substrates and converted by enzymes to produce a disinfecting compound that will in turn inhibit the targeted microorganism. The material shall remain passive until such time as it encounters a microbe which expresses and / or secretes specific metabolites or markers. The enzyme or enzymes embedded in the smart material converts the metabolite into a disinfecting compound, which in turn either kills the microorganism or prevents it from multiplying on the surface of the material.

Description

CROSS-REFERENCE TO RELATED APPLICATION[0001]This utility patent application is a divisional patent application of and claims the benefit of co-pending U.S. patent application Ser. No. 13 / 915,839, filed on Jun. 12, 2013, which claims the benefit of U.S. Provision Patent Application Ser. No. 61 / 660,065, filed on Jun. 15, 2012 (now expired). The entire contents of U.S. patent application Ser. No. 13 / 915,839 and U.S. Provisional Patent Application Ser. No. 61 / 660,065 are incorporated by reference into this utility patent application as if fully written herein.BACKGROUND OF THE INVENTION[0002]1. Field of the Invention[0003]The present invention relates to the production of a smart antimicrobial system to inhibit microbial growth. Endogenous chemicals, such as metabolites produced from bacteria are utilized as chemical substrates and then converted by enzymes to produce disinfecting compounds that in turn inhibit the targeted microorganism.[0004]2. Description of the Background Art[0005]B...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61L15/38A61L15/26A61L15/42A61L15/44
CPCA61L15/38A61L15/44A61L2420/06A61L15/425A61L2300/404A61L15/26A61F13/00059A61F13/00063A61K9/06A61K9/7007A61K38/443A61L15/46A61L2300/434
Inventor LEECH, ANNA M.WALKER, JEREMY P.DONAHUE, SCOTTJOHNSON, JERMAINE D.SINCLAIR, JESSICA J.
Owner FLIR DETECTION