Antimicrobial coating for inhibition of bacterial adhesion and biofilm formation

a technology of antimicrobial coating and biofilm, which is applied in the direction of biocides, paints, prostheses, etc., can solve the problems of affecting the integrity of medical devices, forming biofilms on the surface of medical devices, and serious patient problems, so as to increase the antimicrobial effect of coating and inhibit bacterial adhesion and biofilm formation

Inactive Publication Date: 2008-03-13
BACTERIN
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0010]The present invention is based upon the realization that a substantially water-insoluble antimicrobial material can be incorporated into a hydrophilic polymeric coating in a substantially “solubilized’ form wherein the water insoluble antimicrobial material is dispersed homogeneously in a three dimensional hydrogel network gel, formed by a hydrophilic polymer in a substantia...

Problems solved by technology

Colonization of bacteria on the surfaces of medical devices and healthcare products, particularly in implanted devices, result in serious patient problems, including the need to remove and/or replace the implanted device and to vigorously treat secondary infection conditions.
Formation of biofilms on the surface of medical devices can be detrimental to the integrity of the medical device, present health risks, and prevent sufficient flow through the lumens of medical devices.
Although coating or cleaning medical devices with antimicrobial agents, such as antibiotics or antiseptics, can be effective in killing or inhibiting growth of free-floating or “planktonic” organisms not adhered to the device surface, such antimicrobial agents are generally much less active against the microorganisms that are deeply embedded within the biofilm due to their inability to penetrate the biofilm.
The failure of the antimicrobial agents to sufficiently remove the microorganisms is therefore largely due to the protective effect of the biofilm which prevents diffusion of antimicrobial deep into the biofilm layer to eliminate the microorganisms proliferating within therein.
Biofilm associated problems experienced with implantable medical devices such as catheters, particularly catheters designed for urinary tract infections, pose a significant risk for catheterized patients of acquiring secondary infection such as nosocomial infection in a hospital environment.
Such infections can result in prolonged hospital stay, administration of additional antibiotics, and increased cost of post-operative hospital care.
Although, the use of antimicrobially coated catheters wherein antibiotic agents or antimicrobial compounds are dispersed within the coating have been reported to reduce the incidence of catheter associated bacteriuria, such coatings have proven to be largely ineffective in preventing bacterial adhesion and biofilm formation on the catheter surface for extended periods, and therefore do not sufficiently retard the onset of bacterial infection.
Silver nitrate however, can cause toxic side effects at these concentrations, and does cause discoloration of the skin (Argyria).
Unlike antibiotics, the potential for bacterial to become silver ion resistant is therefore quite low.
However, it is also recognized that silver compounds capable of providing bactericidal levels of silver ion have reduced photostability, and tend to discolor in presence of light and or heat as a result of photoreduction of Ag+ ...

Method used

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  • Antimicrobial coating for inhibition of bacterial adhesion and biofilm formation
  • Antimicrobial coating for inhibition of bacterial adhesion and biofilm formation
  • Antimicrobial coating for inhibition of bacterial adhesion and biofilm formation

Examples

Experimental program
Comparison scheme
Effect test

example 1

Coating Formulation Containing Solubilized Silver Sulfadiazine (AgSD)

[0053]A coating formulation comprising AgSD (20 g / L) was prepared as follows. Nitric acid (64 mL, 70%) was added to 800 mL H2O. The resulting nitric acid solution was then heated to 70° C. using a double boiler. AgSD (20 g) was added to the nitric acid solution with stirring using and overhead stirrer with a dissolving stirring shaft. The AgSD was dissolved in a couple minutes. The final volume of the AgSD solution was brought to 1.0 L with H2O.

[0054]Additional coating ingredients may be added when the AgSD (20 g / L) coating formulation is complete. Higher concentrations of AgSD such as 30 g / L may be prepared using analogous procedures.

example 2

Coating Formulation Preparation

[0055]A liter of coating formulation comprising AgSD (20.0 g) and PVA (50.0 g, MW=124,000 to 186,000, 87-89% hydrolysis) was prepared as follows.

[0056]In an appropriate sized temperature controlled mixing vessel set at moderate mixing, Nitric acid (64 mL, 70%) was added to purified H2O and diluted to 800 mL. The temperature of the circulating heater with oil & pump was set between 65° C. and 70° C. The variable speed overhead mixer with dissolving stirrer attachment was set at 500 rpm. AgSD 20.0 g was added slowly to the mixing water and acid mixture. The solution was mixed for a minimum of 15 minutes. The dissolution was confirmed by turning off the mixer and observing that no solid particles settle out after 60 seconds. The temperature of the circulating heater was set to 80° C. and the stirrer was turned back on. The temperature in temperature controlled vessel containing the drug / acid mixture was allowed to reach at least 75° C. before proceeding.

[...

example 3

Coating Formulation Preparation with TiO2

[0059]A liter of coating formulation comprising AgSD (20.0 g), PVA (50.0 g, MW=124,000 to 186,000, 87-89% hydrolysis) and TiO2 (2.0 g) was prepared as follows.

[0060]In an appropriate sized temperature controlled mixing vessel set at moderate mixing, Nitric acid (64 mL, 70%) was added to purified H2O and diluted to 800 mL. The temperature of the circulating heater with oil & pump was set between 65° C. and 70° C. The variable speed overhead mixer with dissolving stirrer attachment was set at 500 rpm. AgSD 20.0 g was added slowly to the mixing water and acid mixture. The solution was mixed for a minimum of 15 minutes. The dissolution was confirmed by turning off the mixer and observing that no solid particles settle out after 60 seconds. The temperature of the circulating heater was set to 80° C. and the stirrer was turned back on. The temperature in temperature controlled vessel containing the drug / acid mixture was allowed to reach at least ...

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Abstract

The present invention provides antimicrobial coatings for coating substrate surfaces, particularly medical devices, for preventing bacterial adhesion and biofilm formation by inhibiting microbial growth and proliferation on the coating surface. The antimicrobial coatings are composed of a hydrogel and a bioactive agent including a substantially water-insoluble antimicrobial metallic material that is solubilized within the coating. Antimicrobial coating formulations for obtaining such coatings, and coating methods are also described.

Description

RELATED APPLICATION[0001]This application claims the benefit of U.S. Provisional Application No. 60 / 566,576, filed on Apr. 29, 2004. The entire teachings of the above application is incorporated herein by reference.FIELD OF THE INVENTION[0002]The present invention relates to an antimicrobial coating for coating a substrate surface, particularly medical devices that are likely to become contaminated or have become contaminated with microorganisms as a result of bacterial adhesion and proliferation and methods for preventing biofilm formation by inhibiting microbial growth and proliferation on the surface of medical devices.BACKGROUND OF THE INVENTION[0003]Colonization of bacteria on the surfaces of medical devices and healthcare products, particularly in implanted devices, result in serious patient problems, including the need to remove and / or replace the implanted device and to vigorously treat secondary infection conditions. Considerable efforts, therefore, have been directed towar...

Claims

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Application Information

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IPC IPC(8): C09D5/16A61K33/38A01N25/00A01N25/10
CPCA61L2300/104A61L29/16A61L2300/406A61L29/085A61L27/54A61L31/10A01N25/10A61L31/16A61L27/34A61L2300/606A01N59/16B05D3/104B05D3/142C09D5/14
Inventor COOK, GUYTREBELLA, MATT
Owner BACTERIN
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