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Development of a Novel Zinc Oxide/Polyvinyl Chloride Nanocomposite Material for Medical Implant Applications

Published online by Cambridge University Press:  15 April 2014

Benjamin M. Geilich
Affiliation:
Program in Bioengineering, Northeastern University, Boston, MA 02115
Thomas J. Webster
Affiliation:
Program in Department of Chemical Engineering, Northeastern University, Boston, MA 02115 Center of Excellence for Advanced Materials Research, King Abdulaziz University, Jeddah, Saudi Arabia
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Abstract

In hospitals and clinics worldwide, medical device surfaces have become a rapidly growing source of nosocomial infections. Almost immediately after adhering to a device surface, bacteria can begin to form a biofilm, which makes the infection especially difficult to treat and often necessitates device removal. Adding to the severity of this problem is the spread of bacterial genetic tolerance to antibiotics, in part demonstrated by the recent and significant increase in the prevalence of methicillin-resistant Staphylococcus aureus (MRSA).

Nanomaterials are beginning to be used for a wide variety of biomedical applications due to their unique surface properties which have the ability to control initial protein adsorption and subsequent cell behavior. This “nanoroughness” gives nanomaterials a greater functional surface area than conventional materials, which do not have significant features on the nanoscale. In addition, it is theorized that nanoparticles may also have general mechanisms of toxicity towards bacteria that do not cause problems for mammalian cells.

The objective of the present in vitro study was to develop a nanocomposite material by embedding conventional polyvinyl chloride (PVC) with zinc oxide nanoparticles through a simple and inexpensive procedure. The effect of different nanoparticle sizes and %wts were investigated. Results demonstrated that this technique significantly decreased S. aureus density and biofilm formation without the incorporation of antibiotics or other pharmaceuticals, as well as increased the adhesion of human fibroblast cells. Thus, this material could have much promise for use in the manufacture of common implanted medical devices.

Type
Articles
Copyright
Copyright © Materials Research Society 2014 

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References

REFERENCES

Burke, JP. Infection control- a problem for patient safety. N Engl J Med. 2003;348(7):651656.CrossRefGoogle ScholarPubMed
Hall-Stoodley, L, et al. . Bacterial biofilms: from the natural environment to infectious disease. Nat Rev Microbiol. 2004;2(2):95108.CrossRefGoogle Scholar
Izano, EA, et al. . Differential roles of poly-N-acetylglucosamine surface polysaccharide and extracellular DNA in Staphylococcus aureus and Staphylococcus epidermidis biofilms. Appl Environ Microbiol. 2008;74(2):470476.CrossRefGoogle ScholarPubMed
Otto, M. Staphylococcus epidermidis – the ‘accidental’ pathogen. Nat Rev Microbiol. 2009;7(8):555567.CrossRefGoogle ScholarPubMed
Klevens, RM, et al. . Estimating heath care- associated infections and deaths in U.S. hospitals, 2002. Public Health Rep. 2007;122(2):160166.CrossRefGoogle Scholar
Fears, R, et al. . The changing burden of infectious disease in Europe. Sci Transl Med. 2011;3(103):103cm30.CrossRefGoogle Scholar
Ibrahim, EH, et al. . The occurrence of ventilator-associated pneumonia in a community hospital: risk factors and clinical outcomes. Chest. 2001;120(2):555561.CrossRefGoogle Scholar
Klein, E, et al. . Hospitalizations and deaths caused by methicillin-resistant Staphylococcus aureus, United States, 1999–2005. Emerg Infect Dis. 2007;13(12):18401846.CrossRefGoogle ScholarPubMed
Hidron, AI, et al. . NHSN annual update: Antimicrobial-resistant pathogens associated with healthcare-associated infections: annual summary of data reported to the National Healthcare Safety Network at the Centers for Disease Control and Prevention, 2006–2007. Infect Control Hosp Epidemiol. 2008;29(11):9961011.CrossRefGoogle ScholarPubMed
Wood, MA, et al. . The effects of colloidal nanotopography on initial fibroblast adhesion and morphology. IEEE Trans Nanobioscience. 2006;5(1):2031.CrossRefGoogle ScholarPubMed
Kim, P, et al. . Fabrication of nanostructures of polyethylene glycol for applications to protein adsorption and cell adhesion. Nanotechnology. 2005;16(10):24202426.CrossRefGoogle ScholarPubMed
Khang, D, et al. . Enhanced fibronectin adsorption on carbon nanotube/ poly(carbonate) urethane: independent role of surface nano- roughness and associated surface energy. Biomaterials. 2007;28(32): 47564768.CrossRefGoogle ScholarPubMed
Sawai, J, et al. . Detection of active oxygen generated from ceramic powders having antibacterial activity. J Chem Eng Jpn. 1996;29(4):627633.CrossRefGoogle Scholar
Zhang, L, et al. . Nanotechnology and nanomaterials: promises for improved tissue regeneration. Nano Today. 2009;4(1):6680.CrossRefGoogle Scholar
Puckett, SD, et al. . The relationship between the nanostructure of titanium surfaces and bacterial attachment. Bio- materials. 2010;31(4):706713.Google ScholarPubMed
Colon, G, et al. . Increased osteoblast and decreased Staphylococcus epidermidis functions on nanophase ZnO and TiO2. J Biomed Mater Res A. 2006;78(3):595604.CrossRefGoogle ScholarPubMed