Substrate Independent Approach for Immobilisation of Quaternary Ammonium Compounds to Surfaces to Reduce Bio-Burden

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Abstract:

Bacterial contamination of biomedical devices is an ongoing problem. One method to alleviate such contamination is the introduction of surface compounds onto devices which can kill bacteria on contact. Polymers containing quaternary ammonium groups are known for their antimicrobial properties. Here we report a substrate-independent two-step method for the immobilisation of quaternary ammonium groups onto any type of surface. To achieve this glycidlytrimethylammonium chloride was covalently bound to plasma polymerised allylmine interlayer. Changes in the membrane permeability of Escherichia coli were observed by BacLight LIVE\DEAD staining. 30% of E. coli grown on the treated surfaces showed high levels of membrane permeability within 4 hours. Importantly, there was no observable cytotoxic effect on human dermal fibroblasts.

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Periodical:

Materials Science Forum (Volumes 783-786)

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1389-1395

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Online since:

May 2014

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* - Corresponding Author

[1] World Health Organization. Annex Table 2: Deaths by cause, sex and mortality stratum in WHO regions, estimates for 2002. The world health report. (2004).

Google Scholar

[2] McCann MT, Gilmore BF, Gorman SP. Staphylococcus epidermidis device-related infections: pathogenesis and clinical management. Journal of Pharmacy and Pharmacology. 2008; 60: 1551-71.

DOI: 10.1211/jpp.60.12.0001

Google Scholar

[3] Fux CA, Costerton JW, Stewart PS, Stoodley P. Survival strategies of infectious biofilms. Trends in Microbiology. 2005; 13: 34-40.

DOI: 10.1016/j.tim.2004.11.010

Google Scholar

[4] Vasilev K, Cook J, Griesser HJ. Antibacterial surfaces for biomedical devices. Expert Rev Med Devices. 2009; 6: 553-67.

DOI: 10.1586/erd.09.36

Google Scholar

[5] Vasilev K, Griesser SS, Griesser HJ. Antibacterial Surfaces and Coatings Produced by Plasma Techniques. Plasma Processes and Polymers. 2011; 8: 1010-23.

DOI: 10.1002/ppap.201100097

Google Scholar

[6] Tiller JC, Liao C-J, Lewis K, Klibanov AM. Designing surfaces that kill bacteria on contact. Proceedings of the National Academy of Sciences. 2001; 98: 5981-5.

DOI: 10.1073/pnas.111143098

Google Scholar

[7] Gottenbos B, van der Mei HC, Klatter F, Nieuwenhuis P, Busscher HJ. In vitro and in vivo antimicrobial activity of covalently coupled quaternary ammonium silane coatings on silicone rubber. Biomaterials. 2002; 23: 1417-23.

DOI: 10.1016/s0142-9612(01)00263-0

Google Scholar

[8] Isquith AJ, Abbott EA, Walters PA. Surface-bonded antimicrobial activity of an organosilicon quaternary ammonium chloride. Appl Microbiol. 1972; 24: 859-63.

DOI: 10.1128/am.24.6.859-863.1972

Google Scholar

[9] Vasilev K, Michelmore A, Griesser HJ, Short RD. Substrate Influence on the Initial Growth Phase of Plasma-Deposited Polymer Films. Chemical Communications. 2009: 3600 - 2.

DOI: 10.1039/b904367e

Google Scholar

[10] Vasilev K, Michelmore A, Martinek P, Chan J, Sah V, Griesser HJ, et al. Early Stages of Growth of Plasma Polymer Coatings Deposited from Nitrogen- and Oxygen-Containing Monomers. Plasma Processes and Polymers. 2010; 7: 824-35.

DOI: 10.1002/ppap.201000030

Google Scholar

[11] Weinstein RA, Gaynes R, Edwards JR, System NNIS. Overview of Nosocomial Infections Caused by Gram-Negative Bacilli. Clinical Infectious Diseases. 2005; 41: 848-54.

DOI: 10.1086/432803

Google Scholar

[12] Vasilev K, Mierczynska A, Hook AL, Chan J, Voelcker NH, Short RD. Creating gradients of two proteins by differential passive adsorption onto a PEG-density gradient. Biomaterials. 2010; 31: 392-7.

DOI: 10.1016/j.biomaterials.2009.09.056

Google Scholar

[13] Goreham RV, Short RD, Vasilev K. Method for the Generation of Surface-Bound Nanoparticle Density Gradients. Journal of Physical Chemistry C. 2011; 115: 3429-33.

DOI: 10.1021/jp111221g

Google Scholar

[14] Kistamah N, Carr CM, Rosunee S. X-ray photoelectron spectroscopic study of Tencel treated with a cationic β-cyclodextrin derivative. Surface and Interface Analysis. 2009; 41: 710-3.

DOI: 10.1002/sia.3076

Google Scholar

[15] Mierczynska A, Michelmore A, Tripathi A, Goreham RV, Sedev R, Vasilev K. pH-tunable gradients of wettability and surface potential. Soft Matter. 2012; 8: 8399-404.

DOI: 10.1039/c2sm25221j

Google Scholar

[16] Ferreira C, Pereira AM, Pereira MC, Melo LF, Simões M. Physiological changes induced by the quaternary ammonium compound benzyldimethyldodecylammonium chloride on Pseudomonas fluorescens. Journal of Antimicrobial Chemotherapy. (2011).

DOI: 10.1093/jac/dkr028

Google Scholar

[17] Kügler R, Bouloussa O, Rondelez F. Evidence of a charge-density threshold for optimum efficiency of biocidal cationic surfaces. Microbiology. 2005; 151: 1341-8.

DOI: 10.1099/mic.0.27526-0

Google Scholar

[18] Murata H, Koepsel RR, Matyjaszewski K, Russell AJ. Permanent, non-leaching antibacterial surfaces-2: How high density cationic surfaces kill bacterial cells. Biomaterials. 2007; 28: 4870-9.

DOI: 10.1016/j.biomaterials.2007.06.012

Google Scholar

[19] Terada A, Yuasa A, Kushimoto T, Tsuneda S, Katakai A, Tamada M. Bacterial adhesion to and viability on positively charged polymer surfaces. Microbiology. 2006; 152: 3575-83.

DOI: 10.1099/mic.0.28881-0

Google Scholar

[20] Ioannou CJ, Hanlon GW, Denyer SP. Action of disinfectant quaternary ammonium compounds against Staphylococcus aureus. Antimicrob Agents Chemother. 2007; 51: 296-306.

DOI: 10.1128/aac.00375-06

Google Scholar

[21] Delcour AH. Outer membrane permeability and antibiotic resistance. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 2009; 1794: 808-16.

DOI: 10.1016/j.bbapap.2008.11.005

Google Scholar

[22] Hancock REW. The bacterial outer membrane as a drug barrier. Trends in Microbiology. 1997; 5: 37-42.

Google Scholar

[23] Abdull Rasad MSB, Halim AS, Hashim K, Rashid AHA, Yusof N, Shamsuddin S. In vitro evaluation of novel chitosan derivatives sheet and paste cytocompatibility on human dermal fibroblasts. Carbohydrate Polymers. 2010; 79: 1094-100.

DOI: 10.1016/j.carbpol.2009.10.048

Google Scholar

[24] Werner S, Krieg T, Smola H. Keratinocyte-Fibroblast Interactions in Wound Healing. Journal of Investigative Dermatology. 2007; 127: 998-1008.

DOI: 10.1038/sj.jid.5700786

Google Scholar