Controlled extended octenidine release from a bacterial nanocellulose/Poloxamer hybrid system

Alkhatib Y, Dewaldt M, Moritz S, Nitzsche R, Kralisch D, Fischer D (2017)


Publication Type: Journal article

Publication year: 2017

Journal

Book Volume: 112

Pages Range: 164-176

DOI: 10.1016/j.ejpb.2016.11.025

Abstract

Although bacterial nanocellulose (BNC) has been widely investigated in the last 10 years as drug delivery system, up to now no long-term controlled release of drugs could be realized. Therefore, the aim of the present work was the development of a BNC-based drug delivery system that provides prolonged retention time for the antiseptic octenidine up to one week with improved mechanical and antimicrobial properties as well as a high biocompatibility. BNC was modified by incorporation of differently concentrated Poloxamers 338 and 407 as micelles and gels that were extensively investigated regarding size, surface charge, and dynamic viscosity. Depending on type and concentration of the Poloxamer, a retarded octenidine release up to one week could be accomplished. Additionally, superior material properties such as high compression stability and water binding could be achieved. The antimicrobial activity of octenidine against Staphylococcus aureus and Pseudomonas aeruginosa was not changed by the use of Poloxamers. Excellent biocompatibility of the Poloxamer loaded BNC could be demonstrated after local administration in a shell-less hen's egg model. In conclusion, a long-term delivery system consisting of BNC and Poloxamer could be developed for octenidine as a ready-to-use system e.g. for long-term dermal wound treatment.

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How to cite

APA:

Alkhatib, Y., Dewaldt, M., Moritz, S., Nitzsche, R., Kralisch, D., & Fischer, D. (2017). Controlled extended octenidine release from a bacterial nanocellulose/Poloxamer hybrid system. European Journal of Pharmaceutics and Biopharmaceutics, 112, 164-176. https://doi.org/10.1016/j.ejpb.2016.11.025

MLA:

Alkhatib, Y., et al. "Controlled extended octenidine release from a bacterial nanocellulose/Poloxamer hybrid system." European Journal of Pharmaceutics and Biopharmaceutics 112 (2017): 164-176.

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