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Chitosan coated vancomycin hydrochloride liposomes: Characterizations and evaluation

Yang, Zhenlei, Liu, Junli, Gao, Jinhua, Chen, Shilei, Huang, Guihua·2015·International Journal of Pharmaceutics

Abstract

The present work evaluated the feasibility of chitosan coated liposomes (c-Lips) for the intravenous delivery of vancomycin hydrochloride (VANH), a water-soluble antibiotic for the treatment of gram-positive bacterial infections like osteomyelitis, arthritis, endocarditis, pneumonia, etc. The objective of this research was to develop a suitable drug delivery system in vivo which could improve therapeutic efficacy and decrease side effects especially nephrotoxicity. Firstly, the vancomycin hydrochloride liposomes (VANH-Lips) were prepared by modified reverse phase evaporation method, then the chitosan wrapped vancomycin hydrochloride liposomes (c-VANH-Lips) nanosuspension was formulated by the method of electrostatic deposition. Based on the optimized results of single-factor screening experiment, the c-VANH-Lips were found to be relatively uniform in size (220.40 ± 3.56 nm) with a narrow polydispersity index (PI) (0.21 ± 0.03) and a positive zeta potential (25.7 ± 1.12 mV). The average drug entrapment efficiency (EE) and drug loading (DL) were 32.65 ± 0.59% and 2.18 ± 0.04%, respectively. The in vitro release profile of c-VANH-Lips possessed a sustained release Characterization and the release behavior was in accordance with the Weibull equation. Hemolysis experiments showed that its intravenous injection had preliminary safety. In vivo, after intravenous injection to mice, c-VANH-Lips showed a longer retention time and higher AUC values compared with the VANH injection (VANH…

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Research works printed but not linked: 28

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Metadata

Authors
Yang, Z., Liu, J., Gao, J., Chen, S., & Huang, G.
Venue
International Journal of Pharmaceutics
Publisher
Elsevier BV
Published
2015-11
Volume
495
Issue
1
Pages
508-515
ISSN
0378-5173
Cited by
76
References
2
Language
en

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