Liposome preparation using a hollow fiber membrane contactor-Application to spironolactone encapsulation

被引:114
作者
Laouini, A. [1 ,2 ]
Jaafar-Maalej, C. [1 ]
Sfar, S. [2 ]
Charcosset, C. [1 ]
Fessi, H. [1 ]
机构
[1] Univ Lyon 1, Lab Automat & Genie Procedes LAGEP, UMR CNRS 5007, CPE Lyon, F-69622 Villeurbanne, France
[2] Fac Pharm, Pharm Galen Lab, Monastir 5000, Tunisia
关键词
Liposome; Spironolactone; Hollow fiber module; Membrane contactor; Scale-up; REVERSE-PHASE EVAPORATION; SIZE DISTRIBUTION; INJECTION METHOD; DRUG-DELIVERY; PARTICLE-SIZE; STABILITY; VESICLES; TEMPERATURE; NANOPARTICLES; EFFICIENCY;
D O I
10.1016/j.ijpharm.2011.05.034
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In this study, we present a novel liposome preparation technique suitable for the entrapment of pharmaceutical and cosmetic agents. This new method uses a membrane contactor in a hollow fiber configuration. In order to investigate the process, key parameters influence on the liposome characteristics was studied. It has been established that the vesicle size distribution decreased with the organic phase pressure decrease, the phospholipid concentration decreases and the aqueous to organic phase volume ratio increases. Liposomes were filled with a hydrophobic drug model, spironolactone that could be used for a paediatric medication. The mean size of drug-free and drug-loaded liposomes was, respectively, 113 +/- 4 nm and 123 +/- 3 nm. The zeta potential of drug-free and drug-loaded liposomes was, respectively, -43 +/- 0.7 mV and -23 +/- 0.6 mV. High entrapment efficiency values were successfully achieved (93 +/- 1.12%). Transmission electron microscopy images revealed nanometric sized and spherical shaped oligo-lamellar vesicles. The release profile showed a rapid and complete release within about 5 h. Additionally, special attention was paid on process reproducibility and long term lipid vesicles stability. Results confirmed the robustness of the hollow fiber module based technique. Moreover, the technique is simple, fast and has a potential for continuous production of nanosized liposome suspensions at large scale. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:53 / 61
页数:9
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