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

机译:使用中空纤维膜接触器的脂质体制备-螺内酯包封的应用

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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 5h. 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.
机译:在这项研究中,我们提出了一种新型的脂质体制备技术,适用于截留药物和美容剂。这种新方法使用中空纤维结构的膜接触器。为了研究该过程,研究了关键参数对脂质体特性的影响。已经确定,囊泡尺寸分布随着有机相压力的降低而减小,磷脂浓度降低并且水与有机相的体积比增大。脂质体中充满了可用于儿科药物的疏水性药物模型螺内酯。无药物脂质体和载药脂质体的平均大小分别为113 +/- 4 nm和123 +/- 3 nm。无药物和载有药物的脂质体的ζ电势分别为-43 +/- 0.7 mV和-23 +/- 0.6 mV。成功实现了高包封率(93 +/- 1.12%)。透射电子显微镜图像显示了纳米尺寸和球形的寡层囊泡。释放曲线显示约5h内快速完全释放。另外,对过程可重复性和长期脂质囊泡稳定性给予了特别关注。结果证实了基于中空纤维模块的技术的鲁棒性。而且,该技术简单,快速并且具有大规模连续生产纳米级脂质体悬浮液的潜力。

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