Extrusion of electroformed giant unilamellar vesicles through track-etched membranes

被引:15
作者
Patil, Yogita P. [1 ]
Kumbhalkar, Mrunmayi D. [2 ]
Jadhav, Sameer [1 ]
机构
[1] Indian Inst Technol, Dept Chem Engn, Bombay 400076, Maharashtra, India
[2] Birla Inst Technol & Sci, Dept Chem Engn, Pilani 333031, Rajasthan, India
关键词
Phospholipid; Bilayer; Lamellarity; Lysis tension; Encapsulation efficiency; Dynamic light scattering; ENCAPSULATION EFFICIENCY; LIPID VESICLES; LIPOSOMES; SIZE; VOLUME; POLYDISPERSITY; MULTILAMELLAR; SPECTROSCOPY; PRESSURE; BILAYER;
D O I
10.1016/j.chemphyslip.2011.11.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Unilamellar vesicle populations having a narrow size distribution and mean radius below 100 nm are preferred for drug delivery applications. In the present work, 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) was used to prepare giant unilamellar vesicles (GUVs) by electroformation and multilamellar vesicles (MLVs) by thin film hydration. Our experiments show that in contrast to MLVs, a single-pass extrusion of GUVs through track-etched polycarbonate membranes at moderate pressure differences is sufficient to produce small liposomes having low polydispersity index. Moreover, we observe that the drug encapsulating potential of extruded liposomes obtained from GUVs is significantly higher compared to liposomes prepared by extrusion of MLVs. Furthermore, our experiments carried out for varying membrane pore diameters and extrusion pressures suggest that the size of extruded liposomes is a function of the velocity of GUV suspensions in the membrane pore. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:475 / 481
页数:7
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