Physico-chemical characterisation of cationic DOTAP liposomes as drug delivery system for a hydrophilic decapeptide before and after freeze-drying

被引:34
|
作者
Wieber, Alena [1 ,2 ]
Selzer, Torsten [1 ]
Kreuter, Joerg [2 ]
机构
[1] Merck Serono, Formulat & Proc Dev, D-64293 Darmstadt, Germany
[2] Goethe Univ Frankfurt, Inst Pharmaceut Technol, Bioctr, Frankfurt, Germany
关键词
DOTAP; Liposome; Lyophilisation; Hydrophilic peptide; Freeze-drying microscope; Collapse temperature; DRIED LIPOSOMES; IMMUNOSTIMULATION; TEMPERATURE; STABILITY; TREHALOSE; BEHAVIOR; ADJUVANT;
D O I
10.1016/j.ejpb.2011.11.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In the present study, positively charged 1,2-dioleoyloxy-3-trimethylammoniumpropane (DOTAP) liposomes as a delivery system for a hydrophilic decapeptide were developed. The main objective was the preparation of a stable, highly loaded, lyophilised formulation to yield the basis for an acceptable shelf life. The influences of addition of cholesterol, pH value, amounts of lipid and peptide, type and amount of sugar-based cryoprotective agent (trehalose and sucrose), and time point for cryoprotector addition as well as the freeze-drying process parameters were investigated. The collapse temperatures of the liposome dispersions in the presence of the disaccharides trehalose and sucrose were determined using a freeze-drying microscope (Lyostat 2). The liposome morphology before freeze-drying was determined by transmission electron microscopy (TEM). The evidence of intact liposomes after freeze-drying was shown by scanning electron microscope (SEM) imaging. In summary, this study demonstrated the successful development of DOTAP liposomes including their lyophilisation as a drug delivery system for small hydrophilic peptides. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:358 / 367
页数:10
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