Evaluation of liposomes coated with a pH responsive polymer

被引:65
作者
Barea, M. J. [1 ]
Jenkins, M. J. [2 ]
Gaber, M. H. [3 ]
Bridson, R. H. [1 ]
机构
[1] Univ Birmingham, Ctr Formulat Engn, Sch Chem Engn, Birmingham B15 2TT, W Midlands, England
[2] Univ Birmingham, Sch Met & Mat, Edgbaston B15 2TT, W Midlands, England
[3] British Univ Egypt, Cairo 11837, Egypt
基金
英国工程与自然科学研究理事会;
关键词
Colonic drug delivery; Liposomes; Oral drug delivery; Targeted drug delivery; ORAL-DRUG DELIVERY; METHACRYLIC-ACID COPOLYMERS; INFLAMMATORY-BOWEL-DISEASE; IN-VIVO PERFORMANCE; S100; COMBINATIONS; CHARGED LIPOSOMES; COLONIC-MUCOSA; PEPTIDE DRUGS; MANIPULATION; ABSORPTION;
D O I
10.1016/j.ijpharm.2010.09.028
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Liposomes have been coated with the pH responsive polymer, Eudragit S100, and the formulation's potential for lower gastrointestinal (GI) targeting following oral administration assessed. Cationic liposomes were coated with the anionic polymer through simple mixing. The evolution of a polymer coat was studied using zeta potential measurements and laser diffraction size analysis. Further evidence of an association between polymer and liposome was obtained using light and cryo scanning electron microscopy. Drug release studies were carried out at pH 1.4, pH 6.3 and pH 7.8, representing the pH conditions of the stomach, small intestine and ileocaecal junction, respectively. The polymer significantly reduced liposomal drug release at pH 1.4 and pH 6.3 but drug release was equivalent to the uncoated control at pH 7.8, indicating that the formulation displayed appropriate pH responsive release characteristics. While the coating layer was not able to withstand the additional challenge of bile salts this reinforces the importance of evaluating these types of formulations in more complex media. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:89 / 94
页数:6
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