Oral colon-specific drug delivery for bee venom peptide: development of a coated calcium alginate gel beads-entrapped liposome

被引:143
作者
Liu, X
Chen, DW [1 ]
Xie, LP
Zhang, RQ
机构
[1] Shenyang Pharmaceut Univ, Dept Pharmaceut Sci, Sch Pharm, Shenyang 100016, Peoples R China
[2] Tsing Hua Univ, Dept Biol Sci & Biotechnol, Beijing 100084, Peoples R China
关键词
bee venom peptide; coated calcium alginate gel beads; liposome; colon-specific drug delivery;
D O I
10.1016/j.jconrel.2003.08.019
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Colon-specific drug delivery systems (CDDSs) can be used to improve the bioavailability of protein and peptide drugs through the oral route. A novel formulation for oral administration using coated calcium alginate gel beads-entrapped liposome and bee venom peptide as a model drug has been investigated for colon-specific drug delivery in vitro. Drug release studies under conditions mimicking stomach to colon transit have shown that the drug was protected from being released completely in the physiological environment of the stomach and small intestine. The release rate of bee venom from the coated calcium alginate gel beads-entrapped liposome was dependent on the concentration of calcium and sodium alginate, he amount of bee venom in the liposome, as well as the coating. Furthermore, a human gamma-scintigraphy technique was used in vivo to determine drug delivery more precisely. The colonic arrival time of the tablets was found to be 4-5 h. The results clearly demonstrated that the coated calcium alginate gel beads-entrapped liposome is a potential system for colon-specific drug delivery. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:293 / 300
页数:8
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