Drug-Coupled Poly(Amino Acids) as Polymeric Prodrugs

被引:15
作者
Bennett, D. B.
Adams, N. W.
Li, X.
Feijen, J.
Kim, S. W. [1 ]
机构
[1] Univ Utah, Dept Pharmaceut, Salt Lake City, UT 84112 USA
关键词
D O I
10.1177/088391158800300105
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Biodegradable poly(alpha-amino acids) can serve as chemical carriers of active agents. The narcotic antagonist naltrexone and the anti-hypertensive minoxidil were covalently coupled to polymer backbones based upon L-glutamic acid to give polymeric prodrugs. The synthesis and release characteristics of these two systems are reviewed. The rate of hydrolytic cleavage of the polymer-drug linkage should be much slower than the rate of diffusion through the polymer matrix; thus release rates approaching zero order can be achieved. In vitro and in vivo release studies demonstrate the potential for these types of polymeric delivery systems.
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页码:44 / 52
页数:9
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