Poly(ethylene glycol) conjugated drugs and prodrugs: A comprehensive review

被引:115
作者
Greenwald, RB [1 ]
Conover, CD [1 ]
Choe, YH [1 ]
机构
[1] Enzon Inc, Piscataway, NJ 08854 USA
来源
CRITICAL REVIEWS IN THERAPEUTIC DRUG CARRIER SYSTEMS | 2000年 / 17卷 / 02期
关键词
poly(ethylene glycol); anticancer drug conjugates; prodrugs; camptothecin; paclitaxel; EPR effect;
D O I
10.1615/critrevtherdrugcarriersyst.v17.i2.20
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Low molecular weight Poly(ethylene glycol) (PEG) (< 20,000)-drug conjugates, prepared over a 20-year period, have been scrutinized and their properties and efficacy reviewed. No commercial products have thus far been reported for these types of compounds. However, during the past 5 years a renaissance in the field of PEG-(anticancer) drug conjugates has taken place, initiated by the use of higher molecular weight PEGs (> 20,000), especially 40,000, which is estimated to have a plasma circulating half-life of approximately 8-9 h. This recent resuscitation of small organic molecule delivery by high molecular weight PEG conjugates was founded on meaningful in vivo testing using established tumor models and has led to a clinical candidate. Recent applications of high molecular weight PEG prodrug strategies to amino-containing drugs are also detailed.
引用
收藏
页码:101 / 161
页数:61
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