前药
乙二醇
PEG比率
共轭体系
结合
化学
药物输送
文艺复兴
体内
药品
组合化学
药理学
医学
聚乙二醇化
有机化学
聚合物
聚乙二醇
生物
数学分析
艺术
生物技术
经济
艺术史
数学
财务
作者
Richard B. Greenwald,Charles D. Conover,Yun H. Choe
出处
期刊:Critical Reviews in Therapeutic Drug Carrier Systems
[Begell House Inc.]
日期:2000-01-01
卷期号:17 (2): 62-62
被引量:119
标识
DOI:10.1615/critrevtherdrugcarriersyst.v17.i2.20
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.
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