前药
娴熟的
药理学
脂质体
单克隆抗体
化学
癌症
药品
化疗
医学
抗体
生物化学
内科学
免疫学
作者
Xi Chen,Bingyuan Wu,Peng George Wang
出处
期刊:Current medicinal chemistry
[Bentham Science]
日期:2003-03-01
卷期号:3 (2): 139-150
被引量:44
标识
DOI:10.2174/1568011033353470
摘要
Glucuronide prodrugs have shown promising efficacy in anti-cancer therapy due to their increased specificity and reduced systemic toxicity. The prodrugs can be used in prodrug monotherapy (PMT), which is based on elevated tumor β-glucuronidase activity. β-Glucuronidase activates the low-toxic prodrugs into highly cytotoxic agents specifically in the tumor site. The specificity of the prodrugs can be further improved by combined use with monoclonal antibodies against tumor-specific antigens, namely antibody-directed enzyme prodrug therapy (ADEPT), and the potency of the prodrugs can be greatly enhanced with the incorporation of an appropriate radionuclide in the combined chemo- and radio-therapy of cancer (CCRTC) strategy. The prodrugs can also be utilized to modify liposomes for efficient delivery of anti-cancer drugs.
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