拓扑异构酶
药代动力学
药理学
拓扑异构酶抑制剂
化学
酶
癌症治疗
小分子
癌症
生物
生物化学
遗传学
作者
Ali Dehshahri,Milad Ashrafizadeh,Elham Ghasemipour Afshar,Abbas Pardakhty,Ali Mandegary,Reza Mohammadinejad,Gautam Sethi
标识
DOI:10.1016/j.phrs.2019.104551
摘要
Topoisomerase enzymes have shown unique roles in replication and transcription. These enzymes which were initially found in Escherichia coli have attracted considerable attention as target molecules for cancer therapy. Nowadays, there are several topoisomerase inhibitors in the market to treat or at least control the progression of cancer. However, significant toxicity, low solubility and poor pharmacokinetic properties have limited their wide application and these characteristics need to be improved. Nano-delivery systems have provided an opportunity to modify the intrinsic properties of molecules and also to transfer the toxic agent to the target tissues. These delivery systems leads to the re-introduction of existing molecules present in the market as novel therapeutic agents with different physicochemical and pharmacokinetic properties. This review focusses on a variety of nano-delivery vehicles used for the improvement of pharmacological properties of topoisomerase inhibitors and thus enabling their potential application as novel drugs in the market.
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