紫杉烷
多西紫杉醇
紫杉醇
医学
生物利用度
药代动力学
药理学
药品
癌症
内科学
乳腺癌
作者
Nusrat Chowdhury,Mandip Singh
出处
期刊:Critical Reviews in Therapeutic Drug Carrier Systems
[Begell House]
日期:2020-01-01
卷期号:37 (3): 205-227
被引量:6
标识
DOI:10.1615/critrevtherdrugcarriersyst.2020029699
摘要
In this review, we describe the advances in oral drug delivery approaches for taxanes for successful therapeutic outcome. Taxanes (paclitaxel and docetaxel) have unwanted pharmacokinetic profiles when they are given in their current dosage forms. Taxanes have low bioavailability, are extensively metabolized by CYP3A, and have a high affinity for P-glycoprotein. Regardless of dosage schedule, the overall docetaxel or paclitaxel dose that a patient can tolerate at a given interval remains similar. Currently, there are no commercially available oral taxane nanoformulations, and there are still several challenges to overcome. Nano-based formulations may offer the best solutions to problems involving the safety and effectiveness of taxane delivery. Thus, further research is necessary before such taxane nanoformulations can be manufactured for clinical use.
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