心脏毒性
阿霉素
纳米载体
药理学
曲妥珠单抗
地塞米松
蒽环类
医学
柔红霉素
药品
化疗
癌症
内科学
乳腺癌
作者
Michaela Fojtů,Jaromír Gumulec,Tibor Stračina,Martina Raudenská,Anna Skotakova,Markéta Vaculovičová,Vojtěch Adam,Petr Babula,Marie Novàkovâ,Michal Masařík
出处
期刊:Current Drug Metabolism
[Bentham Science]
日期:2017-03-31
卷期号:18 (3): 237-263
被引量:42
标识
DOI:10.2174/1389200218666170105165444
摘要
Background: Anthracycline antibiotic doxorubicin (DOX) is a very potent and extensively prescribed chemotherapeutic drug. It is widely utilized in the therapy of variety of haematological and solid tumours, although its administration is commonly accompanied with several severe side effects. The most serious one is a development of dose-dependent and cumulative cardiotoxicity. In the course of time, many strategies have been investigated in order to avoid or at least to diminish DOX-induced cardiac dysfunction; these include reduction of toxic effect by coadministration with iron chelators (dexrazoxane), trastuzumab, taxanes, statins, and ACE-inhibitors. However, the attenuation of cardiotoxic effect is still not satisfactory yet. Keywords: Doxorubicin, nanoparticles, liposomal, polymeric, protein, gold, cardiotoxicity, nanocarriers.
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