| Literature DB >> 28805085 |
Juan Li1, Bin Zhang1, Chunwen Yue1, Jing Wu1, Lanxia Zhao1, Deqing Sun1, Rongmei Wang1.
Abstract
Doxorubicin (DOX) is one of the most effective cytotoxic anticancer drugs and has been successfully applied in clinics to treat haematological malignancies and a broad range of solid tumours. However, the clinical applications of DOX have long been limited due to severe dose-dependent toxicities. Recent advances in the development of DOX delivery vehicles have addressed some of the non-specific toxicity challenges associated with DOX. These DOX-loaded vehicles are designed to release DOX in cancer cells effectively by cutting off linkers between DOX and carriers response to stimuli. This article focuses on various strategies that serve as potential tools to release DOX from DOX-loaded vehicles efficiently to achieve a higher DOX concentration in tumour tissue and a lower concentration in normal tissue. With a deeper understanding of the differences between normal and tumour tissues, it might be possible to design ever more promising prodrug systems for DOX delivery and cancer therapy in the near future.Entities:
Keywords: Doxorubicin; delivery vehicles; enzyme-catalysed hydrolysis; light-controlled release; pH-controlled release; redox-controlled release
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Year: 2017 PMID: 28805085 DOI: 10.1080/1061186X.2017.1363209
Source DB: PubMed Journal: J Drug Target ISSN: 1026-7158 Impact factor: 5.121