A review of stimuli-responsive polymeric micelles for tumor-targeted delivery of curcumin

被引:20
|
作者
Qiu, Na [1 ]
Du, Xiyou [1 ]
Ji, Jianbo [1 ]
Zhai, Guangxi [1 ]
机构
[1] Shandong Univ, Sch Pharmaceut Sci, Minist Educ, Dept Pharmaceut,Key Lab Chem Biol, Jinan 250012, Peoples R China
关键词
Curcumin; polymeric micelles; antitumor; stimuli-responsive; drug release; targeting; TRIBLOCK COPOLYMER MICELLES; SELF-ASSEMBLED MICELLES; APOPTOTIC CELL-DEATH; DRUG-DELIVERY; IN-VITRO; CO-DELIVERY; ANTICANCER ACTIVITY; MIXED MICELLES; CANCER; NANOPARTICLES;
D O I
10.1080/03639045.2021.1934869
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Despite a potential drug with multiple pharmacological activities, curcumin has disadvantages of the poor water solubility, rapid metabolism, low bioavailability, which considerably limit its clinical application. Currently, polymeric micelles (PMs) have gained widespread concern due to their advantageous physical and chemical properties, easy preparation, and biocompatibility. They can be used to improve drug solubility, prolong blood circulation time, and allow passive targeted drug delivery to tumor through enhanced penetration and retention effect. Moreover, studies focused on tumor microenvironment offer alternatives to design stimulus-responsive smart PMs based on low pH, high levels of glutathione, altered enzyme expression, increased reactive oxygen species production, and hypoxia. There are various external stimuli, such as light, ultrasound, and temperature. These endogenous/exogenous stimuli can be used for the research of intelligent micelles. Intelligent PMs can effectively load curcumin with improved solubility, and intelligently respond to release the drug at a controlled rate at targeted sites such as tumors to avoid early release, which markedly improves the bioavailability of curcumin. The present review is aimed to discuss and summarize recent developments in research of curcumin-loaded intelligent PMs based on endogenous and exogenous stimuli, and facilitates the development of novel delivery systems for future research.
引用
收藏
页码:839 / 856
页数:18
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