Intelligent polymeric micelles for multidrug co-delivery and cancer therapy

被引:71
作者
Yu, Guangping [1 ,2 ]
Ning, Qian [2 ]
Mo, Zhengcheng [3 ]
Tang, Shengsong [1 ,2 ]
机构
[1] Univ South China, Inst Pharm & Pharmacol, Learning Key Lab Pharmacoprote Hunan Prov, Henyang 421001, Peoples R China
[2] Hunan Univ Med, Hunan Prov Key Lab Antibody Based Drug & Intellig, Huaihua, Peoples R China
[3] Univ South China, Hengyang Med Sch, Dept Histol & Embryol, Clin Anat & Reprod Med Applicat Inst, Henyang, Peoples R China
基金
中国国家自然科学基金;
关键词
Polymeric micelles; multidrug co-delivery; tumour targeting; drugs release; uptake; cancer therapy; TARGETED DRUG-DELIVERY; MIXED MICELLES; TUMOR-THERAPY; BREAST-CANCER; COPOLYMER MICELLES; ANTIBODY FRAGMENTS; HYBRID MICELLES; IN-VITRO; DOXORUBICIN; RESISTANCE;
D O I
10.1080/21691401.2019.1601104
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Polymeric micelles (PMs) play a vital role in multidrug co-delivery and cancer treatment. However, the development of intelligent PMs further allows PMs to accurately -target tumour, selectively release cargo multidrug and increase uptake. Therefore, targets, controlled release and uptake of intelligent PMs should be paid more attention to improvement synergistic therapeutic outcomes and minimize side effects. In this review, tumour targeting of co-delivery intelligent PMs and its intracellular trafficking mechanisms were overviewed. And this review provides a comprehensive summarization of several intelligent co-delivery PMs. Such a system could control the multidrug to be released simultaneously or sequentially by special properties of tumour microenvironment (TME) (including acidic PH, redox, overexpressed enzyme, excessive temperature) and external environment trigger. Additionally, limitations, clinical translation and future perspectives of intelligent co-delivery PMs were also being discussed in this article.
引用
收藏
页码:1476 / 1487
页数:12
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