Biointerface engineering nanoplatforms for cancer-targeted drug delivery

被引:54
|
作者
Zhang, Huaiyu [1 ,2 ]
Dong, Shujun [3 ]
Li, Zhongmin [1 ,2 ]
Feng, Xiangru [2 ]
Xu, Weiguo [2 ]
Tulinao, Catrina Mae S. [4 ]
Jiang, Yang [1 ]
Ding, Jianxun [2 ]
机构
[1] Jilin Univ, Dept Gastrointestinal Colorectal & Anal Surg, China Japan Union Hosp, Changchun 130033, Peoples R China
[2] Chinese Acad Sci, Changchun Inst Appl Chem, Key Lab Polymer Ecomat, Changchun 130022, Peoples R China
[3] Jilin Univ, Sch & Hosp Stomatol, VIP Integrated Dept, Changchun 130021, Peoples R China
[4] Far Eastern Univ, Nicanor Reyes Med Fdn, Quezon City 1118, Philippines
基金
中国国家自然科学基金;
关键词
Cell membrane-camouflaged nanoplatform; Biofunctionalization; Tumor microenvironment; Controlled drug delivery; Targeted cancer therapy; MESENCHYMAL STEM-CELLS; MEMBRANE-CAMOUFLAGED NANOPARTICLES; HYALURONIC-ACID; BIOMIMETIC PLATFORM; MACROPHAGE-MEMBRANE; BREAST-CANCER; PHOTODYNAMIC THERAPY; COATED NANOPARTICLES; ERYTHROCYTE-MEMBRANE; GENE NANOCOMPLEX;
D O I
10.1016/j.ajps.2019.11.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Over the past decade, nanoparticle-based therapeutic modalities have become promising strategies in cancer therapy. Selective delivery of anticancer drugs to the lesion sites is critical for elimination of the tumor and an improved prognosis. Innovative design and advanced biointerface engineering have promoted the development of various nanocarriers for optimized drug delivery. Keeping in mind the biological framework of the tumor microenvironment, biomembrane-camouflaged nanoplatforms have been a research focus, reflecting their superiority in cancer targeting. In this review, we summarize the development of various biomimetic cell membrane-camouflaged nanoplatforms for cancer-targeted drug delivery, which are classified according to the membranes from different cells. The challenges and opportunities of the advanced biointerface engineering drug delivery nanosystems in cancer therapy are discussed. (C) 2019 Shenyang Pharmaceutical University. Published by Elsevier B.V.
引用
收藏
页码:397 / 415
页数:19
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