Tumor-on-a-chip model for advancement of anti-cancer nano drug delivery system

被引:31
作者
Tian, Chutong [1 ,2 ]
Zheng, Shunzhe [1 ]
Liu, Xinying [1 ]
Kamei, Ken-ichiro [1 ,3 ]
机构
[1] Shenyang Pharmaceut Univ, Wuya Coll Innovat, Dept Pharmaceut, Shenyang 110016, Peoples R China
[2] Chinese Peoples Liberat Army 210 Hosp, Dalian 116021, Peoples R China
[3] Kyoto Univ, Inst Integrated Cell Mat Sci WPI iCeMS, Sakyo Ku, Yoshida Ushinomiya Cho, Kyoto 6068501, Japan
基金
日本学术振兴会; 中国国家自然科学基金;
关键词
Tumor-on-a-Chip; Microfluidic device; Nanomedicines; Drug delivery process; Preclinical prediction; PROTEIN CORONA; CANCER; NANOPARTICLES; MICROENVIRONMENT; NANOCARRIERS; PLATFORM; OPPORTUNITIES; INFLAMMATION; ANGIOGENESIS; PENETRATION;
D O I
10.1186/s12951-022-01552-0
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
Despite explosive growth in the development of nano-drug delivery systems (NDDS) targeting tumors in the last few decades, clinical translation rates are low owing to the lack of efficient models for evaluating and predicting responses. Microfluidics-based tumor-on-a-chip (TOC) systems provide a promising approach to address these challenges. The integrated engineered platforms can recapitulate complex in vivo tumor features at a microscale level, such as the tumor microenvironment, three-dimensional tissue structure, and dynamic culture conditions, thus improving the correlation between results derived from preclinical and clinical trials in evaluating anticancer nanomedicines. The specific focus of this review is to describe recent advances in TOCs for the evaluation of nanomedicine, categorized into six sections based on the drug delivery process: circulation behavior after infusion, endothelial and matrix barriers, tumor uptake, therapeutic efficacy, safety, and resistance. We also discuss current issues and future directions for an end-use perspective of TOCs.
引用
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页数:16
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