Integrated Array Chip for High-Throughput Screening of Species Differences in Metabolism

被引:15
|
作者
Ai, Xiaoni [1 ]
Zhao, Lin [1 ]
Lu, Yingyuan [1 ]
Hou, Yu [1 ]
Lv, Tian [1 ]
Jiang, Yong [1 ]
Tu, Pengfei [1 ]
Guo, Xiaoyu [1 ]
机构
[1] Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R China
基金
中国国家自然科学基金;
关键词
3D CELL-CULTURE; DRUG-METABOLISM; MICROFLUIDIC DEVICE; HUMAN LIVER; IN-VITRO; TOXICITY; HEPATOTOXICITY; CYTOTOXICITY; SPECTROMETRY; PREDICTION;
D O I
10.1021/acs.analchem.0c01590
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Species differences in metabolism may produce failure prediction of drug efficacy/toxicity in humans. Integration of metabolic competence and cellular effect assays in vitro can provide insight into the species differences in metabolism; however, a coculture platform with features of high throughput, operational simplicity, low sample consumption, and independent layouts is required for potential usage in industrial test settings. Herein, we developed an integrated array chip (IAC) to evaluate the species differences in metabolism through metabolism-induced anticancer bioactivity as a case. The IAC consisted of two functional parts: a micropillar chip for immobilization of liver microsomes and a microwell chip for three-dimensional (3D) tumor cell culture. First, optimized parameters of the micropillar chip for microsomal encapsulation were obtained by cross-shaped protrusions and a 2.5 mu L volume of 3D agarose spots. Next, we examined factors influencing metabolism-induced anticancer bioactivity. Feasibility of the IAC was validated by four model prodrugs using image-based bioactivity detection and mass spectrometry (MS)-based metabolite analysis. Finally, a species-specific IAC was used for selection of animal species that best resembles metabolism-induced drug response to humans at throughputs. Overall, the IAC provides a promising co-culture platform for identifying species differences in metabolism and selection of animal models to accelerate drug discovery.
引用
收藏
页码:11696 / 11704
页数:9
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