A Plug-and-Play, Drug-on-Pillar Platform for Combination Drug Screening Implemented by Microfluidic Adaptive Printing

被引:22
作者
Li, Jiannan [1 ,2 ]
Tan, Wen [1 ,2 ,4 ]
Xiao, Wenwu [3 ]
Carney, Randy P. [3 ]
Men, Yongfan [1 ,2 ,5 ]
Li, Yuanpei [3 ]
Quon, Gerald [6 ]
Ajena, Yousif [3 ]
Lam, Kit S. [3 ]
Pan, Tingrui [1 ,2 ,5 ]
机构
[1] Univ Calif Davis, Dept Biomed Engn, Micronano Innovat MiNI Lab, Davis, CA 95616 USA
[2] Univ Calif Davis, Dept Elect & Comp Engn, Davis, CA 95616 USA
[3] Univ Calif Davis, UC Davis NCI Designated Comprehens Canc Ctr, Sch Med, Dept Biochem & Mol Med, Sacramento, CA 95817 USA
[4] Lanzhou Univ, Sch Pharm, Lanzhou 730000, Gansu, Peoples R China
[5] Chinese Acad Sci, Shenzhen Inst Adv Technol, Shenzhen 518055, Guangdong, Peoples R China
[6] Univ Calif Davis, Dept Mol & Cellular Biol, Davis, CA 95616 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
ALGINATE HYDROGELS; CELL-CULTURE; CANCER; CHEMOTHERAPY; MICROARRAY; INHIBITORS; THERAPY; ARRAY;
D O I
10.1021/acs.analchem.8b03456
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Traditional high-throughput drug combination screening requires automatic pipetting of drugs into high-density microtiter plates. Here, a drug-on-pillar platform is proposed for efficient combination drug screening. Using the proposed approach, combination drug screening can be carried out in a plug-and-play manner, allowing for high-throughput screening of large permutations of drug combinations at various concentrations, such that drug dispensing and cell-based screening can be temporally separated and therefore can potentially be performed at distant laboratories. The dispensing is implemented using our recently developed microfluidic pneumatic printing platform, which features a low-cost disposable cartridge that minimizes cross contamination. Moreover, our previously developed drug nanoformulation method with amphiphilic telodendrimers has been utilized to maintain drug stability in a dry form, allowing for convenient drug storage, shipping, and subsequent rehydration. Combining the features described above, we have implemented a 1260-spot drug combination array to study the effect of paired drugs against MDA-MB-231 triple negative human breast cancer cells. This study supports the feasibility of the drug-on-pillar platform for combination drug screening and has provided valuable insight into drug combination efficacy against breast cancer.
引用
收藏
页码:13969 / 13977
页数:9
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