| Literature DB >> 26334956 |
Yuzhe Ding1, Jiannan Li1, Wenwu Xiao2, Kai Xiao2, Joyce Lee2, Urvashi Bhardwaj2, Zijie Zhu1, Philip Digiglio1, Gaomai Yang1, Kit S Lam2, Tingrui Pan1.
Abstract
Since the 1960s, combination chemotherapy has been widely utilized as a standard method to treat cancer. However, because of the potentially enormous number of drug candidates and combinations, conventional identification methods of the effective drug combinations are usually associated with significantly high operational costs, low throughput screening, laborious and time-consuming procedures, and ethical concerns. In this paper, we present a low-cost, high-efficiency microfluidic print-to-screen (P2S) platform, which integrates combinatorial screening with biomolecular printing for high-throughput screening of anticancer drug combinations. This P2S platform provides several distinct advantages and features, including automatic combinatorial printing, high-throughput parallel drug screening, modular disposable cartridge, and biocompatibility, which can potentially speed up the entire discovery cycle of potent drug combinations. Microfluidic impact printing utilizing plug-and-play microfluidic cartridges is experimentally characterized with controllable droplet volume and accurate positioning. Furthermore, the combinatorial print-to-screen assay is demonstrated in a proof-of-concept biological experiment which can identify the positive hits among the entire drug combination library in a parallel and rapid manner. Overall, this microfluidic print-to-screen platform offers a simple, low-cost, high-efficiency solution for high-throughput large-scale combinatorial screening and can be applicable for various emerging applications in drug cocktail discovery.Entities:
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Year: 2015 PMID: 26334956 DOI: 10.1021/acs.analchem.5b00826
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986