萃取(化学)
吞吐量
质谱法
色谱法
材料科学
炸薯条
纳米技术
巨量平行
药物发现
计算机科学
化学
并行计算
生物化学
电信
无线
作者
Janne J. Wiedmann,Yelda N. Demirdögen,S. Schmidt,Mariia A. Kuzina,Yanchen Wu,Fei Wang,Britta Nestler,Carsten Hopf,Pavel A. Levkin
出处
期刊:Small
[Wiley]
日期:2022-12-20
卷期号:19 (9)
被引量:9
标识
DOI:10.1002/smll.202204512
摘要
Abstract In the current drug discovery process, the synthesis of compound libraries is separated from biological screenings both conceptually and technologically. One of the reasons is that parallel on‐chip high‐throughput purification of synthesized compounds is still a major challenge. Here, on‐chip miniaturized high‐throughput liquid–liquid extraction in volumes down to 150 nL with efficiency comparable to or better than large‐scale extraction utilizing separation funnels is demonstrated. The method is based on automated and programmable merging of arrays of aqueous nanoliter droplets with organic droplets. Multi‐step extraction performed simultaneously or with changing conditions as well as handling of femtomoles of compounds are demonstrated. In addition, the extraction efficiency is analyzed with a fast optical readout as well as matrix‐assisted laser desorption ionization‐mass spectrometry on‐chip detection. The new massively parallel and miniaturized purification method adds another important tool to the chemBIOS concept combining chemical combinatorial synthesis with biological screenings on the same miniaturized droplet microarray platform, which will be essential to accelerate drug discovery.
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