Phapale Prasad B, Blasche Sonja, Patil Kiran R, Alexandrov Theodore
European Molecular Biology Laboratory, Heidelberg, Germany.
Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego, USA.
Bio Protoc. 2021 Nov 5;11(21):e4214. doi: 10.21769/BioProtoc.4214.
Expanding our understanding of drug-gut bacteria interactions requires high-throughput drug measurements in complex bacterial cultures. Quantification of drugs in the cultures, media, and cell pellets is prone to strong matrix effects. We have developed a liquid chromatography-high resolution mass spectrometry (LC-HRMS) method for quantifying duloxetine from high-throughput gut-drug interaction experiments. The method is partially validated for its reproducibility, sensitivity, and accuracy, which makes it suitable for largescale drug screens. We extensively used this method to study biotransformation and bioaccumulation of duloxetine and other drugs in several species of gut bacteria.
拓展我们对药物与肠道细菌相互作用的理解需要在复杂细菌培养物中进行高通量药物测量。对培养物、培养基和细胞沉淀中的药物进行定量容易受到强烈的基质效应影响。我们开发了一种液相色谱-高分辨率质谱(LC-HRMS)方法,用于从高通量肠道-药物相互作用实验中定量度洛西汀。该方法在重现性、灵敏度和准确性方面进行了部分验证,使其适用于大规模药物筛选。我们广泛使用该方法研究度洛西汀和其他药物在几种肠道细菌中的生物转化和生物积累。