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Large Scale Non-targeted Metabolomic Profiling of Serum by Ultra Performance Liquid Chromatography-Mass Spectrometry UPLC-MS
Published on: March 14, 2013
Inclusion of dilution quality control samples in quantitative LC-MS bioanalysis
Wenkui Li1, Yunlin Fu1, Franck Picard2
1Pharmacokinetic Sciences, Novartis Biomedical Research, East Hanover, NJ 07936, USA.
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In LC-MS bioanalysis, sample dilution plays various roles, including bringing analyte concentrations within the validated/qualified dynamic range or alleviating matrix effect for accurate determination of the target analyte(s) in the intended study samples. Adherence to health authority requirements, incorporating good dilution practices, and timely demonstration of dilution integrity whenever samples are diluted in an analytical run are essential to ensure the reliability of bioanalytical results.

