Researchers Improve Sensitivity of Large Volume Urine Injections with HPLC-MS
Researchers at the Chinese Academy of Sciences and Tsingua University have developed an automated on-line HPLC-MS method allowing injection of a large volume of urine for the improvement of sensitivity using estrogens as analytes.
Researchers at the Chinese Academy of Sciences and Tsingua University have developed an automated on-line HPLC-MS method allowing injection of a large volume of urine for the improvement of sensitivity using estrogens as analytes. The injection volume, reporetedly, increased ten times compared with conventional on-line LC-MS methods for biofluid analysis. Moreover, no obvious increase of column pressure was observed after 300 injections. The method was validated by spiking urine. Linearity was determined by sample which was in the range of 1-500 ng/mL. The process efficiency ranged from 70.2 to 106% with RSDs less than 15% with the exception of a few analytes.
Inside the Laboratory: The Richardson Group at the University of South Carolina
November 20th 2024In this edition of “Inside the Laboratory,” Susan Richardson of the University of South Carolina discusses her laboratory’s work with using electron ionization and chemical ionization with gas chromatography–mass spectrometry (GC–MS) to detect DBPs in complex environmental matrices, and how her work advances environmental analysis.
RAFA 2024 Highlights: Cutting-Edge Chromatography Techniques for Food Safety and Food Analysis
November 18th 2024An illuminating session focusing on progress in analytical techniques used in food analysis took place on Wednesday 6 November 2024 at RAFA 2024 in Prague, The Czech Republic, including a talk on the analysis of 1000 toxins in 10 minutes.
Investigating Synthetic Cathinone Positional Isomers using LC–EAD-MS
November 7th 2024Peng Che fom Vrije Universiteit Amsterdam in the Netherlands discusses the benefits of hyphenating liquid chromatography (LC) with electron activated dissociation mass spectrometry (EAD-MS) to analyze cathinone positional isomers.
