Biomedical Engineering Reference
In-Depth Information
21. Carter SJ, Čápka V, Viccarone S An orthogonal approach to increasing assay ruggedness at
low limits of quantition in LC/MS/MS assays, Presented at the 2007 ASMS conference,
Indianapolis, IN, June 2007
22. Voelker T, Tan L, Acheampong A et al Two dimensional PPE/SPE extraction coupled with
three dimensional HPLC/UPLC/MS/MS for a 500 fg/mL LLOQ assay, Presented at the 2011
ASMS conference, Denver, June 2011
23. Tan A, Hussain S, et al (2009) Internal standard response variations during incurred sample
analysis by LC-MS/MS: case by case trouble shooting. J Chromatogr B 877(2):3201-3209
24. Rocci ML, Devanarayan V, Haughey DB et al (2007) Confirmatory reanalysis of incurred
bioanalytical samples. AAPS J 9(3):E336-E343
25. Zhou S, Song Q et al (2005) Critical review of development, validation, and transfer for high
throughput bioanalytical LC-MS/MS methods. Current Pharma Analysis 1:3-14
26. Liu GW, Snapp HM, Ji QC, Arnold ME (2009) Strategy of accelerated method development
for high-throughput bioanalytical assays using ultra high-performance liquid chromatography
coupled with mass spectrometry. Anal Chem 81(22):9225-9232
27. Jemal M, Zheng O, Xia YQ (2010) Systematic LC-MS/MS bioanalytical method development
that incorporated plasma phospholipids risk avoidance, usage of incurred sample and well
thought-out chromatography. Biomed Chromatogr 24(1):2-19
