E
Erin E. Chambers
Researcher at Waters Corporation
Publications - 19
Citations - 1109
Erin E. Chambers is an academic researcher from Waters Corporation. The author has contributed to research in topics: Matrix (chemical analysis) & High-performance liquid chromatography. The author has an hindex of 9, co-authored 18 publications receiving 1002 citations.
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Systematic and comprehensive strategy for reducing matrix effects in LC/MS/MS analyses
TL;DR: The combination of polymeric mixed-mode SPE, the appropriate mobile phase pH and UPLC technology provides significant advantages for reducing matrix effects resulting from plasma matrix components and in improving the ruggedness and sensitivity of bioanalytical methods.
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Performance of plasma free metanephrines measured by liquid chromatography-tandem mass spectrometry in the diagnosis of pheochromocytoma.
TL;DR: Plasma metanephrines measured by LC-MS/MS are a reliable and sensitive test for the biochemical detection of pheochromocytoma.
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Quantitation of amyloid beta peptides Aβ(1-38), Aβ(1-40), and Aβ(1-42) in human cerebrospinal fluid by ultra-performance liquid chromatography-tandem mass spectrometry.
TL;DR: A mixed-mode solid-phase extraction method and an ultra-performance liquid chromatography tandem mass spectrometry (SPE UPLC-MS/MS) assay for the simultaneous quantitation of amyloid beta peptides from human cerebrospinal fluid (CSF).
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Round robin test on quantification of amyloid-β 1–42 in cerebrospinal fluid by mass spectrometry
Josef Pannee,Johan Gobom,Leslie M. Shaw,Magdalena Korecka,Erin E. Chambers,Mary E. Lame,Rand Jenkins,William Mylott,Maria C. Carrillo,Ingrid Zegers,Henrik Zetterberg,Henrik Zetterberg,Kaj Blennow,Erik Portelius +13 more
TL;DR: To overcome problems associated with immunoassays, liquid chromatography‐tandem mass spectrometry (LC‐MS/MS) has emerged as a critical orthogonal alternative.
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Improved sensitivity of the nano ultra-high performance liquid chromatography-tandem mass spectrometric analysis of low-concentrated neuropeptides by reducing aspecific adsorption and optimizing the injection solvent.
Katrien Maes,Joeri Van Liefferinge,Johan Viaene,Jolien Van Schoors,Yannick Van Wanseele,Guillaume Béchade,Erin E. Chambers,Hugo Morren,Yvette Michotte,Yvan Vander Heyden,Jan Claereboudt,Ilse Julia Smolders,Ann Van Eeckhaut +12 more
TL;DR: Since the reduction of peptide adsorption and the optimization of the injection solvent resulted in a clear and quantifiable signal of the three peptides, optimization of both issues should be considered in the early stage of method development, in particular when the analysis of low-concentration peptide solutions is envisaged.