TY - JOUR
T1 - Development of on-line liquid chromatography-biochemical detection for soluble epoxide hydrolase inhibitors in mixtures.
AU - Falck, D.
AU - Schebb, N.H.
AU - Prinatiningtyas, S
AU - Zhang, Jiawen
AU - Heus, F.A.H.
AU - Morisseau, C
AU - Kool, J.
AU - Hammock, B.D.
AU - Niessen, W.M.A.
PY - 2013
Y1 - 2013
N2 - In this study, an end-point-based fluorescence assay for soluble epoxide hydrolase (sEH) was transformed into an on-line continuous-flow format. The on-line biochemical detection system (BCD) was coupled on-line to liquid chromatography (LC) to allow mixture analysis. The on-line BCD was based on a flow system wherein sEH activity was detected by competition of analytes with the substrate hydrolysis. The reaction product was measured by fluorescence detection. In parallel to the BCD data, UV and MS data were obtained through post-column splitting of the LC effluent. The buffer system and reagent concentrations were optimized resulting in a stable on-line BCD with a good assay window and good sensitivity (S/N > 60). The potency of known sEH inhibitors (sEHis) obtained by LC-BCD correlates well with published values. The LC-BCD system was applied to test how oxidative microsomal metabolism affects the potency of three sEHis. After incubation with pig liver microsomes, several metabolites of sEHis were characterized by MS, while their individual potencies were measured by BCD. For all compounds tested, active metabolites were observed. The developed method allows for the first time the detection of sEHis in mixtures providing new opportunities in the development of drug candidates. © 2012 Springer-Verlag Berlin Heidelberg.
AB - In this study, an end-point-based fluorescence assay for soluble epoxide hydrolase (sEH) was transformed into an on-line continuous-flow format. The on-line biochemical detection system (BCD) was coupled on-line to liquid chromatography (LC) to allow mixture analysis. The on-line BCD was based on a flow system wherein sEH activity was detected by competition of analytes with the substrate hydrolysis. The reaction product was measured by fluorescence detection. In parallel to the BCD data, UV and MS data were obtained through post-column splitting of the LC effluent. The buffer system and reagent concentrations were optimized resulting in a stable on-line BCD with a good assay window and good sensitivity (S/N > 60). The potency of known sEH inhibitors (sEHis) obtained by LC-BCD correlates well with published values. The LC-BCD system was applied to test how oxidative microsomal metabolism affects the potency of three sEHis. After incubation with pig liver microsomes, several metabolites of sEHis were characterized by MS, while their individual potencies were measured by BCD. For all compounds tested, active metabolites were observed. The developed method allows for the first time the detection of sEHis in mixtures providing new opportunities in the development of drug candidates. © 2012 Springer-Verlag Berlin Heidelberg.
UR - https://www.scopus.com/pages/publications/84872284267
UR - https://www.scopus.com/inward/citedby.url?scp=84872284267&partnerID=8YFLogxK
U2 - 10.1007/s10337-012-2343-0
DO - 10.1007/s10337-012-2343-0
M3 - Article
SN - 0009-5893
VL - 76
SP - 13
EP - 21
JO - Chromatographia
JF - Chromatographia
ER -