کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2526739 1558061 2010 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Interspecific Difference Assay of UDP-glucuronosyltransferase 1A9 Activities in Liver Microsomes by Ultra-performance Liquid Chromatography-tandem Mass Spectrometry
موضوعات مرتبط
علوم پزشکی و سلامت پزشکی و دندانپزشکی طب مکمل و جایگزین
پیش نمایش صفحه اول مقاله
Interspecific Difference Assay of UDP-glucuronosyltransferase 1A9 Activities in Liver Microsomes by Ultra-performance Liquid Chromatography-tandem Mass Spectrometry
چکیده انگلیسی

AimTo establish a UPLC-ESI-MS method for the assay of UDP-glucuronosyltransferases(UGT) 1A9 activities in human and animal liver microsomes, to investigate the interspecific differences of UGT1A9.MethodsThe probe substrate of propofol (m/z 177.3), II phase metabolite of propofol glucuronide (PG) (m/z 377.3, [M + Na]+), and internal standard (IS) of 3-acetamidophenol (m/z 152.2, [M + H]+) were quantified by selective ion monitor (SIM), using electrospray ionization-MS (ESI-MS), acquity UPLC BEH C18 column (50 mm × 2.1 mm, 1.7 μm) and a mixture of acetonitrile(B)-0.5% acetic acid(A) as flow phase in gradient elution at flow rate of 0.3 mL·min−1.ResultThe linearity was within 0.2 to 12.8 μg·mL−1 for PG. The intra- and inter-day precisions were less than 3% and the accuracies ranged from −3.46% to 3.03%. The recoveries of PG from human liver microsomes (HLMs) were 96.5%-98.6%. The method was successfully used to determine the kinetics of propofol glucuronidation in human and different animals liver microsomes. The results indicated that the kinetics of propofol O-glucuronidation in liver micro-somes from human, mouse, rabbit and sheep were fitted to the substrate inhibition equation, whereas the kinetics in rat liver micro-somes was fitted to the two-enzyme Michaelis–Menten equation. The intrinsic clearance (CLint) of propofol glucuronidation in different liver microsomes was in the order of mice > rats (CLint1 + CLint2)>sheep>rabbits>human.ConclusionThe method is rapid, sensitive and selective for assay of UGT1A9 activities in liver microsomes. The results indicated that the kinetics of propofol O-glucuronidation in rat liver microsomes is different from that in HLMs, and the CLint value for propofol O-glucuronidation in liver microsomes from mice, sheep, and rabbit are remarkably higher than that in HLMs. In animal experiments for drug development, these interspecific differences should be taken into consideration.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Chinese Journal of Natural Medicines - Volume 8, Issue 1, January 2010, Pages 34-39