Propofol glucuronide

 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1989-2016
012319892016

Papers overview

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2017
2017
Besides its clinical application, the anaesthetic agent propofol is being increasingly misused, mostly by healthcare… (More)
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2013
2013
A fast, sensitive and selective liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for the detection and… (More)
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2011
2011
The basis of high intersubject variability of propofol metabolism is unclear. Therefore, we examined the influence of genetic… (More)
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2002
2002
INTRODUCTION Glucuronidation by the uridine diphosphate glucuronosyltransferases (UGTs) plays a pivotal role in the clearance… (More)
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1999
1999
Propofol (P) is metabolized in humans by oxidation to 1,4-di-isopropylquinol (Q). P and Q are in turn conjugated with glucuronic… (More)
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1996
1996
Objective: Results from clinical pharmacokinetic studies of propofol indicate that this i.v. anaesthetic agent may undergo… (More)
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1994
1994
1. Six female Caucasian patients received i.v. doses of propofol (2.7 +/- 0.3 (SE) mg/kg) for induction of anaesthesia… (More)
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1992
1992
1. Propofol glucuronide (PG) is the major human metabolite of the i.v. anaesthetic propofol, 2,6-diisopropylphenol. 2. Bolus i.v… (More)
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1992
1992
We have investigated extrahepatic metabolism of propofol in 10 patients undergoing orthotopic liver transplantation (group 1… (More)
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1992
1992
1. An i.v. dose of 14C-propofol (0.53 mg/kg) was administered to three male and three female patients during the anhepatic phase… (More)
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