Abstract:
PR-104 is a dinitrobenzamide mustard currently in clinical trial as a hypoxia-activated prodrug. It is converted systemically to the corresponding alcohol, PR-104A, which is activated by nitroreduction to the hydroxylamine (PR-104H) and amine (PR-104M). PR-104A is also metabolised to the O-glucuronide (PR-104G), and by oxidative debromoethylation to the semi-mustard PR-1045. We now report a validated ultra-high-pressure liquid chromatography and tandem mass spectrometry (UHPLC-MS/MS) method for the determination of these metabolites in human plasma. Plasma proteins were precipitated with acidified methanol and the supernatant diluted into water. Aliquots were analysed by UHPLC-MS/MS using a Zorbax Eclipse XDB-C18 Rapid Resolution HT (50 nm x 2.1 mm, 1.8 mu m) column and gradient of acetonitrile and 0.01% formic acid with a 6 min run time. The method had a linear range of 0.1-50 mu M for PR-104, PR-104A and PR-104G, 0.05-5 mu M for PR-104H, 0.025-2.5 mu M for PR-104M and 0.01-1 mu M for PR-1045. The intra-day and inter-day precision and accuracy were within 14%. The extraction recovery of all analytes was over 87%. The validated method was illustrated by using it to study the pharmacokinetics of PR-104 and its metabolites in a human patient. (C) 2009 Elsevier B.V. All rights reserved.