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Characterization of human urinary metabolites of the antimalarial piperaquine
Högskolan Dalarna, Akademin Industri och samhälle, Kemiteknik.
Vise andre og tillknytning
2006 (engelsk)Inngår i: Drug Metabolism And Disposition, ISSN 0090-9556, E-ISSN 1521-009X, Vol. 34, nr 12, s. 2011-2019Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Five metabolites of the antimalarial piperaquine (PQ) (1,3-bis-[4-(7chloroquinolyl-4)-piperazinyl-1]-propane) have been identified and their molecular structures characterized. After a p.o. dose of dihydroartemisinin-piperaquine, urine collected over 16 h from two healthy subjects was analyzed using liquid chromatography (LC)/UV, LC/tandem mass spectrometry (MS/MS), Fourier transform ion cyclotron resonance (FTICR)/MS, and H NMR. Five different peaks were recognized as possible metabolites [M1, 320 m/z; M2, M3, and M4, 551 m/z (PQ + 16 m/z); and M5, 567 m/z (PQ + 32 m/z)] using LC/MS/MS with gradient elution. The proposed carboxylic M1 has a theoretical monoisotopic molecular mass of 320.1166 m/z, which is in accordance with the FTICR/MS (320.1168 m/z) findings. The LC/MS/MS results also showed a 551 m/z metabolite (M2) with a distinct difference both in polarity and fragmentation pattern compared with PQ, 7-hydroxypiperaquine, and the other 551 m/z metabolites. We suggest that this is caused by N-oxidation of PQ. The results showed two metabolites (M3 and M4) with a molecular ion at 551 m/z and similar fragmentation pattern as both PQ and 7-hydroxypiperaquine; therefore, they are likely to be hydroxylated PQ metabolites. The molecular structures of M1 and M2 were also confirmed using H NMR. Urinary excretion rate in one subject suggested a terminal elimination half-life of about 53 days for M1. Assuming formation rate-limiting kinetics, this would support recent findings that the terminal elimination half-life of PQ has been underestimated previously.

sted, utgiver, år, opplag, sider
2006. Vol. 34, nr 12, s. 2011-2019
HSV kategori
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URN: urn:nbn:se:du-17541DOI: 10.1124/dmd.106.011494ISI: 000242374700010PubMedID: 16956956OAI: oai:DiVA.org:du-17541DiVA, id: diva2:815124
Tilgjengelig fra: 2015-05-29 Laget: 2015-05-26 Sist oppdatert: 2017-12-04bibliografisk kontrollert

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