An LC/MS/MS method for the quantitation of MTIC (5-(3-N-methyltriazen-1-yl)-imidazole-4-carboxamide), a bioconversion product of temozolomide, in rat and dog plasma
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Chowdhury, SK
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Schering Plough Corp, Res Inst, Drug Metab & Pharmacokinet Dept, Kenilworth, NJ 07033 USASchering Plough Corp, Res Inst, Drug Metab & Pharmacokinet Dept, Kenilworth, NJ 07033 USA
Chowdhury, SK
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Laudicina, D
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Schering Plough Corp, Res Inst, Drug Metab & Pharmacokinet Dept, Kenilworth, NJ 07033 USASchering Plough Corp, Res Inst, Drug Metab & Pharmacokinet Dept, Kenilworth, NJ 07033 USA
Laudicina, D
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Blumenkrantz, N
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Schering Plough Corp, Res Inst, Drug Metab & Pharmacokinet Dept, Kenilworth, NJ 07033 USASchering Plough Corp, Res Inst, Drug Metab & Pharmacokinet Dept, Kenilworth, NJ 07033 USA
Blumenkrantz, N
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Wirth, M
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Schering Plough Corp, Res Inst, Drug Metab & Pharmacokinet Dept, Kenilworth, NJ 07033 USASchering Plough Corp, Res Inst, Drug Metab & Pharmacokinet Dept, Kenilworth, NJ 07033 USA
Wirth, M
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Alton, KB
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Schering Plough Corp, Res Inst, Drug Metab & Pharmacokinet Dept, Kenilworth, NJ 07033 USASchering Plough Corp, Res Inst, Drug Metab & Pharmacokinet Dept, Kenilworth, NJ 07033 USA
Alton, KB
[1
]
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[1] Schering Plough Corp, Res Inst, Drug Metab & Pharmacokinet Dept, Kenilworth, NJ 07033 USA
A sensitive and selective HPLC/electrospray ionization tandem mass spectrometric (LC/ESI/MS/MS) method for the quantitative determination of MTIC (5-(3-N-methyltriazen-1-yl)-imidazole-4- a pharmacologically active hydrolysis product of temozolomide, was developed and validated over a linear range from 10 to 400 ng ml(-1) in dog plasma and from 10 to 500 ng ml(-1) in rat plasma. This HPLC method utilized small plasma volumes (70 mu l), rapid sample processing, and isocratic elusion conditions to achieve sensitive and selective MS/MS detection. Samples were processed and analyzed one at a time every 4.5 min in order to compensate for the inherent instability of MTIC. Both MTIC and the internal standard DTIC [5-(3,3'-N,N'-dimethyltriazen-1-yl)-imidazole-4-carboxamide] were quantitated in the positive ion, selected reaction monitoring (SRM) mode. The lower limit of quantitation (LLOQ) was 10 ng ml(-1) in the plasma from both species. Inter-assay accuracy and precision of all calibration standards and quality control (QC) samples were within +/- 11 and 12%, respectively, with the exception of the LLOQ in rat plasma (17%). The validated method was used to determine the time dependent plasma concentration of MTIC in rats and dogs following a single oral dose of temozolomide. The standard curve and the quality control data indicate that the method performed acceptably throughout the sample analysis period. (C) 1999 Elsevier Science B.V. All rights reserved.