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Sensitive inductively coupled plasma mass spectrometry assay for the determination of platinum originating from cisplatin, carboplatin, and oxaliplatin in human plasma ultrafiltrate

✍ Scribed by E. E. M. Brouwers; M. M. Tibben; H. Rosing; M. J. X. Hillebrand; M. Joerger; J. H. M. Schellens; J. H. Beijnen


Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
210 KB
Volume
41
Category
Article
ISSN
1076-5174

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✦ Synopsis


Abstract

We present a highly sensitive, rapid method for the determination of platinum originating from the anticancer agents cisplatin, carboplatin, and oxaliplatin in human plasma ultrafiltrate. The method is based on the quantification of platinum by inductively coupled plasma mass spectrometry and allows quantification of 7.50 ng l^βˆ’1^ platinum in only 150 Β΅l of matrix. Sample pretreatment involves dilution of samples with 1% HNO~3~. Validation fulfilled the most recent FDA guidelines for bioanalytical method validation. Validated ranges of quantification were 7.50 ng l^βˆ’1^ to 1.00 Γ— 10^5^ ng l^βˆ’1^ in plasma ultrafiltrate for all three platinum compounds. The assay is now successfully used to support pharmacokinetic studies in cancer patients treated with cisplatin, carboplatin, or oxaliplatin. Copyright Β© 2006 John Wiley & Sons, Ltd.


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