| Literature DB >> 25913423 |
Wenkui Li1, John Doherty2, Sarah Favara2, Christopher Breen2, Jimmy Flarakos2, Francis L S Tse2.
Abstract
Quantitative bioanalysis of dried plasma spots (DPS) is not subject to the impact of hematocrit and sample non-homogeneity that are often encountered in dried blood spot (DBS) assay. In the present report, an evaluation of plasma microsampling for DPS has been conducted for the first time using ritonavir as a model compound orally administered to dogs. For this evaluation, an LC-MS/MS method was developed and validated according to the current health authorities' guidance and industry practice for the analysis of ritonavir in DPS samples. The measured ritonavir concentrations in the DPS samples prepared using SAFE-TEC devices and directly from the conventional wet plasma using standard pipette were compared with each other and against those of conventional wet plasma. Both DPS results correlated well with each other and were comparable to those of the wet plasma. Good incurred sample reanalysis results were obtained for the two sets of DPS samples and wet plasma as well. The current plasma microsampling for DPS can serve as an alternative to DPS sampling via standard pipetting and wet plasma in in vivo studies.Entities:
Keywords: Dried matrix card; Dried plasma spot (DPS) sampling; LC-MS/MS; Plasma microsampling; Quantitative bioanalysis; Ritonavir
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Year: 2015 PMID: 25913423 DOI: 10.1016/j.jchromb.2015.03.026
Source DB: PubMed Journal: J Chromatogr B Analyt Technol Biomed Life Sci ISSN: 1570-0232 Impact factor: 3.205