Development and validation of a sensitive LC-MS/MS method with electrospray ionization for quantitation of pramipexole in human plasma: application to a clinical pharmacokinetic study

被引:20
作者
Bharathi, D. Vijaya [2 ,3 ]
Hotha, Kishore Kumar [2 ]
Sagar, P. V. Vidya [2 ]
Kumar, S. Sirish [2 ]
Naidu, A. [3 ]
Mullangi, Ramesh [1 ]
机构
[1] Dr Reddys Labs Ltd, Dept Biopharmaceut, Integrated Prod Dev, Hyderabad 500072, Andhra Pradesh, India
[2] Dr Reddys Labs Ltd, Bioanalyt Dept, Integrated Prod Dev, Hyderabad 500072, Andhra Pradesh, India
[3] JNTU Coll Engn, Dept Chem, Hyderabad 500072, Andhra Pradesh, India
关键词
pramipexole; human plasma; validation; LC-MS/MS; pharmacokinetics; TANDEM MASS-SPECTROMETRY; LIQUID-CHROMATOGRAPHY; BIOANALYSIS;
D O I
10.1002/bmc.1108
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A highly sensitive and specific LC-MS/MS method has been developed and validated for the estimation of pramipexole (PPX) with 500 mu L human plasma using memantine as an internal standard (IS). The API-4000 was operated under multiple-reaction monitoring mode (MRM) using the electrospray ionization technique. Solid-phase extraction was used to extract PPX and IS from human plasma. The resolution of peaks was achieved with 0.01 M ammonium acetate buffer (pH 4.4):acetonitrile (30:70, v/v) on a Discovery CN column. The total chromatographic run time was 3.0 min and the elution of PPX and IS occurred at approximately 2.32 and 2.52, respectively. The MS/MS ion transitions monitored were 212.10 -> 153.10 for PPX and 180.20 -> 107.30 for IS. The method was proved to be accurate and precise at linearity range of 20-3540 pg/mL with a correlation coefficient (r) of >= 0.999. The intra- and inter-day precision and accuracy values found to be within the assay variability limits as per the FDA guidelines. The developed assay method was applied to a pharmacokinetic study in human volunteers following oral administration of 0.25 mg PPX tablet. Copyright (c) 2008 John Wiley & Sons, Ltd.
引用
收藏
页码:212 / 218
页数:7
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