Rapid determination of losartan and losartan acid in human plasma by multiplexed LC-MS/MS

被引:22
|
作者
Shah, Hiten J. [1 ,2 ,3 ]
Kundlik, Mohan L. [1 ]
Patel, Nitesh K. [1 ]
Subbaiah, Gunta [1 ]
Patel, Dasharath M. [2 ]
Suhagia, Bhanubhai N. [3 ]
Patel, Chhagan N. [2 ]
机构
[1] Torrent Pharmaceut Ltd, Bioanalyt Lab, Gandhinagar 382428, Gujarat, India
[2] Shri Sarvajanik Pharm Coll, Mehsana, Gujarat, India
[3] LM Coll Pharm, Ahmadabad, Gujarat, India
关键词
Human plasma; Losartan; Losartan acid; Multiplexed LC-MS/MS; Negative ion electrospray; TANDEM MASS-SPECTROMETRY; PERFORMANCE LIQUID-CHROMATOGRAPHY; II RECEPTOR ANTAGONIST; ACTIVE METABOLITE EXP3174; MAJOR METABOLITE; VOLUNTEERS; THROUGHPUT; SYSTEM; COLUMN; FORMULATIONS;
D O I
10.1002/jssc.200900287
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A rapid LC-MS/MS method has been developed and validated for the determination of losartan (LOS) and its metabolite losartan acid (LA) (EXP-3174) in human plasma using multiplexing technique (two HPLC units connected to one MS/MS). LOS and LA were extracted from human plasma by SPE technique using Oasis HLB circle star cartridge without evaporation and reconstitution steps. Hydroflumethiazide (HFTZ) was used as an internal standard (IS). The analytes were separated on Zorbax SB C-18 column. The mass transition [M-H] ions used for detection were m/z 421.0 -> 127.0 for LOS, m/z 435.0 -> 157.0 for LA, and m/z 330.0 -> 239.0 for HFTZ. The proposed method was validated over the concentration range of 2.5-2000 ng/mL for LOS and 5.0-3000 ng/mL for LA with correlation coefficient >= 0.9993. The overall recoveries for LOS, LA, and IS were 96.53, 99.86, and 94.16%, respectively. Total MS run time was 2.0 min/sample. The validated method has been successfully used to analyze human plasma samples for applications in 100 mg fasted and fed pharmacokinetic studies.
引用
收藏
页码:3388 / 3394
页数:7
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