Simultaneous determination of glimepiride and pioglitazone in human plasma by liquid chromatography-tandem mass spectrometry and its application to pharmacokinetic study

被引:19
作者
Ni, Xiao-Jia [1 ]
Wang, Zhan-Zhang [2 ]
Shang, De-Wei [1 ]
Zhang, Ming [1 ]
Hu, Jin-Qing [2 ]
Qiu, Chang [2 ]
Wen, Yu-Guan [1 ]
机构
[1] Guangzhou Med Univ, Inst Natl Drug Clin Trials, Clin Lab Phase 1, Guangzhou Brain Hosp, Guangzhou 510370, Guangdong, Peoples R China
[2] Guangzhou Med Univ, Clin Pharm Guangzhou Brain Hosp, Guangzhou 510370, Guangdong, Peoples R China
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2014年 / 960卷
关键词
LC-MS/MS; Glimepiride; Pioglitazone; Pharmacokinetic; INSULIN SENSITIVITY; HUMAN SERUM; LC-MS/MS; ALLOPURINOL; OXYPURINOL; METFORMIN; URINE;
D O I
10.1016/j.jchromb.2014.04.039
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The rapid, sensitive, and selective liquid chromatography-electrospray ionization-tandem mass spectrometry method (LC-ESI-MS/MS) for the simultaneous estimation and pharmacokinetic investigation of glimepiride and pioglitazone in human plasma has been developed and fully validated. Glimepiride and pioglitazone, compounds which exert synergistic effects on blood glucose control, were investigated in human plasma using deuterium-labeled analogs as internal standards (IS). Liquid-liquid extraction was carried out on 0.2 mL of human plasma using ethyl acetate, and chromatographic separation was performed on an Agilent Eclipse plus C-18 column (4.6 mm x 100 mm, 3.5 mu m) using a mobile phase consisting of methanol-water-formic acid (95:5:0.1, v/v/v, plus 5 mM ammonium acetate) at a flow rate of 0.8 mL/min. To quantify glimepiride, pioglitazone and their IS, multiple reaction monitoring (MRM) transitions of m/z 491.2 -> 352.2, m/z 496.2 -> 357.2, m/z 357.2 -> 134.2 and m/z 361.2 -> 138.2 were performed in positive mode. The total run time was 3.0 min and the elution time was about 2.4 min. The method exhibited good separation of analytes, without interference from endogenous substances. The linear calibration curves were 0.2-250 ng/mL for glimepiride and 0.2-1250 ng/mL for pioglitazone; the lower limit of quantification (LLOQ) was 0.2 ng/mL for both analytes. Intra- and inter-day reproducibility was less than 10% for glimepiride and less than 5% for pioglitazone, with relative errors ranging from -8.00% to 2.80% at the three concentrations of analytes used for quality control (QC). The matrix effect was negligible and recoveries were similar for each analyte and its IS. Glimepiride and pioglitazone were found to be stable under the assay conditions and the method was successfully applied to the evaluation of pharmacokinetic studies of glimepiride and pioglitazone, following oral doses of 2 mg glimepiride tablets and 15 mg pioglitazone tablets to 16 healthy volunteers. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:247 / 252
页数:6
相关论文
共 24 条
[1]  
Arumugam K., 2008, J PHARM SCI, V21, P421
[2]   ELECTROPHYSIOLOGY OF THE PANCREATIC BETA-CELL [J].
ASHCROFT, FM ;
RORSMAN, P .
PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 1989, 54 (02) :87-143
[3]  
Buchwald A., 2012, MC PHARM TOXICOL, V12, P2
[4]   A rapid and highly sensitive method for the determination of glimepiride in human plasma by liquid chromatography-electrospray ionization tandem mass spectrometry: application to a pre-clinical pharmacokinetic study [J].
Chakradhar, Lagishetty ;
Kallem, Rajareddy ;
Karthik, Arumugam ;
Sundari, Bala Tripura ;
Ramesh, Srirangam ;
Mullangi, Ramesh ;
Srinivas, Nuggehally R. .
BIOMEDICAL CHROMATOGRAPHY, 2008, 22 (01) :58-63
[5]   Simultaneous identification and validated quantification of 11 oral hypoglycaemic drugs in plasma by electrospray ionisation liquid chromatography-mass spectrometry [J].
Hess, Cornelius ;
Musshoff, Frank ;
Madea, Burkhard .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2011, 400 (01) :33-41
[6]   Detection of anti-diabetics in equine plasma and urine by liquid chromatography-tandem mass spectrometry [J].
Ho, ENM ;
Yiu, KCH ;
Wan, TSM ;
Stewart, BD ;
Watkins, KL .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2004, 811 (01) :65-73
[7]   Development and validation of highly selective and robust method for simultaneous estimation of pioglitazone, hydroxypioglitazone and metformin in human plasma by LC-MS/MS: Application to a pharmacokinetic study [J].
Jagadeesh, B. ;
Bharathi, D. Vijaya ;
Pankaj, C. ;
Narayana, V. Satya ;
Venkateswarulu, V. .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2013, 930 :136-145
[8]   Simultaneous estimation of metformin hydrochloride, pioglitazone hydrochloride, and glimepiride by RP-HPLC in tablet formulation [J].
Jain, Deepti ;
Jain, Surendra ;
Jain, Deepak ;
Amin, Maulik .
JOURNAL OF CHROMATOGRAPHIC SCIENCE, 2008, 46 (06) :501-504
[9]   Current clinical evidence on pioglitazone pharmacogenomics [J].
Kawaguchi-Suzuki, Marina ;
Frye, Reginald F. .
FRONTIERS IN PHARMACOLOGY, 2013, 4
[10]   Pioglitazone enhances splanchnic glucose uptake as well as peripheral glucose uptake in non-insulin-dependent diabetes mellitus [J].
Kawamori, R ;
Matsuhisa, M ;
Kinoshita, J ;
Mochizuki, K ;
Niwa, M ;
Arisaka, T ;
Ikeda, M ;
Kubota, M ;
Wada, M ;
Kanda, T ;
Ikebuchi, M ;
Tohda, R ;
Yamasaki, Y .
DIABETES RESEARCH AND CLINICAL PRACTICE, 1998, 41 (01) :35-43