Rapid Simultaneous Determination of Paracetamol, Amantadine Hydrochloride, Caffeine and Chlorpheniramine Maleate in Human Plasma by Liquid Chromatography/Tandem Mass Spectrometry

被引:1
|
作者
Feng, Shudan [1 ,2 ]
Tian, Yuan [1 ,2 ]
Zhang, Zunjian [1 ,2 ]
Zhang, Jingjing [1 ,2 ]
Huang, Meihua [1 ,2 ]
Chen, Yun [3 ,4 ]
机构
[1] China Pharmaceut Univ, Ctr Instrumental Anal, Nanjing 210009, Peoples R China
[2] China Pharmaceut Univ, Key Lab Drug Qual Control & Pharmacovigilance, Minist Educ, Nanjing 210009, Peoples R China
[3] Chinese Acad Med Sci, Inst Dermatol, Nanjing, Peoples R China
[4] Peking Union Med Coll, Nanjing, Peoples R China
来源
ARZNEIMITTELFORSCHUNG-DRUG RESEARCH | 2009年 / 59卷 / 02期
关键词
Amantadine hydrochloride; Caffeine; Chlorpheniramine maleate; HPLC-ESI-MS/MS; Paracetamol; Pharmacokinetics; CAPILLARY ELECTROPHORESIS; URINE; DERIVATIZATION; ACETAMINOPHEN; FORMULATIONS; METABOLITES; SERUM;
D O I
暂无
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A rapid, simple and sensitive high performance liquid chromatography with positive ion electrospray ionization tandem mass spectrometry (HPLC-ESI-MS/MS) was first developed and validated to simultaneously determine paracetamol (PAR, CAS 103-90-2), amantadine hydrochloride (ATH, CAS 665-66-7), caffeine (CAF, CAS 58-08-2) and chlorpheniramine maleate (CPM, CAS 113-92-8) in human plasma using tramadol hydrochloride (TMH, CAS 22204-88-2) as internal standard (IS). Following methanol-induced protein precipitation, the analytes were separated using a mobile phase comprised of methanol: water (0.5% formic acid) = 20:80 (v/v) on a commercially available column (150 mm x 2.1 mm I.D., 5 mu m) and analyzed by electrospray ionization tandem mass spectrometry in the selected reaction monitoring (SRM) mode with the precursor to product ion transitions m/z 152.3 -> 110.2 for PAR, 152.3 -> 135.3 for ATH, 195.1 -> 138.3 for CAF, 275.2 -> 230.3 for CPM and 264.2 -> 58.2 for TMH. The standard curves were linear (r(2) > 0.99) over the concentration range of 0.2-20 mu g/mL for PAR, 20-2000 ng/mL for ATH and CAF, 0.1-10 ng/mL for CPM and had good accuracy and precision, respectively. The within- and between-batch precisions were less than 15% in terms of relative standard deviation (RSD). The lower limit of quantitation (LLOQ) were 0.2 mu g/mL, 20 ng/mL, 20 ng/mL and 0.1 ng/mL for PAR, ATH, CAT and CPM, respectively. The described method has been successfully applied to study the pharmacokinetics of paracetamol-amantadine hydrochloride tablets in Chinese healthy male volunteers with great precision and sensitivity.
引用
收藏
页码:86 / 95
页数:10
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