Simultaneous determination of acetaminophen and dihydrocodeine in human plasma by UPLC-MS/MS: Its pharmacokinetic application

被引:16
作者
Qiu, Xiangjun [1 ]
Lou, Dan [2 ]
Su, Ding [1 ]
Liu, Zebin [1 ]
Gao, Pengtao [1 ]
Zhang, Nan-Sheng [3 ]
机构
[1] Henan Univ Sci & Technol, Coll Med, Luoyang 471003, PR, Peoples R China
[2] Wenzhou Med Univ, Yuying Childrens Hosp, Affiliated Hosp 2, Wenzhou 325027, PR, Peoples R China
[3] Wenzhou Med Univ, Affiliated Hosp 1, Wenzhou 325000, PR, Peoples R China
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2015年 / 992卷
关键词
Acetaminophen; Dihydrocodeine; UPLC-MS/MS; Human plasma; Pharmacokinetic; TANDEM MASS-SPECTROMETRY; RANDOMIZED CONTROLLED-TRIAL; PARACETAMOL ACETAMINOPHEN; HEALTHY-VOLUNTEERS; METABOLITES; PAIN; QUANTIFICATION; VALIDATION; THERAPY; URINE;
D O I
10.1016/j.jchromb.2015.04.031
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) method was developed and validated to determine acetaminophen (AAP) and dihydrocodeine (DHC) in human plasma simultaneously. Plasma samples were prepared using protein precipitation with acetonitrile, the two analytes and the internal standard midazolam were separated on an Acquity UPLC BEH C18 column and mass spectrometric analysis was performed using a QTrap5500 mass spectrometer coupled with an electro-spray ionization (ESI) source in the positive ion mode. The MRM transitions of m/z 151.2 -> 110.0 and m/z 302.3 -> 199.2 were used to quantify for AAP and DHC, respectively. The linearity of this method was found to be within the concentration range of 50-10000 ng/mL for AAP, and 1-100 ng/mL for DHC in human plasma, respectively. The lower limit of quantification (LLOQ) was SO ng/mL. and 1 ng/mL for AAP and DHC in human plasma, respectively. The relative standard deviations (RSD) of intra and inter precision were less than 10% for both AAP and DHC. The analysis time of per sample was 1.0 min. The developed and validated method was successfully applied to a pharmacokinetic study of AAP (500 mg) with DHC (20 mg) capsule in Chinese healthy volunteers (N= 20). (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:91 / 95
页数:5
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