期刊
BIOMEDICAL CHROMATOGRAPHY
卷 26, 期 10, 页码 1176-1182出版社
WILEY
DOI: 10.1002/bmc.2675
关键词
salbutamol; LC-MS; MS; pharmacokinetics; acetaminophen
类别
资金
- Jewim Pharmaceutical (Shandong) Co. Ltd, China
A sensitive and selective liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS) was developed and validated for the determination of salbutamol in human plasma and urine, and successfully applied to the pharmacokinetic study of salbutamol in Chinese healthy volunteers after inhalation of salbutamol sulfate aerosol. Salbutamol and the internal standard (IS) acetaminophen in plasma and urine were extracted with ethyl acetate, separated on a C18 reversed-phase column, eluted with mobile phase of acetonitrileammonium acetate (5?m m; 30:70, v/v), ionized by positive ion pneumatically assisted electrospray and detected in the multi-reaction monitoring mode using precursor ->?product ions of m/z 240.2 -> 148.1 for salbutamol and 152 -> 110 for the IS. The lower limits of quantitation of salbutamol in human plasma and urine by this method were 0.02 and 1?ng/mL, respectively. The specificity, matrix effect, recovery, sensitivity, linearity, accuracy, precision and several stabilities were validated for salbutamol in human plasma and urine. In conclusion, the validation results showed that this method is robust, specific and sensitive, and can successfully fulfill the requirement of clinical pharmacokinetic study of salbutamol in healthy Chinese volunteers. Copyright (c) 2011 John Wiley & Sons, Ltd.
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