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Development of a high performance liquid chromatography-tandem mass method for determination of bis(7)-tacrine, a promising anti-Alzheimer's dimer, in rat blood
Authors:Yu Hua  Ho Jason M K  Kan Kelvin K W  Cheng Bobby W H  Li Wen-Ming  Zhang Li  Lin Ge  Pang Yuan-Ping  Gu Zhe-Ming  Chan Kelvin  Wang Yi-Tao  Han Yi-Fan
Institution:

aDepartment of Biochemistry, Hong Kong University of Science & Technology, Clear Water Bay, Kowloon, Hong Kong, SAR, PR China

bInstitute of Chinese Medical Sciences, University of Macau, Macau SAR, PR China

cBiotechnology Research Institute, Hong Kong University of Science & Technology, Clear Water Bay, Kowloon, Hong Kong, SAR, PR China

dDepartment of Pharmacology, Faculty of Medicine, Chinese University of Hong Kong, Shatin, N.T., Hong Kong, SAR, PR China

eComputer-Aided Molecular Design Laboratory, Mayo Clinic College of Medicine, Rochester, Minnesota, USA

fXenoBiotic Laboratories, Inc., Plainsboro, NJ, USA

gSchool of Applied Sciences, University of Wolverhampton, United Kingdom

Abstract:An analytical method using on-line high performance liquid chromatography-tandem mass spectrometry with electrospray ionization was developed and applied for the quantification of bis(7)-tacrine (B7T) in rat blood. B7T and pimozide (internal standard, IS) were extracted in a single step from 100 μl of alkalized blood with ethyl acetate. Analytes were separated using an Extend C-18 column at 25 °C. The elution was achieved isocratically with a mobile phase composed of 0.05% aqueous formic acid and acetonitrile (60:40, v/v) at a flow rate of 0.35 ml/min. Quantification was achieved by monitoring the selected ions at m/z 247 for B7T and m/z 462 → m/z 328 for pimozide. Retention times were 1.45 and 2.23 min for B7T and IS, respectively. Calibration curves were linear in the range from 86.4 to 2160.0 ng/ml. The established method is rapid, selective and sensitive for the identification and quantification of B7T in biological samples. The assay is accurate (bias <10%) and reproducible (intra- and inter-day variation <10%), with detection and quantification limit of 3.6 and 42.3 ng/ml, respectively. Furthermore, it was successfully applied for the pharmacokinetic measurement of B7T in rat with a single intravenous administration at 0.3 mg/kg.
Keywords:Bis(7)-tacrine  Dimer  Alzheimer's disease  HPLC-MS/MS  Drug monitoring  Pharmacokinetics
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