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Chinese Journal of Clinical Pharmacology and Therapeutics ›› 2012, Vol. 17 ›› Issue (9): 988-995.

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A sensitive and specific UPLC-MS/MS analysis and preliminary pharmacokinetic characterization of S-oxiracetam in Beagle dogs

WANG Wu-san1, JI Hui1, XIE Hai-tang2, DAI Min2, JIA Yuan-wei2, LIANG Da-hu2, YE Lei3, RONG Zu-yuan3   

  1. 1Department of Pharmacology, China Pharmaceutical University, Nanjing 210009,Jiangsu, China;
    2Department of Clinical Pharmacy,Yijishan Hospital,Wannan Medical College , Wuhu 241001, Anhui, China;
    3Dong Ze Pharmaceutical Science and Technology Co. L td, Chongqing 400030 , China
  • Received:2012-06-04 Revised:2012-07-10 Published:2012-09-25
  • Contact: JI Hui, Corresponding author: Professor, Ph.D supervisor, Main research direction: Geriatric pharmacology. Tel: 025-86205849 E-mail: address: huijicpu@163.com
  • About author:Wang Wu-san, Ph.D, Main research direction: Geriatric pharmacology. Tel: 025-86205849 E-mail: wangyue206@yahoo.com.cn

Abstract: AIM: To develop a sensitive and specific ultra performance liquid chromatography-electrospray ionization-tandem mass spectrometry (UPLC-ESI-MS/MS) method for the identification and quantification of S-oxiracetamin in Beagle dog plasma.METHODS: The method involved the addition of piracetam as internal standards, protein-precipitation, UPLC separation, and quantification by MS/MS system using positive electrospray ionization in the multiple reaction monitoring mode (MRM). An HP Amide C18 column (100 mm×3.00 mm, 5 μm) was used as the analytical column, while a mixture of methanol-water was used as the mobile phase. The precursor/product ion transitions selected were m/z 159.0/114.1 for S-oxiracetam and m/z 143.0/126.1 for I.S.RESULTS: The lower limit of quantification of S-oxiracetam was 0.05 μg/mL.The method was linear in the concentration range of 0.05-50 μg/mL.The intra-day and inter-day precisions (RSD) were within 15.0% for the analytes. S-oxiracetam was proved to be stable during all sample storage, preparation and analytical periods.The method was successfully applied to a pharmacokinetic study in dogs after intragastric administration of S-oxiracetam with a dose of 50 mg/kg.CONCLUSION: The proposed method enables unambiguous identification and quantification for the preliminary pharmacokinetic studies of S-oxiracetam.

Key words: S-oxiracetam, UPLC-MS/MS, Pharmacokinetics, Beagle dog, Plasma

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