Development of an LC-MS/MS method for the quantitation of deoxyglycychloxazol in rat plasma and its application in pharmacokinetic study

被引:3
|
作者
Li, Rongshan [1 ]
Ran, Ruixue [1 ]
Li, Quansheng [2 ]
Huang, Yurong [2 ]
Gu, Yuan [2 ]
Si, Duanyun [2 ]
机构
[1] Tianjin Med Univ, Sch Pharm, Tianjin Key Lab Technol Enabling Dev Clin Therape, Tianjin 300070, Peoples R China
[2] Tianjin Inst Pharmaceut Res, State Key Lab Drug Delivery Technol & Pharmacokin, Tianjin 300193, Peoples R China
关键词
Deoxyglycychloxazol (TY501); LC-MS/MS; APCI; Pharmacokinetics; Rat plasma; GLYCYRRHETIC ACID; ESI-MS; LICORICE;
D O I
10.1016/j.jpha.2016.03.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Deoxyglycychloxazol (TY501) is a glycyrrhetinic acid derivative which exhibits high anti-inflammatory activity and reduced pseudoaldosteronism compared to glycyrrhetinic acid. In this study, a sensitive and rapid liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was established for the quantitation of TY501 in rat plasma. Plasma samples were treated by precipitating protein with methanol and supernatants were separated by a Symmetry C-8 column with the mobile phase consisting of methanol and 10 mM ammonium formate (containing 0.1% of formic acid) (90:10, v/v). The selected reaction monitoring (SRM) transitions were performed at m/z 647.4 -> 191.2 for TY501 and m/z 473.3 -> 143.3 for astragaloside aglycone (IS) in the positive ion mode with atmospheric pressure chemical ionization (APCI) source. Calibration curve was linear over the concentration range of 5-5000 ng/mL. The lower limit of quantification was 5 ng/mL. The mean recovery was over 88%. The intra- and inter-day precisions were lower than 6.0% and 12.8%, respectively, and the accuracy was within +/- 1.3%. TY501 was stable under usual storage conditions and handling procedure. The validated method has been successfully applied to a pharmacokinetic study after oral administration of TY501 to rats at a dosage of 10 mg/kg. (C) 2016 Xi'an Jiaotong University. Production and hosting by Elsevier B.V.
引用
收藏
页码:184 / 189
页数:6
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