Determination of armepavine in mouse blood by UPLC-MS/MS and its application to pharmacokinetic study

被引:38
作者
Geng, Peiwu [1 ]
Luo, Jun [2 ]
Weng, Ziwei [3 ]
Fan, Zhehua [3 ]
Zhang, Bin [3 ]
Ma, Jianshe [4 ]
Wang, Xianqin [3 ]
Zhang, Meiling [3 ]
机构
[1] Peoples Hosp Lishui, Lab Clin Pharm, Lishui, Peoples R China
[2] Maternal & Child Hlth Hosp Taizhou, Dept Pharm, Taizhou, Peoples R China
[3] Wenzhou Med Univ, Sch Pharmaceut Sci, Analyt & Testing Ctr, Wenzhou, Peoples R China
[4] Wenzhou Med Univ, Sch Basic Med, Wenzhou, Peoples R China
关键词
armepavine; mouse; pharmacokinetics; UPLC-MS; MS; HPLC-MS ANALYSIS; RAT PLASMA; SIMULTANEOUS QUANTITATION; ALKALOIDS; (S)-ARMEPAVINE; QUANTIFICATION; VALIDATION; EXTRACT;
D O I
10.1002/bmc.4273
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The purpose of this study was to develop an ultra-performance liquid chromatography with tandem mass spectrometry (UPLC-MS/MS) method to determine armepavine in mouse blood. Nuciferine was used as internal standard. Chromatographic separation was performed on a UPLC BEH (2.1x50mm, 1.7m) column with a gradient elution of acetonitrile and 10mmol/L ammonium acetate solution (containing 0.1% formic acid). The quantitative analysis was conducted in multiple reaction monitoring mode with m/z 314.1106.9 for armepavine and m/z 296.2265.1 for nuciferine. Calibration curves were linear (r>0.995) over the concentration range 1-1000ng/mL in mouse blood with a lowest limit of quantitation of 1ng/mL. The intra- and inter-day precisions of armepavine in mouse were<13.5 and 10.8%, respectively. The accuracy ranged between 86.8 and 103.3%. Meanwhile, the average recovery was >70.7% and the matrix effect was within the range 109.5-113.7%. All of the obtained data confirmed the satisfactory sensitivity and selectivity of the developed method which was then successfully applied to evaluate the pharmacokinetic behavior of armepavine in mouse for the first time. The bioavailability of armepavine in mouse was calculated to be 11.3%.
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页数:7
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