首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Simultaneous determination of tetrahydropalmatine, protopine, and palmatine in rat plasma by LC-ESI-MS and its application to a pharmacokinetic study.
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Simultaneous determination of tetrahydropalmatine, protopine, and palmatine in rat plasma by LC-ESI-MS and its application to a pharmacokinetic study.

机译:LC-ESI-MS同时测定大鼠血浆中的四氢巴马汀,原松碱和巴马汀及其在药代动力学研究中的应用。

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A sensitive and specific liquid chromatography-electrospray ionization-mass spectrometry (LC-ESI-MS) method has been developed and validated for the simultaneous quantification of tetrahydropalmatine, protopine and palmatine in rat plasma using phenacetin as the internal standard (IS). Two hundred microliters plasma samples were extracted by dichloromethane under a strong basic condition. The analytes were separated by a C18 column and detected with a single quadrupole mass spectrometer. The used mobile phase was acetonitrile-water (40:60, v/v) containing 5mM ammonium acetate and 0.2% glacial acetic acid. Detection was carried out by positive electrospray ionization in selected ion reaction (SIR) mode at m/z 356.6 for tetrahydropalmatine, 354.6 for protopine, 352.6 for palmatine and 180.4 for the IS, respectively. The method was validated over the concentration range of 1.00-500ngmL(-1) and the lower limit of quantification (LLOQ) was 1.00ngmL(-1) for all three analytes. The intra- and inter-day precision values were less than 9% relative standard deviation (R.S.D.), and the relative error ranged from -7.4 to 4.8%. The extraction recoveries were on average 91.42% for tetrahydropalmatine, 84.75% for protopine, 57.26% for palmatine, and 83.18% for IS. The validated method was successfully applied to a pharmacokinetic study of tetrahydropalmatine, protopine and palmatine in rats after oral administration of Rhizoma Corydalis Decumbentis extract.
机译:已经开发了一种灵敏且特异性的液相色谱-电喷雾电离质谱(LC-ESI-MS)方法,并已使用非那西丁作为内标(IS)进行了大鼠血浆中四氢巴马汀,普鲁托品和棕榈碱的同时定量验证。在强碱性条件下,用二氯甲烷萃取了200微升血浆样品。用C18色谱柱分离分析物,并用单四极杆质谱仪检测。所使用的流动相是含有5mM乙酸铵和0.2%冰醋酸的乙腈-水(40:60,v / v)。通过正电喷雾电离在选定的离子反应(SIR)模式下进行检测,m / z对四氢巴马汀为356.6,对普鲁托品为354.6,对棕榈碱为352.6,对于IS为180.4。该方法在1.00-500ngmL(-1)的浓度范围内得到验证,所有三种分析物的定量下限(LLOQ)为1.00ngmL(-1)。日内和日间精度值均小于9%的相对标准偏差(R.S.D.),相对误差范围为-7.4至4.8%。四氢巴马汀的提取回收率平均为91.42%,普鲁托品的提取回收率平均为84.75%,巴马汀的提取回收率为87.26%,IS的回收率为83.18%。经验证的方法已成功应用于大鼠口服延胡索提取物后四氢巴马汀,原松碱和巴马汀的药代动力学研究。

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