Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Tongji School of Pharmacy, Huazhong University of Science and Technology, 13 Hangkong Road, Wuhan 430030, China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2010 Aug 1;878(23):2067-71. doi: 10.1016/j.jchromb.2010.06.004. Epub 2010 Jun 9.
We have developed and validated a sensitive liquid chromatography-electrospray ionization-mass spectrometric (LC-ESI-MS) method for the quantification of verticinone, a major active constituent from Fritillaria hupehensis Hsiao et KC Hsia., in rat plasma. Verticinone and the internal standard (IS), hupehenine, were extracted from plasma samples by a simple liquid-liquid extraction with ethyl acetate after being alkalified by 1M ammonia hydroxide. Chromatographic separation was achieved on a C(18) column using a gradient elution program with methanol and water as the mobile phase. The detection was performed by selected ion monitoring (SIM) mode via positive electrospray ionization (ESI) interface. The lower limit of quantification (LLOQ) was 0.1 ng/mL. The calibration curves were linear (r(2)>0.998) over the concentration range of 0.1-200 ng/mL. Within- and between-run precision was less than 6.5% and accuracy was within +/-10.7%. The validated method was applied to the pharmacokinetic study of verticinone in rats after a single oral administration of 1 mg/kg.
我们已经开发并验证了一种灵敏的液相色谱-电喷雾电离-质谱(LC-ESI-MS)方法,用于定量测定来自湖北贝母的主要活性成分贝母辛在大鼠血浆中的浓度。贝母辛和内标(IS),湖北贝母碱,在碱性 1M 氨水中用乙酸乙酯进行简单的液-液萃取后,从血浆样品中提取出来。采用甲醇和水作为流动相的梯度洗脱程序,在 C(18)柱上进行色谱分离。检测采用正电喷雾电离(ESI)接口的选择离子监测(SIM)模式。定量下限(LLOQ)为 0.1ng/mL。在 0.1-200ng/mL 的浓度范围内,校准曲线呈线性(r(2)>0.998)。日内和日间精密度均小于 6.5%,准确度在 +/-10.7%范围内。该验证方法应用于大鼠单次口服 1mg/kg 后贝母辛的药代动力学研究。