Department of Pharmaceutical Analysis, School of Pharmacy, Hebei Medical University, Shijiazhuang, Hebei 050017, China.
Anal Biochem. 2010 Dec 1;407(1):111-9. doi: 10.1016/j.ab.2010.07.009. Epub 2010 Jul 17.
A sensitive, specific, and rapid liquid chromatography-mass spectrometry (LC-MS) method was developed and validated for analysis of lasiodonin, oridonin, ponicidin, and rabdoternin A in rat plasma using sulfamethoxazole as an internal standard (IS). The plasma samples were pretreated and extracted by liquid-liquid extraction. Chromatographic separation was performed on a C(18) column with linear gradient elution using water and methanol, both of which were acidified with 0.1% aqueous formic acid, at a flow rate of 0.8 ml/min. Detection was accomplished by scanning with multiple reaction monitoring (MRM) via an electrospray ionization (ESI) source. Higher sensitivity was achieved by setting three scanning periods in a novel detection mode. The optimized mass transition ion pairs (m/z) for quantitation were 365.3/347.3 for lasiodonin and oridonin, 361.2/343.2 for ponicidin, 363.2/283.1 for rabdoternin A, and 254.1/156.0 for IS. The total run time was 13.50 min between injections. The specificity, linearity, accuracy, precision, recovery, matrix effect, and several stabilities were validated for all analytes in the rat plasma samples. In conclusion, the validation results demonstrate that this method is robust and specific. The proposed method was further applied to investigate the pharmacokinetics of all analytes after a single oral administration of Isodon rubescens extract to rats.
建立并验证了一种灵敏、特异、快速的液相色谱-质谱(LC-MS)法,用于分析大鼠血浆中的当药苦苷、冬凌草甲素、落新妇苷和Rabdoterpenin A,以磺胺甲恶唑为内标(IS)。血浆样品经液-液萃取预处理和提取。色谱分离在 C18 柱上进行,采用水和甲醇进行线性梯度洗脱,均用 0.1%甲酸水溶液酸化,流速为 0.8ml/min。通过电喷雾电离(ESI)源的多反应监测(MRM)扫描进行检测。在新型检测模式下设置三个扫描周期,可获得更高的灵敏度。定量的优化质量转移离子对(m/z)分别为 365.3/347.3 用于当药苦苷和冬凌草甲素,361.2/343.2 用于落新妇苷,363.2/283.1 用于 Rabdoterpenin A,254.1/156.0 用于 IS。两次进样之间的总运行时间为 13.50 分钟。对大鼠血浆样品中的所有分析物进行了特异性、线性、准确性、精密度、回收率、基质效应和多种稳定性验证。总之,验证结果表明该方法具有良好的稳定性和特异性。该方法进一步应用于单次灌胃服用当药提取物后大鼠体内所有分析物的药代动力学研究。