Tan Zhi-Rong, Ouyang Dong-Sheng, Zhou Gan, Wang Lian-Sheng, Li Zhi, Wang Dan, Zhou Hong-Hao
Pharmacogenetics Research Institute, Institute of Clinical Pharmacology, Central South University, Xiangya Road 110, Changsha, Hunan 410078, China.
J Pharm Biomed Anal. 2006 Sep 18;42(2):207-12. doi: 10.1016/j.jpba.2006.02.057. Epub 2006 May 19.
A liquid chromatography-ion trap mass spectrometry coupled with electrospray ionization (HPLC-ESI-ion trap mass spectrometry) method for simultaneous determination of cetirizine and pseudoephedrine in human plasma is presented. Chromatographic separation was performed on a Hypurity C18 column (Thermo Hypersil-Keystone 2.1 mm x 150 mm, 5 microm, USA), The mobile phase was composed of 65% methanol and 35% water (contained 0.1% formic acid, 10 mM ammonium formate), which was run with a flow-rate of 0.2 ml/min at 40 degrees C. Quantitation was achieved by monitoring the product ions at m/z 166-->m/z 148 (pseudoephedrine), m/z 389.9-->m/z 201.1 (cetirizine), m/z 264-->m/z 246 (tramadol, IS). The calibration curve of pseudoephedrine and cetirizine was established with standard solutions. The limit of detection for pseudoephedrine and cetirizine each was 5 ng/ml. This simplified analytical method is sensitive, specific and accurate enough for simultaneous determination of pseudoephedrine and cetirizine in human plasma and is successfully applied to the pharmacokinetic study of pseudoephedrine and cetirizine.
本文介绍了一种采用液相色谱-离子阱质谱联用技术结合电喷雾电离(HPLC-ESI-离子阱质谱法)同时测定人血浆中西替利嗪和伪麻黄碱的方法。色谱分离在Hypurity C18柱(美国热电Hypersil-Keystone 2.1 mm×150 mm,5微米)上进行,流动相由65%甲醇和35%水(含0.1%甲酸、10 mM甲酸铵)组成,于40℃以0.2 ml/min的流速运行。通过监测m/z 166→m/z 148(伪麻黄碱)、m/z 389.9→m/z 201.1(西替利嗪)、m/z 264→m/z 246(曲马多,内标)的产物离子进行定量分析。用标准溶液建立伪麻黄碱和西替利嗪的校准曲线。伪麻黄碱和西替利嗪的检测限均为5 ng/ml。这种简化的分析方法灵敏、特异且准确,足以同时测定人血浆中的伪麻黄碱和西替利嗪,并成功应用于伪麻黄碱和西替利嗪的药代动力学研究。