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采用气相色谱-质谱联用技术测定比格犬血浆中痕量斑蝥素及其药代动力学研究。

Determination of trace cantharidin in plasma and pharmacokinetic study in beagle dogs using gas chromatography-mass spectrometry.

作者信息

Dang Yun-Jie, Zhu Chun-Yan

机构信息

Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences, Beijing 100094, China.

出版信息

J Anal Toxicol. 2009 Sep;33(7):384-8. doi: 10.1093/jat/33.7.384.

Abstract

The blister beetle is traditional Chinese medicine that was first discovered and used as anticancer drug in China, and cantharidin proved to be its principal active ingredient. Cantharidin-based pharmaceutical preparations are now widely used in clinics in China with good therapeutic efficacy. As a toxic anticancer drug, the therapeutic dose of cantharidin is low, and no method to determine the blood cantharidin concentration under the therapeutic dose has so far been reported. Here, we present a simple, sensitive, and reliable gas chromatography-mass spectrometry (GC-MS) method to monitor the plasma cantharidin and perform the pharmacokinetic study of cantharidin in beagle dogs. After protein precipitation by hydrochloric acid, a liquid-liquid extraction procedure using ethyl acetate was applied to extract cantharidin from plasma. An elastic quartz capillary GC column DB-5MS was used in GC-MS, the temperature was kept at 60 degrees C for 1 min, then increased to 220 degrees C at the rate of 6 degrees C/min, held there for 1 min, and then to 280 degrees C at the rate of 20 degrees C/min, held for 3 min. The extraction recovery was over 80% for all the tested specimens. The linearity ranged from 2.14 to 314.2 ng/mL, the intra- and interday precisions were both below 20%, the limit of detection was 0.5 ng/mL, and the limit of quantification was 2.14 ng/mL. Cantharidin in plasma proved to be stable during the whole period of storage, treatment, and analysis. Cantharidin demonstrated as one-compartment model after i.v. administration with an elimination half-life of 0.69 +/- 0.03 h and area under curve of 204 +/- 24 h.ng/mL. This GC-MS assay proved to have high precision, accuracy, reliability, and sensitivity, and it was suitable for determination of trace cantharidin in plasma.

摘要

斑蝥是中国传统中药,最早在中国被发现并用作抗癌药物,斑蝥素被证明是其主要活性成分。以斑蝥素为基础的药物制剂目前在中国临床广泛应用,治疗效果良好。作为一种毒性抗癌药物,斑蝥素的治疗剂量较低,目前尚无关于测定治疗剂量下血液中斑蝥素浓度的方法报道。在此,我们提出一种简单、灵敏且可靠的气相色谱-质谱联用(GC-MS)方法来监测血浆中斑蝥素,并进行比格犬体内斑蝥素的药代动力学研究。经盐酸沉淀蛋白后,采用乙酸乙酯液-液萃取法从血浆中提取斑蝥素。GC-MS采用弹性石英毛细管GC柱DB-5MS,温度先在60℃保持1分钟,然后以6℃/分钟的速率升至220℃,保持1分钟,再以20℃/分钟的速率升至280℃,保持3分钟。所有测试样本的提取回收率均超过80%。线性范围为2.14至314.2 ng/mL,日内和日间精密度均低于20%,检测限为0.5 ng/mL,定量限为2.14 ng/mL。血浆中的斑蝥素在整个储存、处理和分析期间均稳定。静脉注射后,斑蝥素呈现一室模型,消除半衰期为0.69±0.03小时,曲线下面积为204±24 h.ng/mL。该GC-MS测定法具有高精度、准确性、可靠性和灵敏性,适用于血浆中痕量斑蝥素的测定。

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