Liang Qionglin, Qu Jun, Luo Guoan, Wang Yiming
Analysis Center, Tsinghua University, Beijing 100084, PR China.
J Pharm Biomed Anal. 2006 Feb 13;40(2):305-11. doi: 10.1016/j.jpba.2005.07.035. Epub 2005 Sep 19.
In recent years, dietary supplements and herbal medicines are increasing in popularity all over the world. However, it is problematic that some manufacturers illegally included synthetic drugs in their products. Due to the extremely complex matrices of those products, most existing methods for screening illegal adulterations are time-consuming and liable to false positive. In this paper, a robust LC/MS/MS method for the high-throughput, sensitive and reliable determination of illegal adulterations from herbal medicines and dietary supplements was established. Minimal LC separation was employed and MRM was used to simultaneously monitor the three transitions under their respective optimal collision energy for each compound. Positive results were determined only if well-defined peaks appeared at all of the three transitions and the ratios among the peak areas were within given threshold. In this study, the method had been applied for the screening of nine most commonly adulterated therapeutic substances, such as sildenafil (Viagra) and famotidine, and the lower limits of detection of these compounds ranged from 0.05 to 1.5 ng/ml. Little sample preparation was needed for this method and the analysis time was less than 5 min/sample. The reliability has been demonstrated by the test with blank matrix. Over 200 products that were under suspicion by SDA of China had been assayed and till now no false negative or positive result was found. This method is rapid, simple, reliable and capable of screening multiple adulterants in one run.
近年来,膳食补充剂和草药在全球范围内越来越受欢迎。然而,一些制造商在其产品中非法添加合成药物的问题也随之出现。由于这些产品的基质极其复杂,大多数现有的非法掺假筛查方法既耗时又容易出现假阳性。本文建立了一种稳健的液相色谱/串联质谱法,用于高通量、灵敏且可靠地测定草药和膳食补充剂中的非法掺假成分。采用了最小化的液相色谱分离,并使用多反应监测(MRM)在各自的最佳碰撞能量下同时监测每种化合物的三个跃迁。只有当在所有三个跃迁处都出现明确的峰且峰面积之比在给定阈值范围内时,才判定为阳性结果。在本研究中,该方法已应用于筛查九种最常见的掺假治疗物质,如西地那非(伟哥)和法莫替丁,这些化合物的检测下限为0.05至1.5 ng/ml。该方法所需的样品前处理很少,每个样品的分析时间不到5分钟。通过空白基质测试证明了其可靠性。对中国国家药品监督管理局(SDA)怀疑的200多种产品进行了检测,截至目前未发现假阴性或假阳性结果。该方法快速、简单、可靠,能够一次运行筛查多种掺假物。