U.S. FDA/CDER/DPA, 1114 Market Street, St. Louis, Missouri 63101, USA.
J Anal Toxicol. 2011 Oct;35(8):545-50. doi: 10.1093/anatox/35.8.545.
The United States Public Health Service Substance Abuse and Mental Health Services Administration is alerting medical professionals that a substantial percentage of cocaine imported into the United States is adulterated with levamisole, a veterinary pharmaceutical that can cause blood cell disorders such as severe neutropenia and agranulocytosis. Levamisole HCl is the active ingredient in a number of veterinary drugs approved to treat worm infestations in animals. Levamisole HCl was also the active ingredient in a human drug for oral administration approved on June 18, 1990, as adjuvant treatment in combination with fluorouracil after surgical resection in patients with Duke's stage C colon cancer. This drug was withdrawn from the U.S. market around 2000, and it has not been marketed in the U.S. since then. The objective of this study was to develop a method to determine the amount of levamisole in urine samples. The procedure will be provided to state health laboratories as needed to be used in the evaluation of patients that have developed neutropenia or agranulocytosis in the setting of recent cocaine use. A gas chromatography-mass spectrometry method was validated and tested at two different laboratories, and the method limit of detection for levamisole is 1 ng/mL in urine when using a 5-mL sample. Confirmation of the stereoisomer of levamisole was done by high-performance liquid chromatography using a chiral column.
美国公共卫生署药物滥用与精神健康服务管理局向医疗专业人员发出警示,称大量进入美国的可卡因中掺杂有左旋咪唑,这是一种兽医药品,可导致血细胞紊乱,如严重中性粒细胞减少症和粒细胞缺乏症。盐酸左旋咪唑是许多兽医药物的有效成分,这些药物被批准用于治疗动物的寄生虫感染。盐酸左旋咪唑也曾是一种用于口服的人类药物的有效成分,该药物于 1990 年 6 月 18 日获得批准,作为 Dukes C 期结肠癌患者手术后与氟尿嘧啶联合使用的辅助治疗药物。该药物已于 2000 年左右从美国市场撤出,此后未在美国上市。本研究的目的是开发一种在尿液样本中测定左旋咪唑含量的方法。该程序将按需提供给州立卫生实验室,以便在评估近期可卡因使用后出现中性粒细胞减少症或粒细胞缺乏症的患者时使用。已在两个不同的实验室验证并测试了一种气相色谱-质谱法,当使用 5 毫升样本时,该方法对尿液中左旋咪唑的检测限为 1 纳克/毫升。通过使用手性柱的高效液相色谱法对左旋咪唑的立体异构体进行了确认。