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开发一种用于在存在一些标签错误药物的情况下检测和定量盐酸曲马多的新型液相色谱-串联质谱法:在假药研究中的应用。

Development of a novel LC-MS/MS method for detection and quantification of tramadol hydrochloride in presence of some mislabeled drugs: Application to counterfeit study.

作者信息

Abdel-Megied Ahmed M, Badr El-Din Khalid M

机构信息

Pharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, Kafrelsheikh University, Kafrelsheikh City, Egypt.

Analytical Chemistry Department, Faculty of Pharmacy, Minia University, El-Minia, Egypt.

出版信息

Biomed Chromatogr. 2019 Jun;33(6):e4486. doi: 10.1002/bmc.4486. Epub 2019 Feb 20.

Abstract

Counterfeiting of pharmaceuticals has become a serious problem all over the world, particularly in developing countries. In the present work, a highly sensitive LC-MS/MS method was developed for simultaneous determination of tramadol hydrochloride in the presence of some suspected mislabeled drugs such as alprazolam, diazepam, chlorpheniramine maleate, diphenylhydramine and paracetamol. The prepared samples were analyzed on an API 4000 mass spectrometer using an Eclipse C column (3.5 μm, 4.6 × 100 mm). The mobile phase consisting of 0.01% formic acid, acetonitrile and methanol (60:20:20 v/v/v) was pumped with an isocratic elution at a flow rate of 0.7 mL min . The detection was achieved on a triple quadruple tandem mass spectrometer in multiple reaction monitoring mode. The proposed method was successfully validated according to International Conference on Harmonization guidelines with respect to accuracy, precision, linearity, limit of detection and limit of quantitation. The calibration linear range for tramadol hydrochloride, alprazolam, diazepam, chlorpheniramine maleate, diphenylhydramine and paracetamol was 5-500 ng mL . The results revealed that the applied method is promising for the differentiation of genuine tramadol tablets from counterfeit ones without prior separation.

摘要

药品造假已成为全球一个严重问题,在发展中国家尤为突出。在本研究中,开发了一种高灵敏度液相色谱 - 串联质谱法,用于在存在一些疑似标签错误的药物(如阿普唑仑、地西泮、马来酸氯苯那敏、苯海拉明和对乙酰氨基酚)的情况下同时测定盐酸曲马多。制备的样品在配备Eclipse C柱(3.5μm,4.6×100mm)的API 4000质谱仪上进行分析。流动相由0.01%甲酸、乙腈和甲醇(60:20:20 v/v/v)组成,以0.7 mL min的流速等度洗脱。检测在三重四极杆串联质谱仪上以多反应监测模式进行。所提出的方法根据国际协调会议指南在准确度、精密度、线性、检测限和定量限方面成功得到验证。盐酸曲马多、阿普唑仑、地西泮、马来酸氯苯那敏、苯海拉明和对乙酰氨基酚的校准线性范围为5 - 500 ng mL。结果表明,所应用的方法有望在无需预先分离的情况下区分正品和假冒的盐酸曲马多片剂。

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