National Institute for Public Health and the Environment, P. O. Box 1, 3721 MA, Bilthoven, the Netherlands.
National Institute for Public Health and the Environment, P. O. Box 1, 3721 MA, Bilthoven, the Netherlands.
J Pharm Biomed Anal. 2020 Jan 30;178:112939. doi: 10.1016/j.jpba.2019.112939. Epub 2019 Oct 21.
Substandard and falsified medical products may cause harm to patients and fail to treat the diseases or conditions for which they were intended. It is therefore required to have analytical methods available to assess medical product quality. Benchtop NMR spectroscopy provides a generic, inherently quantitative, analytical method capable of separating specific signals from those of a matrix. We have developed an analytical method for the analysis of active ingredients in pharmaceutical products and illegal drugs, based on benchtop NMR spectroscopy. Within its resolution limits, benchtop NMR spectroscopy is useful in determining the identity of the active ingredients in products containing acetaminophen, aspirin, caffeine, diclofenac, ibuprofen, naproxen, sildenafil, tadalafil and sibutramine, cocaine, and gamma hydroxybutyric acid, with a limit of detection of about 1 mg/mL. Furthermore, the content of the active ingredient can be determined with an error of 10%. Additionally, a chemometrics approach is shown to be useful to classify spectra in order to identify the active substances present in the sample, reducing the need for expert interpretation of the spectra acquired.
劣质和伪造的医疗产品可能会对患者造成伤害,并不能治疗其预期的疾病或病症。因此,需要有分析方法来评估医疗产品的质量。台式 NMR 光谱提供了一种通用的、固有的定量分析方法,能够将特定信号与基质信号分离。我们已经开发了一种基于台式 NMR 光谱的药物产品和非法药物中活性成分的分析方法。在其分辨率极限内,台式 NMR 光谱可用于确定含有对乙酰氨基酚、阿司匹林、咖啡因、双氯芬酸、布洛芬、萘普生、西地那非、他达拉非和西布曲明、可卡因和γ-羟基丁酸的产品中活性成分的身份,检测限约为 1mg/mL。此外,还可以以 10%的误差确定活性成分的含量。此外,还表明化学计量学方法可用于对光谱进行分类,以识别样品中存在的活性物质,从而减少对获得的光谱进行专家解释的需求。