首页> 美国卫生研究院文献>Molecules >Green Analytical Methods of Antimalarial Artemether-Lumefantrine Analysis for Falsification Detection Using a Low-Cost Handled NIR Spectrometer with DD-SIMCA and Drug Quantification by HPLC
【2h】

Green Analytical Methods of Antimalarial Artemether-Lumefantrine Analysis for Falsification Detection Using a Low-Cost Handled NIR Spectrometer with DD-SIMCA and Drug Quantification by HPLC

机译:使用低成本处理的NIR光谱仪进行DD-SIMCA和HPLC的药物量化伪造伪造的绿色分析方法对伪造检测伪造检测。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Two green analytical approaches have been developed for the analysis of antimalarial fixed dose tablets of artemether and lumefantrine for quality control. The first approach consisted of investigating the qualitative performance of a low-cost handheld near-infrared spectrometer in combination with the principal component analysis as an exploratory tool to identify trends, similarities, and differences between pharmaceutical samples, before applying the data driven soft independent modeling of class analogy (DD-SIMCA) as a one-class classifier for proper drug falsification detection with 100% of both sensitivity and specificity in the studied cases. Despite its limited spectral range and low resolution, the handheld device allowed detecting falsified drugs with no active pharmaceutical ingredient and identifying specifically a pharmaceutical tablet brand name. The second approach was the quantitative analysis based on the green and fast RP-HPLC technique using ethanol as a green organic solvent and acetic acid as a green pH modifier. The optimal separation was achieved in 7 min using a mobile phase composed of ethanol 96% and 10 mM of acetic acid pH 3.35 (63:37, / ). The developed method was validated according to the total error approach based on an accuracy profile, was applied to the analysis of tablets, and allowed confirming falsified drugs detected by spectroscopy.
机译:已经开发了两种绿色分析方法,用于分析促摩尔醚和Lumefantrine的抗疟定剂量片剂,用于质量控制。第一种方法包括调查低成本手持近红外光谱仪的定性性能,结合主要成分分析作为探索工具,以确定药物样本之间的趋势,相似性和差异,在应用数据驱动的软独立建模之前类比类(DD-SIMCA)作为一种单级分类器,用于适当的药物伪造检测,在研究的情况下具有100%的灵敏度和特异性。尽管光谱范围和低分辨率有限,但允许手持设备允许检测伪造的药物,没有活性药物成分,特别是药物平板电脑品牌名称。第二种方法是基于使用乙醇作为绿色有机溶剂和乙酸作为绿色pH调节剂的绿色和快速RP-HPLC技术的定量分析。使用由乙醇96%和10mM的乙酸pH3.35(63:37,/)组成的流动相,在7分钟内实现最佳分离。根据基于精度曲线的总误差方法验证开发方法,应用于片剂的分析,并允许确认通过光谱检测的伪造药物。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号