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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Multi-dimensional fingerprint profiling analysis for screening and quantification of illegal adulterated antidiabetics in hypoglycemic health products by aqueous two-phase extraction and multi-wavelength detection
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Multi-dimensional fingerprint profiling analysis for screening and quantification of illegal adulterated antidiabetics in hypoglycemic health products by aqueous two-phase extraction and multi-wavelength detection

机译:通过两相提取和多波长检测筛选和定量非血糖健康产品中非法掺假抗体的筛选和定量多维指纹分析分析

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摘要

A novel method for screening and quantification of illegal adulterated antidiabetics in hypoglycemic health products was developed by multi-dimensional fingerprint profiling analysis (MDFPA). By means of aqueous two-phase extraction (ATPE), using aqueous two-phase system (ATPS) of butanol-water as the extractant, 11 common antidiabetics could be effectively extracted to the upper and lower phases, respectively. HPLC separation conditions for the extracts from two phases were investigated by multi-wavelength detection before and after p-nitrobenzoyl chloride (p-NBC) and 2,4-dinitrofluorobenzene (DNBF) derivatizations to establish multi-dimensional fingerprints. For high accuracy and reliability, a hierarchical screening approach to screening illegal adulterated antidiabetics in samples was established by MDFPA and spectral purity examination. Meanwhile, detection limits of identification for illegal adulterants were defined by detection limits of spectra (SLOD). The proposed method exhibited good identification and quantification performances. SLODs, LODs and LOQs of 11 antidiabetics were 1.22-8.37 mu g/g, 0.225-4.23 mu g/g and 0.755-14.10 mu g/g, respectively. They had good linearity ranged from 2.0 mu g/g to 300.0 mu g/g (R-2 >= 0.9978). The recoveries and RSDs were 76.83-109.6% and 0.50-6.5%, respectively. The method was successfully applied to screening of 15 batches of samples in different forms. Among them, four samples were detected to contain 5.47 mu g/g of metformin, 6.50 mu g/g of phenformin, 3.69 mu g/g of glibenclamide and 9.11 mu g/g of glimepiride, respectively. The results proved that it was an efficient and feasible alternative to screening and detection of illegal adulterated antidiabetics in hypoglycemic health products. (C) 2020 Elsevier B.V. All rights reserved.
机译:通过多维指纹分析分析(MDFPA)开发了一种新的筛选和定量非法掺杂抗体的筛选和定量非法掺假灭绝剂的方法。通过两相萃取(ATPE),使用丁醇 - 水的水性两相体系(ATP)作为萃取剂,可以分别有效地提取11种常见的抗体剂。通过在硝基苯甲酰氯(P-NBC)(P-NBC)和2,4-二硝基氟苯(DNBF)衍生物之前和之后,通过多波长检测研究来自两相的提取物的HPLC分离条件,以建立多维指纹。对于高精度和可靠性,通过MDFPA和光谱纯度检查建立了一种筛选非法掺假抗体的分层筛选方法。同时,通过光谱(SLOC)的检测限制来定义非法掺杂物的鉴定的检测限。所提出的方法表现出良好的鉴定和量化性能。 11个抗胶质剂的Slod,Lod和Loqs分别为1.22-8.37μg/ g,0.225-4.23μg/ g分别为0.755-14.10μg/ g。它们具有良好的线性,范围为2.0μg/ g至300.0μg/ g(R-2> = 0.9978)。回收率和RSD分别为76.83-109.6%和0.50-6.5%。该方法成功地应用于以不同形式筛选15批样品。其中,检测到四个样品以含有5.47μg/ g的二甲双胍,6.50μg/ g的苯甲酸,3.69μg/ g的Glibenclamide和9.11μg/ g的胶质珠酰胺。结果证明,筛选和检测降血糖健康产品中非法掺假抗体的替代有效和可行的替代品。 (c)2020 Elsevier B.v.保留所有权利。

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