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Determination of Ephedrine and Pseudoephedrine by Field-Amplified Sample Injection Capillary Electrophoresis

机译:场放大样品注射毛细管电泳法测定麻黄碱和伪麻黄碱

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摘要

A simple and rapid capillary electrophoresis method was developed for the separation and determination of ephedrine (E) and pseudoephedrine (PE) in a buffer solution containing 80 mM of NaH_2PO_4 (pH 3.0), 15 mM of β-cyclodextrin and 0.3% of hydroxypropyl methylcellulose. The field-amplified sample injection (FASI) technique was applied to the online concentration of the alkaloids. With FASI in the presence of a low conductivity solvent plug (water), an approximately 1,000-fold improvement in sensitivity was achieved without any loss of separation efficiency when compared to conventional sample injection. Under these optimized conditions, a baseline separation of the two analytes was achieved within 16 min and the detection limits for E and PE were 0.7 and 0.6 μg/L, respectively. Without expensive instruments or labeling of the compounds, the limits of detection for E and PE obtained by the proposed method are comparable with (or even lower than) those obtained by capillary electrophoresis laser-induced fluorescence, liquid chromatography–tandem mass spectrometry and gas chromatography–mass spectrometry. The method was validated in terms of precision, linearity and accuracy, and successfully applied for the determination of the two alkaloids in Ephedra herbs.
机译:建立了一种简单,快速的毛细管电泳方法,用于在含有80 mM NaH_2PO_4(pH 3.0),15 mMβ-环糊精和0.3%羟丙基甲基纤维素的缓冲溶液中分离和测定麻黄碱(E)和伪麻黄碱(PE) 。现场放大样品注射(FASI)技术应用于生物碱的在线浓缩。与常规样品进样相比,使用FASI在低电导率溶剂塞(水)的存在下,灵敏度可提高约1,000倍,而分离效率没有任何损失。在这些优化的条件下,两种分析物的基线分离在16分钟内实现,E和PE的检出限分别为0.7和0.6μg/ L。如果没有昂贵的仪器或化合物的标记,通过本发明方法获得的E和PE的检出限与毛细管电泳激光诱导荧光,液相色谱-串联质谱和气相色谱法所获得的检出限相当(甚至更低) -质谱。该方法在精密度,线性和准确性方面均得到验证,并成功用于麻黄中两种生物碱的测定。

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