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使用带安培检测的微型毛细管电泳快速测定药物制剂中的对乙酰氨基酚和对氨基酚。

Rapid determination of acetaminophen and p-aminophenol in pharmaceutical formulations using miniaturized capillary electrophoresis with amperometric detection.

作者信息

Chu Qingcui, Jiang Lianmei, Tian Xiuhui, Ye Jiannong

机构信息

Department of Chemistry, East China Normal University, 3663 North Zhongshan Road, Shanghai 200062, PR China.

出版信息

Anal Chim Acta. 2008 Jan 14;606(2):246-51. doi: 10.1016/j.aca.2007.11.015. Epub 2007 Nov 17.

Abstract

Capability of fast analysis of a novel miniaturized capillary electrophoresis with carbon disk electrode amperometric detection (mini-CE-AD) system was demonstrated by determining acetaminophen and p-aminophenol in dosage forms. Factors influencing the separation and detection processes were examined and optimized. Under the optimum conditions, the end-capillary 300 microm carbon disc electrode amperometric detector offered favorable signal-to-noise characteristics at a relatively low potential (+600 mV versus Ag/AgCl) for detecting acetaminophen and p-aminophenol. Two analytes can been separated within 150 s in a 8.5 cm length capillary at a separation voltage of 2000V using a Na2B4O7-KH2PO4 running buffer (pH 7.2). Acetaminophen and p-aminophenol could be detected down to the 1.4 x 10(-6)-5.9 x 10(-7) molL(-1) level with linearity up to the 1.0 x 10(-3) molL(-1) level examined. The inter-day repeatability for analytes in peak current (R.S.D.< or =2.3%) and migration times (R.S.D.< or =1.3%) were excellent. The proposed mini-CE-AD system should find a wide range of analytical applications in pharmaceutical formulations as an alternative to conventional CE and mu-CE.

摘要

通过测定剂型中的对乙酰氨基酚和对氨基苯酚,证明了新型小型化毛细管电泳-碳盘电极安培检测(mini-CE-AD)系统的快速分析能力。研究并优化了影响分离和检测过程的因素。在最佳条件下,毛细管末端300微米碳盘电极安培检测器在相对较低的电位(相对于Ag/AgCl为+600 mV)下,对对乙酰氨基酚和对氨基苯酚具有良好的信噪比特性。使用Na2B4O7-KH2PO4运行缓冲液(pH 7.2),在2000V的分离电压下,两种分析物可在8.5厘米长的毛细管中于150秒内分离。对乙酰氨基酚和对氨基苯酚的检测限可达1.4×10(-6)-5.9×10(-7) molL(-1),线性范围可达所检测的1.0×10(-3) molL(-1)水平。分析物的峰电流日内重复性(R.S.D.≤2.3%)和迁移时间日内重复性(R.S.D.≤1.3%)都非常好。所提出的mini-CE-AD系统作为传统CE和μ-CE的替代方法,应在药物制剂中找到广泛的分析应用。

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