Rattanarat Poomrat, Suea-Ngam Akkapol, Ruecha Nipapan, Siangproh Weena, Henry Charles S, Srisa-Art Monpichar, Chailapakul Orawon
Electrochemistry and Optical Spectroscopy Research Unit (EOSRU), Department of Chemistry, Faculty of Science, Chulalongkorn University, Patumwan, Bangkok 10330, Thailand.
Electrochemistry and Optical Spectroscopy Research Unit (EOSRU), Department of Chemistry, Faculty of Science, Chulalongkorn University, Patumwan, Bangkok 10330, Thailand; Chromatography and Separation Research Unit (ChSRU), Department of Chemistry, Faculty of Science, Chulalongkorn University, Patumwan, Bangkok 10330, Thailand.
Anal Chim Acta. 2016 Jun 21;925:51-60. doi: 10.1016/j.aca.2016.03.010. Epub 2016 Apr 8.
We report herein the first development of graphene-polyaniline modified carbon paste electrode (G-PANI/CPE) coupled with droplet-based microfluidic sensor for high-throughput detection of 4-aminophenol (4-AP) in pharmaceutical paracetamol (PA) formulations. A simple T-junction microfluidic platform using an oil flow rate of 1.8 μL/min and an aqueous flow rate of 0.8 μL/min was used to produce aqueous testing microdroplets continuously. The microchannel was designed to extend the aqueous droplet to cover all 3 electrodes, allowing for electrochemical measurements in a single droplet. Parameters including flow rate, water fraction, and applied detection potential (Edet) were investigated to obtain optimal conditions. Using G-PANI/CPE significantly increased the current response for both cyclic voltammetric detections of ferri/ferrocyanide Fe(CN)6 (10 times) and 4-AP (2 times), compared to an unmodified electrode. Using the optimized conditions in the droplet system, 4-AP in the presence of PA was selectively determined. The linear range of 4-AP was 50-500 μM (R(2) = 0.99), limit of detection (LOD, S/N = 3) was 15.68 μM, and limit of quantification (LOQ, S/N = 10) was 52.28 μM. Finally, the system was used to determine 4-AP spiked in commercial PA liquid samples and the amounts of 4-AP were found in good agreement with those obtained from the conventional capillary zone electrophoresis/UV-Visible spectrophotometry (CZE/UV-Vis). The proposed microfluidic device could be employed for a high-throughput screening (at least 60 samples h(-1)) of pharmaceutical purity requiring low sample and reagent consumption.
我们在此报告首次开发出石墨烯 - 聚苯胺修饰碳糊电极(G - PANI/CPE)与基于液滴的微流控传感器相结合,用于高通量检测药物对乙酰氨基酚(PA)制剂中的4 - 氨基酚(4 - AP)。使用一个简单的T型微流控平台,油相流速为1.8 μL/min,水相流速为0.8 μL/min,用于连续产生水性测试微滴。微通道设计为将水滴扩展以覆盖所有3个电极,从而实现对单个液滴的电化学测量。研究了流速、水相分数和施加的检测电位(Edet)等参数以获得最佳条件。与未修饰的电极相比,使用G - PANI/CPE显著提高了亚铁氰化钾/铁氰化钾[Fe(CN)6](3 - /4 - )循环伏安检测(10倍)和4 - AP(2倍)的电流响应。在液滴系统中使用优化条件,选择性地测定了PA存在下的4 - AP。4 - AP的线性范围为50 - 500 μM(R(2) = 0.99),检测限(LOD,S/N = 3)为15.68 μM,定量限(LOQ,S/N = 10)为52.28 μM。最后,该系统用于测定商业PA液体样品中添加的4 - AP,发现4 - AP的含量与通过传统毛细管区带电泳/紫外 - 可见分光光度法(CZE/UV - Vis)获得的结果高度一致。所提出的微流控装置可用于高通量筛选(至少60个样品/h(-1))药物纯度,且所需样品和试剂消耗量低。