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用多壁碳纳米管糊电极通过方波溶出伏安法测定眼科药物丙美卡因

Determination of Ophthalmic Drug Proparacaine Using Multi-walled Carbon Nanotube Paste Electrode by Square Wave Stripping Voltammetry.

作者信息

Demir Ersin, Inam Onur, Inam Recai

机构信息

Department of Food Engineering, Faculty of Engineering, Okan University.

Department of Ophthalmology, Faculty of Medicine, Hacettepe University.

出版信息

Anal Sci. 2018;34(7):771-776. doi: 10.2116/analsci.17P589.

Abstract

Proparacaine, one of the most common local anesthetics to facilitate diagnosis and treatment of eye diseases, was assayed by square wave voltammetry using a paste electrode prepared with carbon nanotubes. In cyclic voltammetric studies, proparacaine has exhibited a single irreversible anodic peak at around + 900 mV vs. Ag/AgCl in pH 6.0 Britton-Robinson buffer solution. It was suggested that the peak had appeared due to the oxidation of the NH group on the proparacaine molecule. Prior to the determination of the proparacaine by square wave stripping voltammetry (SWSV) on the fabricated multi-walled carbon nanotube paste electrode (MWCNTPE), the accumulation potential (E), accumulation time (t), pulse amplitude (ΔE), step potential (ΔE) and frequency (f ) parameters were optimized. The peak currents plotted in the range of 0.5 - 12.5 mg/L proparacaine exhibited two linear sections with a detection limit of 0.11 mg/L. The results for the determination of proparacaine on a pharmaceutical local anesthetic (Alcaine) showed that relative standard deviation (RSD) and relative error (RE) were 4.1 and -2.0%, respectively. Selectivity has also been investigated and results showed recoveries of 5.0 mg/L proparacaine in the presence of 5.0 mg/L dopamine, ascorbic acid and uric acid as 106.9 ± 0.8, 99.9 ± 1.2 and 94.1 ± 0.7, respectively.

摘要

丙美卡因是促进眼科疾病诊断和治疗的最常见局部麻醉剂之一,采用碳纳米管制备的糊剂电极通过方波伏安法对其进行了测定。在循环伏安研究中,在pH 6.0的 Britton-Robinson缓冲溶液中,相对于Ag/AgCl,丙美卡因在约 + 900 mV处表现出一个单一的不可逆阳极峰。据推测,该峰的出现是由于丙美卡因分子上NH基团的氧化。在制备的多壁碳纳米管糊剂电极(MWCNTPE)上通过方波溶出伏安法(SWSV)测定丙美卡因之前,对富集电位(E)、富集时间(t)、脉冲幅度(ΔE)、步长电位(ΔE)和频率(f)参数进行了优化。在0.5 - 12.5 mg/L丙美卡因范围内绘制的峰电流呈现出两个线性部分,检测限为0.11 mg/L。对一种药用局部麻醉剂(爱尔卡因)中丙美卡因的测定结果表明,相对标准偏差(RSD)和相对误差(RE)分别为4.1%和 -2.0%。还研究了选择性,结果表明,在存在5.0 mg/L多巴胺、抗坏血酸和尿酸的情况下,5.0 mg/L丙美卡因的回收率分别为106.9 ± (0.8)、99.9 ± 1.2和94.1 ± 0.7。 (注:原文中“106.9 ± 0.8”括号处疑似少了右括号,翻译时保留原文格式)

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