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制药工业废水中某些抗生素残留的经过验证的电化学和色谱定量分析。

Validated electrochemical and chromatographic quantifications of some antibiotic residues in pharmaceutical industrial waste water.

作者信息

Ibrahim Heba K, Abdel-Moety Mona M, Abdel-Gawad Sherif A, Al-Ghobashy Medhat A, Kawy Mohamed Abdel

机构信息

National Organization for Drug Control and Research, Giza, Egypt.

Pharmaceutical Chemistry Department, College of Pharmacy, Prince Sattam Bin Abdul-Aziz University, Al Kharj, Kingdom of Saudi Arabia.

出版信息

Environ Sci Pollut Res Int. 2017 Mar;24(8):7023-7034. doi: 10.1007/s11356-016-8340-3. Epub 2017 Jan 14.

Abstract

Realistic implementation of ion selective electrodes (ISEs) into environmental monitoring programs has always been a challenging task. This could be largely attributed to difficulties in validation of ISE assay results. In this study, the electrochemical response of amoxicillin trihydrate (AMX), ciprofloxacin hydrochloride (CPLX), trimethoprim (TMP), and norfloxacin (NFLX) was studied by the fabrication of sensitive membrane electrodes belonging to two types of ISEs, which are polyvinyl chloride (PVC) membrane electrodes and glassy carbon (GC) electrodes. Linear response for the membrane electrodes was in the concentration range of 10-10 mol/L. For the PVC membrane electrodes, Nernstian slopes of 55.1, 56.5, 56.5, and 54.0 mV/decade were achieved over a pH 4-8 for AMX, CPLX, and NFLX, respectively, and pH 3-6 for TMP. On the other hand, for GC electrodes, Nernstian slopes of 59.1, 58.2, 57.0, and 58.2 mV/decade were achieved over pH 4-8 for AMX, CPLX, and NFLX, respectively, and pH 3-6 for TMP. In addition to assay validation to international industry standards, the fabricated electrodes were also cross-validated relative to conventional separation techniques; high performance liquid chromatography (HPLC), and thin layer chromatography (TLC)-densitometry. The HPLC assay was applied in concentration range of 0.5-10.0 μg/mL, for all target analytes. The TLC-densitometry was adopted over a concentration range of 0.3-1.0 μg/band, for AMX, and 0.1-0.9 μg/band, for CPLX, NFLX, and TMP. The proposed techniques were successfully applied for quantification of the selected drugs either in pure form or waste water samples obtained from pharmaceutical plants. The actual waste water samples were subjected to solid phase extraction (SPE) for pretreatment prior to the application of chromatographic techniques (HPLC and TLC-densitometry). On the other hand, the fabricated electrodes were successfully applied for quantification of the antibiotic residues in actual waste water samples without any pretreatment. This finding assures the suitability of the fabricated ISEs for environmental analysis.

摘要

将离子选择性电极(ISEs)切实应用于环境监测项目一直是一项具有挑战性的任务。这在很大程度上可归因于ISE分析结果验证方面的困难。在本研究中,通过制备属于两类ISEs的敏感膜电极,即聚氯乙烯(PVC)膜电极和玻碳(GC)电极,研究了三水合阿莫西林(AMX)、盐酸环丙沙星(CPLX)、甲氧苄啶(TMP)和诺氟沙星(NFLX)的电化学响应。膜电极的线性响应浓度范围为10⁻¹⁰ mol/L。对于PVC膜电极,在pH 4 - 8范围内,AMX、CPLX和NFLX的能斯特斜率分别为55.1、56.5和54.0 mV/decade,TMP在pH 3 - 6范围内能斯特斜率为56.5 mV/decade。另一方面,对于GC电极,在pH 4 - 8范围内,AMX、CPLX和NFLX的能斯特斜率分别为59.1、58.2和58.2 mV/decade,TMP在pH 3 - 6范围内能斯特斜率为57.0 mV/decade。除了根据国际行业标准进行分析验证外,所制备的电极还相对于传统分离技术进行了交叉验证;即高效液相色谱(HPLC)和薄层色谱(TLC)-密度测定法。HPLC分析适用于所有目标分析物,浓度范围为0.5 - 10.0 μg/mL。TLC - 密度测定法用于AMX时浓度范围为0.3 - 1.0 μg/条带,用于CPLX、NFLX和TMP时浓度范围为每组0.1 - 0.9 μg/条带。所提出的技术成功应用于纯形式或制药厂废水样品中所选药物的定量分析。实际废水样品在应用色谱技术(HPLC和TLC - 密度测定法)之前先进行固相萃取(SPE)预处理。另一方面,所制备的电极无需任何预处理即可成功应用于实际废水样品中抗生素残留的定量分析。这一发现确保了所制备的ISEs适用于环境分析。

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