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方波阴极吸附溶出伏安法测定药物制剂和生物流体中的呋喃妥因药物

Determination of nitrofurantoin drug in pharmaceutical formulation and biological fluids by square-wave cathodic adsorptive stripping voltammetry.

作者信息

Hammam Essam

机构信息

Department of Chemistry, Faculty of Science, Tanta University, 31527 Tanta, Egypt.

出版信息

J Pharm Biomed Anal. 2002 Oct 15;30(3):651-9. doi: 10.1016/s0731-7085(02)00344-8.

Abstract

Nitrofurnation is an antibacterial drug. It is used in the treatment of initial or recurrent urinary tract infections caused by susceptible organisms. The cyclic voltammogram of the drug in Britton-Robinson buffers (pH 2-11) exhibited a single well-defined cathodic peak at the hanging mercury drop electrode, that due to the reduction of its nitro group to the amine stage. A fully validated, sensitive, and reproducible developed procedure was described for determination of the drug in bulk form, pharmaceutical formulation, human serum and human urine using, square-wave cathodic adsorptive stripping voltammetry. The optimal experimental parameters for the drug assay were: accumulation potential = -0.4 V (vs. Ag/AgCl/ KCl(s)), accumulation time = 40 s, frequency = 120 Hz, pulse amplitude = 50 mV and scan increment = 10 mV in Britton-Robinson buffer (pH 10). A mean percentage recovery of 100.68 +/- 0.17 (n = 5) and a detection limit of 1.32 x 10(-10) M of bulk drug were achieved. Applicability to assay of the drug in pharmaceutical formulation, human serum and human urine was studied and illustrated. The mean percentage recoveries were found as: 101.49 +/- 0.65, 103.94 +/- 0.73 and 101.98 +/- 0.52 (n = 5) in pharmaceutical formulation, human serum and human urine, respectively. Detection limits of 2.86 x 10(-10) M and 5.77 x 10(-10) M nitrofurantoin were achieved in human serum and urine, respectively.

摘要

呋喃妥因是一种抗菌药物。它用于治疗由易感微生物引起的初始或复发性尿路感染。该药物在 Britton-Robinson 缓冲液(pH 2 - 11)中的循环伏安图在悬汞滴电极上呈现出一个明确的阴极峰,这是由于其硝基还原为胺阶段所致。描述了一种经过充分验证、灵敏且可重现的方法,用于使用方波阴极吸附溶出伏安法测定原料药、药物制剂、人血清和人尿中的该药物。药物测定的最佳实验参数为:在 Britton-Robinson 缓冲液(pH 10)中,富集电位 = -0.4 V(相对于 Ag/AgCl/KCl(s)),富集时间 = 40 s,频率 = 120 Hz,脉冲幅度 = 50 mV,扫描增量 = 10 mV。原料药的平均回收率为 100.68 ± 0.17(n = 5),检测限为 1.32×10⁻¹⁰ M。研究并说明了该方法在药物制剂、人血清和人尿中药物测定的适用性。在药物制剂、人血清和人尿中的平均回收率分别为:101.49 ± 0.65、103.94 ± 0.73 和 101.98 ± 0.52(n = 5)。人血清和尿中呋喃妥因的检测限分别为 2.86×10⁻¹⁰ M 和 5.77×10⁻¹⁰ M。

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