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流动注射分光光度法测定福美司特,采用在线热诱导消解和正磷酸盐校准曲线。

Flow injection spectrophotometric determination of fosfestrol, following on-line thermal induced digestion and using an orthophosphate calibration graph.

机构信息

Laboratory of Analytical Chemistry, Department of Chemistry, Aristotle University of Thessaloniki, GR 54124 Thessaloniki, Greece.

出版信息

Talanta. 2003 Jan 2;59(1):207-13. doi: 10.1016/s0039-9140(02)00478-2.

Abstract

A novel flow injection (FI) system for the spectrophotometric determination of diethyl stilbestrol diphosphate (fosfestrol) in pharmaceutical formulations is described. On-line thermal induced digestion of the analyte by peroxodisulfate ion was performed and the orthophosphate ion generated was determined spectrophotometrically (lambda(max)=690 nm) using a molybdenum blue based FI approach. As the achieved conversion of the analyte was quantitative, an orthophosphate calibration graph can be used for its determination as well. The chemical and FI variables affecting the digestion were investigated. A linear calibration graph was obtained in the range 5.0x10(-7)-1.0x10(-4) mol l(-1) fosfestrol. The relative standard deviation was very good (s(r)=0.8% at 5.0x10(-5) mol l(-1) fosfestrol, n=12) and the 3sigma detection limit was 2.5x10(-7) mol l(-1). The sampling rate was 60 injections h(-1). The average accuracies for the determination of the analyte in a pharmaceutical formulation evaluated by comparison of the results with those obtained by the supplier (Asta Medica) and the method recommended by the US Pharmacopoeia were also very good (e(r) of +0.8 and -0.3%, respectively). Average recoveries of known amounts of the analyte ranging between 97.9 and 100.8% were also obtained.

摘要

一种新颖的流动注射(FI)系统,用于分光光度法测定药物制剂中二苯乙烯双磷酸酯(福斯氟酯)。通过过二硫酸盐离子在线热诱导消化分析物,并使用基于钼蓝的 FI 方法在分光光度法(lambda(max)=690nm)下测定生成的正磷酸盐离子。由于分析物的转化率是定量的,因此也可以使用正磷酸盐校准曲线来测定它。研究了影响消化的化学和 FI 变量。在 5.0x10(-7)-1.0x10(-4) mol l(-1)福斯氟酯范围内获得了线性校准曲线。相对标准偏差非常好(在 5.0x10(-5) mol l(-1)福斯氟酯时 s(r)=0.8%,n=12),检测限为 3sigma 为 2.5x10(-7) mol l(-1)。采样率为 60 次/小时。通过将结果与供应商(Asta Medica)和美国药典推荐的方法的结果进行比较,评估该制剂中分析物的测定平均准确度也非常好(分别为 e(r)为+0.8%和-0.3%)。还获得了已知分析物量的平均回收率在 97.9%至 100.8%之间。

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