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采用固相荧光光谱法测定人尿液和血清样本中的环丙沙星。

Determination of ciprofloxacin in human urine and serum samples by solid-phase spectrofluorimetry.

作者信息

Navalón A, Ballesteros O, Blanc R, Vílchez J L

机构信息

Research Group of Solid-Phase Spectrometry, Department of Analytical Chemistry, Faculty of Science, University of Granada, C/Fuentenueva, E-18071 Granada, Spain.

出版信息

Talanta. 2000 Aug 16;52(5):845-52.

Abstract

A method for the determination of trace amounts of ciprofloxacin has been developed, based on solid-phase spectrofluorimetry. The relative fluorescence intensity of ciprofloxacin fixed on Sephadex SP C-25 gel was measured directly after packing the gel beads in a 1-mm silica cell, using a solid-phase attachment. The wavelengths of excitation and emission were 272 and 448 nm, respectively. Using a sample volume of 1000 ml, the linear concentration range of application was 0.3-10.0 ng.ml(-1) of ciprofloxacin, with a R.S.D. of 1.2% (for a level of 4.0 ng.ml(-1)) and a detection limit of 0.1 ng.ml(-1). The method was applied to the determination of ciprofloxacin in human urine and serum samples. It was validated applying the standard addition methodology and using HPLC as a reference method. Recovery levels of the method reached 100% in all cases.

摘要

基于固相荧光光谱法,开发了一种测定痕量环丙沙星的方法。将凝胶珠填充到1毫米的石英池中后,使用固相附件直接测量固定在葡聚糖SP C - 25凝胶上的环丙沙星的相对荧光强度。激发波长和发射波长分别为272纳米和448纳米。使用1000微升的样品体积,环丙沙星的线性应用浓度范围为0.3 - 10.0纳克/毫升,相对标准偏差为1.2%(对于4.0纳克/毫升的水平),检测限为0.1纳克/毫升。该方法应用于测定人尿液和血清样品中的环丙沙星。采用标准加入法并以高效液相色谱法作为参考方法对其进行了验证。在所有情况下,该方法的回收率均达到100%。

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