hplc -荧光法柱前衍生分析妥布霉素的实验设计:在眼液和人血浆中的应用。

Analytical Chemistry Insights Pub Date : 2013-04-16 Print Date: 2013-01-01 DOI:10.4137/ACI.S11612
Asmaa A El-Zaher, Marianne A Mahrouse
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引用次数: 19

摘要

建立了一种新的、选择性的、灵敏的反相高效液相色谱-荧光检测方法,用于检测妥布霉素(tobramycin, TOB)的纯度、眼液和加标血浆。由于TOB缺乏紫外吸收发色团和天然荧光,因此使用荧光胺试剂(0.01%,1.5 mL)和硼酸盐缓冲液(pH 8.5, 2 mL)进行TOB的柱前衍生化。采用实验设计对衍生化步骤进行优化。得到的高荧光稳定衍生物在C18柱上进行色谱分析,用甲醇:水(60:40,v/v)以1 mL min(-1)的流速洗脱。荧光检测器(λex 390和λem 480 nm)。该方法在20 ~ 200 ng mL(-1)浓度范围内呈线性关系。提出了荧光产物的结构,验证了该方法的有效性,并将其应用于人血浆中TOB的测定。结果与参考方法进行统计学比较,差异无统计学意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Utility of Experimental Design in Pre-Column Derivatization for the Analysis of Tobramycin by HPLC-Fluorescence Detection: Application to Ophthalmic Solution and Human Plasma.

A novel, selective, and sensitive reversed phase high-performance liquid chromatography (HPLC) method coupled with fluorescence detection has been developed for the determination of tobramycin (TOB) in pure form, in ophthalmic solution and in spiked human plasma. Since TOB lacks UV absorbing chromophores and native fluorescence, pre-column derivatization of TOB was carried out using fluorescamine reagent (0.01%, 1.5 mL) and borate buffer (pH 8.5, 2 mL). Experimental design was applied for optimization of the derivatization step. The resulting highly fluorescent stable derivative was chromatographed on C18 column and eluted using methanol:water (60:40, v/v) at a flow rate of 1 mL min(-1). A fluorescence detector (λex 390 and λem 480 nm) was used. The method was linear over the concentration range 20-200 ng mL(-1). The structure of the fluorescent product was proposed, the method was then validated and applied for the determination of TOB in human plasma. The results were statistically compared with the reference method, revealing no significant difference.

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