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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

机译:实验设计在柱前衍生化中使用HPLC进行妥布霉素分析的荧光检测—在眼药水和人体血浆中的应用

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摘要

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.
机译:已经开发了一种新颖的,选择性的,灵敏的反相高效液相色谱(HPLC)方法和荧光检测方法,用于测定纯形式,眼药水和加标人体血浆中的妥布霉素(TOB)。由于TOB缺乏吸收紫外线的发色团和天然荧光,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)对TOB进行柱前衍生。实验设计用于优化衍生步骤。将所得的高度荧光稳定的衍生物在C18柱上进行色谱分离,并使用甲醇:水(60:40,v / v)以1 mL min -1 的流速洗脱。使用了荧光检测器(λex390和λem480 nm)。该方法在20–200 ng mL -1 浓度范围内是线性的。提出了荧光产物的结构,然后对该方法进行了验证,并将其用于测定人血浆中的TOB。将结果与参考方法进行统计学比较,发现无显着差异。

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