高效液相色谱-质谱法测定房水中氧氟沙星浓度。

Analytical Chemistry Insights Pub Date : 2014-05-05 eCollection Date: 2014-01-01 DOI:10.4137/ACI.S13857
Panagiotis Plotas, Charalampos Anastasopoulos, Olga E Makri, Michalis Leotsinidis, Constantine D Georgakopoulos
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引用次数: 11

摘要

以妥布霉素为内标,建立了一种快速、简便、特异的超高效液相色谱-质谱法定量分析人房水中氧氟沙星的方法。色谱分离采用Waters Acquity UPLC BEH C18 Shield柱(150 × 2.1 mm, 1.7 μm),以含0.1%甲酸的95:5水:乙腈(v/v)洗脱,流速为0.3 mL/min。总分析时间为3分钟,氧氟沙星洗脱时间为1.67±0.03分钟。方法的线性范围为0.1 ~ 8 μg/mL, r2 = 0.998。根据FDA指南对该方法进行了线性、准确性、精密度、特异性和稳定性的验证。检测限和定量限分别为0.03和0.10 μg/mL。所开发的方法已成功地应用于从患者身上获得的样品的分析。
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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A UPLC-MS Method for the Determination of Ofloxacin Concentrations in Aqueous Humor.

A rapid, simple, and specific method based on ultra performance liquid chromatography (UPLC) with mass spectrometry detection has been developed for quantitative analysis of ofloxacin in human aqueous humor using tobramycin as internal standard (IS). Chromatographic separation was achieved on a Waters Acquity UPLC BEH C18 Shield column (150 × 2.1 mm, 1.7 μm) eluted with 95:5 water: acetonitrile (v/v) containing 0.1% formic acid and a flow rate of 0.3 mL/minute. The total analysis time was three minutes with ofloxacin eluting at 1.67 ± 0.03 minutes. The linearity of the method ranged from 0.1 to 8 μg/mL with r2 = 0.998. The method was validated according to FDA guidelines with respect to linearity, accuracy, precision, specificity, and stability. The limits of detection and quantification were 0.03 and 0.10 μg/mL, respectively. The developed method was successfully applied to the analysis of samples that have been obtained from patients.

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