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采用超临界流体色谱法,用紫外和蒸发光散射检测法测定药物与其反离子的化学计量比:奥丹司琼盐酸盐的应用。

Determination of the stoichiometry between a drug and its counter-ion by supercritical fluid chromatography using ultra-violet and evaporative light scattering detections: Application to ondansetron hydrochloride.

机构信息

Univ Lille, CHU Lille, ULR 7365, GRITA, Groupe de Recherche sur Les Formes Injectables et Technologies Associées, F-59000, Lille, France.

Univ Lille, CHU Lille, ULR 7365, GRITA, Groupe de Recherche sur Les Formes Injectables et Technologies Associées, F-59000, Lille, France.

出版信息

Talanta. 2020 Oct 1;218:121166. doi: 10.1016/j.talanta.2020.121166. Epub 2020 May 22.

Abstract

In this paper, a supercritical fluid chromatography method using ultra-violet and evaporative light scattering detections (SFC-UV/ELSD) has been developed and validated for the stoichiometry determination of an antiemetic drug with its counter-ion i.e. ondansetron hydrochloride. Seven stationary phases were first screened using a CO-methanol-diethylamine mobile phase. Best conditions were determined using Derringer's desirability functions regarding chromatographic separation: selectivity, resolution, peak shape and runtime. The influence of co-solvent composition on resolution was evaluated. After optimization, best chromatographic results were obtained using 2-ethylpyridine stationary phase and a co-solvent composed of 0.2% diethylamine and 2% water in methanol. While ondansetron was quantified using UV detection (214 nm) and an external calibration curve, the determination of chloride was carried out using ELSD and an internal calibration curve. Then, the method was validated using the accuracy profile approach with a total error included in the ±10%. Finally, the proposed method was applied for the determination of the molar ratio between ondansetron and chloride. A value of 1.001 ± 0.003 demonstrated that the stoichiometry of this drug with its counter-ion was 1:1.

摘要

本文建立并验证了一种超临界流体色谱法,采用紫外和蒸发光散射检测(SFC-UV/ELSD),用于测定止吐药物及其反离子盐酸昂丹司琼的化学计量比。首先,使用 CO-甲醇-二乙胺流动相筛选了七种固定相。使用 Derringer 的适宜性函数来评估色谱分离的选择性、分辨率、峰形和运行时间,确定了最佳条件。评估了共溶剂组成对分辨率的影响。优化后,在甲醇中使用 0.2%二乙胺和 2%水组成的共溶剂,在 2-乙基吡啶固定相上获得最佳色谱结果。虽然昂丹司琼采用 UV 检测(214nm)和外标校准曲线进行定量,但是氯离子的测定采用 ELSD 和内标校准曲线。然后,采用准确度轮廓法验证方法,总误差在±10%以内。最后,该方法用于测定昂丹司琼与氯离子的摩尔比。得到的摩尔比为 1.001±0.003,表明该药物与其反离子的化学计量比为 1:1。

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