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中空纤维液相微萃取与原位衍生化法测定生物流体中痕量盐酸二甲双胍(抗糖尿病药物)。

Hollow fiber liquid phase microextraction with in situ derivatization for the determination of trace amounts of metformin hydrochloride (anti-diabetic drug) in biological fluids.

机构信息

School of Chemical Sciences, Universiti Sains Malaysia, 11800 Penang, Malaysia.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2013 Dec 15;941:123-30. doi: 10.1016/j.jchromb.2013.10.007. Epub 2013 Oct 14.

DOI:10.1016/j.jchromb.2013.10.007
PMID:24200841
Abstract

A three phase hollow fiber liquid-phase microextraction with in situ derivatization (in situ HF-LPME) followed by high-performance liquid chromatography-ultraviolet detection (HPLC-UV) method was developed for the trace determination of metformin hydrochloride (MH) in biological fluids. A new derivatization agent pentafluorobenzoyl chloride (PFBC) was used. Several parameters that affect the derivatization and extraction efficiency were studied and optimized (i.e., type of organic solvent, volume of NaOH (4M) and derivatization agent in the donor phase, acceptor phase (HCl) concentration, stirring speed, temperature, time and salt addition). Under the optimum conditions (organic solvent, dihexyl ether; volume of NaOH (4M) and derivatization agent (10mg PFBC in 1mL acetonitrile) in the donor phase, 600 and100μL, respectively; acceptor phase, 100mM HCl (10μL); stirring speed, 300rpm; extraction time, 30min; derivatization temperature, 70°C; without addition of salt) an enrichment factor of 210-fold was achieved. Good linearity was observed over the range of 1-1000ngmL(-1) (r(2)=0.9998). The limits of detection and quantitation were 0.56 and 1.68ngmL(-1), respectively. The proposed method has been applied for the determination of MH in biological fluids (plasma and urine) and water samples. Prior to the microextraction treatment of plasma samples, deproteinization step using acetonitrile was conducted. The proposed method is simple, rapid, sensitive and suitable for the determination of MH in a variety of samples.

摘要

建立了一种采用三相中空纤维液相微萃取(原位 HF-LPME)并结合高效液相色谱-紫外检测(HPLC-UV)的方法,用于痕量测定生物体液中的盐酸二甲双胍(MH)。使用了一种新的衍生化试剂五氟苯甲酰氯(PFBC)。研究并优化了影响衍生化和萃取效率的几个参数(即有机溶剂的类型、供相中的 NaOH(4M)和衍生化试剂的体积、接受相(HCl)的浓度、搅拌速度、温度、时间和加盐)。在最佳条件下(有机溶剂为二己基醚;供相中的 NaOH(4M)和衍生化试剂(10mg PFBC 在 1mL 乙腈中)的体积分别为 600μL 和 10μL;接受相为 100mM HCl(10μL);搅拌速度为 300rpm;萃取时间为 30min;衍生化温度为 70°C;不加盐),可实现 210 倍的富集倍数。在 1-1000ngmL(-1) 范围内呈现良好的线性关系(r(2)=0.9998)。检测限和定量限分别为 0.56 和 1.68ngmL(-1)。该方法已应用于生物体液(血浆和尿液)和水样中 MH 的测定。在对血浆样品进行微萃取处理之前,先用乙腈进行了蛋白质沉淀步骤。该方法简单、快速、灵敏,适用于多种样品中 MH 的测定。

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