一种简单灵敏的基于咪唑离子液体的改良反相液相色谱法,用于同时测定人体血浆样品中的β-受体阻滞剂

IF 1 4区 化学 Q4 CHEMISTRY, ANALYTICAL
Naflaa A. Aldawsari, Hassan M. AlBishri, Basmah H. Alshammari, Deia Abd El-Hady
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引用次数: 0

摘要

β-受体阻滞剂(β-受体阻滞剂)被广泛用于控制心律失常,由于人口老龄化和心脏负担患者人数的增加,β-受体阻滞剂的使用量在未来几年可能会增加。本研究采用离子液体(IL)修饰的反相液相色谱-紫外检测法同时测定了五种β受体阻滞剂(醋丁洛尔、吲哚洛尔、阿替洛尔、纳度洛尔和奥普洛尔),该方法简单、灵敏、可靠。色谱分离采用 ZORBAX® SB-C18 色谱柱,混合流动相为 50 µg/mL 1-丁基-3-甲基氯化咪唑,溶于 0.02 mol/L 磷酸盐缓冲液(pH 3.5)和乙腈(70:30, v/v)。色谱测量采用等度洗脱,流速为 1.0 mL/min,波长为 230 nm,柱温为 25°C。该方法适用于人体血浆基质,直接进样,分析时间短,仅需 12 分钟。阿替洛尔、醋丁洛尔和吲哚洛尔的线性范围为 3-500 ng/L,醋丁洛尔为 7-500 ng/L,奥司洛尔为 10-500 ng/L,测定系数为 0.999。阿替洛尔、纳多洛尔、醋丁洛尔、吲哚洛尔和奥司洛尔的检出限/定量限分别为 1.04/3.00、2.75/7.00、1.03/3.00、1.05/3.00 和 3.47/10.00 ng/L。日内和日间精密度结果均低于 2%。加入IL后,分析物的灵敏度提高了9-41倍。因此,该方法简便灵敏,可用于存在少量IL的β-受体阻滞剂的常规临床分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Simple and Sensitive Imidazolium-Based Ionic Liquid-Modified Reversed-Phase Liquid Chromatography Method for the Simultaneous Determination of Beta-Blockers in Human Plasma Samples

A Simple and Sensitive Imidazolium-Based Ionic Liquid-Modified Reversed-Phase Liquid Chromatography Method for the Simultaneous Determination of Beta-Blockers in Human Plasma Samples

Beta-blockers (β-blockers) are broadly used to manage cardiac arrhythmia, which could increase in the upcoming years due to the aging population and the increase in the number of patients with cardiac burden. In the current work, a simple, sensitive, and reliable simultaneous determination of five β-blockers (acebutolol, pindolol, atenolol, nadolol, and oxprenolol) was accomplished by ionic liquid (IL)-modified reversed-phase liquid chromatography with ultraviolet detection. The chromatographic separation was achieved on a ZORBAX® SB-C18 column using a hybrid mobile phase consisting of 50 µg/mL 1-butyl-3-methylimidazolium chloride dissolved in 0.02 mol/L phosphate buffer (pH 3.5) and acetonitrile (70 : 30, v/v). The chromatographic measurements were performed by isocratic elution at a 1.0 mL/min flow rate, 230 nm wavelength, and 25°C column temperature. The current method was applied to human plasma matrices by direct injection of samples with a short analysis time of 12 min. Good linearity was achieved in the range of 3–500 ng/L for atenolol, acebutolol, and pindolol, 7–500 ng/L for acebutolol, and 10–500 ng/L for oxprenolol with a 0.999 coefficient of determination. The limit of detection/limit of quantification values were 1.04/3.00, 2.75/7.00, 1.03/3.00, 1.05/3.00, and 3.47/10.00 ng/L for atenolol, nadolol, acebutolol, pindolol, and oxprenolol, respectively. Results of intra-day and inter-day precision were found to be less than 2%. The sensitivity enhancement factors of analytes due to the addition of IL ranged between 9- and 41-fold higher than that achieved in the absence of IL. Therefore, the proposed method could be used as a simple and sensitive analytical method for routine clinical analysis of β-blockers with the presence of a small amount of IL.

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来源期刊
Journal of Analytical Chemistry
Journal of Analytical Chemistry 化学-分析化学
CiteScore
2.10
自引率
9.10%
发文量
146
审稿时长
13 months
期刊介绍: The Journal of Analytical Chemistry is an international peer reviewed journal that covers theoretical and applied aspects of analytical chemistry; it informs the reader about new achievements in analytical methods, instruments and reagents. Ample space is devoted to problems arising in the analysis of vital media such as water and air. Consideration is given to the detection and determination of metal ions, anions, and various organic substances. The journal welcomes manuscripts from all countries in the English or Russian language.
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