Development and Validation of Rapid and Cost-Effective RP-HPLC/UV Method for Determination of Cetirizine/Levocetirizine in Blood Plasma of Smokers and Non Smokers: a Two Cohort Comparative Study.

IF 1.5 4区 化学 Q4 BIOCHEMICAL RESEARCH METHODS
Mashal Khattak, Zafar Iqbal, Asif Jan, Niaz Ali, Fazli Nasir, Naila Shahbaz
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Abstract

In this research study, a simple, rapid, sensitive, and cost-effective Reverse Phase High Performance Liquid Chromatography method was developed and validated for determination of Cetirizine and Levocetirizine in human plasma. The drugs were separated on an ACE Generix100-5 C18 RP (250 × 4.6 mm, 5 μm) column, using Acetonitrile and Distilled water pH 7 (59:41 v/v) as mobile phase with a flow rate of 1.5 mL/min, retention time of 3.39 ± 0.02 min, detection wavelength of 230 nm, and column oven temperature at 26°C. The drug was extracted from human plasma using Methanol, the percent recovery was 97%. The LOD and LOQ for Cetirizine and Levocetirizine were 0.5 ng and 1 ng. The method was linear over the concentration range of 0.5-1000 ng /mL for Cetirizine and Levocetirizine. The method was applied for analysis of drugs in plasma following oral administration of Cetirizine (10 mg) and Levocetirizine (5 mg) in smokers and nonsmokers of Pashtun ethnicity belonging from different districts of Khyber Pakhtunkhwa, Pakistan. The difference between Cetirizine plasma levels in smokers and non-smokers was significant with p -value 0.0279.

用于检测吸烟者和非吸烟者血浆中西替利津/左西替利津含量的快速、经济高效的 RP-HPLC/UV 方法的开发与验证:一项双队列比较研究。
本研究开发并验证了一种简单、快速、灵敏且经济高效的反相高效液相色谱法,用于测定人体血浆中的西替利嗪和左西替利嗪。采用 ACE Generix100-5 C18 RP(250 × 4.6 mm,5 μm)色谱柱,以乙腈和 pH 值为 7 的蒸馏水(59:41 v/v)为流动相,流速为 1.5 mL/min,保留时间为 3.39 ± 0.02 min,检测波长为 230 nm,柱温为 26°C。使用甲醇从人体血浆中提取药物,回收率为 97%。西替利嗪和左西替利嗪的检出限和定量限分别为 0.5 ng 和 1 ng。西替利嗪和左西替利嗪在 0.5-1000 纳克/毫升的浓度范围内呈线性关系。该方法用于分析巴基斯坦开伯尔巴图克瓦省不同地区的普什图族吸烟者和非吸烟者口服西替利嗪(10 毫克)和左西替利嗪(5 毫克)后血浆中药物的含量。吸烟者和非吸烟者的西替利嗪血浆水平差异显著,P 值为 0.0279。
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来源期刊
CiteScore
2.90
自引率
7.70%
发文量
94
审稿时长
5.6 months
期刊介绍: The Journal of Chromatographic Science is devoted to the dissemination of information concerning all methods of chromatographic analysis. The standard manuscript is a description of recent original research that covers any or all phases of a specific separation problem, principle, or method. Manuscripts which have a high degree of novelty and fundamental significance to the field of separation science are particularly encouraged. It is expected the authors will clearly state in the Introduction how their method compares in some markedly new and improved way to previous published related methods. Analytical performance characteristics of new methods including sensitivity, tested limits of detection or quantification, accuracy, precision, and specificity should be provided. Manuscripts which describe a straightforward extension of a known analytical method or an application to a previously analyzed and/or uncomplicated sample matrix will not normally be reviewed favorably. Manuscripts in which mass spectrometry is the dominant analytical method and chromatography is of marked secondary importance may be declined.
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