一种灵敏、快速、经济高效的 RP-HPLC-UV 方法,用于检测和定量生理液(pH 值为 7.4)中的贝达喹啉。

IF 2.7 3区 化学 Q2 CHEMISTRY, ANALYTICAL Analytical Methods Pub Date : 2024-09-11 DOI:10.1039/D4AY01143K
Simisola Ayodele, Armorel D. van Eyk, Pradeep Kumar and Yahya E. Choonara
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引用次数: 0

摘要

贝达喹啉是一种高亲脂性分子,用于治疗耐多药结核病。肺结核的一种罕见并发症是结核性心包炎。利用动物心包进行的体内外研究可用于调查这种药物是否能穿过心包组织扩散到模拟心包液(pH 值为 7.4)中,以显示其疗效。要检测生理液体中的贝达喹啉,必须采用快速、经济、灵敏的方法。因此,本研究的目的是开发并验证一种简单灵敏的 RP-HPLC-UV 方法,用于检测和定量包裹在纳米系统中的贝达喹啉在 pH 值为 7.4 时透过切除心包后的含量。采用 HPLC Phenomenex Kinetex RPC18 色谱柱(150 x 4.6 mm,5 µm)进行分析。流动相为 95:5 v/v (A:B),其中 (A) 甲醇:乙腈(85:15 v/v):(B)三乙胺(1% v/v):0.15 mM KH2PO4 缓冲液(pH 7.4)。运行条件如下:进样量 20 µl,流速 1.0 ml.min-1,检测波长 275 nm,温度 25oC,运行时间 5 分钟。贝达喹啉以单个对称峰洗脱,保留时间为 4.17 分钟。该方法在 1 - 50 μg.ml-1 范围内线性关系良好(R2 = 1)。检出限(LOD)和定量限(LOQ)分别为 0.05 μg.ml-1 和 0.15 μg.ml-1(信噪比法)。所有验证参数均在可接受范围内(RSD<2%)。该方法在模拟生理液(pH 7.4)中检测贝达喹啉具有快速、可靠、准确、重现性好和瞬时等特点。因此,该方法可用于轻松检测体液(pH 值为 7.4)(即血液和心包液)中的贝达喹啉,其准确性不会受到分子电离因子的影响。
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 sensitive, rapid and cost-effective RP-HPLC-UV method for detection and quantification of bedaquiline in physiological fluid (pH 7.4)

Bedaquiline, a highly lipophilic molecule, is used in the treatment regimen of multi-drug resistant tuberculosis. A rare complication of pulmonary tuberculosis is tuberculous pericarditis. Ex vivo studies utilising animal pericardium can be used to investigate whether this drug is capable of diffusing across pericardial tissue into simulated pericardial fluid (pH 7.4) to indicate efficacy. For detection of bedaquiline in physiological fluid, a rapid, cost-effective and sensitive method is essential. The aim of this study was thus to develop and validate a simple and sensitive RP-HPLC-UV method for the detection and quantification of bedaquiline, encapsulated in a nanosystem, at pH 7.4 after permeation across excised pericardium. A HPLC Phenomenex Kinetex RPC18 column (150 × 4.6 mm, 5 μm) was utilized for analysis. The mobile phase consisted of 95 : 5 v/v (A : B), where (A) methanol : acetonitrile (85 : 15 v/v) : (B) triethylamine (1% v/v) : 0.15 mM KH2PO4 buffer (pH 7.4). Running conditions included the following: injection volume 20 μl, flow rate 1.0 ml min−1, detection wavelength 275 nm, 25 °C and running time of 5 min. Bedaquiline eluted as a single symmetrical peak at a retention time of 4.17 min. The method was found to be linear within the range of 1–50 μg ml−1 (R2 = 1). The limit of detection (LOD) and limit of quantification (LOQ) were found to be 0.05 μg ml−1 and 0.15 μg ml−1, respectively (signal-to-noise ratio method). All validation parameters were found to be within acceptable limits (RSD < 2%). The method was fast, reliable, accurate, reproducible, and transient for the detection of bedaquiline in simulated physiological fluid (pH 7.4). This method can thus be applied to easily detect bedaquiline in body fluids (pH 7.4) i.e. blood and pericardial fluid without the accuracy being impacted by ionisation factors of the molecule.

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来源期刊
Analytical Methods
Analytical Methods CHEMISTRY, ANALYTICAL-FOOD SCIENCE & TECHNOLOGY
CiteScore
5.10
自引率
3.20%
发文量
569
审稿时长
1.8 months
期刊介绍: Early applied demonstrations of new analytical methods with clear societal impact
期刊最新文献
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