Wits Advanced Drug Delivery Platform Research Unit, Department of Pharmacy and Pharmacology, School of Therapeutic Sciences, Faculty of Health Sciences, University of the Witwatersrand, 7 York Road, Parktown, Johannesburg, 2193, South Africa.
Division of Pharmacology, Department of Pharmacy and Pharmacology, University of the Witwatersrand, 7 York Road, Parktown, Johannesburg, 2193, South Africa.
Anal Methods. 2024 Oct 31;16(42):7169-7177. doi: 10.1039/d4ay01143k.
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. 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 KHPO buffer (pH 7.4). Running conditions included the following: injection volume 20 μl, flow rate 1.0 ml min, 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). The limit of detection (LOD) and limit of quantification (LOQ) were found to be 0.05 μg ml and 0.15 μg ml, 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) blood and pericardial fluid without the accuracy being impacted by ionisation factors of the molecule.
贝达喹啉是一种高度亲脂性分子,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研究可以用来研究这种药物是否能够穿过心包组织扩散到模拟心包液(pH7.4)中,以表明其疗效。为了检测生理液中的贝达喹啉,需要一种快速、经济高效且灵敏的方法。因此,本研究旨在开发和验证一种简单灵敏的反相高效液相色谱-紫外法,用于检测和定量 pH7.4 下穿过离体心包的纳米系统包封的贝达喹啉。采用 Phenomenex Kinetex RPC18 柱(150×4.6mm,5μm)进行分析。流动相由 95:5v/v(A:B)组成,其中(A)甲醇:乙腈(85:15v/v):(B)三乙胺(1%v/v):0.15mM KH2PO4 缓冲液(pH7.4)。运行条件包括:进样体积 20μl,流速 1.0ml min,检测波长 275nm,25°C,运行时间 5min。贝达喹啉在 4.17min 时洗脱为单个对称峰。该方法在 1-50μg ml( = 1)范围内呈线性。检测限(LOD)和定量限(LOQ)分别为 0.05μg ml 和 0.15μg ml(信噪比法)。所有验证参数均在可接受范围内(RSD<2%)。该方法快速、可靠、准确、重现性好,可用于检测模拟生理液(pH7.4)中的贝达喹啉。因此,该方法可用于在不影响分子电离因子的情况下,轻松检测血液和心包液等体液中的贝达喹啉。