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采用经过验证的液相色谱-串联质谱技术测定血浆中的艾氟康唑。

Determination of Efinaconazole in Plasma using Validated LC-MS/MS Technique.

作者信息

Srinivasan Govindarajan, Viswambaran Asharani Indira

机构信息

Department of Chemistry, School of Advanced Sciences, Vellore Institute of Technology, Vellore, 632 014, Tamil Nadu, India.

Advance Characterization Laboratory, Encube Ethicals Private Limited, Mumbai, India.

出版信息

Drug Metab Bioanal Lett. 2024;17(2):76-87. doi: 10.2174/0118723128348675241129100845.

Abstract

BACKGROUND

Efinaconazole is a topical antifungal medication that is effective against fungal infections of the toenails. In addition, due to its application on the skin, minimal systemic absorption takes place on the epidermic layer, which leads to the availability of lower-level concentration in the bloodstream. Although several reported methods in the literature describe the quantification of Efinaconazole using conventional techniques like HPTLC and HPLC, these methods lack the necessary sensitivity and selectivity to be directly applied for quantification in biological samples.

OBJECTIVE

Current research work aimed to develop a rapid, specific, selective, and sensitive method using plasma as one of the biological samples for quantification of Efinaconazole (EZ) in the presence of Fluconazole (FZ) as an internal standard by tandem mass spectrometry (LC-MS/MS).

METHODS

Chromatographic separation was achieved with a Thermo Hypersil Gold (100 mm x 2.1 mm, 1.9 μm) UPLC column using a mobile phase composed of 20% formic acid-water (0.1%) and 80% methanol. Liquid-liquid extraction (LLE) was employed for sample preparation. Efinaconazole and the internal standard were detected using the heated electrospray ionization (HESI) technique in parallel reaction monitoring (PRM) mode.

RESULTS

The developed method displayed a linearity range of 1 to 2000 pg/mL (0.001-2 ng/mL). Precision and accuracy for the lower limit of quantitation, low, mid, and high-quality control (QC) levels demonstrated a variance of less than 5% and an accuracy of 99 to 103%. Long-term stability was confirmed under various conditions, including storage in an auto-sampler, at room temperature, in a deep freezer, and after freeze-thaw cycles.

CONCLUSION

The validated LC-MS/MS method has exceptional sensitivity, specificity, selectivity, rapid analysis, minimal requirement of sample quantity, wide dynamic range of concentration, robustness, and reproducibility, making it an indispensable tool, especially in fields of Permeation Testing (IVPT), Release Testing (IVRT), Pharmacokinetic, Toxicology, Clinical studies, and in drug development program for the quantification of Efinaconazole.

摘要

背景

艾氟康唑是一种局部用抗真菌药物,对趾甲真菌感染有效。此外,由于其应用于皮肤,在表皮层的全身吸收极少,这导致血液中药物浓度较低。尽管文献中报道的几种方法描述了使用高效薄层色谱法(HPTLC)和高效液相色谱法(HPLC)等传统技术对艾氟康唑进行定量,但这些方法缺乏直接用于生物样品定量所需的灵敏度和选择性。

目的

当前的研究工作旨在开发一种快速、特异、选择性和灵敏的方法,以血浆作为生物样品之一,在以氟康唑(FZ)作为内标的情况下,通过串联质谱法(LC-MS/MS)对艾氟康唑(EZ)进行定量。

方法

采用Thermo Hypersil Gold(100 mm×2.1 mm,1.9μm)超高效液相色谱柱进行色谱分离,流动相由20%甲酸-水(0.1%)和80%甲醇组成。采用液-液萃取(LLE)进行样品制备。艾氟康唑和内标采用加热电喷雾电离(HESI)技术在平行反应监测(PRM)模式下进行检测。

结果

所开发的方法线性范围为1至2000 pg/mL(0.001 - 2 ng/mL)。定量下限、低、中、高浓度质量控制(QC)水平的精密度和准确度显示变异小于5%,准确度为99%至103%。在各种条件下均证实了长期稳定性,包括在自动进样器中储存、室温下、深冻冰箱中以及冻融循环后。

结论

经过验证的LC-MS/MS方法具有出色的灵敏度、特异性、选择性、快速分析、样品量要求极少、浓度动态范围宽、稳健性和重现性,使其成为一种不可或缺的工具,尤其在渗透试验(IVPT)、释放试验(IVRT)、药代动力学、毒理学、临床研究以及艾氟康唑定量的药物开发项目等领域。

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