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

Govindarajan Srinivasan, Asharani Indira Viswambaran
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引用次数: 0

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 in vitro Permeation Testing (IVPT), in vitro Release Testing (IVRT), Pharmacokinetic, Toxicology, Clinical studies, and in drug development program for the quantification of Efinaconazole.

验证LC-MS/MS技术测定血浆中艾非那康唑的含量。
背景:艾非那康唑是一种局部抗真菌药物,对脚趾甲真菌感染有效。此外,由于其在皮肤上的应用,表皮层发生最小的全身吸收,这导致血液中的可用浓度较低。虽然文献中报道的几种方法描述了使用HPTLC和HPLC等传统技术对艾菲那康唑进行定量,但这些方法缺乏必要的灵敏度和选择性,无法直接应用于生物样品的定量。目的:建立以血浆为生物样品,以氟康唑(FZ)为内标,采用串联质谱法(LC-MS/MS)定量埃非那康唑(EZ)的快速、特异、选择性和灵敏度高的方法。方法:采用Thermo Hypersil Gold (100 mm × 2.1 mm, 1.9 μm)超高效液相色谱柱,流动相为20%甲酸-水(0.1%)和80%甲醇。采用液液萃取法(LLE)制备样品。采用平行反应监测(PRM)模式下加热电喷雾电离(HESI)技术对艾非那康唑和内标进行检测。结果:该方法在1 ~ 2000 pg/mL (0.001 ~ 2 ng/mL)范围内呈线性关系。定量、低、中、高质量控制(QC)水平下限的精密度和准确度方差小于5%,准确度为99 ~ 103%。在各种条件下,包括在自动进样器中储存、在室温下储存、在深度冷冻室中储存以及在冻融循环后,都证实了长期稳定性。结论:经验证的LC-MS/MS方法具有灵敏度、特异性、选择性、分析速度快、样本量要求低、动态浓度范围宽、稳健性好、重复性好等优点,是体外渗透试验(IVPT)、体外释放试验(IVRT)、药代动力学、毒理学、临床研究、药物开发规划等领域对艾菲那康唑进行定量分析的重要工具。
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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CiteScore
1.60
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