Department of Pharmaceutical Biochemistry, College of Pharmacy, Kyung Hee University, Seoul 02447, Republic of Korea.
Department of Biomedical and Pharmaceutical Science, Graduate School, Kyung Hee University, Seoul 02447, Republic of Korea.
Molecules. 2023 Mar 3;28(5):2352. doi: 10.3390/molecules28052352.
This study aimed to establish a simple and sensitive analytical method to simultaneously quantify donepezil (DPZ) and tadalafil (TAD) in rat plasma using lansoprazole (LPZ) as an internal standard (IS) by using liquid chromatography tandem mass spectrometry. The fragmentation pattern of DPZ, TAD, and IS was elucidated using multiple reaction monitoring in electrospray ionization positive ion mode for the quantification of precursor to production at / 380.1 → 91.2 for DPZ, / 390.2 → 268.1 for TAD, and / 370.3 → 252.0 for LPZ. The extracted DPZ and TAD from plasma using acetonitrile-induced protein precipitation was separated using Kinetex C18 (100 × 2.1 mm, 2.6 µm) column with a gradient mobile phase system consisting of 2 mM ammonium acetate and 0.1% formic acid in acetonitrile at a flow rate of 0.25 mL/min for 4 min. The selectivity, lower limit of quantification, linearity, precision, accuracy, stability, recovery, and matrix effect of this developed method was validated according to the guidelines of the U.S. Food and Drug Administration and the Ministry of Food and Drug Safety of Korea. The established method achieved acceptance criteria in all validation parameters, ensuring reliability, reproducibility, and accuracy, and was successfully implemented in a pharmacokinetic study on the co-administration of DPZ and TAD orally in rats.
本研究旨在建立一种简单灵敏的分析方法,采用兰索拉唑(LPZ)作为内标,通过液相色谱串联质谱法同时定量测定大鼠血浆中的多奈哌齐(DPZ)和他达拉非(TAD)。采用电喷雾正离子模式多反应监测,解析 DPZ、TAD 和 IS 的碎裂模式,用于定量前体到产物的 / 380.1→91.2 DPZ、/ 390.2→268.1 TAD 和 / 370.3→252.0 LPZ。采用乙腈诱导的蛋白沉淀从血浆中提取 DPZ 和 TAD,采用 Kinetex C18(100×2.1mm,2.6µm)柱,以含有 2mM 乙酸铵和 0.1%甲酸的乙腈作为流动相系统,梯度洗脱,流速为 0.25mL/min,洗脱时间为 4min。根据美国食品和药物管理局和韩国食品药品安全部的指导原则,对该方法的选择性、定量下限、线性、精密度、准确度、稳定性、回收率和基质效应进行了验证。该方法在所有验证参数中均达到了可接受标准,确保了可靠性、重现性和准确性,并成功应用于大鼠口服 DPZ 和 TAD 联合给药的药代动力学研究。