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脂质体阿苯达唑在天然细粒棘球蚴感染绵羊体内的药代动力学和组织分布研究:一种经验证的 UPLC-Q-TOF-MS 方法。

Pharmacokinetics and tissue distribution study of liposomal albendazole in naturally Echinococcus granulosus infected sheep by a validated UPLC-Q-TOF-MS method.

机构信息

Department of Pharmacy, The First Affiliated Hospital of Xinjiang Medical University, Urumqi 830054, PR China; College of Pharmacy, Xinjiang Medical University, Urumqi 830011, PR China.

Department of Pharmacy, The First Affiliated Hospital of Xinjiang Medical University, Urumqi 830054, PR China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2020 Mar 15;1141:122016. doi: 10.1016/j.jchromb.2020.122016. Epub 2020 Feb 1.

Abstract

Albendazole (ABZ) is the first-line drug in treating echinococcosis, which is recommended by WHO. To address the poor bioavailability of albendazole, liposomal albendazole was formulated and is available in our hospital for many years. In this study, a sensitive, reliable and accurate UPLC-Q-TOF-MS method was developed and validated for the determination of albendazole and its metabolites, albendazole sulfoxide (ABZSO), albendazole sulfone (ABZSO) and albendazole-2-aminosulfone (ABZSONH) in naturally echinococcus granulosus (E. granulosus) infected sheep plasma and tissues with mebendazole (MBZ) as the internal standard (IS). Plasma and tissues samples were prepared by protein precipitation method. The separation was performed on an ACQUITY UPLC® BEH C18 column (2.1 × 50 mm, 1.7 μm) with a gradient mobile phase consisting of methanol and water containing 0.1% formic acid at 0.4 mL/min. The detection was performed on a quadrupole time-of-flight (Q-TOF) high-resolution mass spectrometer using positive electrospray ionization (ESI) source with a chromatographic run time of 6.0 min. The detection was operated using target ions of [M + H] at m/z 266.096 for ABZ, m/z 282.091 for ABZSO, m/z 298.086 for ABZSO, m/z 240.081 for ABZSONH and m/z 296.104 for IS in selective ion mode, respectively. This method was validated in terms of selectivity, linearity, precision, accuracy, recovery, matrix effect, dilution effect, carryover effects, stability, calibration curve and LLOQ. All validation parameter results were within the acceptable range described in guideline for bioanalytical method validation. This method has been successfully applied to the pharmacokinetic study following single and multiple oral dose of 10 mg/kg liposomal albendazole, and tissue distribution study following multiple oral dose of 10 mg/kg, with emulsion albendazole as the reference preparation. The results in the article will provide valuable information for use in clinical applications of liposomal albendazole and also be beneficial for further development of liposomal albendazole in future studies.

摘要

阿苯达唑(ABZ)是治疗包虫病的一线药物,也是世界卫生组织推荐的药物。为了提高阿苯达唑的生物利用度,我们医院多年来一直使用脂质体阿苯达唑。本研究建立并验证了一种灵敏、可靠和准确的 UPLC-Q-TOF-MS 方法,用于测定自然感染细粒棘球蚴(E. granulosus)的绵羊血浆和组织中的阿苯达唑及其代谢物阿苯达唑砜(ABZSO)、阿苯达唑亚砜(ABZSO)和阿苯达唑-2-氨基砜(ABZSONH),以苯并咪唑(MBZ)为内标(IS)。血浆和组织样品采用蛋白沉淀法制备。采用 ACQUITY UPLC® BEH C18 柱(2.1×50mm,1.7μm)进行分离,流动相为甲醇和含 0.1%甲酸的水,梯度洗脱,流速为 0.4mL/min。采用正离子电喷雾电离源(ESI)在四极杆飞行时间(Q-TOF)高分辨质谱仪上进行检测,色谱运行时间为 6.0min。采用目标离子 [M+H]+,m/z 266.096 用于 ABZ,m/z 282.091 用于 ABZSO,m/z 298.086 用于 ABZSO,m/z 240.081 用于 ABZSONH,m/z 296.104 用于 IS,在选择离子模式下进行检测。本方法对选择性、线性、精密度、准确度、回收率、基质效应、稀释效应、交叉污染效应、稳定性、校准曲线和定量下限进行了验证。所有验证参数的结果均在指导生物分析方法验证的可接受范围内。本方法已成功应用于单剂量和多剂量 10mg/kg 脂质体阿苯达唑口服给药后的药代动力学研究,以及多剂量 10mg/kg 口服给药后的组织分布研究,以乳剂阿苯达唑为参比制剂。本研究结果将为临床应用脂质体阿苯达唑提供有价值的信息,也将有助于未来研究中进一步开发脂质体阿苯达唑。

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