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采用高效液相色谱荧光检测法测定猫血浆中 GS-441524 浓度。

Quantification of GS-441524 concentration in feline plasma using high performance liquid chromatography with fluorescence detection.

机构信息

Sydney School of Veterinary Science, The University of Sydney, Camperdown, New South Wales, Australia.

出版信息

Vet Q. 2023 Dec;43(1):1-9. doi: 10.1080/01652176.2023.2246553.

DOI:10.1080/01652176.2023.2246553
PMID:37556736
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10438854/
Abstract

The adenosine analogue GS-441524 has demonstrated efficacy in treatment of feline infectious peritonitis (FIP). With no commercially registered formulations of GS-441524 available, global focus shifted to its pro-drug remdesivir, as it became more accessible throughout the COVID-19 pandemic. This study developed and validated a simple liquid chromatography equipped with a fluorescence detector to quantify plasma concentrations of GS-441524 applicable for routine therapeutic monitoring of remdesivir or GS-441524 therapy for FIP infected cats. A Waters X-Bridge C18, 5 µm, 150 × 4.6 mm, column was used and mixtures of 20 mM ammonium acetate (pH 4.5) with acetonitrile of 5% and 70% were prepared for gradient mobile phase. With a simple protein precipitation using methanol to clean plasma sample, GS-441524 was monitored at excitation and emission wavelengths of 250 nm and 475 nm, respectively. Using an external standard, the lowest and highest limits of quantification were 19.5 ng/mL to 10,000 ng/mL, respectively. The intra- and inter day trueness of the quality controls (QCs) were within 10% of their nominal concentrations and intra- and inter day precision of the QCs (expressed as the coefficient of variation) ranged from 1.7 to 5.7%, This assay was able to quantify plasma trough levels of GS-441524 (23.7-190.1 ng/mL) after the administration of remdesivir (9.9-15.0 mg/kg BW, IV or SC) in FIP cats ( = 12). Accordingly, this study generated an alternative and cost-effective way to quantify GS-441524 in feline biological fluids at least up to 24 hr after administrations of remdesivir.

摘要

腺苷类似物 GS-441524 已被证明在猫传染性腹膜炎 (FIP) 的治疗中有效。由于没有可商购的 GS-441524 制剂,因此在整个 COVID-19 大流行期间,人们的注意力转向了它的前药瑞德西韦,因为瑞德西韦更容易获得。本研究开发并验证了一种简单的配备荧光检测器的液相色谱法,可定量检测 GS-441524 的血浆浓度,适用于瑞德西韦或 GS-441524 治疗 FIP 感染猫的常规治疗监测。使用 Waters X-Bridge C18,5μm,150×4.6mm 柱,并制备 20mM 乙酸铵 (pH 4.5) 与 5%和 70%乙腈的混合物作为梯度流动相。通过使用甲醇进行简单的蛋白沉淀来净化血浆样品,在激发和发射波长分别为 250nm 和 475nm 时监测 GS-441524。使用外标法,定量下限和定量上限分别为 19.5ng/mL 至 10,000ng/mL。质控 (QC) 的日内和日间准确度均在其名义浓度的 10%以内,QC 的日内和日间精密度(表示为变异系数)在 1.7%至 5.7%之间。该测定法能够在 FIP 猫( = 12)给予瑞德西韦(9.9-15.0mg/kg BW,IV 或 SC)后至少 24 小时内定量检测 GS-441524 的血浆谷水平 (23.7-190.1ng/mL)。因此,本研究提供了一种替代且具有成本效益的方法,可在给予瑞德西韦后至少 24 小时内定量检测猫生物体液中的 GS-441524。

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本文引用的文献

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ADME and Pharmacokinetic Properties of Remdesivir: Its Drug Interaction Potential.瑞德西韦的吸收、分布、代谢、排泄及药代动力学特性:其药物相互作用潜力
Pharmaceuticals (Basel). 2021 Jul 8;14(7):655. doi: 10.3390/ph14070655.
2
Quantitative HPLC-MS/MS determination of Nuc, the active metabolite of remdesivir, and its pharmacokinetics in rat.定量高效液相色谱-串联质谱法测定瑞德西韦的活性代谢产物 Nuc 在大鼠体内的药代动力学。
Anal Bioanal Chem. 2021 Sep;413(23):5811-5820. doi: 10.1007/s00216-021-03561-8. Epub 2021 Jul 24.
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Accelerated stability study of the ester prodrug remdesivir: Recently FDA-approved Covid-19 antiviral using reversed-phase-HPLC with fluorimetric and diode array detection.
Assessing stability of remdesivir (GS-5734) and conversion to GS-441524 in feline plasma and whole blood.
评估瑞德西韦(GS-5734)在猫血浆和全血中的稳定性以及向GS-441524的转化。
Vet Q. 2024 Dec;44(1):1-9. doi: 10.1080/01652176.2024.2305731. Epub 2024 Jan 30.
酯前药瑞德西韦的稳定性加速研究:最近 FDA 批准的用于治疗 COVID-19 的抗病毒药物,采用反相高效液相色谱法,荧光和二极管阵列检测。
Biomed Chromatogr. 2021 Dec;35(12):e5212. doi: 10.1002/bmc.5212. Epub 2021 Aug 9.
4
Simultaneous quantification of seven repurposed COVID-19 drugs remdesivir (plus metabolite GS-441524), chloroquine, hydroxychloroquine, lopinavir, ritonavir, favipiravir and azithromycin by a two-dimensional isotope dilution LC-MS/MS method in human serum.一种二维同位素稀释 LC-MS/MS 方法同时定量测定人血清中的七种已批准用于治疗 COVID-19 的药物:瑞德西韦(及其代谢物 GS-441524)、氯喹、羟氯喹、洛匹那韦、利托那韦、法匹拉韦和阿奇霉素。
J Pharm Biomed Anal. 2021 Mar 20;196:113935. doi: 10.1016/j.jpba.2021.113935. Epub 2021 Jan 28.
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Clin Chem Lab Med. 2020 Jun 22;58(9):1461-1468. doi: 10.1515/cclm-2020-0612. Print 2020 Aug 27.
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Remdesivir for the Treatment of Covid-19 - Final Report.瑞德西韦治疗 COVID-19 的疗效 - 最终报告。
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Probable Molecular Mechanism of Remdesivir for the Treatment of COVID-19: Need to Know More.瑞德西韦治疗 COVID-19 的可能分子机制:需要了解更多。
Arch Med Res. 2020 Aug;51(6):585-586. doi: 10.1016/j.arcmed.2020.05.001. Epub 2020 May 12.