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Talanta. 2020 Jan 1;206:120172. doi: 10.1016/j.talanta.2019.120172. Epub 2019 Jul 27.
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NADPH oxidases as drug targets and biomarkers in neurodegenerative diseases: What is the evidence?NADPH 氧化酶作为神经退行性疾病的药物靶点和生物标志物:有何证据?
Free Radic Biol Med. 2017 Nov;112:387-396. doi: 10.1016/j.freeradbiomed.2017.08.006. Epub 2017 Aug 12.
4
Developing selective histone deacetylases (HDACs) inhibitors through ebselen and analogs.通过依布硒啉及其类似物开发选择性组蛋白去乙酰化酶(HDACs)抑制剂。
Drug Des Devel Ther. 2017 May 2;11:1369-1382. doi: 10.2147/DDDT.S124977. eCollection 2017.
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DNA methylation: a profile of methods and applications.DNA甲基化:方法与应用概述
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一种用于定量研究 NOX 抑制剂 R14 亚硫酸氢盐加合物的稳定性指示 LC-MS/MS 方法,用于药代动力学研究。

A stability indicating LC-MS/MS method for quantification of a NOX Inhibitor R14 in its bisulfite adduct form for pharmacokinetic studies.

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, Texas Southern University, Houston, TX 77004, USA.

Department of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston TX 77030, USA.

出版信息

J Pharm Biomed Anal. 2023 May 10;228:115326. doi: 10.1016/j.jpba.2023.115326. Epub 2023 Mar 6.

DOI:10.1016/j.jpba.2023.115326
PMID:36924633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10079374/
Abstract

R14, also known as NOX Inhibitor VII, is a potent inhibitor of NADPH oxidases (NOX) which has recently been identified as a novel agent targeting to triple-negative breast cancer. It is also rapidly degraded in collected pharmacokinetic plasma and blood samples even stored under - 70 °C. The purpose of this study was to develop a stability indicating LC-MS/MS assay that would be suitable for quantification of R14 in plasma and blood. In the presence of sodium sulfite under acidic pH, R14, an aryl lactam compound which is not a typically reactive compound for bisulfite addition, readily and completely converted to R14 bisulfite adduct, which was more stable in plasma and blood. The adduct has MRM transition at m/z 340.1-127.0 in negative mode and showed high sensitivity in LC-MS/MS quantification. Thus, monitoring the adduct provided a suitable way of quantitating R14 concentrations in mouse whole blood. The reacting conditions were optimized based on detecting R14 bisulfite adduct, and the assay was established and validated on a SCIEX 6500+ Triple Quad LC-MS/MS System. The method was then successfully adapted to pharmacokinetic studies after oral administration of R14 to mice.

摘要

R14,也称为 NOX 抑制剂 VII,是一种有效的烟酰胺腺嘌呤二核苷酸磷酸氧化酶(NOX)抑制剂,最近被确定为一种针对三阴性乳腺癌的新型靶向药物。即使在 -70°C 下储存,它也会在收集的药代动力学血浆和血液样本中迅速降解。本研究旨在开发一种适合于定量测定血浆和血液中 R14 的稳定性指示 LC-MS/MS 测定法。在酸性 pH 下亚硫酸钠的存在下,R14(一种芳基内酰胺化合物,不是通常用于亚硫酸氢盐加成的反应性化合物)很容易且完全转化为 R14 亚硫酸氢盐加合物,在血浆和血液中更稳定。加合物在负离子模式下具有 m/z 340.1-127.0 的 MRM 跃迁,在 LC-MS/MS 定量中具有高灵敏度。因此,监测加合物提供了一种定量测定小鼠全血中 R14 浓度的合适方法。根据检测 R14 亚硫酸氢盐加合物优化了反应条件,并在 SCIEX 6500+三重四极杆 LC-MS/MS 系统上建立和验证了该测定法。然后,该方法成功地适应了 R14 经口给予小鼠后的药代动力学研究。