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采用 LC-MS/MS 定量测定强效香叶基香叶基二磷酸合酶抑制剂:衍生化及应用。

Quantitative determination of a potent geranylgeranyl diphosphate synthase inhibitor using LC-MS/MS: Derivatization and application.

机构信息

Department of Pharmacy Practice, University of Nebraska Medical Center, Omaha, NE 68198, United States.

Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE 68198, United States.

出版信息

J Pharm Biomed Anal. 2018 May 10;153:22-28. doi: 10.1016/j.jpba.2018.02.010. Epub 2018 Feb 6.

Abstract

An isomeric mixture of homogeranyl/homoneryl triazole bisphosphonates (VSW1198) has previously been shown to be a potent inhibitor of geranylgeranyl diphosphate (GGDP) synthase (GGDPS) and of therapeutic interest for the treatment of multiple myeloma. We have developed and validated a selective and sensitive liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) method for the simultaneous quantitation of both the E- and Z- isomers of VSW1198 in cell culture media, mouse plasma and tissues. VSW1198 and internal standard are extracted from the bio-matrices by solid-phase extraction, followed by derivatization using trimethylsilyldiazomethane. The chromatographic separation of analytes was achieved on a Phenomenex Gemini NX column (150 mm * 2.0 mm, 5 μ) with gradient elution using 0.1% acetic acid and methanol/acetonitrile (1:1) as the mobile phase at a flow rate of 0.2 mL/min. Derivatized analytes were ionized with an electrospray ionization source in positive multiple reaction monitoring (MRM) mode and quantitated using MS/MS. The MS/MS response was linear over the concentration range from 0.38-1500 and 0.13-500 ng/mL for the E- and Z-isomers, respectively. The within- and between-day precision (relative standard deviation, % RSD) and accuracy were within the acceptable limits per FDA guidelines. The validated method was used for quantitative determination of the compounds in preclinical studies focused on the development of VSW1198 as a novel anti-cancer agent.

摘要

先前已经证明,同型香叶基/香叶基三唑双膦酸盐(VSW1198)的立体异构体混合物是一种有效的法尼基二磷酸合酶(GGDPS)抑制剂,并且对治疗多发性骨髓瘤具有治疗意义。我们已经开发并验证了一种选择性和灵敏的液相色谱-串联质谱(LC-MS/MS)方法,用于同时定量细胞培养介质、小鼠血浆和组织中 VSW1198 的 E-和 Z-异构体。VSW1198 和内标通过固相萃取从生物基质中提取,然后用三甲基硅基重氮甲烷进行衍生化。分析物的色谱分离在 Phenomenex Gemini NX 柱(150mm*2.0mm,5μm)上实现,使用 0.1%乙酸和甲醇/乙腈(1:1)作为流动相,以 0.2mL/min 的流速进行梯度洗脱。衍生化的分析物在电喷雾电离源中以正多重反应监测(MRM)模式进行离子化,并通过 MS/MS 定量。E-和 Z-异构体的 MS/MS 响应在 0.38-1500 和 0.13-500ng/mL 的浓度范围内呈线性。按照 FDA 指南,日内和日间精密度(相对标准偏差,%RSD)和准确度均在可接受范围内。该验证方法用于定量测定临床前研究中化合物的含量,这些研究专注于开发 VSW1198 作为新型抗癌药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddff/5857472/96a069a5eade/nihms945001f1.jpg

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