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一种用于定量大鼠和狨猴血浆中LY-354,740的高效液相色谱-串联质谱法的开发与验证

Development and validation of a high-performance liquid chromatography-tandem mass spectrometry method to quantify LY-354,740 in rat and marmoset plasma.

作者信息

Gaudette Fleur, Hamadjida Adjia, Bédard Dominique, Nuara Stephen G, Beaudry Francis, Huot Philippe

机构信息

CRCHUM, Centre de Recherche du Centre Hospitalier de l'Université de Montréal, Montreal, Quebec, Canada.

CRCHUM, Centre de Recherche du Centre Hospitalier de l'Université de Montréal, Montreal, Quebec, Canada.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2017 Sep 1;1061-1062:392-398. doi: 10.1016/j.jchromb.2017.07.007. Epub 2017 Jul 15.

DOI:10.1016/j.jchromb.2017.07.007
PMID:28802219
Abstract

LY-354,740 (eglumegad) is a selective and potent agonist of the metabotropic glutamate group II receptors (mGluR2,3) that has already entered clinical trials as a potential anti-psychotic agent and therefore has well-documented pharmacokinetic (PK), safety and tolerability profiles in human. Whereas its development as an anti-psychotic agent has not been pursued, LY-354,740 may have potential in other neuroscience-related fields, notably anxiety and neuro-protection. The common marmoset is a small primate that has long been used in neuroscience. However, given its small size and small circulating blood volume, conducting PK studies to determine the therapeutic effectiveness of LY-354,740 at clinically-relevant doses is challenging. Here, we have developed and validated a simple, sensitive and selective analytical method that enables quantification of LY-354,740 using a small volume of plasma. The analytical method consisted of protein precipitation followed by high-performance liquid chromatography with heat assisted electrospray ionisation mass spectrometry (UHPLC-HESI-MS/MS). The chromatographic separation was achieved using gradient elution with a mobile phase consisting of acetonitrile and 10mM ammonium formate (pH 3) on a Thermo Scientific Acclaim Trinity P1 analytical column (100x3.0mm I.D., 3μm) operating at 45°C and at a flow rate of 900μl/min. The method displays a linear relationship ranging from 20.0 to 5000ng/ml. Intra- and inter-day relative standard deviations are less than 5.7% and 7.0%, respectively and the accuracy ranged from 91.0 to 106.0%. The UHPLC-HESI-MS/MS analytical method we describe here is simple, sensitive, specific and capable of quantifying LY-354,740 in both rat and marmoset plasma, and is suitable to conduct PK studies after a single sub-cutaneous dose of 1.0mg/kg or lower in both species.

摘要

LY-354,740(依格鲁美)是一种对代谢型谷氨酸II组受体(mGluR2,3)具有选择性且强效的激动剂,它已作为一种潜在的抗精神病药物进入临床试验阶段,因此在人体中具有充分记录的药代动力学(PK)、安全性和耐受性特征。尽管其作为抗精神病药物的研发工作尚未继续推进,但LY-354,740可能在其他神经科学相关领域具有潜力,特别是在焦虑症和神经保护方面。普通狨猴是一种长期用于神经科学研究的小型灵长类动物。然而,鉴于其体型小且循环血量少,进行PK研究以确定LY-354,740在临床相关剂量下的治疗效果具有挑战性。在此,我们开发并验证了一种简单、灵敏且具有选择性的分析方法,该方法能够使用少量血浆对LY-354,740进行定量分析。该分析方法包括蛋白沉淀,随后采用热辅助电喷雾电离质谱联用的高效液相色谱法(UHPLC-HESI-MS/MS)。色谱分离通过梯度洗脱实现,流动相由乙腈和10mM甲酸铵(pH 3)组成,在Thermo Scientific Acclaim Trinity P1分析柱(内径100x3.0mm,3μm)上进行,柱温45°C,流速900μl/min。该方法在20.0至5000ng/ml范围内呈线性关系。日内和日间相对标准偏差分别小于5.7%和7.0%,准确度范围为91.0%至106.0%。我们在此描述的UHPLC-HESI-MS/MS分析方法简单、灵敏、特异,能够对大鼠和狨猴血浆中的LY-354,740进行定量分析,适用于在两种动物单次皮下注射1.0mg/kg或更低剂量后进行PK研究。

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