建立并验证大鼠血浆中HR0019含量测定的液质联用分析方法文献综述

 2023-02-21 19:25:26

一、本课题的研究内容及目的基于HR0019这个新的化合物潜在的药理活性,我们需要对它进行药代动力学评价。

而为了准确评价其药理活性,我们必须开发一种该药物的分析方法,能够对其进行准确定量。

目前实验室已经完成了主要的方法开发,本次毕业设计主要是进行方法验证及方法调整。

研究内容主要有:1、对HR0019的HPLC-MS定量分析的方法开发,包括调试MS条件,调试HPLC条件。

2、对开发方法的验证,包括系统适用性、准确度、精密度、选择性、残留、基质效应、稀释可靠性、溶血效应、稳定性、回收率等。

二、主要成果形式 包括色谱条件、样品处理方式,以及方法验证的数据。

三、主要参考文献[1]Qiu,Qiyu;Domarkas,Juozas;Banerjee,Ranjita;Katsoulas,Athanasia;,cNamee,james P;Jean-Claude,Bertrand J.Type Ⅱcombi-molecules:design and binary targeting properties of the novel triazolinium-containing molecules JDD36 and JDE05.[J]ANTI-CABCER DRUGS.Volume 18(2),February 2007,pp 171-177.[2] Heather L.Watt, Zakaria Rachid, and Bertrand J. Jean-Claude.The Concept of Divergent Targeting through the Activation and Inhibition of Receptors as a Novel Chemotherapeutic Strategy: Signaling Responses to Strong DNA-Reactive CombinatorialMimicries.[J] Journal of Signal Transduction Volume 2012, Article ID 282050, 17 pages doi:10.1155/2012/282050.[3] 裴丽,罗艳,李翔,王丽伟。

《吉非替尼含量测定方法研究进展》实用药物与临床2013 年第16卷第7期。

[4] Structure-based ensemble-QSAR model: a novel approach to the study of the EGFR tyrosine kinase and its inhibitors.Xian-qiang SUN, Lei CHEN, Yao-zong LI, Wei-hua LI1, Gui-xia LIU1, Yao-quan TU, Yun TANG.[J]Acta Pharmacologica Sinica (2014) 35: 301310.[5] Malleshappa N. Noolvi* and Harun M. Patel.3D QSAR STUDIES ON A SERIES OF QUINAZOLINE DERRIVATIVES AS TYROSINE KINASE (EGFR) INHIBITOR: THE k-NEAREST NEIGHBOR MOLECULAR FIELD ANALYSIS APPROACH.[J] Journal of Basic and Clinical Pharmacy Vol-001 Issue-003 June 2010 August 2010 153-175.[6] Suman Rao, Anne-Laure Larroque-Lombard,Lisa Peyrard,Cdric Thauvin,Zakaria Rachid,Christopher Williams, Bertrand J. Jean-Claude. Target Modulation by a Kinase Inhibitor Engineered to Induce a Tandem Blockade of the Epidermal Growth Factor Receptor(EGFR) and c-Src: The Concept of Type III Combi-Targeting.[J] PLOS ONE,DOI:10.1371/journal.pone.0117215February 6,2015.[7] Synthesis of half-mustard combi-molecules with fluorescence properties: correlation with EGFR status. Zakaria Rachid, Fouad Brahimi, Juozas Domarkas and Bertrand Jacques Jean-Claude.[J] Bioorganic amp; Medicinal Chemistry Letters 15 (2005) 11351138.[8] A bioanalytical investigation on the exquisitely strong in vitro potency of theEGFRDNA targeting type II combi-molecule ZR2003 and its mitigated in vivo antitumour activity. Nahid Golabi, Fouad Brahimi, Ying Huang, Zakaria Rachid, Qiyu Qiu, Anne-Laure Larroque-Lombard,Bertrand J. Jean-Claude.[J]Journal of Pharmaceutical and Biomedical Analysis. Journal of Pharmaceutical and Biomedical Analysis 56 (2011) 592 599.[9] Ying Huang, Zakaria Rachid, Lisa Peyrard,Zhor Senhaji Mouhri, Christopher,Williams and Bertrand J. Jean-Claude.Positional Isomerization of A Non-Cleavable Combi-Molecule Dramatically Altered Tumor Cell Response Profile.[J]Chem Biol Drug Des 2015; 85: 153162[10] 谢楠_多靶点酪氨酸激酶抑制剂AL_8326抗肿瘤活性及机制研究 浙江大学硕士学位论文 [11] 吉非替尼可能通过EGFR启动子甲基化诱导肺腺癌细胞继发性耐药的研究_王起龙 中南大学硕士学位论文[12] Wang L,Lim MY,Chin T,et al. Rapid determination of gefitinib and its main metabolite,O-desmethyl gefitinib in human plasma using liquid chromatography-tandem mass spectrometry.[J]Journal of Chromatography B,2011,879( 22) : 2155-2161.[13] Guetens G,Prenen H,De Boeck G, et al. Sensitive and specific quantification of the anticancer agent ZD1839( Gefitinib) in plasma by on-column focusing capillary liquid chromatography-tandem mass spectrometry[J]. J Chromatogr A,2005,1082( 1) : 2-5.[14] Chahbouni A,Den Burger JC,Vos RM,et al. Simultaneous quantification of erlotinib,gefitinib,and imatinib in human plasma by liquid chromatography tandem mass spectrometry[J]. Ther Drug Monit,2009,31( 6) : 683-687.[15] Honeywell R,Yarzadah K,Giovannetti E,et al. Simple and selective method for the determination of various tyrosine kinase inhibitors used in the clinical setting by liquid chromatography tandem mass spectrometry[J].Journal of Chromatography B,2010,878( 15-16) : 1059-1068.四、工作进度3月1日~3月25日 资料查找,文献阅读;熟悉生物样品前处理的基本方法、方法验证的主要内容、HPLC-MS仪器操作以及方法开发的相关步骤。

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