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本文引用的文献

1
CHEMICAL SELECTIVITY OF NUCLEOBASE ADDUCTION RELATIVE TO IN VIVO MUTATION SITES ON EXON 7 FRAGMENT OF P53 TUMOR SUPPRESSOR GENE.相对于p53肿瘤抑制基因第7外显子片段体内突变位点的核碱基加合物的化学选择性
Chem Sci. 2015 Oct 1;6(10):5554-5563. doi: 10.1039/C5SC01403D. Epub 2015 Jun 24.
2
Three-Dimensional Cell Culture Assays: Are They More Predictive of In Vivo Efficacy than 2D Monolayer Cell-Based Assays?三维细胞培养分析:与基于二维单层细胞的分析相比,它们对体内疗效的预测性更强吗?
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Elucidating Organ-Specific Metabolic Toxicity Chemistry from Electrochemiluminescent Enzyme/DNA Arrays and Bioreactor Bead-LC-MS/MS.通过电化学发光酶/DNA阵列和生物反应器珠粒液相色谱-串联质谱法阐明器官特异性代谢毒性化学
Chem Sci. 2015;6(4):2457-2468. doi: 10.1039/C4SC03401E.
4
Organs-on-chips at the frontiers of drug discovery.药物研发前沿的器官芯片
Nat Rev Drug Discov. 2015 Apr;14(4):248-60. doi: 10.1038/nrd4539. Epub 2015 Mar 20.
5
Piezotronic-effect enhanced drug metabolism and sensing on a single ZnO nanowire surface with the presence of human cytochrome P450.在人类细胞色素 P450 存在的情况下,基于压电器效应增强的单根 ZnO 纳米线表面上的药物代谢和传感。
ACS Nano. 2015 Mar 24;9(3):3159-68. doi: 10.1021/acsnano.5b00142. Epub 2015 Mar 12.
6
Efficient drug metabolism strategy based on microsome-mesoporous organosilica nanoreactors.基于微粒体-介孔有机硅纳米反应器的高效药物代谢策略。
Anal Chem. 2014 Nov 4;86(21):10870-6. doi: 10.1021/ac503024h. Epub 2014 Oct 27.
7
Thin multicomponent films for functional enzyme devices and bioreactor particles.用于功能性酶装置和生物反应器颗粒的超薄多组分薄膜。
Soft Matter. 2014 Nov 7;10(41):8145-56. doi: 10.1039/c4sm01679c.
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Microfluidic organs-on-chips.微流控器官芯片。
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Three dimensional cellular microarray platform for human neural stem cell differentiation and toxicology.用于人类神经干细胞分化和毒理学研究的三维细胞微阵列平台
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10
Real-time imaging of oxidative and nitrosative stress in the liver of live animals for drug-toxicity testing.用于药物毒性测试的活体动物肝脏中氧化应激和亚硝化应激的实时成像。
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最新代谢毒性筛选及途径评估。

State-of-the-Art Metabolic Toxicity Screening and Pathway Evaluation.

机构信息

Department of Chemistry, East Carolina University Greenville, North Carolina 27858, United States.

Department of Chemistry, University of Connecticut , Storrs, Connecticut 06269, United States.

出版信息

Anal Chem. 2016 May 3;88(9):4584-99. doi: 10.1021/acs.analchem.5b04772. Epub 2016 Apr 14.

DOI:10.1021/acs.analchem.5b04772
PMID:27043322
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4862375/
Abstract

Routine in vitro bioassays and animal toxicity studies of drug and environmental chemical candidates fail to reveal toxicity in ∼30% of cases. This Feature article addresses research on new approaches to in vitro toxicity testing as well as our own efforts to produce high-throughput genotoxicity arrays and LC-MS/MS approaches to reveal possible chemical pathways of toxicity.

摘要

在药物和环境化学候选物的常规体外生物测定和动物毒性研究中,约有 30%的情况未能揭示其毒性。本文介绍了新的体外毒性测试方法的研究,以及我们自己在生产高通量遗传毒性阵列和 LC-MS/MS 方法以揭示可能的毒性化学途径方面的努力。