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EPR Detection of Free Radicals in Vascular Disease: Bruker EMXPlus Spectrometer

EPR Detection of Free Radicals in Vascular Disease: Bruker EMXPlus Spectrometer
EPR 检测血管疾病中的自由基:布鲁克 EMXPlus 光谱仪
批准号:
8447255
负责人:
Eric Eugene Kelley
金额:
$30.4万
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-06-15 至 2014-06-14

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中文摘要
翻译
描述:氧和氮的活性物种越来越受到重视,因为它们对疾病的发生和发展有影响。因此,医学研究机构必须拥有强大的自由基研究技术。目前,匹兹堡大学医学院的研究人员只能在他们的模型系统中使用劣质的方法来批判性地审问自由基物种。例如,目前所有用于检测自由基物种的荧光、比色、发光和化学发光探针都显示出相对较高的灵敏度和重复性,但它们在特异性、氧化还原循环倾向、膜通透性和毒性方面存在显著限制。值得注意的是,电子顺磁共振(EPR)光谱是目前唯一可用的技术,可以直接识别生物系统中的自由基,因此仍然是自由基研究的黄金标准。EPR的用途体现在它能够提供特定的指纹光谱来识别被测量的自由基。因此,EPR可以直接检测和鉴定稳定的自由基物种。对于不太稳定的自由基物种,EPR自旋捕获技术允许在许多体外和体内系统中进行检测和鉴定。事实证明,这项技术对于研究细胞、组织和体内系统中自由基的形成和来源,以及研究蛋白质自由基中间体和研究药物与细胞膜的相互作用非常有用。到目前为止,医学院的研究人员仅限于无法获得这项技术。因此,收购EPR光谱仪将独特地促进当前研究计划的发展,激励新的合作努力,并增强成功实现我们开发治疗疾病的新战略的总体目标的潜力。
英文摘要
DESCRIPTION: Reactive species of oxygen and nitrogen are becoming increasingly appreciated for their impact on the onset and progression of disease. It is therefore imperative for medical research institutions to possess robust free radical research technology. Currently, investigators at the University of Pittsburgh, School of Medicine are relegated to the use of inferior methodologies to critically interrogate free radical species in their model systems. For example, all currently available fluorescent, colorimetric, luminescent and chemiluminescent probes used to detect free radical species demonstrate reproducible results with relatively high sensitivity however, they have significant limitations regarding specificity, the propensity to redox cycle, membrane permeability and toxicity. This being noted, electron paramagnetic resonance (EPR) spectroscopy is the only technique currently available that affords direct identification of free radicals in biological systems and as such remains the gold standard for free radical research. The utility of EPR is exemplified in its capacity to provide specific fingerprint spectra that identify the free radical being measured. Thus, EPR can provide direct detection and identification of stable free radical species. For less stable free radical species, EPR spin trapping techniques permit detection and identification in a multitude of in vitro and in vivo systems. This technique has proven extremely informative for investigating formation and identifying sources of radicals in cellular, tissue and in vivo systems as well as investigating protein radical intermediates and studying drug interactions with cell membranes. To date, investigators in the School of Medicine have limited to no access to this technology. As such, acquisition of an EPR spectrometer would serve to uniquely cultivate the development of current research initiatives, incentivize new collaborative efforts and enhance the potential for success in achieving our overarching goal of developing novel strategies to treat disease.
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