用于神经退行性疾病诊断的等离子体阵列生物传感器

K. Vere, J. Richens, M. Somekh, N. Bajaj, K. Morgan, P. O'shea
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引用次数: 2

摘要

阿尔茨海默病(AD)的影响预计将成为现代社会的主要挑战之一:在未来几年内,仅在英国,AD的发病率就将达到100万人,估计每年的经济成本为300亿英镑。不幸的是,现有的诊断程序不足以早期发现疾病,并不能将阿尔茨海默病与其他痴呆症区分开来。此外,它们耗时、昂贵,而且在专家中心以外的可用性有限。明确的阿尔茨海默病诊断仍然只能在死后获得,因此,开发增强的诊断策略是非常可取的。我们已经确定了一组AD生物标志物,其中包含蛋白质,其诊断能力来自于它们的相互关联模式,我们正在开发一种用于临床环境(社区医疗中心和医院)的即时诊断测试的仪器,作为这些标志物的筛查工具。一种可靠的AD生物标志物检测方法的可用性将提高疾病诊断的准确性,有助于早期疾病检测,包括社区筛查的自动化,并允许改进治疗靶向性。虽然目前还没有治愈阿尔茨海默病的方法,但更早、更准确和更具成本效益的阿尔茨海默病检测将是促进开发和实施更新的疾病修饰疗法(淀粉样蛋白疫苗)的重要组成部分。我们的方法还将使昂贵的资源,特别是新兴的最先进的成像技术得到更有效的利用
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Plasmonic-array-based biosensors for the diagnosis of neurodegenerative diseases
The impact of Alzheimer's disease (AD) is projected to become one of the major challenges to modern society: over the next few years the incidence of AD will reach 1 million people in the UK alone with an estimated annual economic cost of £30 billion. Unfortunately, the existing diagnostic procedures are inadequate for early disease detection and do not always differentiate AD from other dementias. In addition, they are time consuming, expensive and of limited availability outside specialist centres. Definitive AD diagnosis is still only available post-mortem and the development of enhanced diagnostic strategies are, therefore, highly desirable. We have identified a panel of AD biomarkers incorporating proteins whose diagnostic power arises from their interrelated patterns and we are developing an instrument for point-of-care diagnostic tests that can be used in clinical settings (community medical centres and hospitals) as a screening tool for these markers. Availability of a reliable biomarker test for AD would increase the accuracy of disease diagnosis, aid earlier disease detection including automation for community screening and allow for improved treatment targeting. Whilst no cure for AD is currently available, earlier, more accurate and cost-effective detection of AD will be an important component for facilitating development and implementation of newer, disease modifying therapies (amyloid vaccines). Our approach would also allow expensive resources, particularly emerging state-of-the-art imaging technologies, to be more effectively utilised
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High-contrast imaging of moving targets Development of a robust wide field surface plasmon instrument as part of a platform for Alzheimer's disease diagnosis Advances in time-resolved fluorescence microscopy: Simultaneous FRAP, FLIM and tr-FAIM to image rotational and translation diffusion in living cells Confocal surface plasmon resonance microscopy with pupil function engineering Silicon on Insulator photonic wire based evanescent field multi-channelled biosensor array “Lab on a Chip” devices
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