A low-cost, mass-producible point-of-care platform for diagnosing hemoglobin disorders

M. N. Hasan, A. Fraiwan, J. Little, U. Gurkan
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引用次数: 6

Abstract

Sickle Cell Disease (SCD) is a genetically inherited hemoglobin disorder, which can be fatal if left undiagnosed and untreated. Geographically, the most SCD-prevalent regions have the lowest gross domestic product (GDP) and are therefore unable to implement costly, centralized SCD screening programs. In these regions, the early mortality is 50%–90% among children born with sickle cell anemia [1]. According to the World Health Organization (WHO), who passed a resolution naming SCD as a global public health problem in 2006 [2], 70% of these early mortality could be prevented by implementing low-cost SCD screening followed by cost-effective treatments [3]. To address this need, we developed HemeChip, a mass-producible, low-cost, microchip version of electrophoresis, able to detect and quantify hemoglobin type(s) from whole blood at the point of care (POC). The process is fast (<10 minutes), efficient, and can be performed by minimally trained personnel.
用于诊断血红蛋白疾病的低成本、可批量生产的即时护理平台
镰状细胞病(SCD)是一种遗传性血红蛋白疾病,如果不及时诊断和治疗,可能会致命。从地理上看,SCD最流行的地区的国内生产总值(GDP)最低,因此无法实施昂贵的集中式SCD筛查计划。在这些地区,出生时患有镰状细胞性贫血的儿童早期死亡率为50%-90%[1]。世界卫生组织(WHO)在2006年通过了一项决议,将SCD列为全球公共卫生问题[2],其中70%的早期死亡可以通过实施低成本的SCD筛查和高成本效益的治疗来预防[3]。为了满足这一需求,我们开发了HemeChip,这是一种可批量生产、低成本的微芯片电泳技术,能够在护理点(POC)检测和定量全血中的血红蛋白类型。该过程快速(<10分钟),高效,可以由最少训练的人员执行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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