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Long-term dry storage of an enzyme-based reagent system for ELISA in point-of-care devices

机译:即时干燥的点对点设备中用于ELISA的基于酶的试剂系统的长期保存

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摘要

Lateral flow devices are commonly used for many point-of-care (POC) applications in low-resource settings. However, they lack the sensitivity needed for many analytes relevant in the diagnosis of diseases. One approach to achieve higher sensitivity is signal amplification, which is commonly used in laboratory assays, but uses reagents that require refrigeration and inherently requires multiple assay steps not normally compatible with POC settings. Enzyme-based signal amplification, such as the one used in ELISA, could greatly improve the limit of detection if it were translated to a format compatible with POC requirements. A signal-amplified POC device not only requires the reagents to be stored in a stable form, but also requires automation of the multiple sequential steps of signal amplification protocols. Here, we describe a method for the long-term dry storage of ELISA reagents: horseradish peroxidase (HRP) conjugated antibody label and its colorimetric substrate diaminobenzidine (DAB). The HRP conjugate retained ~80% enzymatic activity after dry storage at 45 °C for over 5 months. The DAB substrate was also stable at 45 °C and exhibited no detectable loss of activity over 3 months. These reagents were incorporated into a two-dimensional paper network (2DPN) device that automated the steps of ELISA for the detection of a malarial biomarker. These results demonstrate the potential of enzyme-based signal amplification for enhanced sensitivity in POC devices for low resource settings.
机译:横向流量设备通常在资源匮乏的环境中用于许多即时医疗(POC)应用。但是,它们缺乏与疾病诊断相关的许多分析物所需的灵敏度。一种实现更高灵敏度的方法是信号放大,它通常用于实验室分析,但是使用的试剂需要冷藏,并且固有地需要多个通常与POC设置不兼容的分析步骤。如果将基于酶的信号放大(翻译成与POC要求兼容的格式),例如ELISA中使用的信号放大,则可以大大提高检测限。信号放大的POC设备不仅要求试剂以稳定的形式存储,而且还要求自动化信号放大协议的多个顺序步骤。在这里,我们描述了一种用于ELISA试剂的长期干燥存储的方法:辣根过氧化物酶(HRP)偶联的抗体标记及其比色底物二氨基联苯胺(DAB)。在45°C下干燥保存5个月后,HRP共轭物保留了约80%的酶活性。 DAB底物在45°C时也是稳定的,并且在3个月内未显示出可检测到的活性损失。这些试剂被并入二维纸网络(2DPN)设备中,该设备可以自动执行ELISA步骤来检测疟疾生物标志物。这些结果证明了基于酶的信号放大在低资源设置下提高POC设备灵敏度的潜力。

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