Madhurantakam Sasya, Karnam Jayanth Babu, Muthukumar Sriram, Prasad Shalini
Department of Bioengineering The University of Texas at Dallas Richardson Texas USA.
EnLiSense LLC Allen Texas USA.
Bioeng Transl Med. 2023 Jul 11;8(5):e10566. doi: 10.1002/btm2.10566. eCollection 2023 Sep.
With the evolution of the COVID-19 pandemic, there is now a need for point-of-care devices for the quantification of disease biomarkers toward disease severity assessment. Disease progression has been determined as a multifactor phenomenon and can be treated based on the host immune response within each individual. CoST is an electrochemical immunosensor point-of-care device that can determine disease severity through multiplex measurement and quantification of spike protein, nucleocapsid protein, D-dimer, and IL-2R from 100 μL of plasma samples within a few minutes. The limit of detection was found to be 3 ng/mL and 21 ng/mL for S and N proteins whereas for D-dimer and IL-2R it was 0.0006 ng/mL and 0.242 ng/mL, respectively. Cross-reactivity of all the biomarkers was studied and it was found to be <20%. Inter and intra-assay variability of the CoST sensor was less than <15% confirming its ability to detect the target biomarker in body fluids. In addition, this platform has also been tested to quantify all four biomarkers in 40 patient samples and to predict the severity index. A significant difference was observed between healthy and COVID-19 samples with a -value of 0.0002 for D-dimer and <0.0001 for other proteins confirming the ability of the COST sensor to be used as a point of care device to assess disease severity at clinical sites. This device platform can be modified to impact a wide range of disease indications where prognostic monitoring of the host response can be critical in modulating therapy.
随着新冠疫情的演变,现在需要用于定量疾病生物标志物以评估疾病严重程度的即时检测设备。疾病进展已被确定为一种多因素现象,可以根据每个个体的宿主免疫反应进行治疗。CoST是一种电化学免疫传感器即时检测设备,它可以通过对100微升血浆样本中的刺突蛋白、核衣壳蛋白、D-二聚体和白细胞介素-2受体进行多重测量和定量,在几分钟内确定疾病严重程度。发现S蛋白和N蛋白的检测限分别为3纳克/毫升和21纳克/毫升,而D-二聚体和白细胞介素-2受体的检测限分别为0.0006纳克/毫升和0.242纳克/毫升。研究了所有生物标志物的交叉反应性,发现其小于20%。CoST传感器的批间和批内变异小于15%,证实了其在体液中检测目标生物标志物的能力。此外,该平台还经过测试,用于对40份患者样本中的所有四种生物标志物进行定量,并预测严重程度指数。在健康样本和新冠样本之间观察到显著差异,D-二聚体的p值为0.0002,其他蛋白质的p值<0.0001,证实了COST传感器作为即时检测设备在临床场所评估疾病严重程度的能力。该设备平台可以进行改进,以适用于广泛的疾病适应症,在这些疾病中,宿主反应的预后监测对于调整治疗可能至关重要。