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Point-of-Care Microelectronic Diagnostics for Early Phase Rickettsial Infections

机译:用于早期阶段的高级电子诊断

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Rickettsial diseases (RD) are widely distributed in the world and account for seasonal outbreaks and epidemics. The greatest challenge to clinicians is diagnosing RD at early phases when antibiotic therapy is most effective. This burgeoning problem is further compounded by the unavailability of rapid point-of-care (POC) diagnostics for RD. The focus of this poster will be development and optimization of dielectrophoresis-enhanced microfluidic impedance biosensing (DEP-e-MIB) assay to detect the pathogenic cells in sera. In DEP-e-MIB assays, pathogens are labeled with a DEP label (polystyrene beads) and then injected into the DEP-e-MIB chip for capture of the labeled pathogens and reading impedance changes at the interdigitated electrodes. We have seen detection down to 10^5 cells. However, minor reduction in nonspecific binding can lead to large increment in signal to noise ratio. Specifically, we show how to reduce in the non-specific binding of immunobeads to the electrodes through the choice of bead surface chemistry (epoxy, carboxylate, and aldehyde), and the co-immobilization of polyethylene glycol with antibodies at the electrodes and the beads. Further we also show how this non-specific binding is affected by the use of DEP.
机译:人力儿疾病(RD)广泛分布在世界上,并占季节性爆发和流行病。当抗生素治疗最有效时,对临床医生的最大挑战正在诊断早期阶段。通过RD的快速护理点(POC)诊断的不可用来,该爆炸性问题进一步复杂化。该海报的焦点将是介电泳增强的微流体阻抗生物传感(DEP-E-MIB)测定的开发和优化,以检测血清中的病原细胞。在DEP-E-MIB测定中,病原体用DEP标记(聚苯乙烯珠粒)标记,然后注射到DEP-E-MIB芯片中以捕获标记的病原体和读取的电极处的读取阻抗变化。我们已看到检测到10 ^ 5个细胞。然而,非特异性结合的轻微降低可能导致信号到噪声比例大。具体地,我们展示了如何通过选择珠表面化学(环氧树脂,羧酸盐和醛)和用电极和珠子的抗体的聚乙二醇的共固化来减少免疫形状对电极的非特异性结合电极。 。此外,我们还展示了如何受到DEP的使用影响的这种非特异性绑定。

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