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The design of a microfluidic biochip for the rapid,multiplexed detection of foodborne pathogensby surface plasmon resonance imaging

机译:用于快速,复用检测的微流体Biochip的设计,食物丧失的群体等离子体谐振成像

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The rapid detection of foodborne pathogens is increasingly important due to the rising occurrence of contaminated foodsupplies. We have previously demonstrated the design of a hybrid optical device that has the capability to perform real-time surface plasmon resonance (SPR) and epi-fluorescence imaging. We now present the design of a microfluidicbiochip consisting of a two-dimensional array of functionalized gold spots. The spots on the array have beenfunctionalized with capture peptides that specifically bind E. coli 0157:H7 or Salmonella enterica. This array isenclosed by a PDMS microfluidic flow cell. A magnetically pre-concentrated sample is injected into the biochip, andwhole pathogens will bind to the capture array. The previously constructed optical device is being used to detect thepresence and identity of captured pathogens using SPR imaging. This detection occurs in a label-free manner, and doesnot require the culture of bacterial samples. Molecular imaging can also be performed using the epi-fluorescencecapabilities of the device to determine pathogen state, or to validate the identity of the captured pathogens usingfluorescently labeled antibodies. We demonstrate the real-time screening of a sample for the presence of E. coli0157:H7 and Salmonella enterica. Additionally the mechanical properties of the microfluidic flow cell will be assessed.The effect of these properties on pathogen capture will be examined.
机译:由于污染的食品蛋白酶的出现上升,食物载病原体的快速检测越来越重要。我们之前已经证明了一种混合光学装置的设计,其具有执行实时表面等离子体共振(SPR)和外延荧光成像的能力。我们现在介绍了由二维官能化金斑的二维阵列组成的微流体芯片的设计。阵列上的斑点已经与特异性结合大肠杆菌0157:H7或沙门氏菌的捕获肽的捕获肽已经过分动化。该阵列由PDMS微流体流动细胞缩短。将磁性预浓缩的样品注入生物芯片中,并且伴随捕获阵列的血液病原体。先前构造的光学器件用于使用SPR成像检测捕获病原体的假期和标识。这种检测以无标记的方式发生,并且不需要细菌样品的培养物。分子成像也可以使用装置的外氟脲键可进行测定病原体状态,或者验证捕获的病原体的身份使用氟荧光标记的抗体。我们证明了用于存在大肠杆菌0157:H7和沙门氏菌的样品的实时筛选。另外,将评估微流体流动细胞的机械性能。将研究这些性质对病原体捕获的影响。

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