Evaluation of PPC / mBio Inc.’s Biochip Reader Integrated Circuit Reader System for Diagnosis of HIV / HCV Infection: Preliminary Method

L. Knop, R. Badaró, Chris Myat
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引用次数: 1

Abstract

The technological advances of recent decades in immunodiagnostic techniques have enabled the development of methods capable of detecting the antigen-antibody complex with high efficiency and reliability. However, the cost of such procedures has remained high; they are not easy to handle for an unskilled professional, nor provide immediate results for multiple samples. Precision Photonics Corporation (PPC), with m/Bio Inc. and in partnership with the University of San Diego (UCSD), USA, created an integrated circuit reader (Biochip Reader), which is low cost, fast and easy to handle, based on an optical systems and multiplex arrangements for the detection of biological multi-markers at the same time. This study aimed to evaluate the operation of the integrated circuit reader system (Biochip Reader), the protocols and the results of the multiplex tests for antibodies against HIV and HCV in partnership with the Federal University of Bahia (UFBA). We tested a total of 65 samples in the Biochip reader, and they showed 100% of sensitivity and specificity when compared to the results obtained by ELISA for HIV and HCV. Nevertheless, the protocols and the results obtained in Bahia presented slide instability, such as the formation of crystals and trehalose residues, unnecessary steps and manipulation of the slides. This fact led to changing the protocol and improving the prototype. However, more tests with new biomarkers are needed to validate the method.
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PPC / mBio公司的生物芯片阅读器集成电路阅读器系统用于HIV / HCV感染诊断的评估:初步方法
近几十年来,免疫诊断技术的技术进步使得能够高效可靠地检测抗原-抗体复合物的方法得以发展。但是,这种程序的费用仍然很高;对于不熟练的专业人员来说,它们不容易处理,也不能立即提供多个样品的结果。精密光子公司(PPC)与m/Bio公司以及与美国圣地亚哥大学(UCSD)合作,开发了一种集成电路读取器(Biochip reader),该阅读器基于光学系统和多路配置,可同时检测生物多标记物,成本低,速度快,易于操作。本研究旨在评估与巴伊亚联邦大学(UFBA)合作的集成电路读取器系统(Biochip reader)的运行、方案和抗HIV和HCV抗体多重测试的结果。我们在Biochip阅读器中测试了总共65个样本,与ELISA获得的HIV和HCV结果相比,它们显示出100%的敏感性和特异性。然而,在巴伊亚获得的方案和结果存在玻片不稳定性,例如晶体和海藻糖残留物的形成,不必要的步骤和玻片的操作。这一事实导致了协议的改变和原型的改进。然而,需要用新的生物标志物进行更多的测试来验证该方法。
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