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Engineering of a miniaturized robotic clinical laboratory

机译:小型机器人临床实验室的工程设计

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摘要

The ability to perform laboratory testing near the patient and with smaller blood volumes would benefit patients and physicians alike. We describe our design of a miniaturized clinical laboratory system with three components: a hardware platform (ie, the miniLab) that performs preanalytical and analytical processing steps using miniaturized sample manipulation and detection modules, an assay‐configurable cartridge that provides consumable materials and assay reagents, and a server that communicates bidirectionally with the miniLab to manage assay‐specific protocols and analyze, store, and report results (i.e., the virtual analyzer). The miniLab can detect analytes in blood using multiple methods, including molecular diagnostics, immunoassays, clinical chemistry, and hematology. Analytical performance results show that our qualitative Zika virus assay has a limit of detection of 55 genomic copies/ml. For our anti‐herpes simplex virus type 2 immunoglobulin G, lipid panel, and lymphocyte subset panel assays, the miniLab has low imprecision, and method comparison results agree well with those from the United States Food and Drug Administration‐cleared devices. With its small footprint and versatility, the miniLab has the potential to provide testing of a range of analytes in decentralized locations.
机译:在患者附近并以较小的血液量进行实验室测试的能力将使患者和医生受益。我们描述了一个由三部分组成的小型临床实验室系统的设计:一个硬件平台(即miniLab),该平台使用小型化的样品处理和检测模块执行预分析和分析处理步骤;一个可提供试剂盒的可配置材料,可提供消耗性材料和试剂,以及与miniLab双向通信以管理特定于测定的协议并分析,存储和报告结果的服务器(即虚拟分析仪)。 miniLab可以使用多种方法检测血液中的分析物,包括分子诊断,免疫测定,临床化学和血液学。分析性能结果表明,我们的定性寨卡病毒测定法的检测限为55个基因组拷贝/ ml。对于我们的抗2型单纯疱疹病毒免疫球蛋白G,脂质面板和淋巴细胞亚群面板检测,miniLab的不准确性较低,方法比较结果与美国食品药品监督管理局(FDA)批准的设备的结果相当吻合。 miniLab的占地面积小且用途广泛,因此有潜力在分散的位置提供对各种分析物的测试。

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