Nourse Marilyn B, Engel Kate, Anekal Samartha G, Bailey Jocelyn A, Bhatta Pradeep, Bhave Devayani P, Chandrasekaran Shekar, Chen Yutao, Chow Steven, Das Ushati, Galil Erez, Gong Xinwei, Gessert Steven F, Ha Kevin D, Hu Ran, Hyland Laura, Jammalamadaka Arvind, Jayasurya Karthik, Kemp Timothy M, Kim Andrew N, Lee Lucie S, Liu Yang Lily, Nguyen Alphonso, O'Leary Jared, Pangarkar Chinmay H, Patel Paul J, Quon Ken, Ramachandran Pradeep L, Rappaport Amy R, Roy Joy, Sapida Jerald F, Sergeev Nikolay V, Shee Chandan, Shenoy Renuka, Sivaraman Sharada, Sosa-Padilla Bernardo, Tran Lorraine, Trent Amanda, Waggoner Thomas C, Wodziak Dariusz, Yuan Amy, Zhao Peter, Young Daniel L, Robertson Channing R, Holmes Elizabeth A
Assay Development Theranos, 7373 Gateway Boulevard Newark CA 94560.
Systems Integration Theranos, 7373 Gateway Boulevard Newark CA 94560.
Bioeng Transl Med. 2018 Jan 19;3(1):58-70. doi: 10.1002/btm2.10084. eCollection 2018 Jan.
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.
能够在患者身边进行实验室检测且所需血量较少,这将使患者和医生都受益。我们描述了一种小型化临床实验室系统的设计,该系统由三个部分组成:一个硬件平台(即miniLab),它使用小型化的样本处理和检测模块执行分析前和分析处理步骤;一个可配置检测的试剂盒,提供消耗材料和检测试剂;以及一台服务器,它与miniLab进行双向通信,以管理特定检测的协议并分析、存储和报告结果(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,我们的寨卡病毒定性检测方法的检测限为55个基因组拷贝/毫升。对于我们的抗2型单纯疱疹病毒免疫球蛋白G、血脂检测和淋巴细胞亚群检测,miniLab的不精密度较低,方法比较结果与美国食品药品监督管理局批准的设备的结果非常吻合。凭借其小占地面积和多功能性,miniLab有潜力在分散地点提供一系列分析物的检测。