Chan Kamfai, Coen Mauricio, Hardick Justin, Gaydos Charlotte A, Wong Kah-Yat, Smith Clayton, Wilson Scott A, Vayugundla Siva Praneeth, Wong Season
AI Biosciences, Inc., College Station, Texas, 77845, United States of America.
Division of Infectious Diseases, Department of Medicine, Johns Hopkins University, Baltimore, Maryland, 21205, United States of America.
PLoS One. 2016 Jun 30;11(6):e0158502. doi: 10.1371/journal.pone.0158502. eCollection 2016.
Most molecular diagnostic assays require upfront sample preparation steps to isolate the target's nucleic acids, followed by its amplification and detection using various nucleic acid amplification techniques. Because molecular diagnostic methods are generally rather difficult to perform manually without highly trained users, automated and integrated systems are highly desirable but too costly for use at point-of-care or low-resource settings. Here, we showcase the development of a low-cost and rapid nucleic acid isolation and amplification platform by modifying entry-level 3D printers that cost between $400 and $750. Our modifications consisted of replacing the extruder with a tip-comb attachment that houses magnets to conduct magnetic particle-based nucleic acid extraction. We then programmed the 3D printer to conduct motions that can perform high-quality extraction protocols. Up to 12 samples can be processed simultaneously in under 13 minutes and the efficiency of nucleic acid isolation matches well against gold-standard spin-column-based extraction technology. Additionally, we used the 3D printer's heated bed to supply heat to perform water bath-based polymerase chain reactions (PCRs). Using another attachment to hold PCR tubes, the 3D printer was programmed to automate the process of shuttling PCR tubes between water baths. By eliminating the temperature ramping needed in most commercial thermal cyclers, the run time of a 35-cycle PCR protocol was shortened by 33%. This article demonstrates that for applications in resource-limited settings, expensive nucleic acid extraction devices and thermal cyclers that are used in many central laboratories can be potentially replaced by a device modified from inexpensive entry-level 3D printers.
大多数分子诊断检测需要预先进行样本制备步骤,以分离目标核酸,然后使用各种核酸扩增技术对其进行扩增和检测。由于分子诊断方法通常很难在没有经过高度培训的用户的情况下手动执行,因此自动化和集成系统非常理想,但对于即时检测或资源有限的环境来说成本太高。在这里,我们展示了一种低成本、快速的核酸分离和扩增平台的开发,该平台通过改装价格在400美元至750美元之间的入门级3D打印机实现。我们的改装包括用一个装有磁铁的梳状吸头附件替换挤出机,以进行基于磁性颗粒的核酸提取。然后,我们对3D打印机进行编程,使其执行能够完成高质量提取方案的动作。在不到13分钟的时间内可以同时处理多达12个样本,核酸分离效率与基于金标准旋转柱的提取技术相当。此外,我们利用3D打印机的加热床提供热量,以进行基于水浴的聚合酶链反应(PCR)。使用另一个附件来固定PCR管,对3D打印机进行编程,使其自动执行在水浴之间穿梭PCR管的过程。通过消除大多数商业热循环仪所需的温度梯度,35个循环的PCR方案的运行时间缩短了33%。本文表明,对于资源有限环境中的应用,许多中心实验室使用的昂贵核酸提取设备和热循环仪可能会被由廉价入门级3D打印机改装而成的设备所取代。