Department of Chemistry, University of Virginia, Charlottesville, VA 22904, USA.
TeGrex Technologies, Charlottesville, VA 22910, USA.
Lab Chip. 2016 Nov 15;16(23):4569-4580. doi: 10.1039/c6lc00953k.
Current conventional methods utilized for forensic DNA analysis are time consuming and labor-intensive requiring large and expensive equipment and instrumentation. While more portable Rapid DNA systems have been developed, introducing them to a working laboratory still necessitates a high cost of initiation followed by the recurrent cost of the devices. This has highlighted the need for an inexpensive, rapid and portable DNA analysis tool for human identification in a forensic setting. In order for an integrated DNA analysis system such as this to be realized, device operations must always be concluded by a rapid separation of short-tandem repeat (STR) DNA fragments. Contributing to this, we report the development of a unique, multi-level, centrifugal microdevice that can perform both reagent loading and DNA separation. The fabrication protocol was inspired by the print, cut and laminate (PCL) technique described previously by our group, and in accordance, offers a rapid and inexpensive option compared with existing approaches. The device comprises multiple polyester-toner fluidic layers, a cyclic olefin copolymer separation domain and integrated gold leaf electrodes. All materials are commercially-available and complement the PCL process in a way that permits fabrication of increasingly sought after single-use devices. All reagents, including a viscous sieving matrix, are loaded centrifugally, eliminating external pneumatic pumping, and the sample is separated in <5 minutes using an effective separation length of only 4 cm (reagent loading to completed separation, is <37 minutes). The protocol for gold leaf electrode manufacture yielded up to 30 electrodes for less than $3 (cost of a 79 mm × 79 mm gold leaf sheet) and when using a device combining these electrodes and centrifugal reagent/polymer loading, the electrophoretic separation of STR fragments with two base resolution was demonstrated. This exemplary performance makes the device an ideal candidate for further integration and development of an inexpensive, portable and rapid forensic human identification system.
目前用于法医 DNA 分析的常规方法既耗时又费力,需要大型昂贵的设备和仪器。虽然已经开发出更便携的 Rapid DNA 系统,但将其引入工作实验室仍然需要高昂的启动成本,随后还需要不断支付设备的成本。这凸显了在法医环境中需要一种廉价、快速且便携的 DNA 分析工具来进行人类身份识别。为了实现这种集成 DNA 分析系统,设备操作必须始终通过快速分离短串联重复 (STR) DNA 片段来完成。为此,我们报告了一种独特的、多级、离心微设备的开发,该设备可以进行试剂加载和 DNA 分离。该制造方案受到了我们小组之前描述的打印、切割和层压 (PCL) 技术的启发,与现有方法相比,它提供了一种快速且廉价的选择。该设备由多个聚酯调色剂流体层、环状烯烃共聚物分离域和集成金叶电极组成。所有材料均为市售产品,并与 PCL 工艺相补充,以实现越来越受欢迎的一次性设备的制造。所有试剂,包括粘性筛分基质,都通过离心加载,无需外部气动泵,使用仅 4 厘米的有效分离长度(从试剂加载到完成分离的时间不到 5 分钟)即可完成分离。金叶电极制造的方案可生产多达 30 个电极,成本不到 3 美元(成本为 79 毫米×79 毫米金叶片),并且当使用结合了这些电极和离心试剂/聚合物加载的设备时,展示了具有两个碱基分辨率的 STR 片段的电泳分离。这种出色的性能使该设备成为进一步集成和开发廉价、便携和快速法医人类识别系统的理想候选者。