Woolf M Shane, Cunha Larissa L, Hadley Kevyn C, Moffett Rachel P, Landers James P
Department of Chemistry, University of Virginia, Charlottesville, VA, USA.
Department of Chemistry, University of Virginia, Charlottesville, VA, USA.
Anal Chim Acta. 2023 Apr 8;1249:340826. doi: 10.1016/j.aca.2023.340826. Epub 2023 Jan 20.
Biological evidence originating from victims of sexual assault is often comprised of unbalanced cellular mixtures with significantly higher contributions from the victim's genetic material. Enrichment of the forensically-critical sperm fraction (SF) with single-source male DNA relies on differential extraction (DE), a manually-intensive process that is prone to contamination. Due to DNA losses from sequential washing steps, some existing DE methods often fail to generate sufficient sperm cell DNA recovery for perpetrator(s) identification. Here, we propose an enzymatic, 'swab-in' rotationally-driven microfluidic device to achieve complete, self-contained, on-disc automation of the forensic DE workflow. This 'swab-in' approach retains the sample within the microdevice, enabling lysis of sperm cells directly from the evidence cutting to improve sperm cell DNA yield. We demonstrate clear proof-of-concept of a centrifugal platform that provides for timed reagent release, temperature control for sequential enzymatic reactions, and enclosed fluidic fractionation that allows for objective evaluation of the DE process chain with a total processing time of ≤15 min. On-disc extraction of buccal or sperm swabs establishes compatibility of the prototype disc with: 1) an entirely enzymatic extraction method, and 2) distinct downstream analysis modalities, such as the PicoGreen® DNA assay for nucleic acid detection and the polymerase chain reaction (PCR).
性侵犯受害者的生物证据通常由不平衡的细胞混合物组成,受害者的遗传物质贡献显著更高。利用单源男性DNA富集法医鉴定关键的精子部分(SF)依赖于差异提取(DE),这是一个人工操作密集型过程,容易受到污染。由于连续洗涤步骤导致DNA损失,一些现有的DE方法往往无法产生足够的精子细胞DNA用于识别犯罪者。在此,我们提出一种酶促的“拭子插入式”旋转驱动微流控装置,以实现法医DE工作流程的完整、独立、盘上自动化。这种“拭子插入式”方法将样品保留在微装置内,能够直接从证据切割物中裂解精子细胞,以提高精子细胞DNA产量。我们展示了一个离心平台的明确概念验证,该平台可实现定时试剂释放、顺序酶促反应的温度控制以及封闭的流体分级分离,从而能够在总处理时间≤15分钟的情况下对DE过程链进行客观评估。盘上提取口腔拭子或精子拭子证明了原型盘与以下方面的兼容性:1)完全酶促提取方法,以及2)不同的下游分析模式,如用于核酸检测的PicoGreen® DNA测定和聚合酶链反应(PCR)。