College of Science & Engineering, Flinders University, Adelaide 5042, Australia.
College of Science & Engineering, Flinders University, Adelaide 5042, Australia.
Forensic Sci Int Genet. 2023 Nov;67:102927. doi: 10.1016/j.fsigen.2023.102927. Epub 2023 Aug 10.
The detection of human DNA on and within illicit drug preparations is novel and a focus of current research. Previous studies have indicated that certain drug-related powders present in illicit drug preparations can interfere with downstream DNA analysis when directly added to the PCR. Therefore, it is important to determine if these drug-related powders are effectively removed during the DNA extraction or whether traces of powder remain to interfere with DNA processing. Three extraction methods were selected to assess their efficiency at removing drug-related powders for downstream processes using DNA from both saliva and touch depositions. This is the first study to compare efficiencies of DNA extraction methods from drug-related powders. The extraction methods compared were the DNA IQ™ System, the QIAamp® DNA Investigator Kit and the combination of a simple lysis step followed by use of the Microcon® DNA Fast Flow device. Saliva was added to dimethylsulfone (DMS), nitrostyrene and PROSOLV® tablet mixture to determine the effect of powder type (based on solubility). Saliva was also added to 0, 50, 200 and 400 mg of DMS to determine the effect of an increase in DMS quantity. Trace DNA was deposited onto DMS using a worn glove approach. These samples were re-tested six months post-DNA deposition and profiled for further comparisons. Ten replicates were conducted for each condition with five replicates of saliva positive controls per method (n = 255 samples). A subset of samples was chemically analysed to determine if DMS was present in the final DNA eluant. The readily soluble DMS did not interfere with any of the extraction methods at lower amounts, however increasing the DMS to 400 mg reduced the relative DNA yields using the Microcon® and Investigator methods. The tablet mixture reduced the relative DNA yield of all three methods, however the nitrostyrene (which was relatively insoluble) only reduced the relative DNA yield of the DNA IQ™. The Investigator method performed the best with the trace samples, followed by the Microcon® method and then the DNA IQ™. DMS was detected in all extracts chemically analysed from the DNA IQ™ and Microcon®, whereas only one sample tested from the Investigator kit contained DMS in the extract and was in a relatively low amount compared to the other samples. Not one kit outperformed the others in all comparisons, however the Investigator kit was the most efficient overall at optimising the DNA yield whilst also removing the powders more effectively.
在非法药物制剂中检测人类 DNA 是新颖的,也是当前研究的重点。先前的研究表明,某些与药物相关的粉末存在于非法药物制剂中,当直接添加到 PCR 中时,可能会干扰下游 DNA 分析。因此,确定这些与药物相关的粉末在 DNA 提取过程中是否被有效去除,或者是否有痕迹的粉末残留以干扰 DNA 处理,这一点很重要。选择了三种提取方法来评估它们在使用唾液和接触沉积的 DNA 进行下游处理时从与药物相关的粉末中去除它们的效率。这是首次比较从与药物相关的粉末中提取 DNA 的方法的效率。比较的提取方法是 DNA IQ™系统、QIAamp®DNA Investigator 试剂盒和简单裂解步骤后使用 Microcon®DNA Fast Flow 装置的组合。唾液被添加到二甲基亚砜 (DMS)、硝基苯乙烯和 PROSOLV®片剂混合物中,以确定粉末类型(基于溶解度)的影响。唾液也被添加到 0、50、200 和 400 mg 的 DMS 中,以确定 DMS 量增加的影响。使用磨损的手套方法将痕量 DNA 沉积到 DMS 上。这些样品在 DNA 沉积后六个月重新测试,并进行进一步比较。每种条件进行了 10 次重复,每种方法有 5 次唾液阳性对照重复(n = 255 个样品)。对一部分样品进行了化学分析,以确定最终的 DNA 洗脱液中是否存在 DMS。易溶的 DMS 在较低量下不会干扰任何提取方法,但是将 DMS 增加到 400 mg 会降低 Microcon®和 Investigator 方法的相对 DNA 产量。片剂混合物降低了所有三种方法的相对 DNA 产量,但是相对不溶的硝基苯乙烯仅降低了 DNA IQ™的相对 DNA 产量。微量样品中 Investigator 方法表现最好,其次是 Microcon®方法,然后是 DNA IQ™。从化学分析的所有提取物中都检测到了 DMS,从 DNA IQ™和 Microcon®中提取的所有提取物中都检测到了 DMS,而从 Investigator 试剂盒中提取的只有一个样品中含有 DMS,且含量相对较低与其他样品相比。没有一个试剂盒在所有比较中都表现出色,但是 Investigator 试剂盒在优化 DNA 产量的同时更有效地去除粉末,总体上效率最高。