Graham E A M, Turk E E, Rutty G N
Forensic Pathology Unit, University of Leicester, Robert Kilpatrick Building, Leicester Royal Infirmary, Leicester LE2 7LX, UK.
Forensic Sci Int Genet. 2008 Jan;2(1):29-34. doi: 10.1016/j.fsigen.2007.07.003. Epub 2007 Sep 4.
In mass fatality incidents, for example following a vehicle accident or terrorist event, severe fragmentation of bodies may occur, making identification by the use of traditional techniques such as fingerprinting or odontology difficult. In such situations DNA profiling can be employed for individualization and re-association of fragmented remains. As at times disrupted soft tissue may be the predominate tissue type requiring identification and re-association. We have investigated the use of two buffer solutions for preservation of soft tissue samples that may be collected during such investigations, when buccal cells, blood samples or teeth or bone may not be available. Both buffer solutions have shown sufficient DNA preservation over a 12-month period of storage at room temperature to allow for DNA profiling to be successfully performed when 5-1000 mg muscle tissue was stored in each solution.
在大规模死亡事件中,例如在车辆事故或恐怖袭击事件之后,尸体可能会严重碎裂,使得使用指纹识别或牙科学等传统技术进行身份鉴定变得困难。在这种情况下,可以采用DNA分析来对碎裂遗骸进行个体化识别和重新关联。有时,受损的软组织可能是需要进行识别和重新关联的主要组织类型。我们研究了两种缓冲溶液在保存软组织样本方面的用途,这些样本可能是在这类调查中采集的,此时可能无法获取颊细胞、血液样本或牙齿或骨骼。两种缓冲溶液在室温下储存12个月期间均显示出足够的DNA保存效果,当在每种溶液中储存5 - 1000毫克肌肉组织时,能够成功进行DNA分析。