Khare Parul, Raj Vineet, Chandra Shaleen, Agarwal Suraksha
Department of Oral and Maxillofacial Pathology, Maharana Pratap College of Dentistry and Research Center, Gwalior, Madhya Pradesh, India.
Department of Oral and Maxillofacial Pathology, Saraswati Dental College and Hospital, Lucknow, Uttar Pradesh, India.
J Forensic Dent Sci. 2014 May;6(2):81-5. doi: 10.4103/0975-1475.132529.
Saliva has long been known for its diagnostic value in several diseases. It also has a potential to be used in forensic science.
The objective of this study is to compare the quantity and quality of DNA samples extracted from saliva with those extracted from blood in order to assess the feasibility of extracting sufficient DNA from saliva for its possible use in forensic identification.
Blood and saliva samples were collected from 20 volunteers and DNA extraction was performed through Phenol Chloroform technique. The quantity and quality of isolated DNA was analyzed by spectrophotometery and the samples were then used to amplify short tandem repeat (STR) F13 using the polymerase chain reaction.
Mean quantity of DNA obtained in saliva was 48.4 ± 8.2 μg/ml and in blood was 142.5 ± 45.9 μg/ml. Purity of DNA obtained as assessed by the ratio of optical density 260/280, was found to be optimal in 45% salivary samples while remaining showed minor contamination. Despite this positive F13 STR amplification was achieved in 75% of salivary DNA samples.
Results of this study showed that saliva may prove to be a useful source of DNA for forensic purpose.
长期以来,唾液在多种疾病中的诊断价值已为人所知。它在法医学中也有潜在用途。
本研究的目的是比较从唾液中提取的DNA样本与从血液中提取的DNA样本的数量和质量,以评估从唾液中提取足够的DNA用于法医鉴定的可行性。
从20名志愿者身上采集血液和唾液样本,并通过酚氯仿技术进行DNA提取。通过分光光度法分析分离出的DNA的数量和质量,然后使用聚合酶链反应对样本进行短串联重复序列(STR)F13的扩增。
唾液中获得的DNA平均量为48.4±8.2μg/ml,血液中为142.5±45.9μg/ml。通过光密度260/280比值评估获得的DNA纯度,在45%的唾液样本中被发现是最佳的,而其余样本显示有轻微污染。尽管如此,75%的唾液DNA样本实现了F13 STR的阳性扩增。
本研究结果表明,唾液可能被证明是用于法医目的的有用DNA来源。