Ohta Jun, Noda Nanaka, Sakurada Koichi
Forensic Biology Unit, Scientific Crime Laboratory, Kanagawa Prefectural Police, 155-1 Yamashita-cho, Naka-ku, Yokohama, Kanagawa, 231-0023, Japan.
Department of Forensic Dentistry, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, 113-8510, Japan.
J Forensic Sci. 2019 May;64(3):873-877. doi: 10.1111/1556-4029.13936. Epub 2018 Oct 19.
The stability of salivary α-amylase is a critical factor in both catalytic and immunological method-based forensic saliva identification. This study aimed to assess the sensitivity of catalytic and immunological tests on degraded saliva samples. Degraded saliva stains were prepared by microbial decomposition using humid soil. Salivary α-amylase activity was catalytically detected both qualitatively and quantitatively using the Phadebas amylase test. As immunological methods, we conducted qualitative and quantitative tests using the RSID™-saliva test and ELISA, respectively. Salivary α-amylase activity of degraded samples (incubated at 37°C for 12 h) was significantly lower than that of controls in the quantitative tests. All the degraded samples obtained by the humid soil produced negative results in the Phadebas tests, but showed positive results in the RSID™-saliva test and ELISA. These results suggest that immunological tests are effective for testing degraded saliva samples that have lost their enzymatic activity.
唾液α-淀粉酶的稳定性是基于催化和免疫方法的法医唾液鉴定中的关键因素。本研究旨在评估催化试验和免疫试验对降解唾液样本的敏感性。使用潮湿土壤通过微生物分解制备降解的唾液污渍。使用法德巴斯淀粉酶试验对唾液α-淀粉酶活性进行定性和定量催化检测。作为免疫方法,我们分别使用RSID™-唾液试验和酶联免疫吸附测定进行定性和定量试验。在定量试验中,降解样本(在37°C孵育12小时)的唾液α-淀粉酶活性显著低于对照样本。通过潮湿土壤获得的所有降解样本在法德巴斯试验中均产生阴性结果,但在RSID™-唾液试验和酶联免疫吸附测定中显示阳性结果。这些结果表明,免疫试验对于检测已失去酶活性的降解唾液样本是有效的。