Immunoassay/Immunosensors Lab, Institute of Nuclear&Radiological Sciences&Technology, Energy&Safety, NCSR "Demokritos", GR-15341 Aghia Paraskevi, Greece; Forensic Science Division, Hellenic Police, Athens, Greece.
Forensic Science Division, Hellenic Police, Athens, Greece.
Talanta. 2017 Dec 1;175:443-450. doi: 10.1016/j.talanta.2017.07.074. Epub 2017 Jul 24.
A label-free biosensor based on white light reflectance spectroscopy for the determination of PSA as semen indicator in forensic samples is presented. The sensor is based on a two-step immunoassay which employs the same polyclonal anti-PSA antibody as capture and detection antibody followed by reaction with streptavidin as a signal enhancement step. The whole assay time was set to 10min; 5min reaction of immobilized antibody with the PSA calibrators or the samples, 3min reaction with the biotinylated anti-PSA antibody and 2min reaction with streptavidin. Following this protocol, a detection limit of 0.5ng/mL was achieved and the assay's linear response range extended up to 500ng/mL. Thus, taking into account the quantification limit of 1.0ng/mL and the average PSA concentration in semen (0.2-5.5mg/mL), semen quantities of a few nanoliters could be detected. The accuracy of the sensor developed was demonstrated through recovery (% recovery ranged from 89.6 to 106) and semen dilution experiments. A linear correlation was found for semen dilutions ranging from 5000 to 360,000. The lack of interference by other bodily fluids was confirmed by analysing stains of blood, urine and saliva prior to and after the addition of semen. Finally, the sensor was evaluated by analysing 51 forensic casework samples which were also analysed with a semi-quantitative membrane strip test (Seratec® PSA), through microscopic detection of spermatozoa, and male DNA identification through detection of Y chromosome. The results obtained with the sensor were in excellent agreement with those provided by an immunoradiometric assay kit (PSA-RIACT) and in complete agreement with the findings using the membrane strip assay, spermatozoa and Y chromosome detection. The excellent analytical performance and small size of the instrument make the sensor developed an attractive tool for use in forensic evidence screening for semen detection.
提出了一种基于白光反射光谱的无标记生物传感器,用于测定法医样本中的 PSA 作为精液指示剂。该传感器基于两步免疫测定法,该方法使用相同的多克隆抗 PSA 抗体作为捕获和检测抗体,随后与链霉亲和素反应作为信号增强步骤。整个测定时间设置为 10min;固定化抗体与 PSA 校准品或样品反应 5min,与生物素化抗 PSA 抗体反应 3min,与链霉亲和素反应 2min。按照该方案,检测限达到 0.5ng/mL,测定的线性响应范围扩展至 500ng/mL。因此,考虑到 1.0ng/mL 的定量限和精液中 PSA 的平均浓度(0.2-5.5mg/mL),可以检测到几个纳升的精液量。通过回收率(回收率范围为 89.6%至 106%)和精液稀释实验证明了传感器的准确性。发现精液稀释范围在 5000 至 360000 之间存在线性相关性。通过在添加精液前后分析血液、尿液和唾液的污渍,证实了缺乏其他体液的干扰。最后,通过分析 51 份法医工作样本,并用半定量膜条测试(Seratec®PSA)、通过显微镜检测精子和通过检测 Y 染色体进行男性 DNA 鉴定,对传感器进行了评估。传感器获得的结果与免疫放射测定试剂盒(PSA-RIACT)提供的结果非常吻合,与膜条检测、精子和 Y 染色体检测的结果完全一致。该传感器具有出色的分析性能和仪器的小巧尺寸,使其成为法医证据筛查中用于检测精液的有吸引力的工具。