Nano biotechnology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran; Department of Medical Nanotechnology, Schcool of Advance Medical Scinces and Technologies, Shiraz University of Medical Scinces, Shiraz, Iran.
Nano biotechnology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.
Mater Sci Eng C Mater Biol Appl. 2019 Dec;105:110113. doi: 10.1016/j.msec.2019.110113. Epub 2019 Aug 22.
The highly sensitive and specificity detection are very important in diagnosis of foodborne pathogens and prevention of spread diseases. Therefore, in the present study, a highly sensitive fluorescence Nano-biosensors was designed for detection of Shigella species. For achieved this purpose, DNA probes and gold nanoparticles (AuNPs) were designed and synthesized, respectively. Then, two DNA probes as signal reporter were immobilized on surface of AuNPs. On the other hand, Iron nanoparticles (MNPs) were synthesized and modified with SMCC (Sulfosuccinimidyl 4-Nmaleimidomethyl cyclohexane-1- carboxylate). The 3th DNA probe was immobilized on surface of MNPs for separation of target DNA. The MNP-DNA probe and DNA probe-AuNP-fluorescence DNA probe were added to target DNA. The MNP- DNA probe-target DNA-DNA probe-AuNP-fluorescence DNA probe complex was isolated by a magnet. The fluorescence DNA probe was released on surface of AuNPs and the fluorescence intensity was read by fluorescence spectrophotometry. Sensitivity and specificity of designed Nano-biosensor was determined. The results showed that the fluorescence intensity was increased with increasing of target DNA concentration. Linear related between target DNA and fluorescence intensity was observed in 2.3 × 10 up to 2.3 × 10 CFU mL. The linear equation and regression were Y = 1.8 X + 23.4 and R 0.9953. Limit of detection (LOD) were determined 90 CFUmL. The specificity of Nano-biosensor in present of other bacteria was confirmed.
在食源性病原体的诊断和疾病传播的预防中,高灵敏度和特异性的检测非常重要。因此,在本研究中,设计了一种高灵敏度的荧光纳生物传感器来检测志贺氏菌属。为此,分别设计和合成了 DNA 探针和金纳米粒子(AuNPs)。然后,将两个 DNA 探针作为信号报告分子固定在 AuNPs 的表面。另一方面,合成了铁纳米粒子(MNPs)并用 SMCC(磺基琥珀酰亚胺 4-马来酰亚胺基甲基环己烷-1-羧酸酯)进行了修饰。将第三个 DNA 探针固定在 MNPs 的表面,用于分离目标 DNA。将 MNPs-DNA 探针和 DNA 探针-AuNP-荧光 DNA 探针添加到目标 DNA 中。通过磁铁分离 MNP-DNA 探针-靶 DNA-DNA 探针-AuNP-荧光 DNA 探针复合物。荧光 DNA 探针从 AuNPs 表面释放出来,并通过荧光分光光度法读取荧光强度。测定了设计的纳生物传感器的灵敏度和特异性。结果表明,荧光强度随目标 DNA 浓度的增加而增加。在 2.3×10 至 2.3×10 CFU/mL 的范围内,观察到靶 DNA 与荧光强度之间存在线性关系。线性方程和回归为 Y=1.8X+23.4 和 R 0.9953。检测限(LOD)确定为 90 CFUmL。在存在其他细菌的情况下,确认了纳生物传感器的特异性。