Nadzirah Sh, Azizah N, Hashim Uda, Gopinath Subash C B, Kashif Mohd
Institute of Nano Electronic Engineering,Universiti Malaysia Perlis, 01000 Kangar, Perlis, Malaysia.
Department of Electrical and Electronic Engineering, Faculty of Engineering, Universiti Malaysia Sarawak, 94300 Kota Samarahan, Sarawak, Malaysia.
PLoS One. 2015 Oct 7;10(10):e0139766. doi: 10.1371/journal.pone.0139766. eCollection 2015.
Nanoparticle-mediated bio-sensing promoted the development of novel sensors in the front of medical diagnosis. In the present study, we have generated and examined the potential of titanium dioxide (TiO2) crystalline nanoparticles with aluminium interdigitated electrode biosensor to specifically detect single-stranded E.coli O157:H7 DNA. The performance of this novel DNA biosensor was measured the electrical current response using a picoammeter. The sensor surface was chemically functionalized with (3-aminopropyl) triethoxysilane (APTES) to provide contact between the organic and inorganic surfaces of a single-stranded DNA probe and TiO2 nanoparticles while maintaining the sensing system's physical characteristics. The complement of the target DNA of E. coli O157:H7 to the carboxylate-probe DNA could be translated into electrical signals and confirmed by the increased conductivity in the current-to-voltage curves. The specificity experiments indicate that the biosensor can discriminate between the complementary sequences from the base-mismatched and the non-complementary sequences. After duplex formation, the complementary target sequence can be quantified over a wide range with a detection limit of 1.0 x 10(-13)M. With target DNA from the lysed E. coli O157:H7, we could attain similar sensitivity. Stability of DNA immobilized surface was calculated with the relative standard deviation (4.6%), displayed the retaining with 99% of its original response current until 6 months. This high-performance interdigitated DNA biosensor with high sensitivity, stability and non-fouling on a novel sensing platform is suitable for a wide range of biomolecular interactive analyses.
纳米颗粒介导的生物传感推动了医学诊断领域新型传感器的发展。在本研究中,我们制备并检测了带有铝叉指电极生物传感器的二氧化钛(TiO₂)晶体纳米颗粒特异性检测单链大肠杆菌O157:H7 DNA的潜力。使用皮安计测量该新型DNA生物传感器的电流响应来评估其性能。传感器表面用(3-氨丙基)三乙氧基硅烷(APTES)进行化学功能化,以在单链DNA探针的有机和无机表面与TiO₂纳米颗粒之间提供接触,同时保持传感系统的物理特性。大肠杆菌O157:H7的靶DNA与羧酸盐探针DNA的互补可转化为电信号,并通过电流-电压曲线中电导率的增加得到证实。特异性实验表明,该生物传感器能够区分互补序列与碱基错配序列和非互补序列。双链形成后,互补靶序列可在宽范围内定量,检测限为1.0×10⁻¹³M。对于来自裂解的大肠杆菌O157:H7的靶DNA,我们能够获得相似的灵敏度。固定有DNA的表面稳定性通过相对标准偏差(4.6%)计算得出,显示在6个月内其原始响应电流保留了99%。这种在新型传感平台上具有高灵敏度、稳定性和抗污染性的高性能叉指式DNA生物传感器适用于广泛的生物分子相互作用分析。