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Development of DNA Biosensor Based on TiO_2 Nanoparticles

机译:基于TiO_2纳米粒子的DNA生物传感器的开发

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A novel technique of DNA hybridization on the TiO_2 nanoparticles film was developed by dropping a single droplet of target DNA onto the surface of TiO_2 for the study of various concentrations of target DNA. The surface of TiO_2 nanoparticle film was functionalized with APTES and covalently immobilized with 1 μM probe DNA on the silanized TiO_2 nanoparticles surface. The effect of silanization, immobilization and hybridization were quantitatively measured by the output current signal obtained using a picoammeter. The 1 μM target DNA was found to be the most effective target towards the 1μM probe DNA as the output current signal was within range; while the output current signal of the 10 μM target DNA was observed to beyond the range of the probe DNA control due to the excessive concentration as compared to the probe DNA. This approach has several advantages such as rapid, simple, low cost, and sensitive current signal during detection of different target DNA concentrations.
机译:通过将单滴靶DNA滴到TiO_2的表面上,通过将各种浓度的靶DNA进行研究,通过将单滴液滴滴入TiO_2纳米粒子膜上的DNA杂交技术。 TiO_2纳米颗粒膜的表面用Aptes官能化,并在硅烷化TiO_2纳米颗粒表面上与1μM探针DNA共价固定。通过使用Picoambeter获得的输出电流信号定量测量硅烷化,固定和杂交的效果。发现1μM靶DNA是最有效的靶向1μM探针DNA,因为输出电流信号在范围内;虽然与探针DNA相比,观察到10μM靶DNA的输出电流信号超过探针DNA控制的范围,但由于过量的浓度而过度。在检测到不同靶DNA浓度期间,这种方法具有多种优点,例如快速,简单,低成本和敏感的电流信号。

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