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Development of a DNA Biosensor Using Magnetic Nanoparticles and Giant Magnetoresistance Sensor on Graphene Sheets

机译:在石墨烯片上使用磁性纳米粒子和巨型磁阻传感器的DNA生物传感器的开发。

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Graphene sheets were functionalized with fluorine or oxygen using plasma treatment under C3F8 gas or O-2 gas environment to fabricate DNA micropatterns. The regions on the outer side of the micropatterns were passivated with fluorine, and changes on the two different surfaces, oxygen groups on the inside of the patterned regions and fluorine on the outside of the patterned regions. The plasma treated areas were characterized by spatially resolved X-ray photoelectron spectroscopy (XPS). Probe DNA was selectively immobilized on the oxygenated graphene sheet via bifunctional molecules. Magnetic nanoparticles (MNPs) were used as a label to detect hybridization of specifically sequenced DNA. And we detected the specific sequenced DNA hybridization using giant magnetoresistance (GMR) sensors. The concentration of target DNA was 100 nM in 2x SSC containing 0.2% SDS. The shift voltage of the GMR sensor when the 5' MNP-labeled complementary and noncomplementary target DNA hybridized with the probe DNA was 86.12 +/- 16.37 mV and -24.74 +/- 5.60 mV, respectively.
机译:在C3F8气体或O-2气体环境下使用等离子体处理,通过氟或氧对石墨烯片进行功能化,以制造DNA微图案。微图案外侧的区域被氟钝化,并且在两个不同的表面上发生变化,在图案化区域的内部为氧基,在图案化区域的外部为氟。等离子体处理的区域通过空间分辨X射线光电子能谱(XPS)进行表征。探针DNA通过双功能分子选择性地固定在氧化石墨烯片上。磁性纳米颗粒(MNP)用作标记来检测特定测序DNA的杂交。然后,我们使用巨型磁阻(GMR)传感器检测了特定的测序DNA杂交。在含有0.2%SDS的2x SSC中,目标DNA的浓度为100 nM。当5'MNP标记的互补和非互补靶DNA与探针DNA杂交时,GMR传感器的移位电压分别为86.12 +/- 16.37 mV和-24.74 +/- 5.60 mV。

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