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Fabrication and Characterization of a Test Platform Integrating Nanoporous Structures With Biochemical Functionality

机译:纳米孔结构与生化功能集成的测试平台的制造和表征。

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The application of solid-state nanopore technology for biosensing is a rapidly developing area of research with high commercial potential. Different synthetic materials, including silicon nitride, alumina, and polymers, are employed to fabricate single and multiple pores and offer a good platform for selective biomolecule detection. Two solid-state pore arrays, one with integrated silicon microfluidic system, were considered and an immobilization strategy suitable for detecting a single-stranded DNA (ssDNA) sequence was investigated. For the silicon nitride pores, a modification method based on the use of 3-aminopropyltriethoxysilane for silanization and 1,4-phenylene diisothiocyanate for amine crosslinking was applied to immobilize 100-nM ssDNA (amine C6) and a 100-nM limit of detection for complementary to probe ssDNA (Cy5) was estimated. The polycarbonate pores (the second type of the pore arrays) underwent surface modification based on an oxidation reduction reaction using sodium periodate and sodium borohydride and was used to immobilize 10-nM ssDNA and an estimated 100-nM limit of detection was also achieved. Linear sweep voltammetry was used to characterize the pores and a current potential profile was obtained after both immobilization of probe ssDNA and hybridization of complementary to probe ssDNA on the modified pore array surface. A decrease in current amplitude was measured after surface modification of both pore arrays, and this was attributed to the appearance of an additional layer on the pore surface reducing the pore opening and hindering the current flow. The hybridization event was also supported by contact angle measurements, where an increase in hydrophilicity was recorded at the different surface modification steps that were applied to produce the biofunctionalized nanopore. In addition, fluorescence was observed on the surfaces after hybridization, through incorporation of a CY5 fluorescent tag attached on the 5’ end of the complemen- ary to probe DNA. These results show the potential to use both silicon nitride and polycarbonate nanopores in DNA detection applications.
机译:固态纳米孔技术在生物传感中的应用是具有高商业潜力的快速发展的研究领域。使用包括氮化硅,氧化铝和聚合物在内的不同合成材料来制造单个和多个孔,并为选择性生物分子检测提供了良好的平台。考虑了两个固态孔阵列,其中一个具有集成的硅微流体系统,并研究了适合检测单链DNA(ssDNA)序列的固定策略。对于氮化硅孔,应用了基于3-氨基丙基三乙氧基硅烷进行硅烷化和1,4-亚苯基二异硫氰酸酯用于胺交联的修饰方法,以固定100-nM ssDNA(胺C6)和100-nM的检测限估计与探针ssDNA(Cy5)互补。基于高碘酸钠和硼氢化钠的氧化还原反应,对聚碳酸酯孔(孔阵列的第二种类型)进行了表面修饰,并用于固定10-nM ssDNA,并且估计达到了100-nM的检测限。使用线性扫描伏安法来表征孔,并且在修饰的孔阵列表面上固定探针ssDNA和与探针ssDNA的互补物杂交后,获得了电流势分布。在对两个孔阵列进行表面修饰之后,测量了电流幅度的减小,这归因于孔表面上出现了额外的层,从而减少了孔的开口并阻碍了电流。接触角测量也支持了杂交事件,其中在用于生产生物功能化纳米孔的不同表面改性步骤中记录了亲水性的增加。此外,杂交后,通过在互补序列的5'末端掺入CY5荧光标签来探测DNA,从而在表面上观察到荧光。这些结果表明在DNA检测应用中同时使用氮化硅和聚碳酸酯纳米孔的潜力。

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