Department of Chemistry, Faculty of Science, Yazd University, Yazd, Iran.
Department of Chemistry, Faculty of Science, Yazd University, Yazd, Iran.
Biosens Bioelectron. 2021 May 15;180:113124. doi: 10.1016/j.bios.2021.113124. Epub 2021 Mar 2.
An innovative label-free electrochemical aptasensing platform has been designed for detection of insulin using functionalized mesoporous silica thin-film (MSTF) coated on a glassy carbon electrode through the one-step electrochemically assisted self-assembly (EASA) method. This strategy is contingent upon the covalent attachment of a complementary DNA (cDNA) oligonucleotide sequence on the mesoporous silica surface, for which further hybridization with its labeled aptamer as a gating molecule restricts the diffusion of the electroactive probe (Fe(CN)-) toward the electrode surface by the closing of mesochannels. Upon insulin introduction as the stimulus target molecule, hybridization between aptamer and cDNA is efficiently destroyed, which triggers the opening of nanochannels to facilitate redox probe diffusion toward the electrode with a noticeable increase in differential pulse voltammetry signal. The proposed aptasensor showed a wide detection ranging from 10.0 to 350.0 nM and a suitable detection limit of 3.0 nM. This method offers the sensitive and rapid detection of insulin without the need for cargo (dye/fluorophore) as an electrochemical marker inside the pore, at low cost and with a fast modification time.
一种创新的无标记电化学适体传感平台已被设计用于通过一步电化学辅助自组装 (EASA) 方法在玻碳电极上涂覆功能化介孔硅薄膜 (MSTF) 来检测胰岛素。该策略取决于将互补 DNA (cDNA) 寡核苷酸序列共价连接到介孔硅表面,然后通过封闭介孔来进一步与标记的适体进行杂交作为门控分子,限制了电化学探针 (Fe(CN) 6 3-) 向电极表面的扩散。当胰岛素作为刺激靶分子引入时,适体和 cDNA 之间的杂交被有效地破坏,这触发纳米通道的打开,有利于氧化还原探针向电极扩散,差分脉冲伏安法信号显著增加。所提出的适体传感器显示出从 10.0 到 350.0 nM 的宽检测范围和 3.0 nM 的合适检测限。该方法提供了对胰岛素的灵敏和快速检测,而无需在孔内作为电化学标记物使用货物(染料/荧光团),成本低且修饰时间快。