聚合物使能碳纳米管沉积在细胞审讯中的应用

B. Chu, E. Pierstorff, D. Ho
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引用次数: 0

摘要

我们利用嵌段共聚物薄膜作为模板沉积单壁碳纳米管的模式,以应用于单细胞审讯。细胞活动(如神经元、心肌细胞等)的跨膜研究常常受到探针诱导的膜破裂的侵袭性的限制。这通常排除了慢性活动分析。我们开发了一种共聚物-碳纳米管(P-CNT)混合材料,由于共聚物的仿生刚度加上P-CNT复合物的纳米尺寸,该材料有望应用于非侵入性细胞探测,具有减轻炎症的潜力。我们采用了由聚环氧乙烷-甲基丙烯酸甲酯组成的二嵌段共聚物;PEO-PMMA)以及由聚甲基氯恶唑-聚二甲基硅氧烷-聚甲基氯恶唑啉组成的丙烯酸酯端端两亲性“ABA”三嵌段共聚物;通过Langmuir-Blodgett方法,将PMOXA-PDMS-PMOXA)作为碳纳米管沉积的支撑基质。这使得碳纳米管悬浮在空气-水界面上,转移到金衬底上。循环伏安法测量证实碳纳米管与金衬底直接连接,以实现电气功能。此外,细胞粘附在聚合物底物上,证实了p -碳纳米管材料的生物相容性。碳纳米管涂层电极也被检测为生物电极,用于监测由细胞色素c介质驱动的氧化还原过程,其中碳纳米管/聚合物涂层表面也能够促进抗蛋白质吸附,从而观察到蛋白质和电极之间的可逆电子转移。这是通过采集明显的阳极和阴极峰来证明的,峰间距为64mV,这证实了一个可逆的转移过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Polymer-Enabled Carbon Nanotube Deposition for Cellular Interrogation Applications
We have utilized a block copolymeric thin film as a modality to template the deposition of single-walled carbon nanotubes towards applications in single cell interrogation. Transmembrane studies of cellular activity (e.g. neurons, cardiomyocytes, etc.) have often been limited by the invasiveness of probe-induced membrane rupture. This often precludes chronic activity analysis. We have developed a copolymer-carbon nanotube (P-CNT) hybrid material for potential applications in non-invasive cell probing with attenuated inflammation due to the biomimetic stiffness of the copolymer coupled with nanoscale dimensions of the P-CNT complex. We applied both a diblock copolymer comprised of poly(ethylene oxide-b-methyl methacrylate; PEO-PMMA) as well as an acrylate-terminated amphiphilic `ABA' triblock copolymer comprised of polymethyloxazoline-polydimethylsiloxane-polymethyloxazoline; PMOXA-PDMS-PMOXA) as the supporting matrix for carbon nanotube deposition via the Langmuir-Blodgett methodology. This enabled the suspension of the carbon nanotubes on the air-water interface for transfer to a gold substrate. Cyclic voltammetry measurements confirmed that the CNT's were interfaced directly with the gold substrates to enable electrical functionality. In addition, cellular adhesion to the polymeric substrate was demonstrated, confirming the biocompatibility of the P-CNT material. CNT-coated electrodes were also examined as biological electrodes for the monitoring of oxidation-reduction processes driven by the cytochrome c mediator, where CNT/polymer-coated surfaces were also capable of facilitating anti-protein adsorption, resulting in the observation of reversible electron transfer between the protein and electrode. This was demonstrated via acquisition of pronounced anodic and cathodic peaks with peak separations of 64mV, which confirmed a reversible transfer process.
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