Smail Soren M, Laibinis Paul E, Weiss Sharon M
Interdisciplinary Materials Science Graduate Program, Vanderbilt University, Nashville, Tennessee 37235, United States.
Department of Chemical and Biomolecular Engineering, Vanderbilt University, Nashville, Tennessee 37235, United States.
ACS Omega. 2025 Jul 16;10(29):31932-31939. doi: 10.1021/acsomega.5c03495. eCollection 2025 Jul 29.
Porous silicon (PSi)-based biosensors are a promising platform for quantitative rapid diagnostics, but they have not broadly realized clinically relevant limits of detection due, in part, to poor baseline stability. Baseline instability can be attributed to two major physicochemical challengeshydrolysis of PSi in aqueous solutions and fouling by unwanted biological species, both of which can obscure the detection of target molecules at low concentrations. In this work, PSi was thermally hydrosilated with vinylbenzyl chloride (VBC) to incorporate hydrolytically stable Si-C bonding and to provide an attached alkyl halide termination for further chemistry. Subsequent grafting of zwitterionic poly-(sulfobetaine methacrylate) (SBMA) from this PSi-VBC layer by surface-initiated atom-transfer radical polymerization (siATRP) formed an antifouling coating. Films both with and without the antifouling polymer were exposed to PBS (pH 7.4) and human blood serum, and optical reflectance measurements were used to monitor hydrolysis and nonspecific adsorption. PSi-VBC-polySBMA surfaces exhibited little to no nonspecific binding, as determined by ATR-FTIR and optical reflectance measurements, due to their hydrophilicity. The compatibility of hydrosilylation and siATRP with various chemical groups provides significant versatility in this surface chemistry approach, as well as facilitates the incorporation of highly specific capture agents. By directly addressing the issues of hydrolysis and fouling, this strategy holds promise for reducing the limits of detection in complex biological samples.
基于多孔硅(PSi)的生物传感器是用于定量快速诊断的一个很有前景的平台,但部分由于基线稳定性差,它们尚未广泛实现临床相关的检测限。基线不稳定可归因于两个主要的物理化学挑战——PSi在水溶液中的水解以及不需要的生物物种造成的污染,这两者都可能掩盖低浓度下目标分子的检测。在这项工作中,PSi用乙烯基苄基氯(VBC)进行热硅氢化,以引入水解稳定的Si-C键,并提供连接的卤代烷基端基用于进一步的化学反应。随后通过表面引发的原子转移自由基聚合(siATRP)从该PSi-VBC层接枝两性离子聚(甲基丙烯酸磺酸甜菜碱)(SBMA)形成防污涂层。将有和没有防污聚合物的薄膜暴露于PBS(pH 7.4)和人血清中,并使用光反射率测量来监测水解和非特异性吸附。通过ATR-FTIR和光反射率测量确定,PSi-VBC-polySBMA表面由于其亲水性而几乎没有非特异性结合。硅氢化和siATRP与各种化学基团的兼容性在这种表面化学方法中提供了显著的通用性,并且有助于掺入高度特异性的捕获剂。通过直接解决水解和污染问题,该策略有望降低复杂生物样品中的检测限。