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用于与纳米换能器直接集成的分子印迹聚合物的可见光光引发转移终止剂聚合

Visible-Light Photo-Iniferter Polymerization of Molecularly Imprinted Polymers for Direct Integration with Nanotransducers.

作者信息

Di Giulio Tiziano, Asif Muhammad Ibrar, Corsi Martina, De Benedetto Giuseppe Egidio, Malitesta Cosimino, Haupt Karsten, Barillaro Giuseppe, Gonzato Carlo, Mazzotta Elisabetta

机构信息

Laboratory of Analytical Chemistry, Department of Biological and Environmental Sciences and Technologies (Di.S.Te.B.A.), University of Salento, via Monteroni, Lecce, 73100, Italy.

Information Engineering Department, University of Pisa, via G. Caruso 16, Pisa, 56122, Italy.

出版信息

Small Methods. 2025 Apr;9(4):e2401315. doi: 10.1002/smtd.202401315. Epub 2025 Jan 24.

Abstract

Molecularly Imprinted Polymers (MIPs) have gained prominence as synthetic receptors, combining simplicity of synthesis with robust molecular recognition akin to antibodies and enzymes. One of their main application areas is chemical sensing. However, direct integration of MIPs with nanostructured transducers, crucial for enhancing sensing capabilities and broadening MIPs sensing applications, remains limited. This limitation mainly arises from the need for precise control over the MIP features (such as thickness) during deposition on nanostructured transducers. This work explores the potential of depositing MIPs directly onto nanostructured transducers via controlled radical photopolymerization, focusing on nanoporous silica (PSiO) with pore sizes of 40 nm and aspect ratio exceeding 100 as an interferometric optical nanotransducer. Leveraging the covalent attachment of a photo-iniferter agent onto the PSiO surface, we achieved effective control over the polymerization process, resulting in the deposition of thin and uniform MIP layers on PSiO. As a case study, we developed an MIP-based PSiO optical sensor for propranolol, used as the template molecule, showcasing excellent linearity, a low detection limit, and efficacy in real matrices such as tap water. The results further demonstrate the sensor selectivity for the target molecule, along with its reusability and stability for at least 60 days.

摘要

分子印迹聚合物(MIPs)作为合成受体已受到广泛关注,它兼具合成简便性和类似于抗体及酶的强大分子识别能力。其主要应用领域之一是化学传感。然而,MIPs与纳米结构换能器的直接集成仍然有限,而这种集成对于增强传感能力和拓宽MIPs传感应用至关重要。这种限制主要源于在纳米结构换能器上沉积过程中需要精确控制MIP的特征(如厚度)。这项工作探索了通过可控自由基光聚合将MIPs直接沉积到纳米结构换能器上的潜力,重点研究了孔径为40纳米且纵横比超过100的纳米多孔二氧化硅(PSiO)作为干涉式光学纳米换能器。利用光引发转移终止剂在PSiO表面的共价连接,我们实现了对聚合过程的有效控制,从而在PSiO上沉积了薄而均匀的MIP层。作为一个案例研究,我们开发了一种基于MIP的PSiO光学传感器用于普萘洛尔(用作模板分子),该传感器展示出优异的线性、低检测限以及在诸如自来水等实际基质中的有效性。结果进一步证明了该传感器对目标分子的选择性,以及其至少60天的可重复使用性和稳定性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08c9/12020366/1c2c10ab656f/SMTD-9-2401315-g001.jpg

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