Centre for Sustainable Circular Technologies, Department of Chemistry, University of Bath, Bath BA2 7AY, U.K.
Materials for Health Lab, Department of Chemical Engineering, University of Bath, Bath BA2 7AY, U.K.
ACS Appl Bio Mater. 2021 Sep 20;4(9):7243-7253. doi: 10.1021/acsabm.1c00774. Epub 2021 Aug 19.
Today, we heavily rely on technology and increasingly utilize it to monitor our own health. The identification of sensitive, accurate biosensors that are capable of real-time cortisol analysis is one important potential feature for these technologies to aid us in the maintenance of our physical and mental wellbeing. Detection and quantification of cortisol, a well-known stress biomarker present in sweat, offers a noninvasive and potentially real-time method for monitoring anxiety. Molecularly imprinted polymers are attractive candidates for cortisol recognition elements in such devices as they can selectively rebind a targeted template molecule. However, mechanisms of imprinting and subsequent rebinding depend on the choice and composition of the prepolymerization mixture where the molecular interactions between the template, functional monomer, cross-linker, and solvent molecules are not fully understood. Here, we report the synthesis and evaluation of a molecularly imprinted polymer selective for cortisol detection. Molecular dynamics simulations were used to investigate the interactions between all components in the prepolymerization mixture of the as-synthesized molecularly imprinted polymer. Varying the component ratio of the prepolymerization mixture indicates that the number of cross-linker molecules relative to the template impacts the quality of imprinting. It was determined that a component ratio of 1:6:30 of cortisol, methacrylic acid, and ethylene glycol dimethacrylate, respectively, yields the optimal theoretical complexation of cortisol for the polymeric systems investigated. Experimental synthesis and rebinding results demonstrate an imprinting factor of up to 6.45. The trends in cortisol affinity predicted by molecular dynamics simulations of the prepolymerization mixture were also corroborated through experimental analysis of those modeled molecularly imprinted compositions, demonstrating the predictive capabilities of these simulations.
如今,我们严重依赖技术,并越来越多地利用技术来监测自己的健康。识别敏感、准确的生物传感器,使其能够实时分析皮质醇,是这些技术的一个重要潜在功能,有助于我们保持身心健康。检测和定量汗液中已知的应激生物标志物皮质醇,为监测焦虑提供了一种非侵入性且潜在的实时方法。分子印迹聚合物是这些设备中皮质醇识别元件的有吸引力的候选物,因为它们可以选择性地重新结合靶向模板分子。然而,印迹和随后的重新结合的机制取决于预聚合混合物的选择和组成,其中模板、功能单体、交联剂和溶剂分子之间的分子相互作用尚未完全理解。在这里,我们报告了一种选择性检测皮质醇的分子印迹聚合物的合成和评价。分子动力学模拟用于研究预聚合混合物中所有成分之间的相互作用。改变预聚合混合物的成分比例表明,交联剂分子相对于模板的数量会影响印迹的质量。确定皮质醇、甲基丙烯酸和乙二醇二甲基丙烯酸酯的预聚合混合物的成分比例分别为 1:6:30 时,对于所研究的聚合体系,皮质醇的最佳理论络合效果最佳。实验合成和重新结合结果表明,印迹因子高达 6.45。通过对预聚合混合物进行分子动力学模拟预测的皮质醇亲和力趋势,也通过对模拟的分子印迹成分进行实验分析得到了证实,证明了这些模拟的预测能力。