Escuela de Ingeniería y Ciencias, Tecnologico de Monterrey, Ave. Eugenio Garza Sada 2501, Monterrey 64849, NL, Mexico.
Department of Biomedical Engineering, Faculty of Engineering, University of Malaya, Kuala Lumpur 50603, Malaysia.
Sensors (Basel). 2017 Oct 9;17(10):2292. doi: 10.3390/s17102292.
In this article, a combination of far field electrospinning (FFES) and free-radical polymerization has been used to create a unique platform for protein immobilization via the physical attachment of biomolecules to the surface of the fiber mats. The large specific surface area of the fibers with its tailored chemistry provides a desirable platform for effective analyte-surface interaction. The detailed analysis of protein immobilization on a newly developed bio-receptive surface plays a vital role to gauge its advantages in bio-diagnostic applications. We relied on scanning electron microscopy (SEM), diameter range analysis, and X-ray photoelectron spectroscopy (XPS), along with thermal gravimetric analysis (TGA), water-in-air contact angle analysis (WCA), Fourier transform infrared spectroscopy (FTIR), and atomic force microscopy (AFM) to study our developed platforms and to provide valuable information regarding the presence of biomolecular entities on the surface. Detailed analyses of the fiber mats before and after antibody immobilization have shown obvious changes on the surface of the bioreceptive surface including: (i) an additional peak corresponding to the presence of an antibody in TGA analysis; (ii) extra FTIR peaks corresponding to the presence of antibodies on the coated fiber platforms; and (iii) a clear alteration in surface roughness recorded by AFM analysis. Confirmation analyses on protein immobilization are of great importance as they underlay substantial grounds for various biosensing applications.
本文采用远场电纺(FFES)与自由基聚合相结合的方法,通过生物分子物理附着在纤维垫表面,来创建蛋白质固定化的独特平台。纤维的大比表面积及其定制化学性质为有效分析物-表面相互作用提供了理想的平台。对新开发的生物亲和表面上蛋白质固定化的详细分析对于评估其在生物诊断应用中的优势起着至关重要的作用。我们依靠扫描电子显微镜(SEM)、直径范围分析和 X 射线光电子能谱(XPS),以及热重分析(TGA)、气-水接触角分析(WCA)、傅里叶变换红外光谱(FTIR)和原子力显微镜(AFM)来研究我们开发的平台,并提供有关生物分子实体在表面存在的有价值信息。对抗体固定化前后纤维垫的详细分析表明,生物亲和表面的表面发生了明显变化,包括:(i)TGA 分析中存在抗体的附加峰;(ii)涂覆纤维平台上存在抗体的额外 FTIR 峰;以及(iii)AFM 分析记录的表面粗糙度明显改变。蛋白质固定化的确认分析非常重要,因为它们为各种生物传感应用提供了重要基础。