State and Local Joint Engineering Laboratory for Novel Functional Polymeric Materials, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, PR China.
State and Local Joint Engineering Laboratory for Novel Functional Polymeric Materials, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, PR China.
Colloids Surf B Biointerfaces. 2019 May 1;177:448-453. doi: 10.1016/j.colsurfb.2019.02.030. Epub 2019 Feb 16.
Poly(N-vinylpyrrolidone) (PVP)-modified surfaces have been shown to possess excellent protein resistance and good biocompatibility. However, PVP-modified surfaces with different molecular architectures have not been prepared, and their protein-resistant properties have not been studied. Herein, gold surfaces modified with linear PVP brush and PVP bottle-brush architectures were prepared by photoinitiated surface grafting polymerization. Ellipsometry, X-ray photoelectron spectroscopy (XPS), water contact angle, Fourier transform infrared (FTIR) spectroscopy and atomic force microscopy (AFM) were utilized to characterize the prepared surfaces. The protein-resistant properties were investigated by a quartz crystal microbalance with dissipation (QCM-D) with bovine serum albumin (BSA), fibrinogen (Fg) and lysozyme (Lyz). Compared with the ungrafted QCM-D chips, the PVP bottle-brush-grafted chips (9.3 nm thickness) showed superior protein resistance over linear PVP brush-grafted chips (9.9 nm thickness). Furthermore, the PVP bottle-brushes reduced the levels of BSA, Fg and Lyz adsorption by 97%, 85% and 69%, respectively. Moreover, to demonstrate potential applications as functional biosensors and in the biomedical field, PVP bottle-brushes containing glycopolymer-grafted gold surfaces were fabricated. Laser scanning confocal microscopy (LSCM) demonstrated that these glycopolymer surfaces showed excellent protein resistance and specific ConA binding ability. Overall, we speculate that the data presented here can provide useful information for the development of excellent antifouling materials and functional biosensors.
聚(N-乙烯基吡咯烷酮)(PVP)修饰表面已被证明具有优异的抗蛋白质性能和良好的生物相容性。然而,具有不同分子结构的 PVP 修饰表面尚未被制备,其抗蛋白质性能也尚未被研究。在此,通过光引发表面接枝聚合制备了线性 PVP 刷和 PVP 瓶刷结构修饰的金表面。利用椭偏仪、X 射线光电子能谱(XPS)、水接触角、傅里叶变换红外(FTIR)光谱和原子力显微镜(AFM)对制备的表面进行了表征。通过石英晶体微天平(QCM-D)用牛血清白蛋白(BSA)、纤维蛋白原(Fg)和溶菌酶(Lyz)研究了蛋白质的抗附着性能。与未接枝的 QCM-D 芯片相比,PVP 瓶刷接枝芯片(9.3nm 厚)表现出优于线性 PVP 刷接枝芯片(9.9nm 厚)的抗蛋白质性能。此外,PVP 瓶刷降低了 BSA、Fg 和 Lyz 的吸附水平,分别为 97%、85%和 69%。此外,为了展示作为功能生物传感器和在生物医学领域的潜在应用,制备了含有糖聚合物接枝金表面的 PVP 瓶刷。激光共聚焦显微镜(LSCM)表明,这些糖聚合物表面表现出优异的抗蛋白质性能和特异性 ConA 结合能力。总体而言,我们推测这里提供的数据可以为开发优异的抗污材料和功能生物传感器提供有用的信息。