Bio-Interface & Environmental Engineering Lab, Department of Biosciences and Bioengineering , Indian Institute of Technology Guwahati , Guwahati , Assam 781039 , India.
Langmuir. 2018 Mar 20;34(11):3494-3506. doi: 10.1021/acs.langmuir.7b03152. Epub 2018 Mar 7.
Although metallic biomaterials find numerous biomedical applications, their inherent low bioactivity and poor osteointegration had been a great challenge for decades. Surface modification via silanization can serve as an attractive method for improving the aforementioned properties of such substrates. However, its effect on protein adsorption/conformation and subsequent cell adhesion and spreading has rarely been investigated. This work reports the in-depth study of the effect of Ti6Al4V surface functionalization on protein adsorption and cell behavior. We prepared self-assembled monolayers (SAMs) of five different surfaces (amine, octyl, mixed [1:1 ratio of amine:octyl], hybrid, and COOH). Synthesized surfaces were characterized by Fourier transform infrared-attenuated total reflection (FTIR-ATR) spectroscopy, contact angle goniometry, profilometry, and field emission scanning electron microscopy (FESEM). Quantification of adsorbed mass of bovine serum albumin (BSA) and fibronectin (FN) was determined on different surfaces along with secondary structure analysis. The adsorbed amount of BSA was found to increase with an increase in surface hydrophobicity with the maximum adsorption on the octyl surface while the reverse trend was detected for FN adsorption, having the maximum adsorbed mass on the COOH surface. The α-helix content of adsorbed BSA increased on amine and COOH surfaces while it decreased for other surfaces. Whereas increasing β-turn content of the adsorbed FN with the increase in the surface hydrophobicity was observed. In FN, RGD loops are located in the β-turn and consequently the increase in Δ adhered cells (%) was predominantly increased with the increasing Δ β-turn content (%). We found hybrid surfaces to be the most promising surface modifier due to maximum cell adhesion (%) and proliferation, larger nuclei area, and the least cell circularity. Bacterial density increased with the increasing hydrophobicity and was found maximum for the amine surface (θ = 63 ± 1°) which further decreased with the increasing hydrophobicity. Overall, modified surfaces (in particular hybrid surface) showed better protein adsorption and cell adhesion properties as compared to unmodified Ti6Al4V and can be potentially used for tissue engineering applications.
虽然金属生物材料在众多生物医学应用中得到了广泛应用,但它们固有的低生物活性和较差的骨整合能力在几十年来一直是一个巨大的挑战。通过硅烷化进行表面改性可以作为一种有吸引力的方法,用于改善这些基底的上述性能。然而,其对蛋白质吸附/构象以及随后的细胞黏附和铺展的影响很少被研究。本工作报道了 Ti6Al4V 表面功能化对蛋白质吸附和细胞行为影响的深入研究。我们制备了五种不同表面(胺、辛基、混合[胺:辛基比为 1:1]、杂化和 COOH)的自组装单层(SAM)。通过傅里叶变换衰减全反射(FTIR-ATR)光谱、接触角测角法、轮廓法和场发射扫描电子显微镜(FESEM)对合成表面进行了表征。在不同表面上定量测定了牛血清白蛋白(BSA)和纤维连接蛋白(FN)的吸附量,并进行了二级结构分析。BSA 的吸附量随着表面疏水性的增加而增加,在辛基表面上吸附量最大,而 FN 的吸附量则相反,在 COOH 表面上吸附量最大。吸附的 BSA 的α-螺旋含量在胺和 COOH 表面上增加,而在其他表面上则减少。而吸附的 FN 的β-转角含量随表面疏水性的增加而增加。在 FN 中,RGD 环位于β-转角中,因此,与β-转角含量的增加(%)相关的粘附细胞的增加(%)占主导地位。我们发现杂化表面是最有前途的表面改性剂,因为它具有最高的细胞黏附(%)和增殖率、更大的核面积和最小的细胞圆度。细菌密度随疏水性的增加而增加,在胺表面(θ=63±1°)达到最大值,随后随疏水性的增加而降低。总的来说,与未改性的 Ti6Al4V 相比,改性表面(特别是杂化表面)表现出更好的蛋白质吸附和细胞黏附性能,可潜在用于组织工程应用。