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用于潜在生物医学应用的钴铬合金上纳米尺寸膦酸自组装单层的形成。

Formation of nanosized phosphonic acid self assembled monolayers on cobalt-chromium alloy for potential biomedical applications.

机构信息

Center for Materials Research (CMR), Norfolk State University, Norfolk, Virginia 23508, USA.

出版信息

J Biomed Nanotechnol. 2010 Apr;6(2):117-28. doi: 10.1166/jbn.2010.1106.

Abstract

Formation of nanosized self assembled monolayers (SAMs) of carboxyl terminated 16-Phosphonohexadecanoic acid (16-PA) and methyl terminated Octadecylphosphonic acid (ODPA) on Cobalt-Chromium (Co-Cr) alloy have been successfully demonstrated. Nanosized monolayers were formed by adsorption of these phosphonic acid SAMs on bare Co-Cr alloy by solution deposition technique. The formation of the nanosized monolayers was confirmed by using characterization techniques like Fourier Transform Infrared Spectroscopy (FTIR) with Attenuated Total Reflectance (ATR) attachment, Atomic Force Microscopy (AFM), X-ray Photoelectron Spectroscopy (XPS), Ellipsometry and Contact Angle measurements. FTIR confirmed the SAM formation due to the presence of characteristic stretching vibration of SAM functional groups. FTIR studies suggest the binding of the phosphonic SAMs to be a combination of mono and bidentate binding. XPS showed presence of phosphorous peak and an increase in carbon peak intensity after SAM deposition, while it consequently showed decrease in peak intensity of the metal alloy (Co and Cr) peaks. AFM images gave good understanding of the topography, surface roughness and uniformity of SAM formation. Ellipsometric studies indicate nanosized thickness of the SAMs formed, while contact angle measurements showed changes in surface hydrophilicity/hydrophobicity after SAM formation. By tailoring the terminal functional group of these SAMs on Co-Cr alloy these nanosized monolayers could be potentially used for various biomedical applications such as localized drug delivery, biocompatibility, tissue integration etc.

摘要

成功地展示了羧酸封端的 16-膦酸十六烷酸(16-PA)和十八烷基膦酸(ODPA)的纳米自组装单层(SAM)在钴铬(Co-Cr)合金上的形成。通过溶液沉积技术,这些磷酸 SAM 通过吸附在裸 Co-Cr 合金上形成纳米级单层。通过傅里叶变换红外光谱(FTIR)与衰减全反射(ATR)附件、原子力显微镜(AFM)、X 射线光电子能谱(XPS)、椭圆光度法和接触角测量等特性技术证实了纳米级单层的形成。FTIR 证实了 SAM 的形成,因为存在 SAM 官能团的特征伸缩振动。FTIR 研究表明,磷酸 SAM 的结合是单和双配位的组合。XPS 显示在 SAM 沉积后存在磷峰和碳峰强度增加,而金属合金(Co 和 Cr)峰的峰强度随后降低。AFM 图像很好地了解了 SAM 形成的形貌、表面粗糙度和均匀性。椭圆光度研究表明形成的 SAM 的纳米级厚度,而接触角测量表明 SAM 形成后表面亲水性/疏水性发生变化。通过对 Co-Cr 合金上这些 SAM 的末端官能团进行剪裁,这些纳米级单层可能会在局部药物输送、生物相容性、组织整合等各种生物医学应用中得到应用。

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