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首页> 外文期刊>Journal of biomaterials and nanobiotechnology. >Study of Human Serum Albumin Adsorption and Conformational Change on DLC and Silicon Doped DLC Using XPS and FTIR Spectroscopy
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Study of Human Serum Albumin Adsorption and Conformational Change on DLC and Silicon Doped DLC Using XPS and FTIR Spectroscopy

机译:XPS和FTIR光谱研究人血清白蛋白在DLC和硅掺杂DLC上的吸附和构象变化

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摘要

Diamond-like carbon (DLC) coatings are extremely useful for creating biocompatible surfaces on medical implants. DLC and silicon doped DLC synthesised on silicon wafer substrate by using plasma enhanced chemical vapour deposition (PECVD). The effects of surface morphology on the interaction of HSA with doped and undoped DLC films have been investigated. The chemical composition of the surface before and after adsorption was analysed using X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared (FTIR). Results showed that silicon incorporation DLC tends to increase of sp3/sp2 hybridization ratio by decreasing sp2 hybridized carbon bonding configurations. Following exposure to solutions containing (0.250 μg/ml) HSA, the results indicated that significant changes in the C, N and O levels on the surfaces with reducing of the Si2p band at 100 eV. From FTIR spectrum, the peaks occur the following functional groups were assigned as amide I and II groups at 1650 cm-1 and 1580 cm-1. Both XPS and FTIR spectroscopy confirm that HSA was bound onto the surfaces of the DLC and Si-DLC films via interaction of ionized carboxyl groups and the amino group did not play a significant role in the adsorption of protein. These results from peak intensity show that an adsorbed layer of HSA is higher at high level (19%) silicon doping. Therefore doping of DLC may provide an approach to controlling the protein adsorption.
机译:类金刚石碳(DLC)涂层对于在医疗植入物上创建生物相容性表面非常有用。通过使用等离子体增强化学气相沉积(PECVD)在硅晶片基板上合成DLC和掺杂硅的DLC。研究了表面形态对HSA与掺杂和未掺杂DLC膜相互作用的影响。使用X射线光电子能谱(XPS)和傅里叶变换红外(FTIR)分析了吸附前后的表面化学成分。结果表明,掺入硅的DLC倾向于通过降低sp2杂化碳键构型来提高sp3 / sp2杂化率。暴露于含有(0.250μg/ ml)HSA的溶液后,结果表明表面上C,N和O含量发生了显着变化,且Si2p带在100 eV处减少。根据FTIR光谱,在1650cm-1和1580cm-1处出现以下官能团为酰胺I和II基团的峰。 XPS和FTIR光谱均证实,HSA通过离子化羧基的相互作用结合到DLC和Si-DLC膜的表面上,而氨基在蛋白质的吸附中不起重要作用。这些来自峰值强度的结果表明,在高水平(19%)的硅掺杂下,HSA的吸附层更高。因此,DLC的掺杂可以提供控制蛋白质吸附的方法。

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