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Polymer surface functionalities that control human embryoid body cell adhesion revealed by high throughput surface characterization of combinatorial material microarrays

机译:通过组合材料微阵列的高通量表面表征揭示了控制人胚状体细胞粘附的聚合物表面功能

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摘要

High throughput materials discovery using combinatorial polymer microarrays to screen for new biomaterials with new and improved function is established as a powerful strategy. Here we combine this screening approach with high throughput surface characterization (HT-SC) to identify surface structure function relationships. We explore how this combination can help to identify surface chemical moieties that control protein adsorption and subsequent cellular response. The adhesion of human embryoid body (hEB) cells to a large number (496) of different acrylate polymers synthesized in a microarray format is screened using a high throughput procedure. To determine the role of the polymer surface properties on hEB cell adhesion, detailed HT-SC of these acrylate polymers is carried out using time of flight secondary ion mass spectrometry (ToF SIMS), X-ray photoelectron spectroscopy (XPS), pico litre drop sessile water contact angle (WCA) measurement and atomic force microscopy (AFM). A structure function relationship is identified between the ToF SIMS analysis of the surface chemistry after a fibronectin (Fn) pre-conditioning step and the cell adhesion to each spot using the multivariate analysis technique partial least squares (PLS) regression. Secondary ions indicative of the adsorbed Fn correlate with increased cell adhesion whereas glycol and other functionalities from the polymers are identified that reduce cell adhesion. Furthermore, a strong relationship between the ToF SIMS spectra of bare polymers and the cell adhesion to each spot is identified using PLS regression. This identifies a role for both the surface chemistry of the bare polymer and the pre-adsorbed Fn, as-represented in the ToF SIMS spectra, in controlling cellular adhesion. In contrast, no relationship is found between cell adhesion and wettability, surface roughness, elemental or functional surface composition. The correlation between ToF SIMS data of the surfaces and the cell adhesion demonstrates the ability to identify surface moieties that control protein adsorption and subsequent cell adhesion using ToF SIMS and multivariate analysis. (C) 2010 Elsevier Ltd. All rights reserved.
机译:使用组合聚合物微阵列筛选具有新功能和改进功能的新生物材料的高通量材料发现已被确立为一项强大的策略。在这里,我们将这种筛选方法与高通量表面表征(HT-SC)相结合,以识别表面结构功能关系。我们探索这种组合如何可以帮助识别控制蛋白质吸附和后续细胞反应的表面化学部分。使用高通量方法筛选了人胚状体(hEB)细胞对大量(496)以微阵列形式合成的不同丙烯酸酯聚合物的粘附力。为了确定聚合物表面性质对hEB细胞粘附的作用,使用飞行时间二次离子质谱(ToF SIMS),X射线光电子能谱(XPS),微微升升对这些丙烯酸酯聚合物进行了详细的HT-SC分析。无水接触角(WCA)测量和原子力显微镜(AFM)。使用多元分析技术偏最小二乘(PLS)回归,在纤连蛋白(Fn)预处理步骤后对表面化学进行ToF SIMS分析与细胞粘附于每个斑点之间,确定了结构函数关系。指示吸附的Fn的次级离子与增加的细胞粘附力相关,而从聚合物中分离出的乙二醇和其他官能团可降低细胞粘附力。此外,使用PLS回归可以确定裸露的聚合物的ToF SIMS光谱与细胞粘附于每个斑点之间的密切关系。这确定了ToF SIMS光谱中代表的裸露聚合物的表面化学和预吸附的Fn在控制细胞粘附方面的作用。相反,在细胞粘附性和润湿性,表面粗糙度,元素或功能性表面组成之间未发现任何关系。表面的ToF SIMS数据与细胞粘附之间的相关性证明了使用ToF SIMS和多变量分析能够识别控制蛋白质吸附和后续细胞粘附的表面部分的能力。 (C)2010 Elsevier Ltd.保留所有权利。

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