基于自组装纳米材料的肽表面粘附靶细胞

IF 2.9 Q2 ELECTROCHEMISTRY
Hasret Turkmen
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引用次数: 0

摘要

以纳米颗粒为基础的多肽对电极表面进行非共价修饰不会改变电极的化学性质,但允许对细胞粘附进行电化学测量。本研究探讨了自修饰纳米材料/肽表面对细胞粘附的影响。这种与表面的粘附是由系统中由于-0H、硫、羰基或反应基团的存在而形成的负Gibs自由能引起的。在这项工作中使用了一种更便宜、更实用的电极表面靶向细胞粘附方法,该方法不使用重化学物质和EDC/NHS化学。通过将生物活性材料以可控方式固定在丝网印刷碳电极(SPCE)表面,以及这些材料提供的表面化学特性,构建了一个生物相容性自组装纳米材料肽表面平台,并通过电化学技术测量了细胞粘附性。在表征步骤之后,电化学技术为每个细胞系创建了电流值作为浓度函数的校准曲线。比较研究了所制备的生物活性电极表面与所选细胞系的粘附性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Self-assembling nanomaterial-based peptide surface for target cell adhesion
Non-covalent modification of electrode surfaces with nanoparticle-based peptides does not change the chemical properties of the electrode but allows electrochemical measurement of cell adhesion. This study examines the effect of self-modified nanomaterial/peptide surfaces on cell adhesion. This adhesion to the surface is caused by the negative Gibs free energy formed in the system because of the presence of -0H, sulfur, carbonyl, or reactive groups. A cheaper and more practical method for electrode surfaces targeting cell adhesion, which does not use heavy chemicals and EDC/NHS chemistry, is used in this work. Thanks to the bioactive materials immobilized on the screen-printed carbon electrode (SPCE) surface in a controlled manner and the surface chemistry offered by these materials, a biocompatible self-assembling nanomaterial-based peptide surface platform is created, and cell adhesion is measured by an electrochemical technique. After the characterization steps, electro­chemical techniques created a calibration curve of the current value as a function of concentration for each cell line. The adhesion of the generated bioactive electrode surfaces to the selected cell lines was examined comparatively.
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来源期刊
CiteScore
3.60
自引率
27.30%
发文量
90
审稿时长
6 weeks
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