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Incorporation of proteins and enzymes at different stages of the preparation of calcium phosphate coatings on a degradable substrate by a biomimetic methodology

机译:通过仿生方法在可降解基材上制备磷酸钙涂层的不同阶段掺入蛋白质和酶

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摘要

In this work, the possibility of incorporating proteins into calcium phosphate (Ca-P) coatings, prepared on the surface of starchpolymeric biomaterials by means of a biomimetic route, was investigated. The morphology, chemical composition and crystallinity of Ca-P coatings was assessed and related to the incorporation of the studied biomolecules. For that, bovine serum albumin (BSA) and aamylase were added in concentrations of 1 mg/ml to simulated body fluid (SBF) solutions, being both added at the nucleation or growth stages of the biomimetic coating process. A biodegradable blend of corn starch/ethylene vinyl alcohol (SEVA-C) was used as substrate and bioactive glass (45S5 BioglassR) was used as the nucleating agent. The obtained Ca-P coatings were characterised by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), Fourier transform infrared spectroscopy using an attenuatedreflectance device (FTIR-ATR) and thin-film X-ray diffraction (TF-XRD). Additionally, to evaluate the activity of the incorporatedenzyme and the stability of the Ca-P films, coated samples were immersed in an SBF solution for different periods of time. The enzyme activity was measured and the morphology of the coating examined by SEM. The results obtained showed that the presence of protein molecules, at the nucleation or growth stages, lead to the formation of a dense Ca-P film presenting different morphologies that weredifferent of the selected coating conditions. FTIR-ATR analysis detected the presence of carbonate and phosphate groups on the Ca-Player, indicating the formation of a coating similar to the mineral component of vertebrates bone tissue. When proteins were added, amide I and amide II bands, characteristic groups of protein molecules, were also detected, revealing the efficient incorporation of these biomolecules into the Ca-P coatings.Ca-P coatings, with a-amylase incorporated at the nucleation stage, showed no degradation of the film after incubation in SBF for 28 days. The release of increasing concentration of reducing sugars with degradation time revealed that a-amylase was efficiently incorporated in the coating remaining active throughout the coating preparation. This can be a strategy that will allow, in addition of conferring osteoconductive properties to biodegradable polymers, also simultaneously tailoring their degradation kinetics.
机译:在这项工作中,研究了通过仿生途径将蛋白质掺入在淀粉聚合生物材料表面制备的磷酸钙(Ca-P)涂层中的可能性。评估了Ca-P涂层的形态,化学组成和结晶度,并与所研究的生物分子的掺入有关。为此,将牛血清白蛋白(BSA)和淀粉酶以1 mg / ml的浓度添加到模拟体液(SBF)溶液中,两者均在仿生涂层过程的成核或生长阶段添加。玉米淀粉/乙烯乙烯醇(SEVA-C)的可生物降解混合物用作基质,而生物活性玻璃(45S5 BioglassR)用作成核剂。通过扫描电子显微镜(SEM),能量色散光谱(EDS),使用衰减反射装置(FTIR-ATR)和薄膜X射线衍射(TF-XRD)的傅立叶变换红外光谱对获得的Ca-P涂层进行表征。另外,为了评估掺入的酶的活性和Ca-P膜的稳定性,将涂覆的样品浸入SBF溶液中不同的时间。测量酶活性,并通过SEM检查涂层的形态。获得的结果表明,在成核或生长阶段,蛋白质分子的存在导致形成致密的Ca-P膜,该膜呈现出与所选择的包被条件不同的不同形态。 FTIR-ATR分析检测到Ca-Player上存在碳酸根和磷酸根,这表明涂层的形成类似于脊椎动物骨骼组织的矿物质成分。当添加蛋白质时,还检测到了蛋白质分子的特征基团酰胺I和酰胺II带,表明这些生物分子有效地掺入了Ca-P涂层中.Ca-P涂层在成核阶段掺入了a-淀粉酶在SBF中温育28天后,显示膜未降解。随着降解时间的增加,还原糖浓度的增加释放出α-淀粉酶被有效地掺入包衣中,并在整个包衣制剂中保持活性。这可以是一种策略,除了赋予可生物降解的聚合物以骨传导性,还可以同时调整其降解动力学。

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