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Morphology and Activity of Biological Fabrics Prepared by Electrospray Deposition Method

机译:电喷雾沉积法制备的生物织物的形态和活性

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Protein nanofabrics were prepared by the electrospray deposition (ESD) method from the aqueous solutions of a-lactalbumin (a-LA), invertaze, immunoglobulin (IgG), and orLA with poly(vinyl alcohol) (PVA), and their surface morphologies and biological activities were characterized. The surface morphologies of the deposited films were observed using scanning electron microscopy (SEM) and atomic force microscopy (AFM). The SEM and AFM images showed that the film surfaces had a fine porous structure, in which the pore diameters ranged from 40 to 600 nm. The biological activities were tested by the mechano-chemical method, a microarray-based enzyme linked immunosorbent assay (ELISA), and fluorescence immunoassay (FIA) format. It was demonstrated that the activities of the deposited protein fabrics were preserved during the ESD. The results revealed that the ESD method was useful for producing fine porous protein nanofabrics with biological activities. The porous protein fabric opens a new direction in the application of biomaterials. To improve the sensitivity of the protein nanofabric, it should be attempted to control the nano-scaled structure and fine porous morphology of the fabric surface. ESD technique also can be extended to the protein fabrics combined with polymeric nanofibers.
机译:通过电喷雾沉积(ESD)方法由来自乳蛋白(A-La)的水溶液,拒载,免疫球蛋白(IgG)和用聚(乙烯醇)(PVA)的orla和它们的表面形态和它们的表面形态和蛋白质纳米制剂表征生物活性。使用扫描电子显微镜(SEM)和原子力显微镜(AFM)观察沉积膜的表面形态。 SEM和AFM图像显示膜表面具有精细多孔结构,其中孔径范围为40至600nm。通过机械化学方法,微阵列的酶联免疫吸附测定(ELISA)和荧光免疫测定(FIA)形式进行生物学活性。结果证明,在ESD期间保存了沉积的蛋白质织物的活性。结果表明,ESD方法可用于生产具有生物活性的细多孔蛋白纳米制剂。多孔蛋白质织物在生物材料的应用中打开了新的方向。为了提高蛋白质纳米谱的敏感性,应该试图控制粉底状结构和织物表面的细孔形态。 ESD技术也可以扩展到与聚合物纳米纤维结合的蛋白质织物。

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