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Electrophoretic Characterization and Purification of Silica-Coated Photon-Upconverting Nanoparticles and Their Bioconjugates

机译:二氧化硅包覆的光子上转换纳米粒子及其生物共轭物的电泳表征和纯化

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摘要

Photon-upconverting nanoparticles (UCNPs) have attracted much interest as a new class of luminescent label for the background-free detection in bioanalytical applications. UCNPs and other nanoparticles are commonly coated with a silica shell to improve their dispersibility and chemical stability in aqueous buffer and to incorporate functional groups for subsequent bioconjugation steps. The process of silica coating, however, is difficult to control without suitable analytical and preparative methods. Here, we have introduced agarose gel electrophoresis for the analysis and purification of silica-coated UCNPs. The silica shell can be doped with a fluorescent dye for direct detection in the gel without influencing the structure or electrophoretic mobility of the nanoparticles. The preparation of a bare silica shell by reverse microemulsion resulted in individual nanoparticles but also distinct aggregates that could be separated and isolated from the agarose gel. In contrast, the preparation of an ultrathin carboxylated silica shell yielded non-aggregated UCNPs only that could be directly used for protein conjugation. Agarose gel electrophoresis has also facilitated an efficient separation of protein—UCNP conjugates from excess reagents.
机译:作为用于生物分析应用中无背景检测的新型发光标记,光子上转换纳米颗粒(UCNP)引起了人们的极大兴趣。 UCNP和其他纳米粒子通常涂有二氧化硅外壳,以改善其在水性缓冲液中的分散性和化学稳定性,并为后续的生物缀合步骤引入官能团。但是,如果没有合适的分析和制备方法,则很难控制二氧化硅涂层的过程。在这里,我们介绍了琼脂糖凝胶电泳,用于分析和纯化硅胶包被的UCNP。二氧化硅壳可以掺杂有荧光染料,以便在凝胶中直接检测,而不会影响纳米粒子的结构或电泳迁移率。通过反向微乳液制备二氧化硅裸壳,得到了单个的纳米颗粒,但也产生了可以从琼脂糖凝胶中分离和分离的独特聚集体。相反,超薄羧化二氧化硅壳的制备仅产生非聚集的UCNP,其可直接用于蛋白质偶联。琼脂糖凝胶电泳还促进了蛋白质-UCNP共轭物与过量试剂的有效分离。

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