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Minimalism in Radiation Synthesis of Biomedical Functional Nanogels

机译:极简主义的辐射合成生物医学功能纳米凝胶。

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摘要

A scalable, single-step, synthetic approach for the manufacture of biocompatible, functionalized micro- and nanogels is presented. In particular, poly(N-vmyl pyrrolidone)-grafted-(aminopropyl)methacrylamide microgels and nanogels were generated through e-beam irradiation of PVP aqueous solutions in the presence of a primary amino-group-carrying monomer. Particles with different hydrodynamic diameters and surface charge densities were obtained at the variance of the irradiation conditions. Chemical structure was investigated by different spectroscopic techniques. Fluorescent variants were generated through fluorescein isothiocyanate attachment to the primary amino groups grafted to PVP, to both quantify the available functional groups for bioconjugation and follow nanogels localization in cell cultures. Finally, a model protein, bovine serum albumin, was conjugated to the nanogels to demonstrate the attachment of biologically relevant molecules for targeting purposes in drug delivery. The described approach provides a novel strategy to fabricate biohybrid nanogels with a very promising potential in nanomedicine.
机译:提出了一种可扩展的单步合成方法,用于制造生物相容的功能化微凝胶和纳米凝胶。特别地,在带有伯氨基基团的单体存在下,通过电子束照射PVP水溶液,生成了聚(N-乙烯基吡咯烷酮)-接枝的(氨基丙基)甲基丙烯酰胺微凝胶和纳米凝胶。在照射条件的变化下获得具有不同流体动力学直径和表面电荷密度的颗粒。通过不同的光谱技术研究化学结构。通过将异硫氰酸荧光素附着到接枝到PVP的伯氨基上来产生荧光变体,以量化可用于生物缀合的官能团并遵循纳米凝胶在细胞培养物中的定位。最后,将模型蛋白牛血清白蛋白偶联到纳米凝胶上,以证明生物学上相关分子的附着以靶向药物递送为目的。所描述的方法提供了一种新颖的策略来制造在纳米医学中具有非常有前途潜力的生物杂交纳米凝胶。

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