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Synthesis and bio-applications of carbohydrate-gold nanoconjugates with nanoparticle and nanolayer forms

机译:具有纳米粒子和纳米层形式的糖金纳米复合物的合成及生物应用

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摘要

Carbohydrate-conjugated gold nanopartides (GNPs) and gold nanolayers (GNLs), which have recently attracted increasing attention as innovative nano-biomaterials, were successfully synthesized using carbohydrate thiosemicarbazones in an aqueous N-methylmorpholine N-oxide (NMMO) system. This system can dissolve various types of carbohydrates including structural polysaccharides, e.g., cellulose. We observed that oxidative NMMO solvent unexpectedly promoted the immediate reduction of [Au~Ⅲ Cl_4]~- species to nanosized metallic Au°, that is GNP. One possible mechanism is that the chloride ligand was oxidized to chlorate via the formation of a hypochlorite intermediate. Site-selective S-labeling of sugar reducing ends with thiosemicarbazide may have enabled regulated self-assembly immobilization to the surfaces of GNPs and GNLs. The carbohydrate-gold nanoconjugates possess unique nanoarchitectures and biofunctions for carbohydrate-cell interactions. Novel and simple approaches for the structural design of carbohydrate-decorated GNPs and GNLs in the NMMO system have potential to inspire a new phase in glyco-biomaterials eneineerine.
机译:糖类共轭金纳米粒子(GNP)和金纳米层(GNL)作为创新的纳米生物材料,最近已受到越来越多的关注,它们是在水-N-甲基吗啉N-氧化物(NMMO)系统中成功地使用碳水化合物硫代半氨基甲酮合成的。该系统可以溶解各种类型的碳水化合物,包括结构性多糖,例如纤维素。我们发现,氧化NMMO溶剂出乎意料地促进了[Au〜ⅢCl_4]〜-物种立即还原为纳米级金属Au°,即GNP。一种可能的机理是氯化物配体通过形成次氯酸盐中间体而被氧化成氯酸盐。用硫代氨基脲对糖还原端进行选择性S标记可能使GNP和GNL表面的自组装固定化。碳水化合物-金纳米共轭物具有独特的纳米结构和碳水化合物-细胞相互作用的生物功能。 NMMO系统中糖修饰的GNP和GNL的结构设计的新颖而简单的方法有可能激发糖生物材料烯丙氨酸的新阶段。

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