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Hydroxylamine-O-sulfonic acid as a New Reducing Agent for the Formation of Nearly Monodisperse Gold Nanoparticles in water: Synthesis Characterisation and Bioconjugation

机译:羟胺-O-磺酸作为在水中形成几乎单分散的金纳米颗粒的新型还原剂:合成表征和生物共轭

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Gold nanoparticles (Au NPs), with diameters ranging between 15 and 150 nm have been synthesized in water. 15 and 30 nm Au NPs were obtained by the Turkevich and Frens method using sodium citrate as both a reducing and stabilising agent at high temperature (Au NPs-citrate), while 60, 90 and 150 nm were formed using hydroxylamine-o-sulfonic acid (HOS) as a reducing agent for HAuCl_4 at room temperature. This new method using HOS is an extension of approaches previously reported for producing Au NPs with mean diameters above 40 nm by direct reduction. Functionalised polyethylene glycol-based thiol polymers were used to stabilise the pre-synthesised Au NPs. The nanoparticles obtained were characterised using uv-visible spectroscopy, dynamic light scattering (DLS) and transmission electron microscopy (TEM). Further biocojuguation on 15, 30 and 90 nm PEGylated Au NPs were performed by grafting Bovine Serum Albumin, Transferrin and Apolipoprotein E (ApoE).
机译:已经在水中合成了直径在15到150 nm之间的金纳米颗粒(Au NPs)。通过Turkevich和Frens方法使用柠檬酸钠作为高温的还原剂和稳定剂(柠檬酸Au NPs)获得15和30 nm的Au NPs,而使用羟胺-邻磺酸形成60、90和150 nm的Au NPs。 (HOS)在室温下作为HAuCl_4的还原剂。这种使用HOS的新方法是先前报道的通过直接还原生产平均直径大于40 nm的Au NP的方法的扩展。功能化的基于聚乙二醇的硫醇聚合物用于稳定预合成的金纳米颗粒。使用紫外可见光谱,动态光散射(DLS)和透射电子显微镜(TEM)对获得的纳米颗粒进行表征。通过嫁接牛血清白蛋白,转铁蛋白和载脂蛋白E(ApoE),在15、30和90 nm PEG化的Au NP上进行进一步的生物共轭。

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