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在亲水和疏水基底上原位自组装金纳米粒子用于流感病毒传感平台。

In situ self-assembly of gold nanoparticles on hydrophilic and hydrophobic substrates for influenza virus-sensing platform.

机构信息

Research Institute of Green Science and Technology, Shizuoka University, 836 Ohya Suruga-ku, Shizuoka 422-8529, Japan.

Department of Cogno-Mechatronics Engineering, Pusan National University, Busan 609-735, Korea.

出版信息

Sci Rep. 2017 Mar 14;7:44495. doi: 10.1038/srep44495.

Abstract

Nanomaterials without chemical linkers or physical interactions that reside on a two-dimensional surface are attractive because of their electronic, optical and catalytic properties. An in situ method has been developed to fabricate gold nanoparticle (Au NP) films on different substrates, regardless of whether they are hydrophilic or hydrophobic surfaces, including glass, 96-well polystyrene plates, and polydimethylsiloxane (PDMS). A mixture of sodium formate (HCOONa) and chloroauric acid (HAuCl) solution was used to prepare Au NP films at room temperature. An experimental study of the mechanism revealed that film formation is dependent on surface wettability and inter particle attraction. The as-fabricated Au NP films were further applied to the colorimetric detection of influenza virus. The response to the commercial target, New Caledonia/H1N1/1999 influenza virus, was linear in the range from 10 pg/ml to 10 μg/ml and limit of detection was 50.5 pg/ml. In the presence of clinically isolated influenza A virus (H3N2), the optical density of developed color was dependent on the virus concentration (10-50,000 PFU/ml). The limit of detection of this study was 24.3 PFU/ml, a limit 116 times lower than that of conventional ELISA (2824.3 PFU/ml). The sensitivity was also 500 times greater than that of commercial immunochromatography kits.

摘要

在二维表面上没有化学连接物或物理相互作用的纳米材料因其具有电子、光学和催化性能而受到关注。已经开发出一种原位方法来在不同的基底上制造金纳米颗粒 (Au NP) 薄膜,无论它们是亲水还是疏水表面,包括玻璃、96 孔聚苯乙烯板和聚二甲基硅氧烷 (PDMS)。使用甲酸钠 (HCOONa) 和氯金酸 (HAuCl) 溶液的混合物在室温下制备 Au NP 薄膜。对机制的实验研究表明,薄膜的形成取决于表面润湿性和颗粒间的吸引力。所制备的 Au NP 薄膜进一步应用于流感病毒的比色检测。对商用靶标,新喀里多尼亚/H1N1/1999 流感病毒的响应在 10 pg/ml 至 10 μg/ml 的范围内呈线性,检测限为 50.5 pg/ml。在存在临床分离的甲型流感病毒 (H3N2) 的情况下,显色的光密度取决于病毒浓度 (10-50,000 PFU/ml)。本研究的检测限为 24.3 PFU/ml,比传统 ELISA(2824.3 PFU/ml)低 116 倍。灵敏度也比商用免疫层析试剂盒高 500 倍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2714/5349514/858faff11332/srep44495-f1.jpg

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