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使用磁性形式的金纳米颗粒修饰的单分散多孔二氧化硅微球检测人血清中的谷胱甘肽。

Glutathione detection in human serum using gold nanoparticle decorated, monodisperse porous silica microspheres in the magnetic form.

作者信息

Gökçal Burcu, Hamaloğlu Kadriye Özlem, Kip Çiğdem, Güngör Selen Yağmur, Büber Esra, Tuncel Ali

机构信息

Chemical Engineering Department, Hacettepe University, Ankara, 06800, Turkey.

出版信息

Anal Methods. 2020 Nov 21;12(43):5219-5228. doi: 10.1039/d0ay01292k. Epub 2020 Oct 20.

DOI:10.1039/d0ay01292k
PMID:33079092
Abstract

A nanozyme for glutathione (GSH) detection in a broad concentration range was synthesized. GSH is usually detected up to an upper limit of 100 μM using current noble metal nanozymes due to the sharp decrease in the colorimetric response with the increasing GSH concentration. Strong inhibition of colorimetric reactions by GSH adsorbed onto noble metal based nanozymes in the form of non-porous, nanoscale particulate materials dispersed in an aqueous medium is the reason for the sharp decrease in the colorimetric response. In the present study, a new magnetic nanozyme synthesized by immobilization of Au nanoparticles (Au NPs) on magnetic, monodisperse porous silica microspheres (>5 μm) obtained by a "staged-shape templating sol-gel protocol" exhibited peroxidase-like activity up to a GSH concentration of 5000 μM. A more controlled linear decrease in the peroxidase-like activity with a lower slope with respect to that of similar nanozymes was observed with the increasing GSH concentration. The proposed design allowed the GSH detection in a broader concentration range depending on the adsorption of GSH onto the Au NPs immobilized on magnetic, monodisperse porous silica microspheres. A calibration plot allowing the detection of GSH in a broad concentration range up to 3300 μM was obtained using the magnetic nanozyme. The GSH concentration was also determined in human serum by elevating the upper detection range and adjusting the sensitivity of detection via controlling the nanozyme concentration.

摘要

合成了一种用于在宽浓度范围内检测谷胱甘肽(GSH)的纳米酶。由于随着GSH浓度增加比色响应急剧下降,目前使用贵金属纳米酶检测GSH的上限通常为100μM。以分散在水性介质中的无孔纳米级颗粒材料形式吸附在基于贵金属的纳米酶上的GSH对比色反应有强烈抑制作用,这是比色响应急剧下降的原因。在本研究中,通过将金纳米颗粒(Au NPs)固定在通过“分段形状模板溶胶 - 凝胶方案”获得的磁性、单分散多孔二氧化硅微球(>5μm)上合成的新型磁性纳米酶,在GSH浓度高达5000μM时表现出类过氧化物酶活性。随着GSH浓度增加,观察到类过氧化物酶活性以比类似纳米酶更低的斜率更可控地线性下降。所提出的设计允许根据GSH吸附到固定在磁性、单分散多孔二氧化硅微球上的Au NPs上,在更宽的浓度范围内检测GSH。使用磁性纳米酶获得了一个校准曲线,可在高达3300μM的宽浓度范围内检测GSH。还通过提高检测上限并通过控制纳米酶浓度来调整检测灵敏度,在人血清中测定了GSH浓度。

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