Graphene Oxide-based Magnetic Boronate-affinity Adsorbent for Extraction of Horseradish Peroxidase

被引:6
|
作者
Hou, Xing-Yu [1 ,2 ]
Tong, Yu-Kui [1 ]
Zhu, Fu-Gui [1 ]
Xia, Qin-Fei [1 ]
Tian, Miao-Miao [1 ]
机构
[1] Harbin Normal Univ, Coll Chem & Chem Engn, Key Lab Photochem Biomat & Energy Storage Mat, Harbin 150025, Heilongjiang, Peoples R China
[2] Jiamusi Univ, Coll Pharm, Jiamusi 154007, Peoples R China
关键词
Fe3O4@GO@APBA; Adsorbent; Graphene oxide; 3-Am nophenylboronic acid; Glycoprotein; Horseradish peroxidase; SELECTIVE EXTRACTION; ACID; NANOPARTICLES; SAMPLES; RECOGNITION; ENRICHMENT; BIOSENSOR;
D O I
10.1016/S1872-2040(20)60067-6
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Graphene oxide (GO) is a two-dimensional atom-thick sheet generated from an oxidation of graphene. GO possesses a range of reactive oxygen functional groups on the basal planes and edges, which makes it a good candidate in the field of separation and enrichment through chemical functionalization. In this work, GO-based Fe3O4 magnetic nanoparticles were prepared, and boronic acid groups were introduced by 3-aminophenylboronic acid (APBA) at the same time to improve the enrichment efficiency. Herein, the GO-based magnetic boronate-affinity adsorbent (Fe3O4@GO@APBA) was developed focusing on the specific capture of low abundance of glycoprotein. The composites gathered excellent characters of large specific surface area and biocompatibility of GO, strong magnetic responsiveness, and enhanced affinity properties of boronic acid. The proposed system showed better specificity for glycoprotein even in the presence of non-glycoproteins. As a result, the prepared Fe3O4@GO@APBA not only exhibited high selectivity for horseradish peroxidase (HRP), and an outstanding tolerance for interference, but also showed excellent rebinding rate for an extraction application. Furthermore, this method provided a reliable way to improve conventional magnetic adsorbent, and showed great potential in analysis of low-abundant glycoprotein from even complex samples.
引用
收藏
页码:E20158 / E20164
页数:7
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