An enrichment system for glycoproteins using microfluidic paper-based analytical device with colorimetric detection

被引:0
|
作者
Zhang, Jian [1 ,2 ]
Liu, Yi [1 ]
Peng, Jiayi [1 ]
Li, Wenjing [1 ,2 ]
Miao, Yanqing [1 ,2 ]
Liu, Chunye [1 ,2 ]
机构
[1] Xian Med Univ, Sch Pharm, Xian 710021, Peoples R China
[2] Xian Med Univ, Inst Med, Xian 710021, Peoples R China
基金
中国国家自然科学基金;
关键词
Microfluidic paper-based analytical devices; Glycoproteins; Enrichment; Detachable design; Boronate; AFFINITY MONOLITHIC COLUMN; SELECTIVE ENRICHMENT; CORE; GLYCOSYLATION; RECOGNITION; BIOMARKERS; SEPARATION;
D O I
10.1016/j.microc.2024.110393
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We introduce a facile method for glycoprotein enrichment, separation, and detection using microfluidic paperbased analytical devices (mu PADs). The mu PADs comprise two distinct components: the enrichment region (Chip I) and the detection section (Chip II). The reusable Chip I is fabricated by immobilizing 3-aminophenylboronic acid (APBA) onto a circular paper substrate, demonstrating exceptional glycoprotein affinity. In disposable Chip II, glycoproteins react with periodic acid, generating carbonyl compounds that produce a purple-colored product upon reacting with the Schiff reagent. Alterations in color intensity are captured using an ordinary cell phone and are subsequently analyzed using Photoshop software. Observations note a linear increase in average color intensities from 1.0 x 10- 3 to 5.0 x 10- 3 mol/L, with an R2 value of 0.9927. The relative standard deviations (RSDs) of inter-day (n = 5) and intra-day (n = 5) assessments stand at 1.5 % and 1.4 %, respectively. Our proposed approach can effectively enrich an ovalbumin (OVA) solution with concentrations as low as 1.0 x 10-11 mol/L, resulting in enrichment rates of 107 to 108 times. The interference deviations of five substances relative to OVA lie within the range of - 2.0 % to + 2.0 %. The methodology successfully enriches glycoproteins from egg white samples diluted by a factor of 1 x 106, demonstrating that the proposed method is remarkably suitable for enriching glycoproteins from authentic samples.
引用
收藏
页数:6
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