Department of Chemistry and Institute of BioPhysio Sensor Technology (IBST), Pusan National University, Busan, 46241, Republic of Korea.
Department of Chemistry and Institute of BioPhysio Sensor Technology (IBST), Pusan National University, Busan, 46241, Republic of Korea; Korea Mouse Metabolic Phenotyping Center, Lee Gil Ya Cancer and Diabetes Institute, and Internal Medicine, Gil Medical Center, Gachon University, Incheon, 21565, Republic of Korea.
Biosens Bioelectron. 2019 Oct 1;142:111515. doi: 10.1016/j.bios.2019.111515. Epub 2019 Jul 15.
Separation and detection of hemoglobin (Hb) and glycated hemoglobin fractions (HbA1c, HbAld, HbAle, HbAld3a, HbAl, HbA2, and HbAld3b) was performed using an electrochemical AC field modulated separation channel (EMSC) coupled with a sensor probe. The sensor was fabricated based on immobilization of a redox mediator on the poly(2,2':5',5″-terthiophene-3'-p-benzoic acid, pTTBA) and N,S-doped porous carbon (NSPC) nanocomposite. The different types of catalytic redox mediators such as Nile Blue (NB), toluidine blue O (TBO), and Neutral Red (NR) were evaluated to achieve the efficient detection. Of these, the NB-based sensor showed the best analytical signal for Hb and HbA1c, thus it was characterized using various electrochemical and surface analysis methods. After that, the sensor was coupled with the EMSC to achieve the separation detection of the Hb family. The frequency and amplitude of the AC electrical field applied onto the EMSC walls were the main driving forces for the separation and sensitive detection of the analytes. Under optimized conditions, linear dynamic ranges for Hb and HbA1c among their fractions were obtained between 1.0 × 10 to 3.5 mM and 3.0 × 10 to 0.6 mM with the detection limit of 8.1 × 10 ± 3.0 × 10 and 9.2 × 10 ± 5 × 10 mM, respectively. Interference effects of other biomolecules were also investigated and the clinical applicability of the device was evaluated by the determination of total Hb and % HbA1c in real human blood samples.
采用电化学 AC 场调制分离通道 (EMSC) 与传感器探头相结合的方法,对血红蛋白 (Hb) 和糖化血红蛋白 (HbA1c、HbAld、HbAle、HbAld3a、HbAl、HbA2 和 HbAld3b) 进行分离和检测。该传感器基于聚(2,2':5',5″-三噻吩-3′-对苯二甲酸,pTTBA)和 N,S-掺杂多孔碳 (NSPC) 纳米复合材料上固定氧化还原介体来制备。评估了不同类型的催化氧化还原介体,如尼罗蓝 (NB)、甲苯胺蓝 O (TBO) 和中性红 (NR),以实现高效检测。其中,基于 NB 的传感器对 Hb 和 HbA1c 表现出最佳的分析信号,因此使用各种电化学和表面分析方法对其进行了表征。之后,将传感器与 EMSC 耦合,实现了 Hb 家族的分离检测。施加在 EMSC 壁上的 AC 电场的频率和幅度是分离和敏感检测分析物的主要驱动力。在优化条件下,Hb 和 HbA1c 及其各组分的线性动态范围分别在 1.0×10 到 3.5×10 和 3.0×10 到 0.6×10 mM 之间,检测限分别为 8.1×10±3.0×10 和 9.2×10±5×10 mM。还研究了其他生物分子的干扰效应,并通过测定真实人血样中的总 Hb 和 %HbA1c 评估了该设备的临床适用性。