Lo Ting-Chi, Wang Wen-Jyun, Chen Chih-Yen, Chang Jui-Cheng, Li Wei-Peng
Department of Medicinal and Applied Chemistry, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
Department of Electrophysics, National Yang Ming Chiao Tung University, Hsinchu 300, Taiwan.
Langmuir. 2025 May 20;41(19):12022-12029. doi: 10.1021/acs.langmuir.5c00591. Epub 2025 May 7.
As the global prevalence of diabetes continues to rise, the home health testing market has experienced rapid growth. Although blood glucose monitoring is widespread among diabetic patients, there remains a significant lack of testing methods for diabetic ketoacidosis. The present study developed a feasible electrochemical technique for ketoacid detection using serine-immobilized copper(I) oxide nanoparticles (CuO NPs) as the primary electrode material. Given that the serine on the nanoparticle surface enables conjugation with β-hydroxybutyrate (β-HBA) through an esterification reaction between the hydroxyl group of serine and carboxylic acid of β-HBA and another intramolecular nucleophilic acyl substitution between amine and ester groups to form irreversible amide bonding, thus resulting in the β-HBA deposition on the surface of the CuO NP-coated electrode. The quantification of β-HBA can be determined through current variations in amperometry measurement. The results showed a highly linear relationship between reductive current and β-HBA concentration at 0-20 mM, with a reasonable detection limit of 0.1 mM. Moreover, a reasonable mechanism involving the NP surface covering-mediated electrolysis enhancement was proposed. The present method reveals a promising direction in developing sensors for small molecule detection with high specificity and sensitivity.
随着全球糖尿病患病率持续上升,家庭健康检测市场经历了快速增长。尽管血糖监测在糖尿病患者中广泛存在,但糖尿病酮症酸中毒的检测方法仍严重匮乏。本研究开发了一种可行的电化学技术,以固定丝氨酸的氧化铜纳米颗粒(CuO NPs)作为主要电极材料用于酮酸检测。鉴于纳米颗粒表面的丝氨酸能够通过丝氨酸的羟基与β-羟基丁酸(β-HBA)的羧酸之间的酯化反应以及胺与酯基团之间的另一种分子内亲核酰基取代反应与β-HBA共轭,形成不可逆的酰胺键,从而导致β-HBA沉积在CuO NP修饰电极的表面。β-HBA的定量可以通过安培测量中的电流变化来确定。结果表明,在0-20 mM范围内,还原电流与β-HBA浓度之间存在高度线性关系,合理的检测限为0.1 mM。此外,还提出了一种涉及NP表面覆盖介导的电解增强的合理机制。本方法为开发具有高特异性和灵敏度的小分子检测传感器揭示了一个有前景的方向。