乙二醇二甲基丙烯酸酯
分子印迹聚合物
分析物
分子印迹
甲基丙烯酸
选择性
分子识别
化学
色谱法
乙二醇
检出限
单体
组合化学
聚合物
分子
有机化学
催化作用
作者
Yasemin L. Mustafa,Hannah S. Leese
出处
期刊:ACS omega
[American Chemical Society]
日期:2023-02-21
卷期号:8 (9): 8732-8742
被引量:23
标识
DOI:10.1021/acsomega.2c08127
摘要
The development of sensitive and selective robust sensor materials for targeted biomarker detection aims to contribute to self-health monitoring and management. Molecularly imprinted polymeric (MIP) materials can perform as biomimetic recognition elements via tailored routes of synthesis for specific target analyte extraction and/or detection. In this work, a sensitive- and selective-lactate MIP has been developed utilizing methacrylic acid and ethylene glycol dimethacrylate as the functional monomer and cross-linker, respectively. The sensitivity of the as-synthesized imprinted species was evaluated by determining the target analyte retention, imprinting factor, and selectivity adsorption of up to 63.5%, 6.86, and 0.82, respectively. MIP selectivity elucidated the imprinting mechanism between the functional monomers and target analyte lactate, further experimentally evidenced by using structurally competitive analytes malic acid and sodium 2-hydroxybutyrate, where retentions of 22.6 and 25.2%, respectively, were observed. Understanding the specific intermolecular mechanisms of both the template analyte and structural interferents with the MIP enables experimentalists to make informed decisions regarding monomer-target and porogen selections and possible sites of interaction for improved molecular imprinting. This imprinting system highlights the potential to be further developed into artificial receptor sensor materials for the detection of disease.
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