Boonsriwong Worachote, Chunta Suticha, Thepsimanon Nonthawat, Singsanan Sanita, Lieberzeit Peter A
Faculty of Medicine, Bangkok Thonburi University, Bangkok 10170, Thailand.
Department of Clinical Chemistry, Faculty of Medical Technology, Prince of Songkla University, Songkhla 90110, Thailand.
Polymers (Basel). 2021 May 27;13(11):1763. doi: 10.3390/polym13111763.
Herein we demonstrate molecularly imprinted polymers (MIP) as plastic antibodies for a microplate-based assay. As the most abundant plasma protein, human serum albumin (HSA) was selected as the target analyte model. Thin film MIP was synthesized by the surface molecular imprinting approach using HSA as the template. The optimized polymer consisted of acrylic acid (AA) and -vinylpyrrolidone (VP) in a 2:3 (/) ratio, crosslinked with -(1,2-dihydroxyethylene) bisacrylamide (DHEBA) and then coated on the microplate well. The binding of MIP toward the bound HSA was achieved via the Bradford reaction. The assay revealed a dynamic detection range toward HSA standards in the clinically relevant 1-10 g/dL range, with a 0.01 g/dL detection limit. HSA-MIP showed minimal interference from other serum protein components: γ-globulin had 11% of the HSA response, α-globulin of high-density lipoprotein had 9%, and β-globulin of low-density lipoprotein had 7%. The analytical accuracy of the assay was 89-106% at the 95% confidence interval, with precision at 4-9%. The MIP-coated microplate was stored for 2 months at room temperature without losing its binding ability. The results suggest that the thin film plastic antibody system can be successfully applied to analytical/pseudoimmunological HSA determinations in clinical applications.
在此,我们展示了分子印迹聚合物(MIP)作为用于基于微孔板分析的塑料抗体。作为最丰富的血浆蛋白,人血清白蛋白(HSA)被选作目标分析物模型。采用表面分子印迹法以HSA为模板合成了薄膜MIP。优化后的聚合物由丙烯酸(AA)和N-乙烯基吡咯烷酮(VP)按2:3(体积比)的比例组成,用N,N'-(1,2-二羟基亚乙基)双丙烯酰胺(DHEBA)交联,然后涂覆在微孔板孔上。MIP与结合的HSA的结合通过考马斯亮蓝反应实现。该分析方法对临床相关的1-10 μg/dL范围内的HSA标准品显示出动态检测范围,检测限为0.01 μg/dL。HSA-MIP对其他血清蛋白成分的干扰极小:γ-球蛋白的响应为HSA的11%,高密度脂蛋白的α-球蛋白为9%,低密度脂蛋白的β-球蛋白为7%。在95%置信区间下,该分析方法的分析准确度为89-106%,精密度为4-9%。涂有MIP的微孔板在室温下储存2个月后仍未丧失其结合能力。结果表明,薄膜塑料抗体系统可成功应用于临床分析/假免疫HSA测定。