BioMark Sensor Research, School of Engineering of the Polytechnic Institute of Porto, 4249-015 Porto, Portugal.
CEB, Centre of Biological Engineering, Minho University, 4710-057 Braga, Portugal.
ACS Appl Bio Mater. 2021 May 17;4(5):4224-4235. doi: 10.1021/acsabm.1c00039. Epub 2021 Apr 19.
In this work, the conjugation of molecularly imprinted polymers (MIPs) to quantum dots (QDs) was successfully applied in the assembly of an imprinted cellulose membrane [hydroxy ethyl cellulose (HEC)/MIP@QDs] for the specific recognition of the cardiac biomarker myoglobin (Myo) as a sensitive, user-friendly, and portable system with the potential for point-of-care (POC) applications. The concept is to use the MIPs as biorecognition elements, previously prepared on the surface of semiconductor cadmium telluride QDs as detection particles. The fluorescent quenching of the membrane occurred with increasing concentrations of Myo, showing linearity in the interval range of 7.39-291.3 pg/mL in a1000-fold diluted human serum. The best membrane showed a linear response below the cutoff values for myocardial infarction (23 ng/mL), a limit of detection of 3.08 pg/mL, and an imprinting factor of 1.65. The incorporation of the biorecognition element MIPs on the cellulose substrate brings an approach toward a portable and user-friendly device in a sustainable manner. Overall, the imprinted membranes display good stability and selectivity toward Myo when compared with the nonimprinted membranes (HEC/NIP@QDs) and have the potential to be applied as a sensitive system for Myo detection in the presence of other proteins. Moreover, the conjugation of MIPs to QDs increases the sensitivity of the system for an optical label-free detection method, reaching concentration levels with clinical significance.
在这项工作中,成功地将分子印迹聚合物(MIPs)与量子点(QDs)结合在一起,组装了一种印迹纤维素膜[羟乙基纤维素(HEC)/MIP@QDs],用于特异性识别心脏生物标志物肌红蛋白(Myo),作为一种敏感、用户友好且便携的系统,具有即时检测(POC)应用的潜力。该概念是使用 MIPs 作为生物识别元件,预先制备在半导体碲化镉 QDs 的表面作为检测粒子。随着 Myo 浓度的增加,膜的荧光猝灭发生,在稀释 1000 倍的人血清中,在 7.39-291.3 pg/mL 的区间内呈现线性关系。最佳膜在心肌梗死(23 ng/mL)的截止值以下显示出线性响应,检测限为 3.08 pg/mL,印迹因子为 1.65。将生物识别元件 MIPs 掺入纤维素基质中,为便携式和用户友好的设备提供了一种可持续的方法。总体而言,与非印迹膜(HEC/NIP@QDs)相比,印迹膜对 Myo 具有良好的稳定性和选择性,并且有可能作为一种在存在其他蛋白质时检测 Myo 的敏感系统。此外,MIPs 与 QDs 的结合增加了系统对光学无标记检测方法的灵敏度,达到了具有临床意义的浓度水平。