Cabrero-Martín Andrea, Santiago Sara, Serafín Verónica, Montero-Calle Ana, Pingarrón José M, Barderas Rodrigo, Campuzano Susana
Departamento de Química Analítica, Facultad de CC. Químicas, Universidad Complutense de Madrid, Pza. de Las Ciencias 2, 28040, Madrid, Spain.
Chronic Disease Programme, UFIEC, Institute of Health Carlos III, 28220, Majadahonda, Madrid, Spain.
Mikrochim Acta. 2025 May 27;192(6):377. doi: 10.1007/s00604-025-07232-8.
The use of gold-silica nanoconjugates (Au@SiO₂NCs) decorated with biotinylated detection antibodies (b-dAb) and horseradish peroxidase (HRP) is reported for the improved electrochemical immunosensing of chemokine ligand-12 (CXCL12), a relevant chemokine implicated in colorectal cancer (CRC) progression. Implemented on an amperometric sandwich immunoplatform the resulting nanobioconjugates provided significant signal amplification which is attributed to the high enzyme loading capacity and improved antibody orientation. The role played by each of the nanomaterials forming the nanohybrid was evaluated. Under optimized conditions, the developed immunoplatform exhibited a linear response ranging from 72 to 1000 pg mL, a 4 times higher sensitivity than the conventional labeling-based immunoplatform, a LOD of 22 pg mL, and a storage stability of 1 month. The immunoplatform was applied to the determination of CXCL12 in plasma from healthy individuals and CRC patients. The clinically relevant results obtained demonstrate the potential of plasma CXCL12 levels as a biomarker for both the early diagnosis of CRC and the monitoring of its progression.
报道了使用用生物素化检测抗体(b-dAb)和辣根过氧化物酶(HRP)修饰的金-二氧化硅纳米共轭物(Au@SiO₂NCs)来改进对趋化因子配体-12(CXCL12)的电化学免疫传感,CXCL12是一种与结直肠癌(CRC)进展相关的趋化因子。在电流型夹心免疫平台上实施后,所得的纳米生物共轭物提供了显著的信号放大,这归因于高酶负载能力和改进的抗体取向。评估了构成纳米杂化物的每种纳米材料所起的作用。在优化条件下,所开发的免疫平台表现出72至1000 pg mL的线性响应,灵敏度比传统的基于标记的免疫平台高4倍,检测限为22 pg mL,储存稳定性为1个月。该免疫平台应用于健康个体和CRC患者血浆中CXCL12的测定。所获得的具有临床相关性的结果证明了血浆CXCL12水平作为CRC早期诊断和进展监测生物标志物的潜力。