Plasmonic nanosized molecularly imprinted polymer (nanoMIP) as innovative optical lateral flow immunoassay probes

被引:1
作者
Serra, Thea [1 ,5 ]
Nieddu, Salvatore [1 ]
Cavalera, Simone [1 ,6 ]
Perez-Juste, Jorge [7 ]
Pastoriza-Santos, Isabel [2 ,3 ,4 ,7 ]
Di Nardo, Fabio [1 ,6 ]
Testa, Valentina [1 ,8 ]
Baggiani, Claudio [1 ,6 ]
Anfossi, Laura [1 ,6 ]
机构
[1] Univ Turin, Dept Chem, Via Giuria 7, I-10125 Turin, Italy
[2] Univ Vigo, CINBIO, Campus Lagoas, Vigo 36310, Spain
[3] Univ Vigo, Dept Phys Chem, Campus Lagoas, Vigo 36310, Spain
[4] Galicia Hlth Res Inst IIS Galicia Sur, Vigo 36310, Spain
[5] Univ Torino, Dept Chem, Pharmaceut & Biomol Sci, Turin, Italy
[6] Univ Torino, Dept Chem, Analyt Chem, Turin, Italy
[7] Univ Vigo, Dept Phys Chem, Phys Chem, CINBIO, Vigo, Spain
[8] Univ Torino, Dept Chem, Chem & Mat Sci, Turin, Italy
来源
SENSORS AND ACTUATORS B-CHEMICAL | 2025年 / 428卷
关键词
Gold nanoparticles; Colorimetric sensor; Immunoglobulins G detection; Milk; LFIA; SOLID-PHASE SYNTHESIS; RECOMBINANT ANTIBODIES; PROTEIN-A; NANOPARTICLES; BINDING; ASSAY; ELISA;
D O I
10.1016/j.snb.2025.137249
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Lateral flow immunoassays (LFIAs) are very popular as diagnostics, especially for point-of-care testing; they use antibodies as high affinity and specific ligands and therefore suffer from limited stability, batch variability, crossreactivity, high production costs, limited shelf life, and ethical concerns associated with antibody production. This study addresses these issues by introducing nanosized molecularly imprinted polymers (nanoMIPs) as specific ligands to replace antibodies in LFIA. Silica-coated gold nanoparticles (Au@SiO2 NPs) and nanoMIPs that recognize bovine immunoglobulins G (BIgGs) were synthesized and conjugated to prepare a novel probe with optical properties and specific binding capabilities. The successful synthesis of this nanosized hybrid material was confirmed by transmission electron microscopy and dynamic light scattering. The probe was incorporated into a model LFIA containing a bacterial protein that binds to mammalian immunoglobulins as a reactive test line. Visual and instrumental detection of BIgG showed detection limits of 0.25 mu g/mL and 0.1 mu g/mLl, respectively, in 15 minutes, meeting the requirements for rapid testing. The probe demonstrated high selectivity for IgGs from different animal species, with cross-reactivities of 1.1 % and 1.8 % for mouse and horse IgGs, respectively. The potential of the new nanoMIP-based probe was further validated by successfully detecting BIgGs in whole soy and goat milk samples.
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页数:9
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