6533b834fe1ef96bd129d76e

RESEARCH PRODUCT

Colorimetric detection of normetanephrine, a pheochromocytoma biomarker, using bifunctionalised gold nanoparticles.

Ramón Martínez-máñezTania M. Godoy-reyesFélix SancenónPablo GaviñaPablo GaviñaAna M. Costero

subject

OxazolidineMetaboliteAdrenal Gland NeoplasmsMetal Nanoparticles02 engineering and technologyPheochromocytomaNormetanephrine01 natural sciencesBiochemistryAnalytical ChemistryAggregationchemistry.chemical_compoundQUIMICA ORGANICAMolecular recognitionLimit of DetectionCell Line TumorBiomarkers TumorGold nanoparticlesEnvironmental ChemistryHumansSpectroscopychemistry.chemical_classificationChromatographyBiomoleculeQUIMICA INORGANICA010401 analytical chemistryHomovanillic acid021001 nanoscience & nanotechnology0104 chemical sciencesNormetanephrinechemistryColloidal goldColorimetryNaked eyeGold0210 nano-technologyColorimetric detection

description

[EN] A simple and effective colorimetric method for the detection of normetanephrine (NMN), an O-methylated metabolite of norepinephrine, using functionalised gold nanoparticles is described. This metabolite is an important biomarker in the diagnosis of adrenal tumours such as pheocromocytoma or paraganglioma. The colorimetric probe consists of spherical gold nanoparticles (AuNPs) functionalised with two different ligands, which specifically recognize different functional groups in normetanephrine. Thus, a benzaldehyde-terminated ligand was used for the recognition of the amino alcohol moiety in NMN, by forming the corresponding oxazolidine. On the other hand, N-acetyl-cysteine was chosen for the recognition of the phenolic hydroxyl group through the formation of hydrogen bonds. The selective double molecular recognition between the probe and the hydroxyl and the amino-alcohol moieties of normetanephrine led to interparticle-crosslinking aggregation resulting in a change in the color of the solution, from red to blue, which could be observed by naked eye. The probe was highly selective towards normetanephrine and no color changes were observed in the presence of other neurotransmitter metabolites such as homovanillic acid (HVA) (dopamine metabolite), 5-hydroxyindoleacetic acid (5-HIAA) (serotonin metabolite), or other biomolecules present in urine such as glucose (Glc), uric acid (U.A), and urea. Finally, the probe was evaluated in synthetic urine with constituents that mimic human urine, where a limit of detection of 0.5 mu M was achieved.

10.1016/j.aca.2019.01.003https://pubmed.ncbi.nlm.nih.gov/30797455