: The rapid, precise identification and quantification of specific biomarkers, toxins, or pathogens is currently a key strategy for achieving more efficient diagnoses. Herein a dopamine-biotin monomer was synthetized and oxidized in the presence of hexamethylenediamine, to obtain adhesive coatings based on polydopamine-biotin (PDA-BT) on different materials to be used in targeted molecular therapy. Insight into the structure of the PDA-BT coating was obtained by solid-state 13C NMR spectroscopy acquired, for the first time, directly onto the coating, deposited on alumina spheres. The receptor binding capacity of the PDA-BT coating toward 4-hydroxyazobenzene-2-carboxylic acid/Avidin complex was verified by means of UV-vis spectroscopy. Different deposition cycles of avidin onto the PDA-BT coating by layer-by-layer assembly showed that the film retains its receptor binding capacity for at least eight consecutive cycles. Finally, the feasibility of PDA-BT coating to recognize cell lines with different grade of overexpression of biotin receptors (BR) was investigated by tumor cell capture experiments by using MCF-7 (BR+) and HL-60 (BR-) cell lines. The results show that the developed system can selectively capture MCF-7 cells indicating that it could represent a first approach for the development of future more sophisticated biosensors easily accessible, low cost and recyclable with the dual and rapid detection of both proteins and cells.

Notarbartolo di Villarosa M., Alfieri M.L., Avolio R., Ball V., Errico M.E., Massaro M., et al. (2025). Design of innovative and low-cost dopamine-biotin conjugate sensor for the efficient detection of protein and cancer cells. JOURNAL OF COLLOID AND INTERFACE SCIENCE, 678(Pt C), 766-775 [10.1016/j.jcis.2024.09.145].

Design of innovative and low-cost dopamine-biotin conjugate sensor for the efficient detection of protein and cancer cells

Notarbartolo di Villarosa M.;Massaro M.;
2025-01-15

Abstract

: The rapid, precise identification and quantification of specific biomarkers, toxins, or pathogens is currently a key strategy for achieving more efficient diagnoses. Herein a dopamine-biotin monomer was synthetized and oxidized in the presence of hexamethylenediamine, to obtain adhesive coatings based on polydopamine-biotin (PDA-BT) on different materials to be used in targeted molecular therapy. Insight into the structure of the PDA-BT coating was obtained by solid-state 13C NMR spectroscopy acquired, for the first time, directly onto the coating, deposited on alumina spheres. The receptor binding capacity of the PDA-BT coating toward 4-hydroxyazobenzene-2-carboxylic acid/Avidin complex was verified by means of UV-vis spectroscopy. Different deposition cycles of avidin onto the PDA-BT coating by layer-by-layer assembly showed that the film retains its receptor binding capacity for at least eight consecutive cycles. Finally, the feasibility of PDA-BT coating to recognize cell lines with different grade of overexpression of biotin receptors (BR) was investigated by tumor cell capture experiments by using MCF-7 (BR+) and HL-60 (BR-) cell lines. The results show that the developed system can selectively capture MCF-7 cells indicating that it could represent a first approach for the development of future more sophisticated biosensors easily accessible, low cost and recyclable with the dual and rapid detection of both proteins and cells.
15-gen-2025
Settore CHEM-05/A - Chimica organica
Notarbartolo di Villarosa M., Alfieri M.L., Avolio R., Ball V., Errico M.E., Massaro M., et al. (2025). Design of innovative and low-cost dopamine-biotin conjugate sensor for the efficient detection of protein and cancer cells. JOURNAL OF COLLOID AND INTERFACE SCIENCE, 678(Pt C), 766-775 [10.1016/j.jcis.2024.09.145].
File in questo prodotto:
File Dimensione Formato  
J. Coll. Interf. Sci., 2025 678, 766–775.pdf

accesso aperto

Tipologia: Versione Editoriale
Dimensione 5.8 MB
Formato Adobe PDF
5.8 MB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10447/657233
Citazioni
  • ???jsp.display-item.citation.pmc??? 0
  • Scopus 0
  • ???jsp.display-item.citation.isi??? ND
social impact