Szczegóły publikacji

Opis bibliograficzny

Surface modification of titanium with a gold nanoparticle monolayer: AFM-IR insights into tryptophan and cysteine adsorption / Dominika ŚWIĘCH, Natalia Piergies, Magdalena Oćwieja, Monika Wasilewska, Jérémie Mathurin, Alexandre Dazzi, Ariane Deniset-Besseau // Journal of Physical Chemistry . C ; ISSN  1932-7447. — 2025 — vol. 129 iss. 46, s. 20768–20776. — Bibliogr. s. 20775–20776, Abstr. — Publikacja dostępna online od: 2025-11-06

Autorzy (7)

  • AGHŚwięch Dominika
  • Piergies Natalia
  • Oćwieja Magdalena
  • Wasilewska Monika
  • Mathurin Jérémie
  • Dazzi Alexandre
  • Deniset-Besseau Ariane

Dane bibliometryczne

ID BaDAP164775
Data dodania do BaDAP2025-12-10
Tekst źródłowyURL
DOI10.1021/acs.jpcc.5c06070
Rok publikacji2025
Typ publikacjiartykuł w czasopiśmie
Otwarty dostęptak
Czasopismo/seriaJournal of Physical Chemistry, C

Abstract

Titanium (Ti) is widely used in biomedical implants due to its high strength, corrosion resistance, and excellent biocompatibility. However, surface functionalization is essential to enhancing its interaction with biological environments. In this study, monolayers of citrate-stabilized, negatively charged gold nanoparticles (TCAuNPs(−)) were fabricated on Ti substrates precoated with poly(allylamine hydrochloride) (PAH) to facilitate electrostatically driven adsorption. The adsorption behavior of two amino acids, cysteine (Cys) and tryptophan (Trp) on TCAuNPs(−) deposited on the modified Ti surface, was investigated using atomic force microscopy combined with surface-enhanced infrared absorption (AFM-SEIRA) spectroscopy, enabling nanoscale chemical analysis of biomolecular interactions on the modified surface. The AFM-SEIRA spectra revealed characteristic bands associated with COO–and NH3+groups for both amino acids. In addition, Trp exhibited prominent signals from the aromatic indole ring, suggesting that these molecular fragments were adsorbed onto the TCAuNPs(−)/Ti surface. AFM-SEIRA results indicate that the strongest amino acid signals were localized at the nanoparticle apexes. The results provide insight into the early stage molecular interactions at the bionano interface and offer a framework for designing new functionalized implant surfaces.

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