Conjugation of Kahalalide F with Gold Nanoparticles to Enhance in Vitro Antitumoral Activity

Hosta, L; Pla-Roca, M; Arbiol, J; Lopez-Iglesias, C; Samitier J.; Cruz, LJ; Kogan, MJ; Albericio, F.

Abstract

Two Cys-containing analogues of the anticancer drug Kahalalide F are synthesized and conjugated to 20 and 40 nm gold nanoparticles (GNPs). The resulting complexes are characterized by different analytical techniques to confirm the attachment of peptide to the GNPs. The self-assembly capacity of a peptide dramatically influences the final ratio number of molecules per nanoparticle, saturating the nanoparticle surface and prompting multilayered capping on the surface. In such way, the nanoparticle could act as a concentrator for the delivery of drugs, thereby increasing bioactivity. The GNP sizes and the conjugation have influence on the biological activities. Kahalalide F analogues conjugated with GNPs are located subcellularly at lysosome-like bodies, which may be related to the action mechanism of Kahalalide F. The results suggest that the selective delivery and activity of Kahalalide F analogues can be improved by conjugating the peptides to GNPs.

Más información

Título según WOS: Conjugation of Kahalalide F with Gold Nanoparticles to Enhance in Vitro Antitumoral Activity
Título según SCOPUS: Conjugation of Kahalalide F with gold nanoparticles to enhance in vitro antitumoral activity
Título de la Revista: BIOCONJUGATE CHEMISTRY
Volumen: 20
Número: 1
Editorial: AMER CHEMICAL SOC
Fecha de publicación: 2009
Página de inicio: 138
Página final: 146
Idioma: English
URL: http://pubs.acs.org/doi/abs/10.1021/bc800362j
DOI:

10.1021/bc800362j

Notas: ISI, SCOPUS