J 2015

Oleyl-hyaluronan micelles loaded with upconverting nanoparticles for bio-imaging

POSPISILOVA, M; J MRAZEK; V MATUSKA; Sofiane KETTOU; Milada DUSÍKOVÁ et al.

Základní údaje

Originální název

Oleyl-hyaluronan micelles loaded with upconverting nanoparticles for bio-imaging

Autoři

POSPISILOVA, M; J MRAZEK; V MATUSKA; Sofiane KETTOU; Milada DUSÍKOVÁ; V SVOZIL; Kristina NEŠPOROVÁ; G HUERTA-ANGELES; H VAGNEROVA a V VELEBNY

Vydání

Journal of Nanoparticle Research, Dordrecht, Springer Netherlands, 2015, 1388-0764

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Impakt faktor

Impact factor: 2.101

Označené pro přenos do RIV

Ne

Klíčová slova anglicky

Upconverting nanoparticles; Hyaluronan; Micelle; Luminescence imaging; Biomedicine
Změněno: 6. 8. 2016 13:27, Mgr. Kristina Nešporová, Ph.D.

Anotace

V originále

Hyaluronan (HA) represents an interesting polymer for nanoparticle coating due to its biocompatibility and enhanced cell interaction via CD44 receptor. Here, we describe incorporation of oleate-capped beta-NaYF4:Yb3+, Er3+ nanoparticles (UCNP-OA) into amphiphilic HA by microemulsion method. Resulting structures have a spherical, micelle-like appearance with a hydrodynamic diameter of 180 nm. UCNP-OA-loaded HA micelles show a good stability in PBS buffer and cell culture media. The intensity of green emission of UCNP-OA-loaded HA micelles in water is about five times higher than that of ligand-free UCNP, indicating that amphiphilic HA effectively protects UCNP luminescence from quenching by water molecules. We found that UCNP-OA-loaded HA micelles in concentrations up to 50 mu g mL(-1) increase cell viability of normal human dermal fibroblasts (NHDF), while viability of human breast adenocarcinoma cells MDA-MB-231 is reduced at these concentrations. The utility of UCNP-OA-loaded HA micelles as a bio-imaging probe was demonstrated in vitro by successful labelling of NHDF and MDA-MB-231 cells overexpressing the CD44 receptor.