Bimodal Fucoidan-Coated Zinc Oxide/Iron Oxide-Based Nanoparticles for the Imaging of Atherothrombosis
Hoang Nguyen,
Eric Tinet,
Thierry Chauveau,
Frédéric Geinguenaud,
Yoann Lalatonne,
Aude Michel,
Rachida Aid-Launais,
Clément Journé,
Caroline Lefèbvre,
Teresa Simon-Yarza,
Laurence Motte,
Noureddine Jouini,
Jean-Michel Tualle,
Frédéric Chaubet
Affiliations
Hoang Nguyen
Laboratory for Vascular Translational Science, Inserm U1148, Institut Galilée—Université Paris Diderot, Université Paris 13, Sorbonne-Paris-Cité, 99 av JB Clément, 93430 Villetaneuse, France
Eric Tinet
Laboratoire de Physique des Lasers, UMR CNRS 7538, Institut Galilée—Université Paris 13, Sorbonne-Paris-Cité, 99 av JB Clément, 93430 Villetaneuse, France
Thierry Chauveau
Laboratoire des Sciences des Procédés et des Matériaux, UPR CNRS 3407, Institut Galilée—Université Paris 13, Sorbonne-Paris-Cité, 99 av JB Clément, 93430 Villetaneuse, France
Frédéric Geinguenaud
Laboratory for Vascular Translational Science, Inserm U1148, Institut Galilée—Université Paris Diderot, Université Paris 13, Sorbonne-Paris-Cité, 99 av JB Clément, 93430 Villetaneuse, France
Yoann Lalatonne
Laboratory for Vascular Translational Science, Inserm U1148, Institut Galilée—Université Paris Diderot, Université Paris 13, Sorbonne-Paris-Cité, 99 av JB Clément, 93430 Villetaneuse, France
Aude Michel
Laboratoire Phénix, UMR 8234, UPMC, 4 place Jussieu, 75252 Paris Cedex 05, France
Rachida Aid-Launais
Laboratory for Vascular Translational Science, Inserm U1148, Institut Galilée—Université Paris Diderot, Université Paris 13, Sorbonne-Paris-Cité, 99 av JB Clément, 93430 Villetaneuse, France
Clément Journé
Laboratory for Vascular Translational Science, Inserm U1148, Institut Galilée—Université Paris Diderot, Université Paris 13, Sorbonne-Paris-Cité, 99 av JB Clément, 93430 Villetaneuse, France
Caroline Lefèbvre
Université de Technologie de Compiègne, Service d’Analyse Physico-Chimique, Direction à la Recherche, Rue du Dr Schweitzer, CS 60319, 60203 Compiègne cedex, France
Teresa Simon-Yarza
Laboratory for Vascular Translational Science, Inserm U1148, Institut Galilée—Université Paris Diderot, Université Paris 13, Sorbonne-Paris-Cité, 99 av JB Clément, 93430 Villetaneuse, France
Laurence Motte
Laboratory for Vascular Translational Science, Inserm U1148, Institut Galilée—Université Paris Diderot, Université Paris 13, Sorbonne-Paris-Cité, 99 av JB Clément, 93430 Villetaneuse, France
Noureddine Jouini
Laboratoire des Sciences des Procédés et des Matériaux, UPR CNRS 3407, Institut Galilée—Université Paris 13, Sorbonne-Paris-Cité, 99 av JB Clément, 93430 Villetaneuse, France
Jean-Michel Tualle
Laboratoire de Physique des Lasers, UMR CNRS 7538, Institut Galilée—Université Paris 13, Sorbonne-Paris-Cité, 99 av JB Clément, 93430 Villetaneuse, France
Frédéric Chaubet
Laboratory for Vascular Translational Science, Inserm U1148, Institut Galilée—Université Paris Diderot, Université Paris 13, Sorbonne-Paris-Cité, 99 av JB Clément, 93430 Villetaneuse, France
A polyol method was used to obtain ultrasmall ZnO nanoparticles (NPs) doped with iron ions and coated with a low molecular weight fucoidan in order to perform in vivo MR and ex vivo fluorescence imaging of athrothrombosis. During the synthesis, the early elimination of water by azeotropic distillation with toluene allowed us to produce NPs which size, determined by XRD and TEM, decreased from 7 nm to 4 nm with the increase of iron/zinc ratios from 0.05 to 0.50 respectively. For the highest iron content (NP-0.50) NPs were evidenced as a mixture of nanocrystals made of wurtzite and cubic phase with a molar ratio of 2.57:1, although it was not possible to distinguish one from the other by TEM. NP-0.50 were superparamagnetic and exhibited a large emission spectrum at 470 nm when excited at 370 nm. After surface functionalization of NP-0.50 with fucoidan (fuco-0.50), the hydrodynamic size in the physiological medium was 162.0 ± 0.4 nm, with a corresponding negative zeta potential of −48.7 ± 0.4 mV, respectively. The coating was evidenced by FT-IR spectra and thermogravimetric analysis. Aqueous suspensions of fuco-0.50 revealed high transverse proton relaxivities (T2) with an r2 value of 173.5 mM−1 s−1 (300 K, 7.0 T) and remained stable for more than 3 months in water or in phosphate buffer saline without evolution of the hydrodynamic size and size distribution. No cytotoxic effect was observed on human endothelial cells up to 48 h with these NPs at a dose of 0.1 mg/mL. After injection into a rat model of atherothrombosis, MR imaging allowed the localization of diseased areas and the subsequent fluorescence imaging of thrombus on tissue slices.