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Fluorinated Mesoporous Silica Nanoparticles for Binuclear Probes in 1H and 19F Magnetic Resonance Imaging.
Bouchoucha, Meryem; van Heeswijk, Ruud B; Gossuin, Yves; Kleitz, Freddy; Fortin, Marc-André.
Afiliação
  • Bouchoucha M; Department of Mining, Metallurgy and Materials Engineering, Université Laval and Centre de Recherche du Centre Hospitalier Universitaire de Québec (CR-CHUQ), Axe Médecine Régénératrice , Québec, Quebec G1L 3L5, Canada.
  • van Heeswijk RB; Department of Radiology, Centre Hospitalier Universitaire Vaudois (CHUV) , 1011 Lausanne, Switzerland.
  • Gossuin Y; Service de Physique Expérimentale et Biologique, Université de Mons , 24 Avenue du Champ-de-Mars, 7000 Mons, Belgium.
  • Fortin MA; Department of Mining, Metallurgy and Materials Engineering, Université Laval and Centre de Recherche du Centre Hospitalier Universitaire de Québec (CR-CHUQ), Axe Médecine Régénératrice , Québec, Quebec G1L 3L5, Canada.
Langmuir ; 33(40): 10531-10542, 2017 10 10.
Article em En | MEDLINE | ID: mdl-28869376
The development of molecular and cellular magnetic resonance imaging (MRI) procedures has always represented a challenge because of the fact that conventional MRI contrast agents are not directly detected in vivo; in proton MRI (e.g., with the nucleus 1H), their local concentration is measured through the effect they exert on the signal of hydrogen protons present in their immediate vicinity. Because the contrast effects generated by conventional MRI probes superpose to and can often impede the anatomical information contained in 1H MRI images, new probes based on a nucleus other than 1H, are being developed. In this study, we report on the development of fluorinated mesoporous silica nanoparticles (MSNs), which could represent an interesting dual probe that allows two MRI modes: 1H for high-resolution anatomical information and 19F for the detection of MSNs used as drug delivery agents. MSNs were synthesized and covalently functionalized either with fluorosilane (FMSNs) or polyfluorosiloxane (polyFMSNs) to enable their detection in 19F MRI. Then, gadolinium chelates were grafted on the particles to enhance their detectability in 1H MRI. The physicochemical, textural, and relaxometric properties (1H and 19F relaxation times) of the nanoparticles were measured and compared. The 19F relaxation properties were found to be dependent on the concentration of fluorine; they were also highly sensitive to the presence of gadolinium. The shortest relaxation times were obtained with polyFMSNs. At clinical magnetic field strengths, high 1H relaxivities and low relaxometric ratios (r2/r1 = 1.45; 2.2 for nanoparticles entrapped in hydrogel) were found for both nanoparticle systems. Finally, the visibility of both systems was confirmed in 1H, and the detectability of polyFMSNs was confirmed in 19F MRI. This physicochemical and relaxometric study opens the door to the applications of fluorinated silica nanoparticles as theranostic materials allowing dual MRI (1H and 19F).
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Nanopartículas Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Nanopartículas Idioma: En Ano de publicação: 2017 Tipo de documento: Article