Pharmaceutical Sciences - Posters F
Dr. Laszlo, Forgach
T9PTOD
SU Dpt. of Biophysics and Radiation Biology
+36308921791
laszlo.forgach@gmail.com
Prussian Blue Nanoparticles as isotope-labeled and fluorescent contrast material
László Forgách1, Nikolett Hegedűs1, Anikó Kubovje1, Zoltán Varga1,2, Noémi Kovács1,3, Ildikó Horváth1, Domokos Máthé1,3, Krisztián Szigeti1
1: Dept. Biophysics and Radiation Biology, Semmelweis University, Budapest, Hungary
2: Research Center for Natural Sciences, ELKH, Budapest, Hungary
3: In Vivo Imaging ACF, Hungarian Center of Excellence for Molecular Medicine, Szeged, Hungary
Poszter
Pharmaceutical Sciences - Posters F
English
Pharmaceutical Sciences
INTRODUCTION Prussian Blue Nanoparticles (PBNPs) have proven their capabilities as radiolabeled and fluorescently labelled nanoparticulate systems,. The mesoporous structure allows the doping of radioisotopes into the PBNP crystalline, while the net negative charge helps the conjugation of the positively charged IR820 onto the nanoparticle surface.
AIMS The study presents the synthesis and development of a Prussian Blue based biocompatible and chemically stable T1 magnetic resonance imaging (MRI) contrast agent with near infrared (NIR) optical contrast for preclinical application.
METHODS The physical properties of the Prussian blue nanoparticles (PBNPs) (iron (II); iron (III);octadecacyanide) were characterized with dynamic light scattering (DLS), zeta potential measurement, atomic force microscopy (AFM), and transmission electron microscopy (TEM). In vitro contrast enhancement properties of PBNPs were determined by MRI.
RESULTS In vivo T1-weighted contrast of the prepared PBNPs was investigated by MRI and optical imaging modality after intravenous administration to mice. PBNP-s doped with 201Tl isotope have also been synthetised and biodistribution in mice was determined by using SPECT and MRI. Activity concentrations (MBq/cm3) were calculated from the SPECT scans for each dedicated volume of interest (VOI) of liver, kidneys, salivary glands, heart, lungs, and brain. Isotope-labeled citrate-coated PBNP accumulation peaked at 2 hours after injection in the kidneys and the liver followed by a gradual decrease in activity in later time points.
CONCLUSION We synthetized, characterized, and radiolabeled a Prussian blue-based nanoparticle platform for contrast material applications. In vivo radiochemical stability and biodistribution open up the way for further diagnostic applications. The presence and detectability of PBNPs during initial biodistribution in the cardiovascular system indicates vascular contrast material applications, too.
FUNDING The research was financed by the Higher Education Institutional Excellence Programme of the Ministry for Innovation and Technology in Hungary, within the framework of the Therapeutic Development thematic programme of the Semmelweis University. The study was supported by EFOP-3.6.3-VEKOP-16-2017-00009 grant of the National Research, Development and Innovation Office, Hungary. The research leading to these results has received funding from the Semmelweis University (STIA-KFI-2020).
Semmelweis University, Doctoral School of Pharmaceutical Sciences
Dr. Krisztian Szigeti
I do not give consent to the publication of my abstract on the website of the congress.
Szabad
elfogadva
poszter
nem rendelkezett róla
5927
12:00
12:05
László Forgách1, Nikolett Hegedűs1, Anikó Kubovje1, Zoltán Varga1,2, Noémi Kovács1,3, Ildikó Horváth1, Domokos Máthé1,3, Krisztián Szigeti1
1: Dept. Biophysics and Radiation Biology, Semmelweis University, Budapest, Hungary
2: Research Center for Natural Sciences, ELKH, Budapest, Hungary
3: In Vivo Imaging ACF, Hungarian Center of Excellence for Molecular Medicine, Szeged, Hungary