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Albumin-based nanoparticles as magnetic resonance contrast agents: I. Concept, first syntheses and characterisation
Authors:M M Stollenwerk  I Pashkunova-Martic  C Kremser  H Talasz  G C Thurner  A A Abdelmoez  E A Wallnöfer  A Helbok  E Neuhauser  N Klammsteiner  L Klimaschewski  E von Guggenberg  E Fröhlich  B Keppler  W Jaschke  P Debbage
Institution:1. Faculty of Health and Society, Malm? University, 205 06, Malm?, Sweden
2. Institute of Inorganic Chemistry, University of Vienna, W?hringer Str. 42, 1090, Vienna, Austria
3. Department of Radiology, Innsbruck Medical University, Anichstrasse 35, 6020, Innsbruck, Austria
4. Section for Clinical Biochemistry, Biozentrum of the Medical University Innsbruck, Fritz-Pregl-Stra?e 3, 6020, Innsbruck, Austria
5. Department of Anatomy, Histology and Embryology, Innsbruck Medical University, Müllerstrasse 59, 6020, Innsbruck, Austria
8. Department of Pharmaceutical Organic Chemistry, Assiut University, Assiut, Egypt
6. Department of Nuclear Medicine, Innsbruck Medical University, Anichstrasse 35, 6020, Innsbruck, Austria
9. Division of Neuroanatomy, Department of Anatomy, Histology and Embryology, Innsbruck Medical University, Müllerstrasse 59, 6020, Innsbruck, Austria
7. Center for Medical Research, Stiftingtalstrasse 24, 8010, Graz, Austria
Abstract:To develop a platform for molecular magnetic resonance imaging, we prepared gadolinium-bearing albumin-polylactic acid nanoparticles in the size range 20–40 nm diameter. Iterative cycles of design and testing upscaled the synthesis procedures to gram amounts for physicochemical characterisation and for pharmacokinetic testing. Morphological analyses showed that the nanoparticles were spheroidal with rough surfaces. Particle sizes were measured by direct transmission electron microscopical measurements from negatively contrasted preparations, and by use of photon correlation spectroscopy; the two methods each documented nanoparticle sizes less than 100 nm and generally 10–40 nm diameter, though with significant intrabatch and interbatch variability. The particles’ charge sufficed to hold them in suspension. HSA retained its tertiary structure in the particles. The nanoparticles were stable against turbulent flow conditions and against heat, though not against detergents. MRI imaging of liquid columns was possible at nanoparticle concentrations below 10 mg/ml. The particles were non-cytotoxic, non-thrombogenic and non-immunogenic in a range of assay systems developed for toxicity testing of nanoparticles. They were micellar prior to lyophilisation, but loosely structured aggregated masses after lyophilisation and subsequent resuspension. These nanoparticles provide a platform for further development, based on non-toxic materials of low immunogenicity already in clinical use, not expensive, and synthesized using methods which can be upscaled for industrial production.
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