
Magnetite colloids for drug delivery and magnetic resonance imaging (thesis Dagmar Schütt).
Magnetic Resonance Tomography (MRT) is a modern technique of diagnostic imaging, which
allows visualization of cross-sectional images of the human body. MRT is a non-invasive
imaging of the tissues, which provides a better resolution for soft tissue imaging than
classic radiation-based imaging techniques. However, it was shown, that the resolution of
the MRT images could be even more improved using additional contrast agents. For example,
iron-based ferrofluids colloids made of magnetite or maghemit nanoparticles are powerful
contrast agents for MRT. But usually, such contrast agents are only useful for liver
imaging. The latter is a consequence of a fast clearance of the particles out of the
bloodstream into the liver reticulo-endothelial system. Thus, iron-based colloids usually
only permit to distinguish healthy liver cells from tumor liver cells.
The main goal of our project is to design new ferrofluids-based organ-specific MRT
contrast agents, which won't be only restricted to liver imaging. For achieving such goal,
the surfaces of the nanoparticles should be functionalized with various organ-specific
ligands but also modified in order to increase the lifetime of the particle in the
bloodstream. The latter can be done by coating the particles surfaces with polyethylene
oxide (PEO), a polymer known to prevent plasma protein adsorption in vivo. Thus, our
contrast agents are made of magnetite particle possessing a nanometer scale diameter
coated with chimera diblock copolymer PEO-polypeptide. The first role of the negatively
charged polypeptide (poly(glutamic acid) or poly(aspartic acid)) is to interact with the
positively charged surface of the magnetite particles. But also, these polypeptide layers
could be potentially used as a drug containers for drug delivery. Therefore, our colloids
combine diagnostic and therapy possibilities. Such concept is extremely innovative and is
currently under investigation in vitro (cell culture) and in vivo (rats).
