Membrane Pharmacy Structure Dynamics 

Research group : Priv.Doz. Dr. Thomas Nawroth 

Nanoparticles   


Nanoparticles depice a size (mass) between single molecules and cells, i.e. a size of 10-1000 nm, or 500,000 to 1012 g/mol particle mass. The size is between that of large protein complexes, e.g. ATP-synthase, and cells. The corresponding native biostructures are cellular compartiments, i.e. mitochondria, chloroplasts and transport vesicles, and the cytosceleton elements, i.e. actin fibres and microtubuli with the associated molecular motor systems, supplying active motion and transport.

- BioNanoparticles for therapy, imaging and diagnosis of cancer and other diseases lead an entrapped or bound therapeutic or diagnostic target material (T)  to the area of interest, e.g. a tumor. The destination may be found by physical forces (magnetic) or with surface-bound antibodies (cell/tissue specific). BioNanoparticles may be: liposomes, magnetic liposomes, shell poly-Ferrofluids or polymers. As a consequence of the particle size (30-300 nm), the number of transported target molecules is very high: 106 - 109 / liposome in case of liposomes  and poly-Ferrofluid applications.

- Motile Polymers and Membranes - a long term concept for technical application of molecular motion (Polymers and chimeric membranes, capable of active motion). Nanoparticles are structure components of those motile systems, which can supply the system with the energy required for motion, e.g. by magnetic forces.

The Nanoparticle applications, BioNanoparticles as well as motile polymers, use the following nanoparticles structure elements as components:

- Magnetic liposomes - Liposomes with an internal ferromagnetic iron oxide shell, entrapped magnetic domains or lipid-bound paramagnetic ions: These magnetic target carrier particles can be used for cancer therapy (neutron capture of entrapped boron compounds), magnetic drug targeting (drug entrapped in the liposome lumen), bioanalytics (analytical target signal, imaging), and biophysical experiments (membranes, Rheology, cellular traffic and transport). Magnetic liposomes of 30 - 300 nm size can be used for targeting  in vivo, i.e. magnetic drug targeting MDT, and magnetic radiation targeting for X-rays (PXT, photodynamic X-ray therapy), neutrons (NCT, neutron capture therapy) and isotopes (PET, pertubed angular correlation).

- Liposomes  - Hollow spheres of biogenic lipids : entrapping of drugs, radiation targets and other labels, immuno-reactive particles (with membrane anchored antigenes or antibodies), investigations on biological membranes (response to membrane potentials). Antibody liposomes of 30 - 300 nm size can be used for targeting  in vivo, i.e. cell specific drug targeting MDT, and radiation targeting for X-rays (PXT, photodynamic X-ray therapy), neutrons (NCT, neutron capture therapy) and isotopes (PET, pertubed angular correlation).

- Ferrofluids - Nanoparticles constructed from massive iron oxide spheres for magnetic drug targeting (cancer therapy), spectroscopy, magnetic imaging (MR) and technical applications. Biocompatible Ferrofluids are water-based and contain only endogenous or bio-inert materials. Small Ferrofluid particles (single domains of 5 - 20 nm size) are suitable for hyperthermic cancer therapy (overheating by RF-application). For biomedical target applications the magnetic effect of simple Ferrofluids is too small. Thus only poly-Ferrofluids of 30 - 300 nm size, depicting a large macroscopic magnetic moment and magnetic structure generation, can be used for targeting  in vivo, i.e. magnetic drug targeting MDT, and magnetic radiation targeting for X-rays (PXT, photodynamic X-ray therapy) and neutrons (NCT, neutron capture therapy).


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email to: nawroth@MPSD.de   update : 11.2.2014