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NANOFOL

Folate-based nanobiodevices for integrated diagnosis/therapy targeting chronic inflammatory diseases

Context and project objectives


It is estimated that inflammatory diseases affect more than 80 million people worldwide leading to untold suffering, economic loss and premature death. Considering life expectancy in Europe, these numbers are expected to increase in the next 20 years. Moreover, studies have shown that disorders such as rheumatoid arthritis (RA) can shorten life span by 10 years. The treatment of chronic inflammatory disorders, including RA, remains a challenge for the medical and scientific community. The emergence of new drugs creates new options though it also entails high costs, complicated drug administration, allergic reactions and potentially fatal side effects. Therefore more efficient strategies have to be identified in order to improve inflammatory disease treatment while decreasing the side effects with an improved cost-benefit ratio. Nano-enabled drug delivery systems will take therapy of chronic inflammatory disorders to a new level by creating a new, highly specific and efficient strategy, with reduced treatment costs. The NANOFOL project has adopted a specific risk amelioration strategy to attain objectives in a step-by-step approach in order to gradually improve the concept (specificity, stability, side effects and efficacy) from lower to higher risk solutions ensuring reduced animal testing and high human safety. NANOFOL will improve treatment of chronic inflammatory diseases by fulfilling the following objectives: Design, development and production of nanobiodevices directly targeting effector cells Experimental design that will enable minimal animal experimentation. Development of a strategy to assess potential life cycle risks ensuring safe nanobiodevice-mediated delivery. Setting-up better citizen awareness on nanomedicine-based therapies and training activities.

Work performed and main results achieved


NANOFOL has acomplished until now the overall objectives established in the initial plan. The consortium defined several possibilities for the global nanodevice strategy, in order to reach delivery technology products with therapeutic potential. In the last 6 months (M18 to M24) the consortium produced FBN (liposomal, protein-based and PLA (poly (L-lactic acid)) nanoparticles) with encapsulated anti-inflammatory drugs that showed to be biologically active, non cytotoxic and capable of specifically targeting folate receptor (FR)-positive cells. The consortium also showed that FR might be exclusively expressed on a certain subset of
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macrophages present in several types of inflammatory conditions. Special attention is being given to minimizing the use of animal testing by establishing adequate in vitro models. The newly produced FR mAb proved invaluable for development of the immunoprecipitation protocol that is suitable for mass spectrometry analysis. Recombinant Fab fragments are being produced in order to facilitate the production of the final bispecific antibody to be used in the surface of the FBN.

Expected final results, intensions for use and impact


NANOFOL nanobiodevices targeting activated macrophages may become an interesting theranostics solution, i.e. simultaneous treatment and diagnosis site of inflammation in RA patients. The production of a validated, stable, specific FBN with incorporated imaging agent and therapeutic agent (drugs or siRNAs) by the NANOFOL consortium will have immediate application in all inflammatory diseases where activated macrophages contribute to the disease process.

NANOFOL Consortium Coordinator


Pr. Artur CAVACO-PAULO, artur@det.uminho.pt, Universidade do Minho Portugal

www.nanofol.eu Partners
Suanfarma SA Spain Technische Universitaet Graz Austria Nederlandse Organisatie Voor Toegepast Natuurwetenschappelijk Onderzoek Netherlands Instituto de Biologia Molecular e Celular Portugal Institut National de la Sant et de la Recherche Mdicale France Medizinische Universitaet Wien Austria Aurel Vlaicu University of Arad Romania Synovo GmbH Germany Institut National de lEnvironnement et des risques France Exbio Praha AS Czech Republic ALMA Consulting Group SAS France ALFAMA Investigacao e Desenvolvimento de Produtos Farmaceuticos, Lda Portugal

Acknowledgements
The research leading to these results has received funding from the European Union Seventh Framework Programme (FP7/2007-2013) under grant agreement n NMP4-LA-2009-228827 NANOFOL.

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