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Nanotherapeutics in the EU: an overview on current state and future directions

Authors Hafner A, Lovrić J, Lakoš G, Pepić I

Received 4 October 2013

Accepted for publication 28 November 2013

Published 19 February 2014 Volume 2014:9(1) Pages 1005—1023


Checked for plagiarism Yes

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Peer reviewer comments 7

Anita Hafner,1,* Jasmina Lovrić,1,* Gorana Perina Lakoš,2 Ivan Pepić1,3

1Department of Pharmaceutical Technology, University of Zagreb, Faculty of Pharmacy and Biochemistry, Zagreb, Croatia; 2Medicines Authorisation Division, Agency for Medicinal Products and Medical Devices, Zagreb, Croatia; 3Centre for Applied Pharmacy, University of Zagreb, Faculty of Pharmacy and Biochemistry, Zagreb, Croatia

*These authors contributed equally to this work

Abstract: The application of nanotechnology in areas of drug delivery and therapy (ie, nanotherapeutics) is envisioned to have a great impact on public health. The ability of nanotherapeutics to provide targeted drug delivery, improve drug solubility, extend drug half-life, improve a drug’s therapeutic index, and reduce a drug’s immunogenicity has resulted in the potential to revolutionize the treatment of many diseases. In this paper, we review the liposome-, nanocrystal-, virosome-, polymer therapeutic-, nanoemulsion-, and nanoparticle-based approaches to nanotherapeutics, which represent the most successful and commercialized categories within the field of nanomedicine. We discuss the regulatory pathway and initiatives endeavoring to ensure the safe and timely clinical translation of emerging nanotherapeutics and realization of health care benefits. Emerging trends are expected to confirm that this nano-concept can exert a macro-impact on patient benefits, treatment options, and the EU economy.

Keywords: nanotechnology, drug delivery, EU approval procedures, EU marketed products

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