Methodological needs in the quality and safety characterisation of nanotechnology-based health products: Priorities for method development and standardisation

Journal of Controlled Release - Tập 336 - Trang 192-206 - 2021
B. Halamoda-Kenzaoui1, R.J. Vandebriel2, A. Howarth3, M. Siccardi3, C.A.W. David3, N.J. Liptrott3, M. Santin4, S.E. Borgos5, S. Bremer-Hoffmann1, F. Caputo5
1European Commission, Joint Research Centre (JRC), Ispra, Italy
2National Institute of Public Health and the Environment (RIVM), Bilthoven, The Netherlands
3Department of Pharmacology and Therapeutics, Institute of Systems, Molecular, and Integrative Biology, University of Liverpool, Liverpool, UK
4Centre for Regenerative Medicine and Devices, School of Pharmacy and Biomolecular Sciences, University of Brighton, Brighton, UK
5Department of Biotechnology and Nanomedicine, SINTEF Industry, Trondheim, Norway

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