Hyaluronic acid–amphotericin B nanocomplexes: a promising anti-leishmanial drug delivery system

Author:

Silva-Carvalho R.12ORCID,Leão T.34ORCID,Bourbon A. I.5ORCID,Gonçalves C.5ORCID,Pastrana L. M.5,Parpot P.126ORCID,Amorim I.7,Tomás A. M.347,Gama F. M.12ORCID

Affiliation:

1. CEB – Centre of Biological Engineering, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal

2. LABBELS – Associate Laboratory, Braga, Guimarães, Portugal

3. i3S – Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Rua Alfredo Allen 208, 4200-135 Porto, Portugal

4. IBMC – Instituto de Biologia Molecular e Celular, Universidade do Porto, Rua Alfredo Allen 208, 4200-135 Porto, Portugal

5. International Iberian Nanotechnology Laboratory, Av. Mestre José Veiga s/n, 4715-330 Braga, Portugal

6. Centre of Chemistry, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal

7. ICBAS – Instituto de Ciências Biomédicas Abel Salazar, Universidade do Porto, Rua de Jorge Viterbo Ferreira 228, 4050-313 Porto, Portugal

Abstract

Hyaluronic acid-Amphotericin B self-assembled nanocomplexes obtained by a simple drug-polysaccharide non-covalent association in an amorphous state exhibit potent anti-leishmanial activity and can overcome drug toxicity.

Funder

Fundação para a Ciência e a Tecnologia

Publisher

Royal Society of Chemistry (RSC)

Subject

General Materials Science,Biomedical Engineering

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