Natural based eumelanin nanoparticles functionalization and preliminary evaluation as carrier for gentamicin

last updated: 2017-05-05
ProjectFoReCaST :: publications list
TitleNatural based eumelanin nanoparticles functionalization and preliminary evaluation as carrier for gentamicin
Publication TypePapers in Scientific Journals
Year of Publication2017
AuthorsDe Trizio A., Srisuk P., Costa R. R., Fraga A. G., Modena T., Genta I., Dorati R., Pedrosa J., Conti B., Correlo V. M., and Reis R. L.
Abstract

Purpose of the work was to modified natural based eumelanin nanoparticles surface by dopamine self-polymerization (FEUNp), facilitating conjugation through polydopamine bioactive functional groups and improving nanoparticle surface hydrophilicity. SEM, TEM, and AFM characterization confirmed FEUNp spherical shape (230.04 ± 8.25 nm) and their polydopamine coating. Individual indole or indoline structure spectrum at 1600 cm− 1 and C:N mass 9.08 was highlighted by FTIR and XPS analysis respectively. Quartz-crystal microbalance with dissipation monitoring (QCM-D) and thermal gravimetric analysis (TGA) showed successful polydopamine adsorption to eumelanin nanoparticles surface, a weight ratio of eumelanin nanoparticles/dopamine of 1/2.46 in the wet state and 1/0.20 in the dry state; the − 36.60 ± 0.45 mV negatively surface charges confirms the presence of PD covering. FEUNp were loaded with gentamicin sulfate, for application in infectious diseases therapies, such as osteomyelitis. Nanoparticles drug entrapment efficiency was 32.42 ± 3.21%, and ζ-potential close to neutrality (− 1.84 ± 0.58 mV). FEUNp-GS antimicrobial effect was tested on Staphylococcusaureus and Escherichiacoli showing gentamicin 24 h sustained release from FEUNp-GS. IC50 and IC90 were 110.60 μg/mL and 216.39 μg/mL against Saureus, and 54.13 μg/mL and 101.25 μg/mL against Ecoli. The results are promising for FEUNp-GS as delivery system potentially useful diverse administration routes.

JournalReactive & Functional Polymers
Volume114
Pagination38-48
Date Published2017-03-01
PublisherElsevier
ISSN1381-5148
DOI10.1016/j.reactfunctpolym.2017.03.004
URLwww.sciencedirect.com/science/article/pii/S1381514817300391
KeywordsDrug delivery systems, Eumelanin nanoparticles, gentamicin, Polydopamine, Surface modification
RightsrestrictedAccess
Peer reviewedyes
Statuspublished

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