Nanoporous silicon microparticles embedded into oxidized hyaluronic acid/adipic acid dihydrazide hydrogel for enhanced controlled drug delivery
Entity
UAM. Departamento de Física AplicadaPublisher
ElsevierDate
2020-09-13Citation
10.1016/j.micromeso.2020.110634
Microporous and Mesoporous Materials 310 (2021): 110634
ISSN
1387-1811 (print)DOI
10.1016/j.micromeso.2020.110634Funded by
This work was financially supported by FONDECYT–Chile (grant number 11180395), CONICYT PFCHA/DOCTORADO/2017-21172001 (Nelson Naveas) and CNPq 140924/2017-5 (Carla França). We thank Fig. 8. A) Cytotoxicity of nPSi microparticles. B) Cell viability of hydrogels. C.G. Franca ̧ et al. Microporous and Mesoporous Materials 310 (2021) 110634 11 Dr. Héctor Pesenti for providing the DRX facility (FONDEQUIP–Chile, project 160152), and Dr. Luis Sanhueza for optical measurements of UVVis spectroscopyEditor's Version
https://doi.org/10.1016/j.micromeso.2020.110634Subjects
Adipic acid dihydrazide; Drug delivery; Hydrogel; Mechanical resistance; Nanoporous silicon; Oxidized hyaluronic acid; FísicaRights
© 2020 Elsevier Inc.
Esta obra está bajo una licencia de Creative Commons Reconocimiento-NoComercial-SinObraDerivada 4.0 Internacional.
Abstract
Oxidized hyaluronic acid cross-linked with adipic acid dihydrazide (oxi-HA/ADH) forms an injectable and biocompatible hydrogel suitable for treatment of musculoskeletal diseases and for drug delivery applications. In that sense, nanoporous silicon (nPSi) can be combined with biopolymers, such as oxi-HA/ADH hydrogel, to display new characteristics, which are not exhibited by the individual constituents alone. Under this context, in this work nPSi microparticles at concentrations from 0.1% to 1% m/v were embedded into oxi-HA/ADH hydrogel to improve its mechanical stability and enhance its control over drug release kinetics using Rose Bengal (RB) as a model drug because its cytotoxic effect in different cancer cell lines and tumors has been previously reported. Our results showed, for both compressive force and stress strength tests, that oxi-HA/ADH hydrogel with 1% nPSi microparticles doubled the values of control samples. Moreover, samples of oxi-HA/ADH with nPSi microparticles improved RB release kinetics control over pure oxi-HA/ADH hydrogel. Finally, the cell viability of nPSi microparticles embedded into oxi-HA/ADH hydrogel was confirmed using fibroblasts
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Google Scholar:França, Carla Giometti
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Plaza, Tanya
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Naveas, Nelson
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Andrade Santana, Maria Helena
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Manso Silván, Miguel
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Recio, Gonzalo
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Hernández-Montelongo, Jacobo
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