Hyaluronan Graft Copolymers Bearing Fatty-Acid Residues as Self-Assembling Nanoparticles for Olanzapine Delivery

dc.bibliographicCitation.firstPage675eng
dc.bibliographicCitation.issue12eng
dc.bibliographicCitation.journalTitlePharmaceuticseng
dc.bibliographicCitation.volume11eng
dc.contributor.authorPaolino, Marco
dc.contributor.authorLicciardi, Mariano
dc.contributor.authorSavoca, Cristina
dc.contributor.authorGiammona, Gaetano
dc.contributor.authorDe Mohac, Laura Modica
dc.contributor.authorReale, Annalisa
dc.contributor.authorGiuliani, Germano
dc.contributor.authorKomber, Hartmut
dc.contributor.authorDonati, Alessandro
dc.contributor.authorLeone, Gemma
dc.contributor.authorMagnani, Agnese
dc.contributor.authorAnzini, Maurizio
dc.contributor.authorCappelli, Andrea
dc.date.accessioned2021-12-02T06:06:21Z
dc.date.available2021-12-02T06:06:21Z
dc.date.issued2019
dc.description.abstractIn order to evaluate the potential of a technology platform based on hyaluronan copolymers grafted with propargylated ferulate fluorophores (HA-FA-Pg) in the development of drug delivery systems, the propargyl groups of HA-FA-Pg derivatives were employed with oleic acid (OA) or stearic acid (SA) residues across a biocompatible hexa(ethylene glycol) (HEG) spacer. The designed materials (i.e., HA-FA-HEG-OA or HA-FA-HEG-SA) showed clear-cut aggregation features in an aqueous environment, as confirmed by dynamic light scattering (DLS) and transmission electron microscopy (TEM), generating nanoaggregate systems. In fact, HA-FA-HEG-OA and HA-FA-HEG-SA derivatives showed the property to create self-assembled cytocompatible nanostructured aggregates in water, thanks to the simultaneous presence of hydrophilic portions in the polymeric backbone, such as hyaluronic acid, and hydrophobic portions in the side chains. Furthermore, the designed materials interact with living cells showing a high degree of cytocompatibility. The potential ability of nanosystems to load pharmacologically active molecules was assessed by the physical entrapment of olanzapine into both polymeric systems. The drug loading evaluation demonstrated that the nanoparticles are able to incorporate a good quantity of olanzapine, as well as improve drug solubility, release profile, and cytocompatibility. © 2019 by the authors. Licensee MDPI, Basel, Switzerland.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/7593
dc.identifier.urihttps://doi.org/10.34657/6640
dc.language.isoengeng
dc.publisherBasel : MDPIeng
dc.relation.doihttps://doi.org/10.3390/pharmaceutics11120675
dc.relation.essn1999-4923
dc.rights.licenseCC BY 4.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/eng
dc.subject.ddc610eng
dc.subject.otherDrug delivery systemseng
dc.subject.otherFerulic acideng
dc.subject.otherHyaluronic acideng
dc.subject.otherOlanzapineeng
dc.subject.otherOleic acideng
dc.subject.otherSelf-assembling nanocarrierseng
dc.subject.otherStearic acideng
dc.titleHyaluronan Graft Copolymers Bearing Fatty-Acid Residues as Self-Assembling Nanoparticles for Olanzapine Deliveryeng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorIPFeng
wgl.subjectMedizin, Gesundheiteng
wgl.typeZeitschriftenartikeleng
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