6533b7dcfe1ef96bd1272b1b

RESEARCH PRODUCT

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

Andrea CappelliGaetano GiammonaGermano GiulianiHartmut KomberAnnalisa RealeMaurizio AnziniMarco PaolinoGemma LeoneAlessandro DonatiLaura Modica De MohacMariano LicciardiAgnese MagnaniCristina Savoca

subject

olanzapinePharmaceutical Science02 engineering and technologyself-assembling nanocarrier010402 general chemistry01 natural sciencesArticlechemistry.chemical_compounddrug delivery systemsDynamic light scatteringhyaluronic acidCopolymerSide chainSolubilityDrug delivery systems; Ferulic acid; Hyaluronic acid; Olanzapine; Oleic acid; Self-assembling nanocarriers; Stearic acidSelf-assembling nanocarriersstearic acid021001 nanoscience & nanotechnology0104 chemical sciencesOleic acidchemistryChemical engineeringoleic acidDrug deliveryStearic acid0210 nano-technologyEthylene glycolferulic acid

description

In 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.

10.3390/pharmaceutics11120675http://hdl.handle.net/10447/387574