| Literature DB >> 30664999 |
Ana Henriques Mota1, Rosa Direito1, Marta P Carrasco1, Patrícia Rijo2, Lia Ascensão3, Ana Silveira Viana4, João Rocha1, Maria Eduardo-Figueira1, Maria João Rodrigues5, Luísa Custódio5, Nataliya Kuplennik6, Alejandro Sosnik6, António José Almeida1, Maria Manuela Gaspar1, Catarina Pinto Reis7.
Abstract
Hyaluronic acid (HA) is commonly used through intra-articular administration for viscosupplementation in osteoarthritis and other disorders. HA is generally supplied as an injection commonly reported as painful, with strong limitations after treatment. In this study, an alternative delivery system was constructed based on HA hydrogel and poly(lactic-co-glycolic acid) (PLGA) particles with oleic acid. Development studies included the determination of particle toxicity, hemolytic activity, in vitro and in vivo anti-inflammatory activity using macrophages and a murine model, respectively. This study showed that empty PLGA particles presented a mean size of 373 nm, while particles containing HA and oleic acid showed a marked particle size increase. The HA association efficiency was of 73.6% and 86.2% for PLGA particles without and with oleic acid, respectively. The in vitro HA release from PLGA particles revealed a sustained profile. Particles showed a good in vitro cell compatibility and the risk of hemolysis was less <1%, ensuring their safety. The in vivo anti-inflammatory study showed a higher inhibition for HA-loaded PLGA particles when compared to HA solution (78% versus 60%) and they were not different from the positive control, clearly suggesting that this formulation may be a promising alternative to the current HA commercial dosage form.Entities:
Keywords: Hyaluronic Acid Sodium Salt (PubChem CID3084049); Hyaluronic acid; In vitro release; In vivo anti-inflammatory activity; Oleic acid (PubChem CID445639); Osteoarthritis; PLGA (PubChem CID71391); PLGA particles; Pluronic® F68 (PubChem CID24751)
Mesh:
Substances:
Year: 2019 PMID: 30664999 DOI: 10.1016/j.ijpharm.2019.01.017
Source DB: PubMed Journal: Int J Pharm ISSN: 0378-5173 Impact factor: 5.875