| Literature DB >> 30772432 |
Barbara Crivelli1, Elia Bari1, Sara Perteghella2, Laura Catenacci1, Milena Sorrenti1, Michela Mocchi3, Silvio Faragò4, Giuseppe Tripodo1, Adriele Prina-Mello5, Maria Luisa Torre6.
Abstract
This paper aims at demonstrating silk fibroin nanoparticles (SFNs) promote anti-inflammatory properties of celecoxib (CXB) or curcumin (CUR), and could be exploited for osteoarthritis (OA) treatment. Nanoparticles were prepared by desolvation method and physico-chemically characterized (FT-IR, DSC, TGA, SEM, size distribution and drug release); empty and drug loaded nanoparticles were tested for their ROS-scavenging activity, hemolytic properties, cytotoxicity, and anti-inflammatory potency in an OA in vitro model. Results indicate that a controlled drug release has been achieved by varying the drug loading. Curcumin plus SFNs exhibited a synergistic antioxidant effect, while CXB was, in some manner, inhibitory. Both free drugs resulted highly cytotoxic while cell viability reached high values when encapsulated in SFNs. No appreciable differences in anti-inflammatory activity was evidenced between CUR loaded SFNs and CXB. In conclusion, SFNs is an optimal carrier to improve cyto- and hemo-compatibility of both CUR and CXB.Entities:
Keywords: Celecoxib; Curcumin; Drug delivery systems; Nanoparticles; Osteoarthritis; Silk fibroin
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Year: 2019 PMID: 30772432 DOI: 10.1016/j.ejpb.2019.02.008
Source DB: PubMed Journal: Eur J Pharm Biopharm ISSN: 0939-6411 Impact factor: 5.571