TY - JOUR
T1 - Silk fibroin nanoparticles for celecoxib and curcumin delivery
T2 - ROS-scavenging and anti-inflammatory activities in an in vitro model of osteoarthritis
AU - Crivelli, Barbara
AU - Bari, Elia
AU - Perteghella, Sara
AU - Catenacci, Laura
AU - Sorrenti, Milena
AU - Mocchi, Michela
AU - Faragò, Silvio
AU - Tripodo, Giuseppe
AU - Prina-Mello, Adriele
AU - Torre, Maria Luisa
N1 - Publisher Copyright:
© 2019 Elsevier B.V.
PY - 2019/4
Y1 - 2019/4
N2 - 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.
AB - 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.
KW - Celecoxib
KW - Curcumin
KW - Drug delivery systems
KW - Nanoparticles
KW - Osteoarthritis
KW - Silk fibroin
UR - https://www.scopus.com/pages/publications/85061662460
U2 - 10.1016/j.ejpb.2019.02.008
DO - 10.1016/j.ejpb.2019.02.008
M3 - Article
SN - 0939-6411
VL - 137
SP - 37
EP - 45
JO - European Journal of Pharmaceutics and Biopharmaceutics
JF - European Journal of Pharmaceutics and Biopharmaceutics
ER -