Dexamethasone-containing biodegradable superparamagnetic microparticles for intra-articular administration: Physicochemical and magnetic properties, in vitro and in vivo drug release
PLGA microparticles;
Dexamethasone acetate;
Superparamagnetic iron oxide nanoparticles (SPIONs);
Microscopy;
SQUID;
EELS;
Drug release;
Dorsal air pouch model;
Arthritis;
Intra-articular;
IRON-OXIDE NANOPARTICLES;
DELIVERY SYSTEM;
AIR POUCH;
MICROSPHERES;
ENCAPSULATION;
INFLAMMATION;
PARTICLES;
INJECTION;
ARTHRITIS;
MINERALS;
D O I:
10.1016/j.ejpb.2009.03.003
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Compared with traditional drug Solutions or suspensions, polymeric microparticles represent a Valuable means to achieve controlled and prolonged drug delivery into joints, but still suffer from the drawback of limited retention duration in the articular cavity. In this Study, Our aim was to prepare and characterize magnetic biodegradable microparticles containing dexamethasone acetate (DXM) lot intra-articular administration. The superparamagnetic Properties, which result from the encapsulation of superparamagnetic iron oxide nanoparticles (SPIONs), allow for microparticle retention with air external magnetic field, thus possibly reducing their clearance from the joint. Two molecular weights of poly(lactic-co-glycolic acid) (PLGA) were used, 12 and 19 kDa. The prepared batches were similar in size (around 10 pm), inner morphology surface morphology, charge (neutral) and superparamagnetic behaviour. The SPION, distribution in the microparticles assessed by TEM indicates a homogeneous distribution and the absence of aggregation, an important factor for preserving superparamagnetic properties. DXM release Profiles were shown to be quite similar in vitro (ca. 6 days) and in Vivo, using a mouse dorsal air pouch model (ca. 5 days). (C) 2009 Elsevier B.V. All rights reserved.