Infliximab microencapsulation: an innovative approach for intra-articular administration of biologics in the management of rheumatoid arthritis-in vitro evaluation

Microencapsulation of the therapeutical monoclonal antibody infliximab (INF) was investigated as an innovative approach to improve its stability and to achieve formulations with convenient features for intra-articular administration. Ultrasonic atomization (UA), a novel alternative to microencapsulate labile drugs, was compared with the conventional emulsion/ evaporation method (Em/Ev) using biodegradable polymers, specifically Polyactive ((R)) 1000PEOT70PBT30 [poly(ethyleneoxide-terephthalate)/poly(butylene-terephthalate); PEOT-PBT] and its polymeric blends with poly-(D, L-lactide-co-glycolide) (PLGA) RG502 and RG503 (PEOT-PBT:PLGA; 65:35). Six different formulations of spherical core-shell microcapsules were successfully developed and characterized. The UA method achieved a significantly higher encapsulation efficiency (69.7-80.25%) than Em/Ev (17.3-23.0%). Mean particle size, strongly determined by the microencapsulation method and to a lesser extent by polymeric composition, ranged from 26.6 to 49.9 mu m for UA and 1.5-2.1 mu m for Em/Ev. All formulations demonstrated sustained INF release in vitro for up to 24 days, with release rates modulated by polymeric composition and microencapsulation technique. Both methods preserved INF biological activity, with microencapsulated INF showing higher efficacy than commercial formulations at comparable doses regarding bioactive tumor necrosis factor-alpha (TNF alpha) neutralization according to WEHI-13VAR bioassay. Microparticles ' biocompatibility and extensive internalization by THP-1-derived macrophages was demonstrated. Furthermore, high in vitro anti-inflammatory activity was achieved after treatment of THP-1 cells with INF-loaded microcapsules, significatively reducing in vitro production of TNF-alpha and interleucine-6 (Il-6).

Automated summary

Microencapsulation of infliximab (INF), a monoclonal antibody, using ultrasonic atomization (UA) and conventional emulsion/evaporation method (Em/Ev) was investigated for improved stability and intra-articular administration. UA achieved higher encapsulation efficiency (69.7-80.25%) compared to Em/Ev (17.3-23.0%). Particle size ranged from 26.6 to 49.9 μm for UA and 1.5-2.1 μm for Em/Ev. Both methods demonstrated sustained INF release and preserved biological activity. Microencapsulated INF exhibited higher efficacy in tumor necrosis factor-alpha (TNF alpha) neutralization and anti-inflammatory activity.