VANİ SETTY, VİJAYA GOPALACHAR JOSHI, SANDANAPALLİ BASAVARAJAİAH CHANDRASEKAR
Turkish Journal of Pharmaceutical Sciences - 2025;22(4):279-293
Objectives The study aimed to combine instant-release and mini-tablet methodologies to develop novel orally disintegrating mini-tablets (ODMTs) for a frequently pescribed antibiotic, cefixime trihydrate (CT), in paediatric patients. Materials and Methods CT-loaded microcapsules were prepared using Eudragit® EPO and Hydroxy Propyl Methyl Cellulose E50 by spray drying technique. The optimized microcapsules were mixed with co-processed ready-to-use tableting excipients, Ludiflash and Pearlitol 200SD, in different proportions and then compressed into ODMTs and evaluated. RESULTS The particle size of CT microcapsules was found to be between 111.8 and 225.87 µm, suitable for oral delivery. The entrapment efficiency was found to be between 94.8% and 95.45%. Pre-compression and post-compression parameters indicated suitability for formulation. In vitro evaluation of ODMTs showed immediate disintegration within 15 seconds in the oral cavity as soon as they came in contact with saliva. Upon swallowing these microcapsules, the microcapsules completely dissolve in the gastrointestinal tract, releasing 100% of the drug (CT) within 15 minutes. The release kinetics of ODMTs were found to follow Hixson-Crowell kinetics for Eudragit® EPO and Korsmeyer-Peppas kinetics for Hydroxy Propyl Methyl Cellulose E50 microcapsules. Scanning electron microscopy images demonstrated that the microcapsules were intact even after compression into ODMTs. Stability studies proved that the formulations were stable as per the International Council for Harmonisation guidelines. CONCLUSION A novel solid oral dosage form of CT ODMTs of 2 mm diameter was successfully developed using Eudragit® EPO and Hydroxy Propyl Methyl Cellulose E50 in combination with co-processed ready-to-use tableting excipients such as Ludiflash and Pearlitol 200SD.
