Effects of porosity on drug release kinetics of swellable and erodible porous pharmaceutical solid dosage forms fabricated by hot melt droplet deposition 3D printing
نویسندگان
چکیده
3D printing has the unique ability to produce porous pharmaceutical solid dosage forms on-demand. Although using porosity alter drug release kinetics been proposed in literature, effects of on swellable and erodible have not explored. This study used a model formulation containing hypromellose acetate succinate (HPMCAS), polyethylene oxide (PEO) paracetamol newly developed hot melt droplet deposition method, Arburg plastic free-forming (APF), examine vitro release. is first reporting use APF tablets. With pellet feeding mechanism APF, it important explore its potential applications additive manufacturing. The pores were created by altering infill percentages (%) between 20 100% generate quality these tablets was examined. printed swelled pH 1.2 HCl eroded 6.8 PBS. During dissolution at 1.2, swelling pathway led gradual decreases open pore area complete closure for with high infills. In buffer media, direct correlation rate infills observed less than 60%. results revealed that controlled complex interplay dynamic changes caused erosion. It also implied impact fluid hydrodynamics data collection interpretation solids.
منابع مشابه
3D Printing by Fused Deposition Modeling of Capsular Devices for Oral Pulsatile Release Based on Swellable/Erodible Polymers
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ژورنال
عنوان ژورنال: International Journal of Pharmaceutics
سال: 2021
ISSN: ['0378-5173', '1873-3476']
DOI: https://doi.org/10.1016/j.ijpharm.2021.120626