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Study of particle rearrangement compression behavior and dissolution properties after melt dispersion of ibuprofen Avicel and Aerosil

机译:布洛芬Avicel和Aerosil熔融分散后的颗粒重排压缩行为和溶解特性的研究

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摘要

Particle rearrangements, compaction under pressure and in vitro dissolution have been evaluated after melt dispersion of ibuprofen, Avicel and Aerosil. The Cooper–Eaton and Kuno equations were utilized for the determination of particle rearrangement and compression behavior from tap density and compact data. Particle rearrangement could be divided into two stages as primary and secondary rearrangement. Transitional tapping between the stages was found to be 20–25 taps in ibuprofen crystalline powder, which was increased up to 45 taps with all formulated powders. Compaction in the rearrangement stages was increased in all the formulations with respect to pure ibuprofen. Significantly increased compaction of ibuprofen under pressure can be achieved using Avicel by melt dispersion technique, which could be beneficial in ibuprofen tablet manufacturing by direct compression. SEM, FTIR and DSC have been utilized for physicochemical characterization of the melt dispersion powder materials. Dissolution of ibuprofen from compacted tablet of physical mixture and melt dispersion particles has also been improved greatly in the following order: Ibc<Ibsmd1<Ibsmd2<Ibsmp10<Ibsmd5<Ibsmd10.
机译:在布洛芬,Avicel和Aerosil熔融分散后,已评估了颗粒重排,加压下的压实和体外溶解。 Cooper-Eaton和Kuno方程用于根据振实密度和紧密数据确定颗粒重排和压缩行为。粒子重排可以分为两个阶段:一次和二次重排。发现各阶段之间的过渡攻丝为布洛芬结晶粉末中的20–25个攻丝,使用所有配制的粉末,最多可增加到45个攻丝。对于纯布洛芬,所有配方的重排阶段的压实度均增加。使用Avicel的熔体分散技术可显着提高布洛芬在压力下的压实度,这可能对通过直接压制法生产布洛芬片剂有利。 SEM,FTIR和DSC已用于熔体分散粉末材料的物理化学表征。布洛芬从物理混合物和熔融分散体颗粒的压实片中的溶解也按以下顺序大大改善:Ibc

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