Aqueous film coating to reduce recrystallization of guaifenesin from hot-melt extruded acrylic matrices

被引:6
|
作者
Bruce, Caroline D. [1 ]
Fegely, Kurt A. [2 ]
Rajabi-Siahboomi, Ali R. [2 ]
McGinity, James W. [3 ]
机构
[1] PharmaForm LLC, Austin, TX 78758 USA
[2] Colorcon, West Point, PA USA
[3] Univ Texas Austin, Coll Pharm, Dept Pharmaceut, Austin, TX 78712 USA
关键词
Acryl-EZE (R); curing; diffusion; Eudragit (R) L100-55; film coating; guaifenesin; hot-melt extrusion; matrix tablets; physical stability; recrystallization; AMORPHOUS POLY(ETHYLENE-TEREPHTHALATE); MOLECULAR MOBILITY; DIFFUSION; MEMBRANES; WATER; PERMEABILITY; SIMULATION; GAS; CRYSTALLIZATION; POLYESTERS;
D O I
10.3109/03639040903271277
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Objectives: This study investigated the effect of aqueous film coating on the recrystallization of guaifenesin from acrylic, hot-melt extruded matrix tablets. Methods: After hot-melt extrusion, matrix tablets were film-coated with either hypromellose or ethylcellulose. The effects of the coating polymer, curing and storage conditions, polymer weight gain, and core guaifenesin concentration on guaifenesin recrystallization were investigated. Results: The presence of either film coating on the guaifenesin-containing tablets was found to prolong the onset time of drug crystallization. The coating polymer was the most important factor determining the delay in the onset of crystallization, with the more hydrophilic polymer, hypromellose, having a higher solubilization potential for the guaifenesin and delaying crystallization for longer period (3 or 6 months in tablets stored at 40 degrees C or 25 degrees C, respectively) than the more hydrophobic ethylcellulose, which displayed a lower solubilization potential for guaifenesin (crystal growth on tablets cured for 2 hours at 60 degrees C occurred within 3 weeks, whereas uncoated tablets displayed surface crystal growth after 30 minutes). Crystal morphology was also affected by the film coating. Elevated temperatures during both curing and storage, incomplete film coalescence, and high core drug concentrations all contributed to an earlier onset of crystal growth.
引用
收藏
页码:218 / 226
页数:9
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