Tres Francesco, Coombes Steven R, Phillips Andrew R, Hughes Leslie P, Wren Stephen A C, Aylott Jonathan W, Burley Jonathan C
School of Pharmacy, Boots Science Building, University of Nottingham, Nottingham NG7 2RD, UK.
Pharmaceutical Development, AstraZeneca, Macclesfield SK10 2NA, UK.
Molecules. 2015 Sep 10;20(9):16404-18. doi: 10.3390/molecules200916404.
We have investigated the dissolution performance of amorphous solid dispersions of poorly water-soluble bicalutamide in a Kollidon VA64 polymeric matrix as a function of the drug loading (5% vs. 30% bicalutamide). A combined suite of state-of-the-art analytical techniques were employed to obtain a clear picture of the drug release, including an integrated magnetic resonance imaging UV-Vis flow cell system and 1H-NMR. Off-line 1H-NMR was used for the first time to simultaneously measure the dissolution profiles and rates of both the drug and the polymer from a solid dispersion. MRI and 1H-NMR data showed that the 5% drug loading compact erodes linearly, and that bicalutamide and Kollidon VA64 are released at approximately the same rate from the molecular dispersion. For the 30% extrudate, data indicated a slower water ingress into the compact which corresponds to a slower dissolution rate of both bicalutamide and Kollidon VA64.
我们研究了难溶性比卡鲁胺在聚乙烯吡咯烷酮VA64聚合物基质中的无定形固体分散体的溶出性能与载药量(5%比卡鲁胺与30%比卡鲁胺)的关系。采用一套先进的分析技术组合来清晰了解药物释放情况,包括集成磁共振成像紫外 - 可见流通池系统和1H - NMR。首次使用离线1H - NMR同时测量固体分散体中药物和聚合物的溶出曲线及速率。MRI和1H - NMR数据表明,5%载药量的制剂呈线性侵蚀,比卡鲁胺和聚乙烯吡咯烷酮VA64从分子分散体中以大致相同的速率释放。对于30%挤出物的数据表明,水进入制剂的速度较慢,这对应于比卡鲁胺和聚乙烯吡咯烷酮VA64较慢的溶出速率。