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灰黄霉素的超临界流体结晶:用选择性生长抑制剂改变晶体习性

Supercritical fluid crystallization of griseofulvin: crystal habit modification with a selective growth inhibitor.

作者信息

Jarmer Daniel J, Lengsfeld Corinne S, Anseth Kristi S, Randolph Theodore W

机构信息

Department of Chemical and Biological Engineering, University of Colorado at Boulder, Center for Pharmaceutical Biotechnology, Boulder, Colorado, USA.

出版信息

J Pharm Sci. 2005 Dec;94(12):2688-702. doi: 10.1002/jps.20463.

DOI:10.1002/jps.20463
PMID:16258994
Abstract

Poly (sebacic anhydride) (PSA) was used as a growth inhibitor to selectively modify habit of griseofulvin crystals formed via the Precipitation with a compressed-fluid antisolvent (PCA) process. PSA and griseofulvin were coprecipitated within a PCA injector, which provided efficient mixing between the solution and compressed antisolvent process streams. Griseofulvin crystal habit was modified from acicular to bipyramidal when the mass ratio of PSA/griseofulvin in the solution feed stream was <or=1:1. The habit modification was attributed to the preferential adsorption of PSA to the fastest growing crystal face of the acicular crystal form, which inhibited growth. Scanning electron microscopy (SEM) was used to characterize the griseofulvin and PSA particles, and gave results consistent with a selective growth inhibition mechanism. SEM micrographs showed regions on griseofulvin crystals where PSA microparticles had preferentially adsorbed. X-ray powder diffraction (XRPD) and differential scanning calorimetry (DSC) analysis of the griseofulvin crystals indicated no changes in the crystalline form after the habit modification. Powder compressibility decreased from 49 +/- 3% to 28 +/- 7% with the modification in crystal habit. No change in the physical stability of the processed powder was observed after being stored at 25 degrees C/60% RH and 40 degrees C/70% RH for 23 days. Despite the change in crystal habit, griseofulvin crystals achieved 100% dissolution within 60 min in a simulated gastric fluid.

摘要

聚(癸二酸酐)(PSA)被用作生长抑制剂,以选择性地改变通过压缩流体抗溶剂沉淀法(PCA)形成的灰黄霉素晶体的习性。PSA和灰黄霉素在PCA注射器内共沉淀,该注射器能使溶液和压缩抗溶剂工艺流之间实现高效混合。当溶液进料流中PSA/灰黄霉素的质量比≤1:1时,灰黄霉素晶体习性从针状变为双锥体状。习性的改变归因于PSA优先吸附到针状晶体形式生长最快的晶面上,从而抑制了生长。扫描电子显微镜(SEM)用于表征灰黄霉素和PSA颗粒,结果与选择性生长抑制机制一致。SEM显微照片显示了灰黄霉素晶体上PSA微粒优先吸附的区域。对灰黄霉素晶体的X射线粉末衍射(XRPD)和差示扫描量热法(DSC)分析表明,习性改变后晶体形式没有变化。随着晶体习性的改变,粉末可压性从49±3%降至28±7%。在25℃/60%相对湿度和40℃/70%相对湿度下储存23天后,未观察到加工后粉末的物理稳定性发生变化。尽管晶体习性发生了变化,但灰黄霉素晶体在模拟胃液中60分钟内实现了100%溶解。

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