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由于制备动力学,苯妥英在硅胶表面呈现一种多晶型及多种形态。

One Polymorph and Various Morphologies of Phenytoin at a Silica Surface Due to Preparation Kinetics.

作者信息

Ehmann Heike M A, Baumgartner Ramona, Reischl Daniela, Roblegg Eva, Zimmer Andreas, Resel Roland, Werzer Oliver

机构信息

Institute of Pharmaceutical Sciences, Department of Pharmaceutical Technology, Graz University , 8010 Graz, Austria.

Institute of Pharmaceutical Sciences, Department of Pharmaceutical Technology, Graz University , 8010 Graz, Austria ; Research Center Pharmaceutical Engineering GmbH, 8010 Graz, Austria.

出版信息

Cryst Growth Des. 2015 Jan 7;15(1):326-332. doi: 10.1021/cg501391j. Epub 2014 Nov 25.

DOI:10.1021/cg501391j
PMID:25593545
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4288062/
Abstract

The preparation of solid crystalline films at surfaces is of great interest in a variety of fields. Within this work the preparation of pharmaceutically relevant thin films containing the active pharmaceutical ingredient phenytoin is demonstrated. The preparation techniques applied include drop casting, spin coating, and vacuum deposition. For the solution processed samples a decisive impact of the solution concentration and the applied film fabrication technique is observed; particular films form for all samples but with their extensions along different crystallographic directions strongly altered. Vacuum deposition of phenytoin reveals amorphous films, which over time crystallize into needle-like or particular-type structures whereby a nominal thickness of 50 nm is required to achieve a fully closed layer. Independent of all preparation techniques, the resulting polymorph is the same for each sample as confirmed by specular X-ray diffraction scans. Thus, morphologies observed via optical and atomic force microscope techniques are therefore a result of the preparation technique. This shows that the different time scales for which crystallization is obtained is the driving force for the various morphologies in phenytoin thin films rather than the presence of another polymorph forming.

摘要

在各种领域中,在表面制备固态结晶膜都备受关注。在这项工作中,展示了含有活性药物成分苯妥英的药学相关薄膜的制备。所应用的制备技术包括滴铸、旋涂和真空沉积。对于溶液处理的样品,观察到溶液浓度和所应用的薄膜制造技术具有决定性影响;所有样品都形成了特定的薄膜,但它们沿不同晶体学方向的延伸有很大改变。苯妥英的真空沉积显示出非晶薄膜,随着时间的推移,这些薄膜会结晶成针状或特定类型的结构,从而需要50纳米的标称厚度才能形成完全封闭的层。通过镜面X射线衍射扫描证实,与所有制备技术无关,每个样品得到的多晶型物都是相同的。因此,通过光学和原子力显微镜技术观察到的形态是制备技术的结果。这表明,获得结晶的不同时间尺度是苯妥英薄膜中各种形态的驱动力,而不是另一种多晶型物形成的存在。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d43a/4288062/fcf34ecc0032/cg-2014-01391j_0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d43a/4288062/9106c3d9da5a/cg-2014-01391j_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d43a/4288062/fcf34ecc0032/cg-2014-01391j_0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d43a/4288062/9106c3d9da5a/cg-2014-01391j_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d43a/4288062/fcf34ecc0032/cg-2014-01391j_0008.jpg

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