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The influence of the crystallization on the properties of a hydrophobic drug.

作者信息

Ludwig A, Van Ooteghem M

出版信息

Pharm Weekbl Sci. 1982 Feb 19;4(1):5-11. doi: 10.1007/BF02112350.

DOI:10.1007/BF02112350
PMID:7070948
Abstract
摘要

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本文引用的文献

1
New in vitro disintegration and dissolution test method for tablets and capsules.片剂和胶囊的新型体外崩解和溶出度测试方法。
J Pharm Sci. 1973 Feb;62(2):304-10. doi: 10.1002/jps.2600620227.
2
Effect of compaction pressure on the dissolution efficiency of some direct compression systems.压制压力对某些直接压片系统溶出效率的影响。
Pharm Acta Helv. 1972 Oct;47(10):594-607.
3
Characterization of habits and crystalline modification of solids and their pharmaceutical applications.固体的习性、晶型表征及其药物应用
J Pharm Sci. 1975 Aug;64(8):1269-88. doi: 10.1002/jps.2600640805.
4
Enhancement of dissolution rates of poorly water-soluble drugs by crystallization in aqueous surfactant solutions I: Sulfathiazole, prednisone, and chloramphenicol.通过在水性表面活性剂溶液中结晶提高难溶性药物的溶出速率I:磺胺噻唑、泼尼松和氯霉素。
J Pharm Sci. 1976 Nov;65(11):1702-4. doi: 10.1002/jps.2600651137.
5
The use of the carbon replica technique to investigate the surface of pharmaceutical powders by transmission electron microscopy.利用碳复型技术通过透射电子显微镜研究药用粉末的表面。
J Pharm Belg. 1978 Sep-Oct;33(5):292-6.
6
The in vitro bioavailability of various drugs formulated as hard gelatin capsules.各种制成硬明胶胶囊的药物的体外生物利用度。
J Pharm Pharmacol. 1977 Apr;29(4):205-8. doi: 10.1111/j.2042-7158.1977.tb11289.x.