Influence of processing-induced phase transformations on the dissolution of theophylline tablets-Reference-Cited by-同舟云学术

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Influence of processing-induced phase transformations on the dissolution of theophylline tablets

Published:2004-03 Issue:1 Volume:5 Page:39-49
ISSN:1530-9932
Container-title:AAPS PharmSciTech
language:en
Short-container-title:AAPS PharmSciTech

Author:

Debnath Smita,Suryanarayanan Raj

Publisher

Springer Science and Business Media LLC

Subject

Drug Discovery,Pharmaceutical Science,Agronomy and Crop Science,Ecology,Aquatic Science,General Medicine,Ecology, Evolution, Behavior and Systematics

Link

http://link.springer.com/content/pdf/10.1208/pt050108.pdf

Reference30 articles.

1. Shefter E, Higuchi T. Dissolution behavior of crystalline solvated and nonsolvated forms of some pharmaceuticals.J. Pharm Sci. 1963;52:781–791.

2. Urakami K, Shono Y, Higashi A, Umemoto K, Godo M. A novel method for estimation of transition temperature for polymorphic pairs in phamaceuticals using heat of solution and solutibility data.Chem Pharm Bull. 2002;50:263–267.

3. Hancock BC, Parks M. What is the true solubility advantage for amorphous pharmaceuticals?Pharm Res. 2000;17:397–404.

4. Elamin AA, Ahlneck C, Alderborn G, Nystrom C. Increased metastable solubility of milled griseofulvin, depending on the formation of a disordered surface structure.Int J. Pharm. 1994;111:159–170.

5. Brittain HG, Morris KR, Bugay DE, Thakur AB, Serajuddin ATM. Solid-state NMR and IR for the analysis of pharmaceutical solids: polymorphs of fosinopril sodium.J. Pharm Biomed Anal. 1993;11:1063–1069.

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