Improvement of the in vitro dissolution characteristics of famotidine by inclusion in β-cyclodextrin-Reference-Cited by-同舟云学术

Improvement of the in vitro dissolution characteristics of famotidine by inclusion in β-cyclodextrin

Published:1990-01 Issue:1 Volume:58 Page:19-24
ISSN:0378-5173
Container-title:International Journal of Pharmaceutics
language:en
Short-container-title:International Journal of Pharmaceutics

Author:

Hassan Mohammad A.,Suleiman Mohammad S.,Najib Naji M.

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference15 articles.

1. Phannacodynamic and phannacokinetic properties and a preliminary review of its therapeutic use in peptic ulcer disease and Zollinger-Ellison syndrome;Campeli-Richards;Drugs,1986

2. Mechanism of drug dissolution rate enhancement from β-cyclodextrin drug systems;Corrigan;J Pharm. Pharmacol,1982

3. Cyclodextrins, their value in pharmaceutical technology;Duchene;Drug. Dev. Ind. Pharm.,1986

4. Improvement in availability and stability of a dermocorticoid by inclusion in β-cyclodextrin;Glomot;Int. J. Pharm.,1988

5. Increasing dissolution rates and gastrointestinal absorption of drugs IV: chloramphenicol-urea system;Goldberg;J. Pharm. Sci.,1966

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