Novel peroral dosage forms with protease inhibitory activities. I. Design of capsules with fast gel-forming and fast drug-releasing properties
Author:
Publisher
Elsevier BV
Subject
Pharmaceutical Science
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1. Peroral delivery systems based on superporous hydrogel polymers: release characteristics for the peptide drugs buserelin, octreotide and insulin;European Journal of Pharmaceutical Sciences;2002-06
2. Azocrosslinked poly(acrylic acid) for colonic delivery and adhesion specificity: in vitro degradation and preliminary ex vivo bioadhesion studies;Journal of Controlled Release;1998-06
3. The effect of Eudragit RL-100 on the mechanical and mucoadhesion properties of polycarbophil dosage forms1The results reported here form part of the dissertation projects of M.B. and T.N., completed in partial fulfilment of the requirements of their respective PhD and MSc degrees at the Hebrew University of Jerusalem. The study has been presented in part at the 22nd International Symposium on Controlled Release of Bioactive Materials, Seattle, WA, 1995.1;Journal of Controlled Release;1997-03
4. Mucoadhesive polymers in peroral peptide drug delivery. V. Effect of poly(acrylates) on the enzymatic degradation of peptide drugs by intestinal brush border membrane vesicles;International Journal of Pharmaceutics;1996-09
5. Novel peroral dosage forms with protease inhibitory activities. II. Design of fast dissolving poly(acrylate) and controlled drug-releasing capsule formulations with trypsin inhibiting properties;International Journal of Pharmaceutics;1996-07-12
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