Development of a rebamipide solid dispersion system with improved dissolution and oral bioavailability

Author:

Pradhan Roshan,Tran Tuan Hiep,Choi Ju Yeon,Choi Im Soon,Choi Han-Gon,Yong Chul Soon,Kim Jong Oh

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,Drug Discovery,Molecular Medicine

Reference48 articles.

1. Alam, M.A., R. Ali, F.I. Al-Jenoobi, and A.M. Al-Mohizea. 2012. Solid dispersions: A strategy for poorly aqueous soluble drugs and technology updates. Expert Opinion on Drug Delivery 9: 1419–1440.

2. Anderson, N.R., G.S. Banker, and G.E. Peck. 1982. Quantitative evaluation of pharmaceutical effervescent systems I: Design of testing apparatus. Journal of Pharmaceutical Sciences 71: 3–6.

3. Arakawa, T., K. Kobayashi, T. Yoshikawa, and A. Tarnawski. 1998. Rebamipide: overview of its mechanisms of action and efficacy in mucosal protection and ulcer healing. Digestive Diseases and Sciences 43: 5–13.

4. Atkinson, R.M., C. Bedford, K.J. Child, and E.G. Tomich. 1962. The effect of griseofulvin particle size on blood levels in man. Antibiotics and Chemotherapy 12: 232–238.

5. Bassi, P., and G. Kaur. 2010. pH modulation: A mechanism to obtain pH-independent drug release. Expert Opinion on Drug Delivery 7: 845–857.

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