Formulation and Evaluation of a Protein-loaded Solid Dispersions by Non-destructive Methods

Author:

Rahman Ziyaur,Zidan Ahmed S.,Khan Mansoor A.

Publisher

Springer Science and Business Media LLC

Subject

Pharmaceutical Science

Reference47 articles.

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2. Taylor NE, Mark AE, Vallat P, Brunne RM, Testa B, Van Gunteren WF. Solvent dependent conformation and hydrogen bounding capacity of cyclosporin A: evidence from partition coefficient and molecular dynamic simulations. J Med Chem. 1993;36:3753–64.

3. Amidon GL, Lennernas H, Shah VP, Crison JR. A theoretical basis for biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm Res. 1995;12:413–20.

4. Chiu YY, Higaki K, Neudeck BL, Barnett JL, Welage LS, Amidon GL. Human jejunal permeability of cyclosporin A: influence of surfactants on P-glycoprotein efflux in Caco-2 cells. Pharm Res. 2003;20:749–56.

5. Liu C, Zhu SJ, Zhou Y, Wei YP, Pei YY. Enhancement of dissolution of cyclosporine A using solid dispersions with polyoxyethylene (40) stearate. Pharmazie. 2006;61:681–4.

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