References
- Amidon L. G., Lennernas H., Shah V. P., Crison J. R. A. Theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm. Res. 1995; 12(3)413–420
- Cohen J., et al. The development of USP dissolution and drug release standards. Pharm. Res. 1990; 7(10)983–987
- Banakar U. V., Lathia C. D., Wood J. H. Interpretation of dissolution rate data and techniques of in vivo dissolution. Pharmaceutical Dissolution Testing, U. V. Banakar. Marcel Dekker, Inc., New York 1992; 202–203
- Rudman A., et al. Guidance for industry: immediate-release solid dosage forms/scale-up and postapproval changes: chemistry, manufacturing, and controls; in vitro dissolution testing; in vivo bioequivaience documentation. Pharm. Technol. 1996; 20(3)50–233