Abstract
Intrinsic dissolution rates were determined for different grades of commonly used calcium salt fillers and lactose. Typical tablet formulations of low-dose drugs were studied to determine the influence of this property on drug dissolution.
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REFERENCES
A. D. Koparkar. The Modification of an Automated Dissolution Test Apparatus for the Rotating Disk Method of Intrinsic Dissolution Rate Measurement, Its Validation and Use in Evaluating Tablet Diluents, Ph.D. dissertation, University of Maryland, Baltimore, 1983.
D. P. Gregory and A. C. Riddiford. J. Chem. Soc. Lond. 3:3756 (1956).
Pharmacopoeia Helvetica, 6th ed., Pharmacopoekommission, Bern, Switzerland, 1971.
British Pharmacopoeia, Her Majesty's Stationery Office at the University Press, London, 1980.
United States Pharmacopeia, 21st revision, United States Pharmacopeial Convention, Rockville, Md., 1985.
K. Diem and C. Lentner (eds.). Scientific Tables, 7th ed., Documenta Geigy, Ardsley, N.Y. 1970, p. 176.
K. Diem and C. Lentner (eds.). Scientific Tables, 7th ed., Documenta Geigy, Ardsley, N.Y. 1970, p. 648.
Remington's Pharmaceutical Sciences, 15th ed., Mack, Easton, Pa., 1975.
L. L. Augsburger, Dissolution of Thiazides, Final Technical Report, RFP 223-76-3009, F.D.A., Health and Human Services, Washington, D.C.
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Koparkar, A.D., Augsburger, L.L. & Shangraw, R.F. Intrinsic Dissolution Rates of Tablet Filler-Binders and Their Influence on the Dissolution of Drugs from Tablet Formulations. Pharm Res 7, 80–86 (1990). https://doi.org/10.1023/A:1015895827989
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DOI: https://doi.org/10.1023/A:1015895827989