Predicting dissolution via hydrodynamics: Salicylic acid tablets in flow through cell dissolution

International Journal of Pharmaceutics

Volumn 201, Issue 2, 2000, Pages 199-209

  Cammarn, Stephen R ^a   Sakr, Adel ^b  

^a PROCTER AND GAMBLE PHARMACEUTICALS   (United States)

^b UNIVERSITY OF CINCINNATI   (United States)

Author keywords

Dissolution; Flow through cell dissolution; Hydrodynamics; Reynold's number

Indexed keywords

SALICYLIC ACID;

ARTICLE; CONTROLLED STUDY; DISSOLUTION; DRUG SOLUBILITY; HYDRODYNAMICS; MATHEMATICAL MODEL; MODEL; PREDICTION; PRIORITY JOURNAL; TABLET; THEORY; TURBULENT FLOW;

MODELS, THEORETICAL; PHARMACOPOEIAS; SALICYLIC ACID; SOLUBILITY; SOLVENTS; SPECTROPHOTOMETRY, ULTRAVIOLET; TABLETS; UNITED STATES;

EID: 0034713283     PISSN: 03785173     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-5173(00)00415-4     Document Type: Article

References (18)

1. Cooper A., Kingery W. Kinetics of solution in high viscosity liquids: sodium chloride-glycerol. J. Phys. Chem. 65:1962;665-669.
2. Cox D., Furman W. Systematic error associated with apparatus 2 of the USP dissolution test I: effects of physical alignment of the dissolution apparatus. J. Pharm. Sci. 71(4):1982;451-452.
3. Cox, D., Douglas, C., Furman, W., Kirchoefer, R., Myrick, J., Wells, C., 1978. Guidelines for Dissolution Testing, Pharm Tech, pp. 41-53.
4. Cox D., Wells C., Furman W., Savage T., King A. Systematic errors associated with apparatus 2 of the USP dissolution test II: effects of deviation in vessel curvature from that of a sphere. J. Pharm. Sci. 71 (4):1982;395-399.
5. Garner, F., Grafton, R., 1954. Proc. Roy. Soc. (Lond.) A224, 64.
6. Garner, F., Suckling, R., 1958. AIChEJ 4, 114.
7. Handbook of Chemistry and Physics, 1991. 71st Ed., CRC Press, Boston, pp. 6-18.
8. Handbook of Chemistry and Physics, 1998. 78th Ed., CRC Press, Boston, pp. 5-95.
9. Hanson, W., 1991. Dissolution Testing, 2nd Edition, Aster Publishing Corporation, Eugene Oregon.
10. Levy G., Leonard J., Procknal J. Development of in vitro test which correlate quantitatively with dissolution rate-limited drug absorption in man. J. Pharm. Sci. 54 (12):1965;1719-1722.
11. Levy G., Leonard J., Procknal J. Interpretation of in vitro dissolution data relative to gastrointestinal absorption characteristics of drugs in tablets. J. Pharm Sci. 56 (10):1967;1365-1367.
12. Mannin, V., Ojala, K., Reissel, P., The Lancet, October 28, 1972, p. 922, as referenced in Leeson, L., Carstensen, J., Dissolution Technology, The Industrial Pharmaceutical Technology Section of the Academy of Pharmaceutical Sciences, Washington, D.C., 1974, p. 60.
13. Mannin, V., Ojala, K., Reissel, P., The Lancet, October 28, 1972, p. 922, as referenced in Leeson, L., Carstensen, J., Dissolution Technology, The Industrial Pharmaceutical Technology Section of the Academy of Pharmaceutical Sciences, Washington, D.C., 1974, p. 60.
14. Nelson, E., 1957. J Pharm Assoc Sci Ed, 46, 607, as referenced in Abdou, H., Dissolution, Bioavailability & Bioequivalence, Chapter 1, Mack Printing Co., Easton PA, 1989.
15. Nelson, E., 1957. J Pharm Assoc Sci Ed, 46, 607, as referenced in Abdou, H., Dissolution, Bioavailability & Bioequivalence, Chapter 1, Mack Printing Co., Easton PA, 1989.
16. Neter, J., Kutner, M., Nachtsheim C., Wasserman, W., Applied Linear Statistical Models, 4th Ed., Richard D. Irwin, Chicago, IL, 1996, p. 1096.
17. United States Pharmacopeia, correspondence received from USP on receipt of Lot N of USP Dissolution Calibrators. United States Pharmacopeia, Rockville MD, December 9, 1997.
18. United States Pharmacopeia 23/National Formulary 18, 1995. United States Pharmacopeial Convention Inc., Rockville MD, pp. 1794-1795.