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Journal of Quality Technology
A Quarterly Journal of Methods, Applications and Related Topics
Volume 12, 1980 - Issue 3
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Reviews of Standards and Specifications

Evaluation of U. S. Pharmacopeia Sampling Plans for Dissolution

Pages 158-164 | Published online: 22 Feb 2018

References

  • Carstensen, J. T., Wright, J. L., Blessel, K. W., and Sheridan, J., “USP Dissolution Test II: Sigmoid Dissolution Profiles from Directly Compressed Tablets,” Journal of Pharmaceutical Sciences, Vol. 67, No. 1, 1978, pp. 48–50.
  • Cox, D. C., Douglas, C. C., et al, “Guidelines for Dissolution Testing,” Pharmaceutical Technology, Vol. 2, No. 4, 1978, pp. 40–53.
  • Duncan, A. J., Quality Control and Industrial Statistics, 4th ed., Richard D. Irwin, Inc., Homewood, Illinois, 1974, pp. 179–198.
  • Kahn, K. A., “The Concept of Dissolution Efficiency,” Journal of Pharmacy and Pharmacology, Vol. 27, No. 1, 1975, pp. 48–49.
  • Knuth, D. E., The Art of Computer Programming, Vol. 2, Addison-Wesley, Reading, Massachusetts, 1969, pp. 105–113.
  • Leeson, L. J. and Carstensen, J. T., Dissolution Technology, The Industrial Pharmaceutical Technology Section of the Academy of Pharmaceutical Sciences, Washington, D. C., 1974, pp. 187–193.
  • “Minutes of the Fall Meeting 1977 of the Quality Control Section of the Pharmaceutical Manufacturers Association,” Pharmaceutical Manufacturers Association, White Sulphur Springs, West Virginia, September 1977, pp. 54–77.
  • Nelson, K. G. and Wang, L. Y., “Determination of Time Course of Tablet Disintegration II: Method Using Continuous Functions,” Journal of Pharmaceutical Sciences, Vol. 67, No. 1, 1978, pp. 86–89.
  • “Sampling Procedures and Tables for Inspection by Variables for Percent Defective,” MIL-STD-414, Department of Defense, Washington, D.C., 1957.
  • Schilling, E. G. and Dodge, H. F., “Procedures and Tables for Evaluating Dependent Mixed Acceptance Sampling Plans,” Technometrics, Vol. 11, No. 2, May 1969, pp. 341–372.
  • Shepherd, R. E., Price, J. C., and Luzzi, L. A., “Dissolution Profiles for Capsules and Tablets Using a Magnetic Basket Dissolution Apparatus,” Journal of Pharmaceutical Sciences, Vol. 61, No. 7, 1972, pp. 1152–1156.
  • The IMSL Library, Volume 1, International Mathematical and Statistical Libraries, Inc., Houston, Texas, 1977.
  • The United States Pharmacopeia XIX, Mack Printing Company, Easton, Pennsylvania, 1974, p. 651.
  • The United States Pharmacopeia XIX, 5th Supplement, Mack Printing Company, Easton, Pennsylvania, February 15, 1979.
  • Wagner, J. G. “Interpretation of Percent Dissolved-Time Plots Derived from In Vitro Testing of Conventional Tablets and Capsules,” Journal of Pharmaceutical Sciences, Vol. 58, No. 10, 1969, pp. 1253–1257.
  • Wood, J. H., “In Vitro Evaluation of Physiological Availability of Compressed Tablets,” Pharmaceutica Acta Helvetian Vol. 42, No. 3, 1967, pp. 129–151.

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