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Drug Development and Industrial Pharmacy Volume 26, 2000 - Issue 7
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Research Article

Dissolution of Omeprazole from Delayed-Release Solid Oral Dosage Forms

A. Farinha Laboratório de Estudos Farmacêuticos, Rua Alto do Duque, 67, Lisboa, 1400, Portugal
,
A. Bica Laboratório de Estudos Farmacêuticos, Rua Alto do Duque, 67, Lisboa, 1400, Portugal
,
J. M. Martins Laboratório de Estudos Farmacêuticos, Rua Alto do Duque, 67, Lisboa, 1400, Portugal
&
J. P. Pais Laboratório de Estudos Farmacêuticos, Rua Alto do Duque, 67, Lisboa, 1400, Portugal
Pages 785-790 | Published online: 06 May 2000

REFERENCES

  • Hardman J. G., Molinoff P. B., Gilman A. G. Goodman and Gilman's the Pharmacological Basis of Therapeutics, McGraw-Hill, Interamericana Editores, S.A.Mexico 1996; 667
  • Dighe S. V. Bio-International: Bioavailability, Bioequivalence and Pharmacokinetics, K. K. Midha, H. H. Blume. Medpharm Scientific, Stuttgart 1993; 247–255
  • U.S. Pharmacopeial Convention. The United States Pharmacopeia. 23rd rev., Author, Rockville, MD 1995
  • Farmacopeia Portuguesa VIImprensa Nacional Casa da Moeda Lisbon, 1997
  • British PharmacopoeiaHer Majesty's Stationery Office London, 1998
  • European Pharmacopoeia. 3rd ed., Council of Europe, Strasbourg 1997
  • FIP (Féderation Internationale Pharmaceutique)Guidelines for Dissolution Testing of Oral Products 1995
  • Lehman K. Acta Pharm. 1984; 93: 55–74
  • Davidson A. G., McCallum A. Drug Dev. Ind. Pharm. 1996; 22: 1173–1185

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