JPET xPharm- The Comprehensive Pharmacology Reference

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Shore, P. A.
Right arrow Articles by Hogben, C. A. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Shore, P. A.
Right arrow Articles by Hogben, C. A. M.
Journal of Pharmacology And Experimental Therapeutics, Vol. 119, Issue 3, 361-369, 1957
Copyright © 1957 by American Society for Pharmacology and Experimental Therapeutics


THE GASTRIC SECRETION OF DRUGS: A pH PARTITION HYPOTHESIS

Parkhurst A. Shore 1, Bernard B. Brodie 1, and C. Adrain M. Hogben 1

1 Laboratory of Chemical Pharmacology and Laboratory of Kidney and Electrolyte Metabolism, National Heart Institute, National Institutes of Health, Public Health Service, U. S. Department of Health, Education, and Welfare, Bethesda, Maryland

Parenterally administered drugs are secreted directly into the gastric juice. The concentration ratio (concentration of drug in gastric juice divided by concentration in plasma) depends on the dissociation constant of the drug. Thus strong acids appear in gastric juice in negligible concentration, weak acids and weak bases in measurable amount and stronger bases in highest concentration. The stronger bases appear in a limiting concentration ratio of about 40 to 1 when gastric juice flow is maximal, the limitation apparently being due to complete clearance by the gastric mucosa.

The pattern of drug secretion can be explained by the concept that the membrane separating plasma from gastric juice has the characteristics of a lipoid membrane that allows the passage of drugs in their undissociated form while restricting passage of dissociated form.

Submitted on September 5, 1956




This article has been cited by other articles:


Home page
Antimicrob. Agents Chemother.Home page
F. Mégraud, A. Occhialini, and J. F. Rossignol
Nitazoxanide, a Potential Drug for Eradication of Helicobacter pylori with No Cross-Resistance to Metronidazole
Antimicrob. Agents Chemother., November 1, 1998; 42(11): 2836 - 2840.
[Abstract] [Full Text]


Home page
Drug Metab. Dispos.Home page
M. G. Lee and W. L. Chiou
Mechanism of Ascorbic Acid Enhancement of the Bioavailability and Diuretic Effect of Furosemide
Drug Metab. Dispos., May 1, 1998; 26(5): 401 - 407.
[Abstract] [Full Text]




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
All ASPET Journals Molecular Pharmacology Pharmacological Reviews
 Molecular Interventions Drug Metabolism and Disposition

Copyright © 1957 by the American Society for Pharmacology and Experimental Therapeutics.