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Influence of acid-base balance on efficacy and toxicity of drugs.

M. D. Milne
- 01 Nov 1965 - 
- Vol. 58, pp 961-963
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TLDR
The excretion of natural metabolites is less likely to be influenced by urinary pH, as these substances are usually less lipoid-soluble than many widely used drugs, and pH-dependent excretion is, however, of practical importance in relation to the urinary content of many indolic metabolites and also in theexcretion of pigments derived from the degradation of hæmoglobin.
Abstract
Changes in acid-base balance have a profound influence on many aspects of the action of drugs. This is illustrated by data on the absorption of drugs from the stomach and intestine, in changes in distribution of drugs between plasma and cells, and the effect of change in urinary pH.As a general principle, these changes in the pharmacology of weak acids and bases are governed by physicochemical principles, which influence the proportion of the ionized and unionized components according to the pH of the medium and also to the peculiar property of biological membranes which allow the free passage of the lipoid-soluble unionized component and impede transfer of the water-soluble ionized fraction.Lipoid-soluble weak acids are excreted at higher clearances in alkaline urine, and conversely weak bases in acid urine. This is shown to be of practical importance in the treatment of poisoning, in the diagnosis of addiction to drugs and in studies of drug metabolism. In general, the excretion of natural metabolites is less likely to be influenced by urinary pH, as these substances are usually less lipoid-soluble than many widely used drugs. pH-dependent excretion is, however, of practical importance in relation to the urinary content of many indolic metabolites and also in the excretion of pigments derived from the degradation of haemoglobin. Urobilinogen excretion is certainly pH-dependent, a higher clearance rate occurring in alkaline urine. However, work is necessary to decide whether some of the porphyrins also show this important physiological property.

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References
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Journal Article

THE GASTRIC SECRETION OF DRUGS: A pH PARTITION HYPOTHESIS

TL;DR: 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.
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Absorption of drugs from the rat small intestine.

TL;DR: The relative rates of absorption of a large number of drugs have been measured by perfusing solutions of drugs through the entire small intestine of the anesthetized rat and the degree of ionization of an organic electrolyte in solution appears to be one of the most important factors determining its absorption from the rat small intestine.
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Absorption of short chain fatty acids in man.

TL;DR: The longer the chain length the faster the acids were absorbed, probably reflected their greater solubility in lipid as shown by their partition into chloroform from an aqueous solution.
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TL;DR: The results suggest that many drugs are absorbed from the colon by simple diffusion of the unionized moiety across a lipoidal harrier, indicating a common mechanism for the gastrointestinal absorption of drugs.
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