Enhanced intestinal absorption of amino acids and amino acid-like drug by possible formation of enamine in administered solution by the presence of ethylacetoacetate.
- 1 January 1984
- journal article
- research article
- Published by Pharmaceutical Society of Japan in Journal of Pharmacobio-Dynamics
- Vol. 7 (3), 143-150
- https://doi.org/10.1248/bpb1978.7.143
Abstract
Ethylacetoacetate promoted the colonic and the jejunal absorption of amino acids such as L-phenylalanine and D-phenylalanine when administered to rats in aqueous solution. Enhanced absorption of these isomers of amino acid might occur via a formation of enamine, which was observed in aqueous solution by monitoring UV absorbance at 288 nm. Since mixture of L- or D-phenylalanine and ethylacetoacetate in aqueous solution enhanced colonic absorption of cefmetazole while the solution did not affect so much on the jejunal absorption of cefmetazole compared to the colonic absorption of it, enhancing action of enamine probably produced in aqueous solution may be more effective at the colonic compartment.This publication has 3 references indexed in Scilit:
- Studies of absorption promoters for rectal delivery preparations. II. A possible mechanism of promoting efficacy of enamine derivatives in rectal absorption.CHEMICAL & PHARMACEUTICAL BULLETIN, 1982
- Study of enamine derivatives of phenylglycine as adjuvants for the rectal absorption of insulin.CHEMICAL & PHARMACEUTICAL BULLETIN, 1981
- Biopharmaceutical study on the oral and rectal administrations of enamine prodrugs of amino acid-like .BETA.-lactam antibiotics in rabbits.CHEMICAL & PHARMACEUTICAL BULLETIN, 1981