Transport of Model Compounds across the Peritoneal Membrane in the Rat
- 1 January 1978
- journal article
- research article
- Published by S. Karger AG in Pharmacology
- Vol. 17 (6) , 330-340
- https://doi.org/10.1159/000136874
Abstract
The absorption into the systemic circulation of compounds administered i.p. in large volumes was investigated in the rat. The influence on absorption of MW, lipid-water partition coefficient (K), and dissociation constant (pKa) was studied. Neutral compounds (9) ranging in MW from 18-2 million demonstrated absorptions that decreased with increasing MW. Five compounds were tested with variable lipid partition (K) values (0.001-3.3) and the absorptions increased from 57 to 96% as the K values increased. A series of 9 acids and bases covering a wide range of pKa values (0.9-9.9) were investigated. For the acids, absorption increased with increasing pKa value, while for the bases absorption decreased with increasing pKa. For both groups of compounds absorption was directly related to the extent of ionization at physiologic pH. As has been documented for other biological membranes, the peritoneal membrane in the rat behaved in a lipoid manner. Unionized or lipid-soluble compounds are absorbed to a greater extent than ionized or lipid-insoluble compounds, and neutral compounds are absorbed in relation to their MW.This publication has 1 reference indexed in Scilit: