The disappearance of various β‐lactam antibiotics from in situ rat small intestinal loops was studied at pH 7.4. For monobasic penicillins, despite the wide variety of apparent partition coefficients in is isobutyl alcohol‐water, the disappearance from the jejunal loops was almost 30% (±5% SD). On the other hand, the disappearance of amphoteric derivatives of penicillins and cephalosporins having very low lipid solubility varied widely between 12 and 80%. The peak blood levels after intraduodenal administration to the rats correlated well with the extent of disappearance of amphoteric penicillins from the intestinal loops. Absorption studies utilizing in situ intestinal loops were performed at variable dose ranges to yield a clear dose‐dependent disappearance. It is suggested that certain carrier‐mediated transport systems underlie the absorption mechanisms of amphoteric β‐lactam antibiotics.
- Absorption, intestinal—mechanism proposed for saturable transport of amphoteric amino‐β‐lactam antibiotics, in situ rat intestinal loops
- Aminocephalosporins—intestinal absorption mechanism proposed, compared with monobasic penicillins, in situ rat intestinal loops
- Aminopenicillins—intestinal absorption mechanism proposed, compared with monobasic penicillins, in situ rat intestinal loops
- Antibiotics, amino‐β‐lactam—compared with monobasic penicillins, intestinal absorption mechanism proposed, in situ rat intestinal loops
ASJC Scopus subject areas
- Pharmaceutical Science