AUTHOR=Yerasi Neelima , Vurimindi Himabindu , Devarakonda Krishna 

TITLE=Frog intestinal perfusion to evaluate drug permeability: application to p-gp and cyp3a4 substrates

JOURNAL=Frontiers in Pharmacology

VOLUME=6

YEAR=2015

URL=https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2015.00141

DOI=10.3389/fphar.2015.00141

ISSN=1663-9812

ABSTRACT=<p>To evaluate the reliability of using <italic>in situ</italic> frog intestinal perfusion technique for permeability assessment of carrier transported drugs which are also substrates for CYP enzymes. Single Pass Intestinal Perfusion (SPIP) studies were performed in frogs of the species <italic>Rana tigrina</italic> using established method for rats with some modifications after inducing anesthesia. Effective permeability coefficient (<italic>P</italic><sub>eff</sub>) of losartan and midazolam was calculated in the presence and absence of inhibitors using the parallel-tube model. P<sub>eff</sub> of losartan when perfused alone was found to be 0.427 ± 0.27 × 10<sup>-4</sup>cm/s and when it was co-perfused with inhibitors, significant change in <italic>P</italic><sub>eff</sub> was observed. P<sub>eff</sub> of midazolam when perfused alone was found to be 2.03 ± 0.07 × 10<sup>-4</sup>cm/s and when it was co-perfused with inhibitors, no significant change in <italic>P</italic><sub>eff</sub> was observed. Comparison of <italic>P</italic><sub>eff</sub> calculated in frog with that of other available models and also humans suggested that the <italic>P</italic><sub>eff</sub>-values are comparable and reflected well with human intestinal permeability. It is possible to determine the <italic>P</italic><sub>eff</sub>-value for compounds which are dual substrates of <italic>P</italic>-glycoprotein and CYP3A4 using <italic>in situ</italic> frog intestinal perfusion technique. The calculated <italic>P</italic><sub>eff</sub>-values correlated well with reported <italic>P</italic><sub>eff</sub>-values of probe drugs. comparison of the <italic>P</italic><sub>eff</sub>-value of losartan obtained with that of reported human’s <italic>P</italic><sub>eff</sub> and Caco 2 cell data, and comparison of the <italic>P</italic><sub>eff</sub>-value of midazolam with that of reported rat’s <italic>P</italic><sub>eff</sub>, we could conclude that SPIP from model can be reliably used in preclinical studies for permeability estimation. This model may represent a valuable alternative to the low speed and high cost of conventional animal models (typically rodents) for the assessment of intestinal permeability.</p>