CriticalSorb™ promotes permeation of flux markers across isolated rat intestinal mucosae and Caco-2 monolayers

DJ Brayden, VA Bzik, AL Lewis, L Illum - Pharmaceutical research, 2012 - Springer
Pharmaceutical research, 2012Springer
Purpose CriticalSorb™ is a novel absorption enhancer based on Solutol® HS15, one that
has been found to enhance the nasal transport. It is in clinical trials for nasal delivery of
human growth hormone. The hypothesis was that permeating enhancement effects of the
Solutol® HS15 component would translate to the intestine. Methods Rat colonic mucosae
were mounted in Ussing chambers and Papp values of [14 C]-mannitol,[14 C]-antipyrine,
FITC-dextran 4000 (FD-4), and TEER values were calculated in the presence of …
Purpose
CriticalSorb™ is a novel absorption enhancer based on Solutol® HS15, one that has been found to enhance the nasal transport. It is in clinical trials for nasal delivery of human growth hormone. The hypothesis was that permeating enhancement effects of the Solutol®HS15 component would translate to the intestine.
Methods
Rat colonic mucosae were mounted in Ussing chambers and Papp values of [14C]-mannitol, [14C]-antipyrine, FITC-dextran 4000 (FD-4), and TEER values were calculated in the presence of CriticalSorb™. Tissues were fixed for H & E staining. Caco-2 monolayers were grown on Transwells™ for similar experiments.
Results
CriticalSorb™(0.01% v/v) significantly increased the Papp of [14C]-mannitol, FD-4 [14C]-antipyrine across ileal and colonic mucosae, accompanied by a decrease in TEER. In Caco-2 monolayers, it also increased the Papp of [14C]-mannitol FD-4 and [14C]-antipyrine over 120 min. In both monolayers and tissues, it acted as a moderately effective P-glycoprotein inhibitor. There was no evidence of cytotoxicity in Caco-2 at concentrations of 0.01% for up to 24 h and histology of tissues showed intact epithelia at 120 min.
Conclusions
Solutol® HS15 is the key component in CriticalSorb™ that enables non-cytotoxic in vitro intestinal permeation and its mechanism of action is a combination of increased paracellular and transcellular flux.
Springer
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