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Study breakdown

How Well Do Opioid Peptides Cross the Gut Barrier? Transport Across Intestinal Cell Monolayers

In VitroPreliminary evidence
The takeaway

Mu-opioid receptor agonist and antagonist peptides showed varying permeability across Caco-2 intestinal monolayers, with some achieving meaningful transport — assessing the oral bioavailability potential of opioid peptides.

Key finding

Mu-opioid peptide agonists and antagonists showed variable Caco-2 monolayer permeability, with some achieving transcellular transport — assessing oral

What the researchers found

Mu-opioid peptide agonists and antagonists showed variable Caco-2 monolayer permeability, with some achieving transcellular transport — assessing oral bioavailability potential and identifying which opioid peptide structures achieve gut barrier crossing.

Why it matters

Relevant for opioid-peptides, bioactive-food-peptides, bioavailability.

How the study worked

in-vitro study.

What this study cannot tell us

See abstract.

How to read the evidence

preliminary evidence.

When this study was published

Published in 2008.

The bigger picture

Advances peptide research.

Questions still open

  • Further research needed.
  • Clinical translation to evaluate.

Common questions

What was studied?
How Well Do Opioid Peptides Cross the Gut Barrier? Transport Across Intestinal Cell Monolayers
What was found?
Mu-opioid receptor agonist and antagonist peptides showed varying permeability across Caco-2 intestinal monolayers, with some achieving meaningful transport — assessing the oral bioavailability potential of opioid peptides.

Read the original research

Transport of micro-opioid receptor agonists and antagonist peptides across Caco-2 monolayer.

Peptides, 29(6), 1042-7

Citation

Iwan, Małgorzata; Jarmołowska, Beata; Bielikowicz, Krzysztof; Kostyra, Elzbieta; Kostyra, Henryk; Kaczmarski, Maciej. (2008). Transport of micro-opioid receptor agonists and antagonist peptides across Caco-2 monolayer.. Peptides, 29(6), 1042-7. https://doi.org/10.1016/j.peptides.2008.01.018