Development and validation of a porcine artificial colonic mucus model reflecting the properties of native colonic mucus in pigs

Colonic mucus plays a key role in colonic drug absorption. Mucus permeation assays could therefore provide useful insights and support rational formulation development in the early stages of drug development. However, the collection of native colonic mucus from animal sources is labor-intensive, doe...

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Published inEuropean journal of pharmaceutical sciences Vol. 181; p. 106361
Main Authors Barmpatsalou, Vicky, Rodler, Agnes, Jacobson, Magdalena, Karlsson, Eva Marie-Louise, Pedersen, Betty Lomstein, Bergström, Christel Anna Sofie
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.02.2023
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Summary:Colonic mucus plays a key role in colonic drug absorption. Mucus permeation assays could therefore provide useful insights and support rational formulation development in the early stages of drug development. However, the collection of native colonic mucus from animal sources is labor-intensive, does not yield amounts that allow for routine experimentation, and raises ethical concerns. In the present study, we developed an in vitro porcine artificial colonic mucus model based on the characterization of native colonic mucus. The structural properties of the artificial colonic mucus were validated against the native secretion for their ability to capture key diffusion patterns of macromolecules in native mucus. Moreover, the artificial colonic mucus could be stored under common laboratory conditions, without compromising its barrier properties. In conclusion, the porcine artificial colonic mucus model can be considered a biorelevant way to study the diffusion behavior of drug candidates in colonic mucus. It is a cost-efficient screening tool easily incorporated into the early stages of drug development and it contributes to the implementation of the 3Rs (refinement, reduction, and replacement of animals) in the drug development process. [Display omitted]
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ISSN:0928-0987
1879-0720
1879-0720
DOI:10.1016/j.ejps.2022.106361