dc.contributor.author | Falavigna, Margherita | |
dc.contributor.author | Klitgaard, Mette | |
dc.contributor.author | Brase, Christina | |
dc.contributor.author | Ternullo, Selenia | |
dc.contributor.author | Skalko-Basnet, Natasa | |
dc.contributor.author | Flaten, Gøril Eide | |
dc.date.accessioned | 2019-01-31T10:19:16Z | |
dc.date.available | 2019-01-31T10:19:16Z | |
dc.date.issued | 2017-12-26 | |
dc.description.abstract | The mucus layer covering all mucosal surfaces in our body is the first barrier encountered by drugs before their potential absorption through epithelial tissues, and could thus affect the drugs’ permeability and their effectiveness. Therefore, it is of key importance to have in vitro permeability models that can mimic this specific environment. For this purpose, the novel mucus phospholipid vesicle-based permeation assay (mucus-PVPA) has been developed and used for permeability screening of drugs and formulations. The model proved to be stable under the chosen conditions and demonstrated the ability to discriminate between compounds with different chemical structures and properties. Overall, a decrease in drug permeability was found in the presence of mucus on top of the PVPA barriers, as expected. Moreover, mucoadhesive (chitosan-coated) and mucopenetrating (PEGylated) liposomes were investigated in the newly developed model. The mucus-PVPA was able to distinguish between the different liposomal formulations, confirming the penetration potential of the tested formulations and the related drug permeability. The mucus-PVPA model appears to be a promising in vitro tool able to mimic the environment of mucosal tissues, and could therefore be used for further drug permeability screening and formulation development. | en_US |
dc.description.sponsorship | The Arctic University of Norway
Lipoid GmbH | en_US |
dc.description | Accepted manuscript version, licensed <a href=http://creativecommons.org/licenses/by-nc-nd/4.0/> CC BY-NC-ND 4.0.</a> Published version available at <a href=https://doi.org/10.1016/j.ijpharm.2017.12.038> https://doi.org/10.1016/j.ijpharm.2017.12.038</a>. | en_US |
dc.identifier.citation | Falavigna, M., Klitgaard, M., Brase, C., Ternullo, S., Škalko-Basnet, N. & Flaten, G.E.F. (2018). Mucus-PVPA (mucus Phospholipid Vesicle-based Permeation Assay): An artificial permeability tool for drug screening and formulation development. <i>International Journal of Pharmaceutics, 537</i>(1-2), 213-222. https://doi.org/10.1016/j.ijpharm.2017.12.038 | en_US |
dc.identifier.cristinID | FRIDAID 1535820 | |
dc.identifier.doi | 10.1016/j.ijpharm.2017.12.038 | |
dc.identifier.issn | 0378-5173 | |
dc.identifier.issn | 1873-3476 | |
dc.identifier.uri | https://hdl.handle.net/10037/14570 | |
dc.language.iso | eng | en_US |
dc.publisher | Elsevier | en_US |
dc.relation.ispartof | Falavigna, M. (2021). The development journey of an artificial intestinal model predicting oral drug absorption: the mucus-PVPA model. (Doctoral thesis). <a href=https://hdl.handle.net/10037/20754>https://hdl.handle.net/10037/20754</a>. | |
dc.relation.journal | International Journal of Pharmaceutics | |
dc.rights.accessRights | openAccess | en_US |
dc.subject | VDP::Medical disciplines: 700::Basic medical, dental and veterinary science disciplines: 710::Pharmacology: 728 | en_US |
dc.subject | VDP::Medisinske Fag: 700::Basale medisinske, odontologiske og veterinærmedisinske fag: 710::Farmakologi: 728 | en_US |
dc.subject | In vitro model | en_US |
dc.subject | Permeability | en_US |
dc.subject | Mucosal administration | en_US |
dc.subject | Mucus | en_US |
dc.subject | Liposomes | en_US |
dc.subject | Mucoadhesive | en_US |
dc.subject | Mucopenetrating | en_US |
dc.title | Mucus-PVPA (mucus Phospholipid Vesicle-based Permeation Assay): An artificial permeability tool for drug screening and formulation development | en_US |
dc.type | Journal article | en_US |
dc.type | Tidsskriftartikkel | en_US |
dc.type | Peer reviewed | en_US |