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  3. Temperature-triggered in situ forming lipid mesophase gel for local treatment of ulcerative colitis.
 

Temperature-triggered in situ forming lipid mesophase gel for local treatment of ulcerative colitis.

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BORIS DOI
10.48350/183412
Date of Publication
June 13, 2023
Publication Type
Article
Division/Institute

DCBP Gruppe Prof. Luc...

Institut für Gewebeme...

Institut für Gewebeme...

Contributor
Carone, Marianna
DCBP Gruppe Prof. Luciani
Departement für Chemie, Biochemie und Pharmazie (DCBP) Universität Bern
Spalinger, Marianne R
Gaultney, Robert Anthony
Institut für Gewebemedizin und Pathologie - Administration Forschung
Institut für Gewebemedizin und Pathologie
Mezzenga, Raffaele
Hlavacková, Kristyna
Institut für Gewebemedizin und Pathologie - Administration Forschung
Institut für Gewebemedizin und Pathologie
Mookhoek, Aart
Institut für Gewebemedizin und Pathologie
Institut für Gewebemedizin und Pathologie - Klinische Pathologie
Krebs, Philippeorcid-logo
Institut für Gewebemedizin und Pathologie - Administration Forschung
Institut für Gewebemedizin und Pathologie
Rogler, Gerhard
Luciani, Paolaorcid-logo
DCBP Gruppe Prof. Luciani
Departement für Chemie, Biochemie und Pharmazie (DCBP) Universität Bern
Aleandri, Simone
DCBP Gruppe Prof. Luciani
Departement für Chemie, Biochemie und Pharmazie (DCBP) Universität Bern
Subject(s)

500 - Science::570 - ...

600 - Technology::610...

500 - Science::540 - ...

Series
Nature Communications
ISSN or ISBN (if monograph)
2041-1723
Publisher
Springer Nature
Language
English
Publisher DOI
10.1038/s41467-023-39013-3
PubMed ID
37311749
Description
Ulcerative colitis is a chronic inflammatory bowel disease that strongly affects patient quality of life. Side effects of current therapies necessitate new treatment strategies that maximise the drug concentration at the site of inflammation, while minimizing systemic exposure. Capitalizing on the biocompatible and biodegradable structure of lipid mesophases, we present a temperature-triggered in situ forming lipid gel for topical treatment of colitis. We show that the gel is versatile and can host and release drugs of different polarities, including tofacitinib and tacrolimus, in a sustained manner. Further, we demonstrate its adherence to the colonic wall for at least 6 h, thus preventing leakage and improving drug bioavailability. Importantly, we find that loading known colitis treatment drugs into the temperature-triggered gel improves animal health in two mouse models of acute colitis. Overall, our temperature-triggered gel may prove beneficial in ameliorating colitis and decreasing adverse effects associated with systemic application of immunosuppressive treatments.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/167839
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File(s)
FileFile TypeFormatSizeLicensePublisher/Copright statementContent
s41467-023-39013-3.pdftextAdobe PDF2.71 MBpublishedOpen
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