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  3. Mucoadhesive 3D printed vaginal ovules to treat endometriosis and fibrotic uterine diseases.
 

Mucoadhesive 3D printed vaginal ovules to treat endometriosis and fibrotic uterine diseases.

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BORIS DOI
10.48350/183579
Date of Publication
September 1, 2023
Publication Type
Article
Division/Institute

Departement für Chemi...

Contributor
Teworte, Sarah
Departement für Chemie, Biochemie und Pharmazie (DCBP) Universität Bern
Aleandri, Simone
Departement für Chemie, Biochemie und Pharmazie (DCBP) Universität Bern
Weber, Jessica
Carone, Marianna
Departement für Chemie, Biochemie und Pharmazie (DCBP) Universität Bern
Luciani, Paolaorcid-logo
Departement für Chemie, Biochemie und Pharmazie (DCBP) Universität Bern
Subject(s)

500 - Science::570 - ...

500 - Science::540 - ...

Series
European journal of pharmaceutical sciences
ISSN or ISBN (if monograph)
1879-0720
Publisher
Elsevier
Language
English
Publisher DOI
10.1016/j.ejps.2023.106501
PubMed ID
37339708
Uncontrolled Keywords

3D printing drug repu...

Description
Gynaecological health is a neglected field of research that includes conditions such as endometriosis, uterine fibroids, infertility, viral and bacterial infections, and cancers. There is a clinical need to develop dosage forms for gynecological diseases that increase efficacy and reduce side effects and explore new materials with properties tailored to the vaginal mucosa and milieu. Here, we developed a 3D printed semisolid vaginal ovule containing pirfenidone, a repurposed drug candidate for endometriosis. Vaginal drug delivery allows direct targeting of the reproductive organs via the first uterine pass effect, but vaginal dosage forms can be challenging to self-administer and retain in situ for periods of more than 1-3 h. Here, we show that a semisoft alginate-based vaginal suppository manufactured using semisolid extrusion additive manufacturing is superior to vaginal ovules made using standard excipients. The 3D-printed ovule showed a controlled release profile of pirfenidone in vitro in standard and biorelevant release tests, as well as better mucoadhesive properties ex vivo. An exposure time of 24 h of pirfenidone to a monolayer culture of an endometriotic epithelial cell line, 12Z, is necessary to reduce the cells' metabolic activity, which demonstrates the need for a sustained release formulation of pirfenidone. 3D printing allowed us to formulate mucoadhesive polymers into a semisolid ovule with controlled release of pirfenidone. This work enables further preclinical and clinical studies into vaginally administered pirfenidone to assess its efficacy as a repurposed endometriosis treatment.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/167971
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1-s2.0-S0928098723001318-main.pdftextAdobe PDF1.17 MBAttribution-NonCommercial-NoDerivatives (CC BY-NC-ND 4.0)publishedOpen
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