Dissolving Microneedles Loaded with Lipid Nanocarriers for Vaginal Delivery of Clotrimazole: <i>In Vitro</i> and <i>Ex Vivo</i> Evaluation

Vaginal yeast infections, such as vulvovaginal candidiasis (VVC), affect nearly three out of four women worldwide. Reoccurrence is frequent and requires repeated treatments with oral, antifungal medications at high doses. Prolonged treatments contribute to development of resistant fungal strains and the risk of systemic adverse effects. Vaginal drug delivery can overcome several of the disadvantages associated with oral drug administration. However, current dosage forms, such as vaginal creams and gels, are rapidly expelled from the vaginal tract and require daily dosing to ensure therapeutic outcome, thus jeopardizing patient compliance. Therefore, we developed rapidly dissolving microneedle arrays with a microneedle height reduction by 50% within 5 min, for local, vaginal delivery of antifungal drugs. Clotrimazole, a poorly water-soluble antifungal agent, was formulated in lipid-based nanocarriers (LNCs) and incorporated in the tips of microneedles. The antifungal activity was then tested against the most common VVC fungal strains, <i>C. albicans</i> and <i>C. glabrata</i>, using an <i>in vitro</i> disk diffusion assay and an explant model from bovine vaginal tissue. LNC loaded microneedles showed consistent significant inhibition of <i>Candida spp</i>. in comparison to blank microneedles and LNCs alone, with an inhibition diameter of 20-30 mm <i>in vitro</i> and a reduction of 3-5-fold fungal colonies <i>ex vivo</i>. Notably, the LNC-loaded microneedles inhibited fungal growth at a 10-fold lower drug dose than a commercial clotrimazole cream. Finally, a device prototype was developed in the form of an intravaginal ring incorporating multiple microneedle arrays on its surface, delivering a total drug dose of 0.1 mg per ring with 600 μm microneedle height. Local vaginal drug delivery using such microneedle-based devices could enable more effective treatment strategies for VVC.

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Journal
Molecular Pharmaceutics
Published
2026-03-16
DOI
https://doi.org/10.1021/acs.molpharmaceut.5c01721
Primary Topic
Advancements in Transdermal Drug Delivery
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article
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article

Dissolving Microneedles Loaded with Lipid Nanocarriers for Vaginal Delivery of Clotrimazole: In Vitro and Ex Vivo Evaluation

Lisa Myrseth Hemmingsen, Georgios A. Sotiriou, Alexandra Teleki, Natasa Skalko-Basnet et al.
Molecular Pharmaceutics
Advancements in Transdermal Drug Delivery
article

Dissolving Microneedles Loaded with Lipid Nanocarriers for Vaginal Delivery of Clotrimazole: In Vitro and Ex Vivo Evaluation

Lisa Myrseth Hemmingsen, Georgios A. Sotiriou, Alexandra Teleki, Natasa Skalko-Basnet, Paarkavi Udayakumar, Cristhian Fernando Salas Cotaquispe, Veronica Rondahl, Juan Du
article en

Abstract

Vaginal yeast infections, such as vulvovaginal candidiasis (VVC), affect nearly three out of four women worldwide. Reoccurrence is frequent and requires repeated treatments with oral, antifungal medications at high doses. Prolonged treatments contribute to development of resistant fungal strains and the risk of systemic adverse effects. Vaginal drug delivery can overcome several of the disadvantages associated with oral drug administration. However, current dosage forms, such as vaginal creams and gels, are rapidly expelled from the vaginal tract and require daily dosing to ensure therapeutic outcome, thus jeopardizing patient compliance. Therefore, we developed rapidly dissolving microneedle arrays with a microneedle height reduction by 50% within 5 min, for local, vaginal delivery of antifungal drugs. Clotrimazole, a poorly water-soluble antifungal agent, was formulated in lipid-based nanocarriers (LNCs) and incorporated in the tips of microneedles. The antifungal activity was then tested against the most common VVC fungal strains, <i>C. albicans</i> and <i>C. glabrata</i>, using an <i>in vitro</i> disk diffusion assay and an explant model from bovine vaginal tissue. LNC loaded microneedles showed consistent significant inhibition of <i>Candida spp</i>. in comparison to blank microneedles and LNCs alone, with an inhibition diameter of 20-30 mm <i>in vitro</i> and a reduction of 3-5-fold fungal colonies <i>ex vivo</i>. Notably, the LNC-loaded microneedles inhibited fungal growth at a 10-fold lower drug dose than a commercial clotrimazole cream. Finally, a device prototype was developed in the form of an intravaginal ring incorporating multiple microneedle arrays on its surface, delivering a total drug dose of 0.1 mg per ring with 600 μm microneedle height. Local vaginal drug delivery using such microneedle-based devices could enable more effective treatment strategies for VVC.

Molecular Pharmaceutics
Uppsala University (SE), Stockholm University (SE), Science for Life Laboratory (SE), Karolinska Institutet (SE), Swedish University of Agricultural Sciences (SE), Institute of Immunology and Physiology (RU), UiT The Arctic University of Norway (NO)
Good health and well-being
Openalex Percentile: Top 18%
Advancements in Transdermal Drug Delivery
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