Helmholtz Gemeinschaft

Search
Browse
Statistics
Feeds

Characterization of an ester-based core-multishell (CMS) nanocarrier for the topical application at the oral mucosa

[img]
Preview
PDF (Original Article) - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader
12MB
[img] Other (Supplementary Information)
1MB

Item Type:Article
Title:Characterization of an ester-based core-multishell (CMS) nanocarrier for the topical application at the oral mucosa
Creators Name:Dommisch, H. and Stolte, K.N. and Jager, J. and Vogel, K. and Müller, R. and Hedtrich, S. and Unbehauen, M. and Haag, R. and Danker, K.
Abstract:OBJECTIVES: Topical drug administration is commonly applied to control oral inflammation. However, it requires sufficient drug adherence and a high degree of bioavailability. Here, we tested the hypothesis whether an ester-based core-multishell (CMS) nanocarrier is a suitable nontoxic drug-delivery system that penetrates efficiently to oral mucosal tissues, and thereby, increase the bioavailability of topically applied drugs. MATERIAL AND METHODS: To evaluate adhesion and penetration, the fluorescence-labeled CMS 10-E-15-350 nanocarrier was applied to ex vivo porcine masticatory and lining mucosa in a Franz cell diffusion assay and to an in vitro 3D model. In gingival epithelial cells, potential cytotoxicity and proliferative effects of the nanocarrier were determined by MTT and sulphorhodamine B assays, respectively. Transepithelial electrical resistance (TEER) was measured in presence and absence of CMS 10-E-15-350 using an Endohm-12 chamber and a volt-ohm-meter. Cellular nanocarrier uptake was analyzed by laser scanning microscopy. Inflammatory responses were determined by monitoring pro-inflammatory cytokines using real-time PCR and ELISA. RESULTS: CMS nanocarrier adhered to mucosal tissues within 5 min in an in vitro model and in ex vivo porcine tissues. The CMS nanocarrier exhibited no cytotoxic effects and induced no inflammatory responses. Furthermore, the physical barrier expressed by the TEER remained unaffected by the nanocarrier. CONCLUSIONS: CMS 10-E-15-350 adhered to the oral mucosa and adhesion increased over time which is a prerequisite for an efficient drug release. Since TEER is unaffected, CMS nanocarrier may enter the oral mucosa transcellularly. CLINICAL RELEVANCE: Nanocarrier technology is a novel and innovative approach for efficient topical drug delivery at the oral mucosa.
Keywords:Core-Multishell Nanocarrier, Transepithelial resistance, Penetration, Oral Mucosal Equivalents, Animals, Swine
Source:Clinical Oral Investigations
ISSN:1432-6981
Publisher:Springer
Volume:25
Number:10
Page Range:5795-5805
Date:October 2021
Official Publication:https://doi.org/10.1007/s00784-021-03884-x
PubMed:View item in PubMed

Repository Staff Only: item control page

Downloads

Downloads per month over past year

Open Access
MDC Library