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1000 Titel
  • Characterization of an ester-based core-multishell (CMS) nanocarrier for the topical application at the oral mucosa
1000 Autor/in
  1. Dommisch, Henrik |
  2. Stolte, KN. |
  3. Jager, J. |
  4. Vogel, K. |
  5. Müller, R. |
  6. Hedtrich, S. |
  7. Unbehauen, M. |
  8. Haag, R. |
  9. Danker, K. |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-04-05
1000 Erschienen in
1000 Quellenangabe
  • 25(10):5795-5805
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00784-021-03884-x |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8443517/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • 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.
1000 Sacherschließung
lokal Penetration
lokal Mouth Mucosa [MeSH]
lokal Swine [MeSH]
lokal Transepithelial resistance
lokal Administration, Cutaneous [MeSH]
lokal Animals [MeSH]
lokal Skin Absorption [MeSH]
lokal Skin [MeSH]
lokal Original Article
lokal Esters/metabolism [MeSH]
lokal Core-multishell nanocarrier
lokal Oral mucosal equivalents
lokal Drug Carriers/metabolism [MeSH]
lokal Nanoparticles [MeSH]
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0003-1043-2651|https://frl.publisso.de/adhoc/uri/U3RvbHRlLCBLTi4=|https://frl.publisso.de/adhoc/uri/SmFnZXIsIEou|https://frl.publisso.de/adhoc/uri/Vm9nZWwsIEsu|https://frl.publisso.de/adhoc/uri/TcO8bGxlciwgUi4=|https://frl.publisso.de/adhoc/uri/SGVkdHJpY2gsIFMu|https://frl.publisso.de/adhoc/uri/VW5iZWhhdWVuLCBNLg==|https://frl.publisso.de/adhoc/uri/SGFhZywgUi4=|https://frl.publisso.de/adhoc/uri/RGFua2VyLCBLLg==
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1000 @id frl:6449226.rdf
1000 Erstellt am 2023-05-04T11:39:19.273+0200
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1000 Zuletzt bearbeitet Sat Oct 21 00:42:38 CEST 2023
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