4.7 Article

Improved In Vitro Model for Intranasal Mucosal Drug Delivery: Primary Olfactory and Respiratory Epithelial Cells Compared with the Permanent Nasal Cell Line RPMI 2650

期刊

PHARMACEUTICS
卷 11, 期 8, 页码 -

出版社

MDPI
DOI: 10.3390/pharmaceutics11080367

关键词

barrier model; nose-to-brain; primary cells; RPMI 2650; olfactory epithelium; respiratory epithelium

资金

  1. EU grant N2B-patch under the European Framework Programme for Research and Innovation Horizon 2020 [721,098]
  2. grant FcRn in Drug Delivery - Baden-Wurttemberg State Ministry of Science, Research and Arts
  3. grant ALIVE - Federal Ministry for Economic Affairs and Energy (BMWi)
  4. Stiftung der Deutschen Wirtschaft

向作者/读者索取更多资源

Background: The epithelial layer of the nasal mucosa is the first barrier for drug permeation during intranasal drug delivery. With increasing interest for intranasal pathways, adequate in vitro models are required. Here, porcine olfactory (OEPC) and respiratory (REPC) primary cells were characterised against the nasal tumour cell line RPMI 2650. Methods: Culture conditions for primary cells from porcine nasal mucosa were optimized and the cells characterised via light microscope, RT-PCR and immunofluorescence. Epithelial barrier function was analysed via transepithelial electrical resistance (TEER), and FITC-dextran was used as model substance for transepithelial permeation. Beating cilia necessary for mucociliary clearance were studied by immunoreactivity against acetylated tubulin. Results: OEPC and REPC barrier models differ in TEER, transepithelial permeation and MUC5AC levels. In contrast, RPMI 2650 displayed lower levels of MUC5AC, cilia markers and TEER, and higher FITC-dextran flux rates. Conclusion: To screen pharmaceutical formulations for intranasal delivery in vitro, translational mucosal models are needed. Here, a novel and comprehensive characterisation of OEPC and REPC against RPMI 2650 is presented. The established primary models display an appropriate model for nasal mucosa with secreted MUC5AC, beating cilia and a functional epithelial barrier, which is suitable for long-term evaluation of sustained release dosage forms.

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