Combining mucilair™ and vitrocell® powder chamber for the in vitro evaluation of nasal ointments in the context of aerosolized pollen

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Abstract

Hay fever is notoriously triggered when nasal mucosa is exposed to allergenic pollen. One possibility to overcome this pollen exposure may be the application of an ointment with physical protective effects. In this context, we have investigated Bepanthen® Eye and Nose Ointment and the ointment basis petrolatum as reference while using contemporary in vitro techniques. Pollen from false ragweed (Iva xanthiifolia) was used as an allergy-causing model deposited as aerosol using the Vitrocell® Powder Chamber (VPC) on Transwell® inserts, while being coated with either Bepanthen® Eye and Nose Ointment and petrolatum. No pollen penetration into ointments was observed upon confocal scanning laser microscopy during an incubation period of 2 h at 37 ºC. The cellular response was further investigated by integrating the MucilAir™ cell system in the VPC and by applying pollen to Bepanthen® Eye and Nose Ointment covered cell cultures. For comparison, MucilAir™ were stimulated by lipopolysaccharides (LPS). No increased cytokine release of IL-6, TNF-α, or IL-8 was found after 4 h of pollen exposure, which demonstrates the safety of such ointments. Since nasal ointments act as a physical barrier against pollen, such preparations might support the prevention and management of hay fever.

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Metz, J., Knoth, K., Groß, H., Lehr, C. M., Stäbler, C., Bock, U., & Hittinger, M. (2018). Combining mucilairTM and vitrocell® powder chamber for the in vitro evaluation of nasal ointments in the context of aerosolized pollen. Pharmaceutics, 10(2). https://doi.org/10.3390/pharmaceutics10020056

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