Enhanced in situ availability of Aphanizomenon Flos-Aquae constituents entrapped in buccal films for the treatment of oxidative stress-related oral diseases: Biomechanical characterization and in vitro/ex vivo evaluation

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Abstract

In recent years, the key role of oxidative stress in pathogenesis of oral diseases has been emphasized and the use of antioxidant agents has been encouraged. Aphanizomenon flos-aquae (AFA) is a unicellular blue-green alga with antioxidant and anti-inflammatory properties. The aim of this study was the formulation and characterization of mucoadhesive thin layer films loaded with AFA, finalized to the treatment of oxidative stress (OS)-related oral diseases. First, to enhance the bioavailability of AFA constituents, the raw food grade material was appropriately treated by a high frequency homogenization able to disrupt cell walls. Thus, Eudragit® E100-based buccal films were produced by the solvent casting method, containing 7% and 18% of AFA. The films, characterized by uniformity in thickness, weight, and drug content, showed low swelling degree, good muco-adhesiveness and controlled drug release. The mechanical tests showed elastic moduli of films of almost 5 MPa that is well-suitable for human buccal applications without discomfort, besides biaxial tests highlighted a marked material isotropy. Permeation studies through porcine mucosae demonstrated the ability of films to promote AFA penetration in the tissues, and when sublingually administered, they produced a drug flux up to six-fold higher than an AFA solution. The new formulations represent an interesting alternative for the development of cosmetics and nutraceuticals with a functional appeal containing plant extracts.

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Caro, V. D., Murgia, D., Seidita, F., Bologna, E., Alotta, G., Zingales, M., & Campisi, G. (2019). Enhanced in situ availability of Aphanizomenon Flos-Aquae constituents entrapped in buccal films for the treatment of oxidative stress-related oral diseases: Biomechanical characterization and in vitro/ex vivo evaluation. Pharmaceutics, 11(1). https://doi.org/10.3390/pharmaceutics11010035

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