Assessing α-Bisabolol as a Transmucosal Permeation Enhancer of Buccal Local Anesthetics
Renê Oliveira do Couto,
Douglas Vieira Thomaz,
Maira Perez Ferreira Duarte,
Renata Fonseca Vianna Lopez,
Vinícius Pedrazzi,
Osvaldo de Freitas,
Gianluca Martino Tartaglia
Affiliations
Renê Oliveira do Couto
“Dona Lindu” Midwest Campus, Universidade Federal de São João del-Rei (UFSJ), Divinopolis 35501-296, MG, Brazil
Douglas Vieira Thomaz
Department of Biomedical, Surgical and Dental Sciences, School of Dentistry, University of Milan, 20129 Milan, Italy
Maira Perez Ferreira Duarte
School of Pharmaceutical Sciences of Ribeirao Preto, Department of Pharmaceutical Sciences, Universidade de São Paulo (USP), Ribeirão Preto 14040-900, SP, Brazil
Renata Fonseca Vianna Lopez
School of Pharmaceutical Sciences of Ribeirao Preto, Department of Pharmaceutical Sciences, Universidade de São Paulo (USP), Ribeirão Preto 14040-900, SP, Brazil
Vinícius Pedrazzi
School of Dentistry of Ribeirao Preto, Department of Dental Materials and Prosthodontics, Universidade de São Paulo (USP), Ribeirão Preto 14040-904, SP, Brazil
Osvaldo de Freitas
School of Pharmaceutical Sciences of Ribeirao Preto, Department of Pharmaceutical Sciences, Universidade de São Paulo (USP), Ribeirão Preto 14040-900, SP, Brazil
Gianluca Martino Tartaglia
Department of Biomedical, Surgical and Dental Sciences, School of Dentistry, University of Milan, 20129 Milan, Italy
Needle-free buccal anesthesia improves dental treatment outcomes for both patients and dentists. In this study, we report on an assessment of the enhancement effects of α-bisabolol on the in vitro transmucosal permeation of prilocaine hydrochloride (PCl) and lidocaine hydrochloride (LCl) from needleless buccal films. We also evaluated the mechanical properties of the film, which consisted of Methocel™ K100 LV as the film-forming polymer (3% m·m−1), PEG 400 as a cosolvent (15% m·m−1 based on drug loading), α-bisabolol (15 and 30% m·m−1 based on drug loading), and the drugs combined at a 1:1 ratio (15 mg·unit−1). The porcine esophageal epithelium was used as a membrane barrier, and artificial saliva was the release medium. After a 1 h experiment at 25 ± 2 °C, α-bisabolol significantly decreased, rather than enhanced, the permeation fluxes (five-fold), permeability coefficients (seven-fold), and retentions (two-fold) of both PCl and LCl through the epithelium, regardless of the concentration. Moreover, the resistance and flexibility of the films markedly decreased compared to those without α-bisabolol. Therefore, under the experimental conditions, using α-bisabolol as a buccal permeation enhancer for the hydrophilic local anesthetics PCl and LCl from buccal films is not feasible.