In Vitro Characterization of Chitosan Gels for Buccal Delivery of Celecoxib: Influence of a Penetration Enhancer


Autoria(s): Cid, Yara Peluso; Pedrazzi, Vinicius; Sousa, Valeria Pereira de; Pierre, Maria Bernadete Riemma
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

07/11/2013

07/11/2013

2012

Resumo

Celecoxib (Cx) shows high efficacy in the treatment of osteoarthritis and rheumatoid arthritis as a result of its high specificity for COX-2, without gastrolesivity or interference with platelet function at therapeutic concentrations. Besides of anti-inflammatory effects, Cx also has a potential role for oral cancer chemoprevention. For these conditions, oral administration in long-term treatment is a concern due to its systemic side effects. However, local application at the site of injury (e.g., buccal inflammation conditions or chemoprevention of oral cancer) is a promising way to reduce its toxicity. In this study, the in vitro characterization of mucoadhesive chitosan (CHT) gels associated to AzoneA (R) was assessed to explore the potential buccal mucosal administration of Cx in this tissue. Rheological properties of gels were analyzed by a rheometer with cone-plate geometry. In vitro Cx release and permeability studies used artificial membranes and pig cheek mucosa, respectively. Mucoadhesion were measured with a universal test machine. CHT gels (3.0%) containing 2.0% or 3.0% Az showed more appropriate characteristics compared to the others: pH values, rheology, higher amount of Cx retained in the mucosa, and minimal permeation through mucosa, besides the highest mucoadhesion values, ideal for buccal application. Moreover, the flux (J) and amounts of drug released decreased with increased CHT and Az concentrations. CHT gels (3.0%) associated with 2.0% or 3.0% Az may be considered potential delivery systems for buccal administration of Cx.

Fundacao de Amparo a Pesquisa do Estado do Rio de Janeiro (FAPERJ) Brazil [E-26/171.254/2006]

Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES), Brazil

Identificador

AAPS PHARMSCITECH, NEW YORK, v. 13, n. 1, p. 101-111, MAR, 2012

1530-9932

http://www.producao.usp.br/handle/BDPI/43045

10.1208/s12249-011-9725-8

http://dx.doi.org/10.1208/s12249-011-9725-8

Idioma(s)

eng

Publicador

SPRINGER

NEW YORK

Relação

AAPS PHARMSCITECH

Direitos

restrictedAccess

Copyright SPRINGER

Palavras-Chave #AZONE #BUCCAL MUCOSA #CELECOXIB #CHITOSAN #IN VITRO PERMEABILITY #IN VITRO RELEASE #MUCOADHESION #RHEOLOGY #NONSTEROIDAL ANTIINFLAMMATORY DRUGS #ORAL-CARCINOMA CELL #PERCUTANEOUS-ABSORPTION #CANCER CHEMOPREVENTION #PERMEATION ENHANCERS #VIVO #SKIN #MUCOSA #CYCLOOXYGENASE-2 #PERMEABILITY #PHARMACOLOGY & PHARMACY
Tipo

article

original article

publishedVersion