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Current Drug Delivery

Editor-in-Chief

ISSN (Print): 1567-2018
ISSN (Online): 1875-5704

Research Article

Copaiba Oil: Chemical Composition and Influence on In-vitro Cutaneous Permeability of Celecoxib

Author(s): Oliesia Gonzalez Quinones, Renata Pereira Abranches, Marcos Jun Nakamura, Monica Freiman de Souza Ramos and Maria Bernadete Riemma Pierre*

Volume 15, Issue 3, 2018

Page: [357 - 366] Pages: 10

DOI: 10.2174/1567201814666170825154453

Price: $65

Abstract

Background: Use of topical or transdermal administration of Celecoxib (Cxb) is an interesting strategy in cutaneous treatments since it reduces or avoids side effects of the oral route. However, Cxb´s high lipophilicity and the stratum corneum (SC) barrier impair cutaneous penetration.

Objective: Evaluation of copaiba oil (C.O) as a potential skin penetration enhancer (P.E) for Cxb.

Methods: The chemical composition of C.O was evaluated by GC-MS. Both in-vitro release and permeability assay of Cxb in Polyethylene glycol 400/ propylene glycol (PEG 400/PG) vehicle associated to C.O (1-50% w/w) were determined in a modified diffusion cell fitted with a synthetic hydrophobic membrane and pig ear skin as model, respectively.

Results: GC-MS analysis of C.O showed that it is composed of sesquiterpenes (68.65%) and diterpenes (22.26%). Formulations containing 25% C.O (F4) and 50% C.O (F5) have shown in-vitro burst release in the first 2 h, but only F4 released 100% of drug after 24 h. The highest Cxb permeation across skin was obtained from F4 and the highest skin retentions for F4 and F5 in the stratum corneum and epidermis plus dermis.

Conclusion: The increased Cxb permeability through skin and its retention for an extended time (24h) at 25% C.O suggest that it could be a promising adjuvant for the development of transdermal formulations of Cxb.

Keywords: Copaiba oil, chemical composition, GC-MS methodology, in-vitro cutaneous permeability, celecoxib, topical route, transdermal route.

Graphical Abstract

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