Quinones Oliesia Gonzalez, Abranches Renata Pereira, Nakamura Marcos Jun, de Souza Ramos Monica Freiman, Riemma Pierre Maria Bernadete
School of Pharmacy, Federal University of Rio de Janeiro, 21.941.902, Rio de Janeiro, RJ, Brazil.
Farmanguinhos, Fundacao Osvaldo Cruz (FIOCRUZ), 21. 041.250, Rio de Janeiro, RJ, Brazil.
Curr Drug Deliv. 2018;15(3):357-366. doi: 10.2174/1567201814666170825154453.
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.
Evaluation of copaiba oil (C.O) as a potential skin penetration enhancer (P.E) for Cxb.
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.
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.
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.
塞来昔布(Cxb)的局部或透皮给药是皮肤治疗中一种有趣的策略,因为它减少或避免了口服途径的副作用。然而,Cxb的高亲脂性和角质层(SC)屏障会损害其皮肤渗透。
评估巴西香脂油(C.O)作为Cxb潜在的皮肤渗透促进剂(P.E)。
通过气相色谱-质谱联用(GC-MS)评估C.O的化学成分。分别在装有合成疏水膜的改良扩散池和以猪耳皮肤为模型的情况下,测定Cxb在与C.O(1-50% w/w)相关的聚乙二醇400/丙二醇(PEG 400/PG)载体中的体外释放和渗透率。
C.O的GC-MS分析表明,它由倍半萜(68.65%)和二萜(22.26%)组成。含有25% C.O(F4)和50% C.O(F5)的制剂在前2小时表现出体外突释,但只有F4在24小时后释放了100%的药物。F4实现了Cxb在皮肤中的最高渗透,F4和F5在角质层以及表皮加真皮中的皮肤滞留量最高。
25% C.O使Cxb的皮肤渗透率增加,并使其在24小时内长时间滞留,这表明它可能是开发Cxb透皮制剂的一种有前景的佐剂。