Mucoadhesive emulgel systems containing curcumin for oral squamous cell carcinoma treatment: From pre -formulation to cytotoxicity in tissue-engineering oral mucosa

被引:28
|
作者
de Souza Ferreira, Sabrina Barbosa [1 ]
Slowik, Klaudia M. [2 ]
de Castro Hoshino, Lidiane Vizioli [3 ]
Baesso, Mauro Luciano [3 ]
Murdoch, Craig [2 ]
Colley, Helen Elizabeth [2 ]
Bruschi, Marcos Luciano [1 ]
机构
[1] Univ Estadual Maringa, Dept Pharm, Lab Res & Dev Drug Delivery Syst, Postgrad Program Pharmaceut Sci, Colombo Ave 5790, BR-97020900 Maringa, Parana, Brazil
[2] Univ Sheffield, Sch Clin Dent, 19 Claremont, Sheffield S10 2TA, S Yorkshire, England
[3] Univ Estadual Maringa, Dept Phys, Colombo Ave 5790, BR-97020900 Maringa, Parana, Brazil
关键词
Emulgel; Curcumin; Tissue-engineering; Oral squamous cell carcinoma; Ex vivo permeation; Mucoadhesion; DRUG-DELIVERY SYSTEMS; IN-VITRO; PHOTODYNAMIC THERAPY; RHEOLOGICAL PROPERTIES; METHYLENE-BLUE; EX-VIVO; PHYSICOCHEMICAL STABILITY; POLYMERIC SYSTEMS; ESSENTIAL OIL; POLOXAMER; 407;
D O I
10.1016/j.ejps.2020.105372
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Current oral squamous cell carcinoma chemotherapies demonstrate off -target toxicity, which could be reduced by local delivery. Curcumin acts via many cellular targets to give anti -cancer properties; however the bioa- vailability is hindered by its physicochemical characteristics. The incorporation of curcumin into emulgel sys- tems could be a promising approach for its solubilization and delivery. The aim of this work was to develop emulgel systems containing curcumin for the treatment of oral cancer. The emulgels containing curcumin were prepared with poloxamer 407, acrylic acid derivatives, oil phase (sesame oil or isopropyl myristate). The more stable system was evaluated for mechanical and rheological properties, as well as, the in vitro drug release profile, permeation and cytotoxic potential to oral mucosa models. The flow -throw system evidenced that the formulations could keep 5 min over porcine oral mucosa. Emulgel showed pseudoplastic behavior and a gelation temperature of 33 degrees C, which ensure their higher consistency. In addition, 70% of the incorporated curcumin was released within 24 h in an in vitro drug release study and could permeate porcine oral mucosa. Monolayers cultures and tissue -engineered models showed the selectivity of the drug and systems for tumor cells. The physicochemical properties, subsequent release and permeation of curcumin to selectivity kill cancer cells could be improved by the incorporation into emulgel systems.
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页数:15
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