Development and in vitro evaluation of mucoadhesive patches of methotrexate for targeted delivery in oral cancer

被引:40
作者
Jin, Bao-Zhong [1 ]
Dong, Xiao-Qi [2 ]
Xu, Xin [2 ]
Zhang, Feng-He [1 ]
机构
[1] Shandong Univ, Dept Oral Surg, Stomatol Hosp, 44 Wenhua West Rd, Jinan 250012, Shandong, Peoples R China
[2] Zhejiang Univ, Dept Oral Surg, Affiliated Hosp 2, Sch Med, Hangzhou 310009, Zhejiang, Peoples R China
关键词
mucoadhesive patch; liposomes; MTT assay; methotrexate; targeted delivery; DRUG-DELIVERY; COLON-CANCER; CELLS; LIPOSOMES; SYSTEMS; NANOPARTICLES; RELEASE; ENCAPSULATION; CHEMOTHERAPY; EXPRESSION;
D O I
10.3892/ol.2017.7613
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The present study focused on the development of a mucoadhesive patch of methotrexate (MTX) for targeted delivery in oral cancer. Initially, MTX-loaded liposomes were prepared using the thin film hydration method, and had a mean diameter of 105.7-137.4 nm and percentage entrapment efficiency of 54.6 3.5. These liposomes were cast in optimized mucoadhesive film. The film was characterized by its release pattern, thickness, weight and percentage swelling index and the sustained release profile of the optimized film was evaluated. The developed liposomes and liposomes cast in the film formulation were evaluated for cytotoxicity in HSC-3 cells using an MTT assay, and a significant decrease in the half maximal inhibitory concentration of MTX was identified with the MTX-entrapped liposomal film, M-LP-F7. The results of the mitochondria-dependent intrinsic pathway demonstrated that there was significant mitochondrial membrane potential disruption with M-LP-F7 compared with the plain drug. M-LP-F7 increased the rate of apoptosis in HSC-3 cells by almost 3-fold. Elevated levels of reactive oxygen species provided evidence that M-LP-F7 exerts a pro-oxidant effect in HSC-3 cells.
引用
收藏
页码:2541 / 2549
页数:9
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