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用于口腔癌靶向递送的甲氨蝶呤粘膜粘附贴片的研制与评价

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

作者信息

Jin Bao-Zhong, Dong Xiao-Qi, Xu Xin, Zhang Feng-He

机构信息

Department of Oral Surgery, Stomatological Hospital of Shandong University, Jinan, Shandong 250012, P.R. China.

Department of Oral Surgery, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang 310009, P.R. China.

出版信息

Oncol Lett. 2018 Feb;15(2):2541-2549. doi: 10.3892/ol.2017.7613. Epub 2017 Dec 13.

Abstract

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.

摘要

本研究聚焦于开发一种用于口腔癌靶向递送的甲氨蝶呤(MTX)粘膜粘附贴片。最初,采用薄膜水化法制备了载有MTX的脂质体,其平均直径为105.7 - 137.4 nm,包封率为54.6±3.5%。将这些脂质体浇铸在优化的粘膜粘附膜中。通过其释放模式、厚度、重量和膨胀指数百分比对该膜进行表征,并评估优化膜的缓释特性。使用MTT法评估了所制备的脂质体以及浇铸在膜制剂中的脂质体对HSC - 3细胞的细胞毒性,结果发现载有MTX的脂质体膜M - LP - F7使MTX的半数最大抑制浓度显著降低。线粒体依赖性内源性途径的结果表明,与普通药物相比,M - LP - F7导致线粒体膜电位显著破坏。M - LP - F7使HSC - 3细胞中的凋亡率提高了近3倍。活性氧水平升高表明M - LP - F7在HSC - 3细胞中发挥促氧化作用。

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