Nazaruk Ewa, Majkowska-Pilip Agnieszka, Bilewicz Renata
Faculty of Chemistry, University of Warsaw, Pasteura 1, 02-093, Warsaw, Poland.
Centre of Radiochemistry and Nuclear Chemistry, Institute of Nuclear Chemistry and Technology, Dorodna 16, 03-195, Warsaw, Poland.
Chempluschem. 2017 Apr;82(4):570-575. doi: 10.1002/cplu.201600534. Epub 2017 Jan 6.
Self-assembled lipid liquid-crystalline nanoparticles, known as cubosomes, were used for the delivery of the anticancer drug doxorubicin (DOX). Several properties make cubosomes a promising alternative in the development of controlled-release systems for drug delivery. They have a larger internal surface area than other carriers, hence deliver more drug molecules to the affected cells and maintain the cubic symmetry of the parent lipidic cubic phase, but at the same time they have a lower viscosity thereby facilitating transport of the drug. The pH-dependent drug release profiles, evaluated by voltammetry, demonstrated triggered drug release from the cubosome carrier to the environment of the cancer cells, where pH is lower. The anticancer effect of a DOX-loaded cubosome on the glioblastoma T98G cell line was found to be highly efficient and required lower concentrations of DOX to inhibit the proliferation of cancer cells than the effective concentrations of free DOX.
自组装脂质液晶纳米颗粒,即立方液晶纳米粒,被用于递送抗癌药物阿霉素(DOX)。立方液晶纳米粒的多种特性使其成为药物递送控释系统开发中一种很有前景的选择。它们的内表面积比其他载体更大,因此能将更多药物分子递送至受影响的细胞,并保持母体脂质立方相的立方对称性,但与此同时它们的粘度较低,从而便于药物运输。通过伏安法评估的pH依赖性药物释放曲线表明,药物从立方液晶纳米粒载体触发释放到癌细胞所处的pH较低的环境中。结果发现,载有阿霉素的立方液晶纳米粒对胶质母细胞瘤T98G细胞系具有高效的抗癌作用,与游离阿霉素的有效浓度相比,抑制癌细胞增殖所需的阿霉素浓度更低。