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Solid Lipid Nanoparticles of Albendazole for Enhancing Cellular Uptake and Cytotoxicity against U-87 MG Glioma Cell Lines

机译:阿苯达唑固体脂质纳米粒可增强细胞对U-87 MG神经胶质瘤细胞的摄取和细胞毒性。

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Albendazole (ABZ) is an antihelminthic drug used for the treatment of several parasitic infestations. In addition to this, there are reports on the anticancer activity of ABZ against a wide range of cancer types. However, its effect on glioma has not yet been reported. In the present study, cytotoxicity of ABZ and ABZ loaded solid lipid nanoparticles (ASLNs) was tested in human glioma/astrocytoma cell line (U-87 MG). Using glyceryl trimyristate as lipid carrier and tween 80 as surfactant spherical ASLNs with an average size of 218.4 ± 5.1 nm were prepared by a combination of high shear homogenization and probe sonication methods. A biphasic in vitro release pattern of ABZ from ASLNs was observed, where 82% of ABZ was released in 24 h. In vitro cell line studies have shown that ABZ in the form of ASLNs was more cytotoxic (IC50 = 4.90 μg/mL) to U-87 MG cells compared to ABZ in the free form (IC50 = 13.30 μg/mL) due to the efficient uptake of the former by these cells. View Full-Text
机译:阿苯达唑(ABZ)是一种抗蠕虫药,用于治疗多种寄生虫感染。除此之外,还有关于ABZ对多种癌症的抗癌活性的报道。然而,尚未报道其对神经胶质瘤的作用。在本研究中,在人胶质瘤/星形细胞瘤细胞系(U-87 MG)中测试了ABZ和负载ABZ的固体脂质纳米颗粒(ASLNs)的细胞毒性。采用高剪切均质化和探针超声处理相结合的方法,以偏苯三酸甘油酯为脂质载体,以吐温80为表面活性剂,制备了平均粒径为218.4±5.1 nm的球形ASLN。观察到ABZ从ASLNs的双相体外释放模式,其中82%的ABZ在24小时内释放。体外细胞系研究表明,与游离形式的ABZ(IC50 = 13.30μg/ mL)相比,呈ASLNs形式的ABZ对U-87 MG细胞的细胞毒性更大(IC50 = 4.90μg/ mL)。这些细胞对前者的摄取。查看全文

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