Paclitaxel loaded liposomes decorated with a multifunctional tandem peptide for glioma targeting

胶质瘤 紫杉醇 体内 脂质体 癌症研究 药物输送 血脑屏障 细胞凋亡 化学 体外 药理学 医学 材料科学 化疗 生物 中枢神经系统 生物化学 内科学 纳米技术 生物技术
作者
Yayuan Liu,Rui Ran,Jiantao Chen,Qifang Kuang,Jie Tang,Ling Mei,Qianyu Zhang,Huile Gao,Zhirong Zhang,Qin He
出处
期刊:Biomaterials [Elsevier BV]
卷期号:35 (17): 4835-4847 被引量:247
标识
DOI:10.1016/j.biomaterials.2014.02.031
摘要

The treatment of glioma is a great challenge because of the existence of the blood-brain barrier (BBB). In order to reduce toxicity to the normal brain tissue and achieve efficient treatment, it is also important for drugs to specifically accumulate in the glioma foci and penetrate into the tumor core after entering into the brain. In this study, a specific ligand cyclic RGD peptide was conjugated to a cell penetrating peptide R8 to develop a multifunctional peptide R8-RGD. R8-RGD increased the cellular uptake of liposomes by 2-fold and nearly 30-fold compared to separate R8 and RGD respectively, and displayed effective penetration of three-dimensional glioma spheroids and BBB model in vitro. In vivo studies showed that R8-RGD-lipo could be efficiently delivered into the brain and selectively accumulated in the glioma foci after systemic administration in C6 glioma bearing mice. When paclitaxel (PTX) was loaded in liposomes, R8-RGD-lipo could induce the strongest inhibition and apoptosis against C6 cells and finally achieved the longest survival in intracranial C6 glioma bearing mice. In conclusion, all the results indicated that the tandem peptide R8-RGD was a promising ligand possessing multi functions including BBB transporting, glioma targeting and tumor penetrating. And R8-RGD-lipo was proved to be a potential anti-glioma drug delivery system.

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