Lipid-Based Nanocarriers for The Treatment of Glioblastoma

被引:22
|
作者
Iturrioz-Rodriguez, Nerea [1 ]
Bertorelli, Rosalia [2 ]
Ciofani, Gianni [1 ]
机构
[1] Ist Italian Tecnol, Smart Biointerfaces, Viale Rinaldo Piaggio 34, I-56025 Pontedera, Italy
[2] Ist Italian Tecnol, Translat Pharmacol, Via Morego 30, I-16163 Genoa, Italy
来源
ADVANCED NANOBIOMED RESEARCH | 2021年 / 1卷 / 02期
基金
欧洲研究理事会;
关键词
blood-brain barrier; glioblastoma multiforme; invivo studies; lipid-based nanocarriers; BLOOD-BRAIN-BARRIER; NEURAL STEM-CELLS; DRUG-DELIVERY; MALIGNANT GLIOMAS; GROWTH-FACTOR; IN-VITRO; ANTICANCER DRUGS; RECEPTOR; CARRIERS; NANOPARTICLES;
D O I
10.1002/anbr.202000054
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Glioblastoma multiforme (GBM) is the most common and malignant neoplasia having origin in the brain. The current treatments involve surgery, radiotherapy, and chemotherapy, being complete surgical resection the best option for the patient survival chances. However, in those cases where a complete removal is not possible, radiation and chemotherapy are applied. Herein, the main challenges of chemotherapy, and how they can be overcome with the help of nanomedicine, are approached. Natural pathways to cross the blood-brain barrier (BBB) are detailed, and different invivo studies where these pathways are mimicked functionalizing the nanomaterial surface are shown. Later, lipid-based nanocarriers, such as liposomes, solid lipid nanoparticles, and nanostructured lipid carriers, are presented. To finish, recent studies that have used lipid-based nanosystems carrying not only therapeutic agents, yet also magnetic nanoparticles, are described. Although the advantages of using these types of nanosystems are explained, including their biocompatibility, the possibility of modifying their surface to enhance the cell targeting, and their intrinsic ability of BBB crossing, it is important to mention that research in this field is still at its early stage, and extensive preclinical and clinical investigations are mandatory in the close future.
引用
收藏
页数:13
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