替莫唑胺
胶质母细胞瘤
化疗
药物输送
放射治疗
热疗
体内
医学
达卡巴嗪
药品
癌症研究
药理学
U87型
肿瘤科
生物医学工程
材料科学
内科学
纳米技术
生物
生物技术
作者
Lilianne Beola,Nerea Iturrioz-Rodríguez,Carlotta Pucci,Rosalia Bertorelli,Gianni Ciofani
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-09-12
卷期号:17 (18): 18441-18455
被引量:16
标识
DOI:10.1021/acsnano.3c06085
摘要
Glioblastoma multiforme (GBM) is a devastating tumor of the central nervous system, currently missing an effective treatment. The therapeutic gold standard consists of surgical resection followed by chemotherapy (usually with temozolomide, TMZ) and/or radiotherapy. TMZ does not, however, provide significant survival benefit after completion of treatment because of development of chemoresistance and of heavy side effects of systemic administration. Improvement of conventional treatments and complementary therapies are urgently needed to increase patient survival and quality of life. Stimuli-responsive lipid-based drug delivery systems offer promising prospects to overcome the limitations of the current treatments. In this work, multifunctional lipid-based magnetic nanovectors functionalized with the peptide angiopep-2 and loaded with TMZ (Ang-TMZ-LMNVs) were tested to enhance specific GBM therapy on an in vivo model. Exposure to alternating magnetic fields (AMFs) enabled magnetic hyperthermia to be performed, that works in synergy with the chemotherapeutic agent. Studies on orthotopic human U-87 MG-Luc2 tumors in nude mice have shown that Ang-TMZ-LMNVs can accumulate and remain in the tumor after local administration without crossing over into healthy tissue, effectively suppressing tumor invasion and proliferation and significantly prolonging the median survival time when combined with the AMF stimulation. This powerful synergistic approach has proven to be a robust and versatile nanoplatform for an effective GBM treatment.
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