Antibody Delivery into the Brain by Radiosensitizer Nanoparticles for Targeted Glioblastoma Therapy.

Omer Gal, Oshra Betzer, Liat Rousso-Noori, Tamar Sadan, Menachem Motiei, Maxim Nikitin, Dinorah Friedmann-Morvinski, Rachela Popovtzer, Aron Popovtzer
{"title":"Antibody Delivery into the Brain by Radiosensitizer Nanoparticles for Targeted Glioblastoma Therapy.","authors":"Omer Gal,&nbsp;Oshra Betzer,&nbsp;Liat Rousso-Noori,&nbsp;Tamar Sadan,&nbsp;Menachem Motiei,&nbsp;Maxim Nikitin,&nbsp;Dinorah Friedmann-Morvinski,&nbsp;Rachela Popovtzer,&nbsp;Aron Popovtzer","doi":"10.3390/jnt3040012","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Glioblastoma is the most lethal primary brain malignancy in adults. Standard of care treatment, consisting of temozolomide (TMZ) and adjuvant radiotherapy (RT), mostly does not prevent local recurrence. The inability of drugs to enter the brain, in particular antibody-based drugs and radiosensitizers, is a crucial limitation to effective glioblastoma therapy.</p><p><strong>Methods: </strong>Here, we developed a combined strategy using radiosensitizer gold nanoparticles coated with insulin to cross the blood-brain barrier and shuttle tumor-targeting antibodies (cetuximab) into the brain.</p><p><strong>Results: </strong>Following intravenous injection to an orthotopic glioblastoma mouse model, the nanoparticles specifically accumulated within the tumor. Combining targeted nanoparticle injection with TMZ and RT standard of care significantly inhibited tumor growth and extended survival, as compared to standard of care alone. Histological analysis of tumors showed that the combined treatment eradicated tumor cells, and decreased tumor vascularization, proliferation, and repair.</p><p><strong>Conclusions: </strong>Our findings demonstrate radiosensitizer nanoparticles that effectively deliver antibodies into the brain, target the tumor, and effectively improve standard of care treatment outcome in glioblastoma.</p>","PeriodicalId":73846,"journal":{"name":"Journal of nanotheranostics","volume":"3 4","pages":"177-188"},"PeriodicalIF":0.0000,"publicationDate":"2022-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7613745/pdf/","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of nanotheranostics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/jnt3040012","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 4

Abstract

Background: Glioblastoma is the most lethal primary brain malignancy in adults. Standard of care treatment, consisting of temozolomide (TMZ) and adjuvant radiotherapy (RT), mostly does not prevent local recurrence. The inability of drugs to enter the brain, in particular antibody-based drugs and radiosensitizers, is a crucial limitation to effective glioblastoma therapy.

Methods: Here, we developed a combined strategy using radiosensitizer gold nanoparticles coated with insulin to cross the blood-brain barrier and shuttle tumor-targeting antibodies (cetuximab) into the brain.

Results: Following intravenous injection to an orthotopic glioblastoma mouse model, the nanoparticles specifically accumulated within the tumor. Combining targeted nanoparticle injection with TMZ and RT standard of care significantly inhibited tumor growth and extended survival, as compared to standard of care alone. Histological analysis of tumors showed that the combined treatment eradicated tumor cells, and decreased tumor vascularization, proliferation, and repair.

Conclusions: Our findings demonstrate radiosensitizer nanoparticles that effectively deliver antibodies into the brain, target the tumor, and effectively improve standard of care treatment outcome in glioblastoma.

Abstract Image

Abstract Image

Abstract Image

靶向胶质母细胞瘤治疗用放射增敏剂纳米颗粒将抗体输送到大脑。
背景:胶质母细胞瘤是成人最致命的原发性脑恶性肿瘤。标准的护理治疗,包括替莫唑胺(TMZ)和辅助放疗(RT),大多不能预防局部复发。药物不能进入大脑,特别是基于抗体的药物和放射增敏剂,是有效治疗胶质母细胞瘤的一个关键限制。方法:在这里,我们开发了一种联合策略,使用涂有胰岛素的放射增敏剂金纳米颗粒穿过血脑屏障,将肿瘤靶向抗体(西妥昔单抗)输送到大脑。结果:静脉注射到原位胶质母细胞瘤小鼠模型后,纳米颗粒在肿瘤内特异性积累。与单独标准治疗相比,靶向纳米颗粒注射联合TMZ和RT标准治疗可显著抑制肿瘤生长并延长生存期。肿瘤的组织学分析表明,联合治疗可以根除肿瘤细胞,减少肿瘤的血管化、增殖和修复。结论:我们的研究结果表明,放射增敏剂纳米颗粒可以有效地将抗体传递到大脑,靶向肿瘤,并有效地提高胶质母细胞瘤的护理标准治疗结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信