{"title":"Nanoparticle-mediated Therapeutic Inventions against Glioblastoma: A Narrative Review on Current Perspectives.","authors":"Bida Joshua John, Dauda Maibasha, Ratnakar Shukla, Adil Husain, Afza Ahmad, Shambhavi Kumari, Vidhi Arora, Gungun Sherawat, Rohit Kumar Tiwari","doi":"10.2174/0118715273453180260908055829","DOIUrl":null,"url":null,"abstract":"<p><p>Glioblastoma (GB) is a highly aggressive tumor that demonstrates significant treatment resistance due to the blood-brain barrier (BBB) and resistance mechanisms of the tumor. Nanoparticle- based drug delivery systems (NDDS) can enhance drug bioavailability, enable targeted delivery, and provide controlled release. These nanoparticles can be engineered to target GB-specific biomarkers, such as EGFRvIII, which is expressed on glioma stem cells, to enhance treatment precision. A comprehensive literature review was conducted using the keywords \"Glioblastoma,\" \"Nanoparticles,\" \"Pathogenesis,\" and \"Treatment Resistance\" across PubMed, MEDLINE, Web of Science, ClinicalTrial. gov, Science Direct, and Google Scholar databases. Engineered nanoparticles have considerable potential to overcome major therapeutic obstacles in GB. Techniques such as surface functionalization (e.g., with cRGD or transferrin) and biomimetic coatings enable nanoparticles to cross the BBB, significantly increasing drug accumulation within brain tumors by up to 12-fold. This leads to improved anti-tumor efficacy, demonstrating significant reductions in tumor burden and improved survival in animal models. Additionally, these platforms are used to deliver genetic therapies, such as siRNA and miRNA, to specific cancer-driving genes. The ability to deliver drugs intranasally further enhances the therapeutic potential. Nanoparticle-based therapies have emerged as a promising approach in the treatment of GB and have successfully overcome barriers such as the BBB and treatment resistance. These methods have demonstrated robust preclinical outcomes, which emphasize their potential for clinical translation. Ongoing research is important to maximize the potential of these technologies and improve survival rates for patients with GB.</p>","PeriodicalId":93947,"journal":{"name":"CNS & neurological disorders drug targets","volume":" ","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2026-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"CNS & neurological disorders drug targets","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/0118715273453180260908055829","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Glioblastoma (GB) is a highly aggressive tumor that demonstrates significant treatment resistance due to the blood-brain barrier (BBB) and resistance mechanisms of the tumor. Nanoparticle- based drug delivery systems (NDDS) can enhance drug bioavailability, enable targeted delivery, and provide controlled release. These nanoparticles can be engineered to target GB-specific biomarkers, such as EGFRvIII, which is expressed on glioma stem cells, to enhance treatment precision. A comprehensive literature review was conducted using the keywords "Glioblastoma," "Nanoparticles," "Pathogenesis," and "Treatment Resistance" across PubMed, MEDLINE, Web of Science, ClinicalTrial. gov, Science Direct, and Google Scholar databases. Engineered nanoparticles have considerable potential to overcome major therapeutic obstacles in GB. Techniques such as surface functionalization (e.g., with cRGD or transferrin) and biomimetic coatings enable nanoparticles to cross the BBB, significantly increasing drug accumulation within brain tumors by up to 12-fold. This leads to improved anti-tumor efficacy, demonstrating significant reductions in tumor burden and improved survival in animal models. Additionally, these platforms are used to deliver genetic therapies, such as siRNA and miRNA, to specific cancer-driving genes. The ability to deliver drugs intranasally further enhances the therapeutic potential. Nanoparticle-based therapies have emerged as a promising approach in the treatment of GB and have successfully overcome barriers such as the BBB and treatment resistance. These methods have demonstrated robust preclinical outcomes, which emphasize their potential for clinical translation. Ongoing research is important to maximize the potential of these technologies and improve survival rates for patients with GB.
胶质母细胞瘤(GB)是一种高度侵袭性的肿瘤,由于血脑屏障(BBB)和肿瘤的耐药机制而表现出明显的治疗耐药性。基于纳米颗粒的药物递送系统(NDDS)可以提高药物的生物利用度,实现靶向递送,并提供控制释放。这些纳米颗粒可以被设计成针对gb特异性生物标志物,如在胶质瘤干细胞上表达的EGFRvIII,以提高治疗精度。我们使用PubMed、MEDLINE、Web of Science、ClinicalTrial等关键词对“胶质母细胞瘤”、“纳米颗粒”、“发病机制”和“治疗耐药性”进行了全面的文献综述。gov, Science Direct和b谷歌Scholar数据库。工程纳米颗粒具有克服GB主要治疗障碍的巨大潜力。表面功能化(例如,用cRGD或转铁蛋白)和仿生涂层等技术使纳米颗粒能够穿过血脑屏障,显著增加脑肿瘤内药物积累,最多可增加12倍。这导致了抗肿瘤功效的提高,在动物模型中显示出肿瘤负荷的显著减少和生存率的提高。此外,这些平台还用于向特定的癌症驱动基因提供遗传疗法,如siRNA和miRNA。鼻内给药的能力进一步提高了治疗潜力。基于纳米颗粒的治疗方法已经成为治疗GB的一种很有前途的方法,并且已经成功地克服了血脑屏障和治疗耐药性等障碍。这些方法已经证明了强大的临床前结果,这强调了它们在临床转化方面的潜力。正在进行的研究对于最大限度地发挥这些技术的潜力和提高GB患者的生存率非常重要。