利用聚苹果酸衍生的纳米硼靶向硼中子俘获治疗胶质母细胞瘤。

Journal of oncology research and therapy Pub Date : 2024-01-01 Epub Date: 2024-06-17 DOI:10.29011/2574-710x.10226
R Patil, T Sun, O Chepurna, M Khoobchandani, S Rudensky, E Holler, J Y Ljubimova, K L Black
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引用次数: 0

摘要

尽管做出了广泛的努力,多形性胶质母细胞瘤(GBM),最恶性的脑癌,继续对有效治疗构成重大挑战,在过去的三十年中,患者生存率的进展有限。这项研究解决了传统疗法的缺点,特别是放射治疗(RT),它面临着由于放射抗性和有毒辐射剂量的限制。硼中子俘获疗法(BNCT)是一种很有前途的替代疗法,它可以在对健康组织损伤最小的情况下向肿瘤细胞提供靶向辐射。然而,关键的挑战在于如何在肿瘤细胞中选择性地获得足够的硼。我们开发了一种基于纳米医学的新方法,利用聚苹果酸(PMLA)作为递送载体,每个纳米缀合物携带多个硼-10分子,以增加细胞内硼-10的浓度,从而有效地进行硼中子捕获治疗。我们的新型纳米药物(纳米硼)含有同位素富集的4-硼苯丙氨酸(BPA)作为硼-10和AP2 (Angiopep-2)肽的来源,用于穿透血脑屏障和靶向肿瘤。PMLA平台允许附着大量的硼-10,提高细胞内硼浓度,从而提高BNCT的疗效。这种创新的方法有可能解决GBM治疗中未满足的临床需求,并提高患者的生存率和生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeted Boron Neutron Capture Therapy Using Polymalic Acid Derived Nano-Boron to Treat Glioblastoma.

Despite extensive efforts, glioblastoma multiforme (GBM), the most malignant brain cancer, continues to pose significant challenges to effective treatment, with limited progress in patient survival over the last three decades. This study addresses shortcomings of conventional therapies, particularly radiotherapy (RT), which faces limitations due to radio-resistance and toxic radiation doses. Boron neutron capture therapy (BNCT) is a promising alternative, delivering targeted radiation to tumor cells with minimal damage to healthy tissue. However, the key challenge lies in achieving sufficient boron uptake selectively in tumor cells. We have developed a novel nanomedicine-based approach, utilizing polymalic acid (PMLA) as a delivery vehicle, carrying multiple boron-10 molecules per nanoconjugate to increase the intracellular concentration of boron-10 for effective boron neutron capture therapy. Our novel nanodrug (Nano-Boron) incorporates isotopically enriched 4-boronophenylalanine (BPA) as a source of boron-10 and Angiopep-2 (AP2) peptide for blood-brain barrier penetration and tumor targeting. The PMLA platform allows for the attachment of a large quantity of boron-10, enhancing the intracellular boron concentration and, consequently, the efficacy of BNCT. This innovative approach holds the potential to address the unmet clinical need in GBM treatment and improve patient survival and quality of life.

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