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用于治疗和诊断的聚合物包覆纳米颗粒 非富集的聚合物包覆氮氧化硼碳(BCNO)纳米颗粒作为有效的硼中子俘获疗法药物

Polymer-Coated Nanoparticles for Therapeutic and Diagnostic Non-B Enriched Polymer-Coated Boron Carbon Oxynitride (BCNO) Nanoparticles as Potent BNCT Drug.

作者信息

Chiang Chen-Wei, Chien Yun-Chen, Yu Wen-Jui, Ho Chia-Yu, Wang Chih-Yi, Wang Tzu-Wei, Chiang Chi-Shiun, Keng Pei-Yuin

机构信息

Department of Material Science and Engineering, National Tsing Hua University, Hsinchu City 300, Taiwan.

Department of Biomedical Engineering and Environmental Science, National Tsing Hua University, Hsinchu City 300, Taiwan.

出版信息

Nanomaterials (Basel). 2021 Nov 2;11(11):2936. doi: 10.3390/nano11112936.

Abstract

Boron neutron capture therapy (BNCT) is a powerful and selective anti-cancer therapy utilizing B-enriched boron drugs. However, clinical advancement of BCNT is hampered by the insufficient loading of B-10 drugs throughout the solid tumor. Furthermore, the preparation of boron drugs for BNCT relies on the use of the costly B-10 enriched precursor. To overcome these challenges, polymer-coated boron carbon oxynitride (BCNO) nanoparticles, with ~30% of boron, were developed with enhanced biocompatibility, cell uptake, and tumoricidal effect via BNCT. Using the ALTS1C1 cancer cell line, the IC of the PEG@BCNO, bare, PEI@BCNO were determined to be 0.3 mg/mL, 0.1 mg/mL, and 0.05 mg/mL, respectively. As a proof-of-concept, the engineered non-B enriched polymer-coated BCNO exhibited excellent anti-tumor effect via BNCT due to their high boron content per nanoparticle and due to the enhanced cellular internalization and retention compared to small molecular B-BPA drug. The astrocytoma ALTS1C1 cells treated with bare, polyethyleneimine-, and polyethylene glycol-coated BCNO exhibited an acute cell death of 24, 37, and 43%, respectively, upon 30 min of neutron irradiation compared to the negligible cell death in PBS-treated and non-irradiated cells. The radical approach proposed in this study addresses the expensive and complex issues of B-10 isotope enrichment process; thus, enabling the preparation of boron drugs at a significantly lower cost, which will facilitate the development of boron drugs for BNCT.

摘要

硼中子俘获疗法(BNCT)是一种利用富含硼的硼药物的强大且选择性的抗癌疗法。然而,BCNT的临床进展受到实体瘤中硼 - 10药物负载不足的阻碍。此外,用于BNCT的硼药物制备依赖于使用昂贵的富含硼 - 10的前体。为了克服这些挑战,开发了含硼量约为30%的聚合物包覆的硼碳氮氧化物(BCNO)纳米颗粒,其通过BNCT具有增强的生物相容性、细胞摄取和杀肿瘤效果。使用ALTS1C1癌细胞系,测定PEG@BCNO、裸BCNO、PEI@BCNO的半数抑制浓度分别为0.3 mg/mL、0.1 mg/mL和0.05 mg/mL。作为概念验证,工程化的非富硼聚合物包覆的BCNO通过BNCT表现出优异的抗肿瘤效果,这是由于其每个纳米颗粒的硼含量高,并且与小分子B - BPA药物相比,细胞内化和保留增强。与PBS处理且未辐照的细胞中可忽略不计的细胞死亡相比,用裸BCNO、聚乙烯亚胺和聚乙二醇包覆的BCNO处理的星形细胞瘤ALTS1C1细胞在中子辐照30分钟后分别表现出24%、37%和43%的急性细胞死亡。本研究中提出的激进方法解决了硼 - 10同位素富集过程昂贵且复杂的问题;因此,能够以显著更低的成本制备硼药物,这将促进用于BNCT的硼药物的开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7891/8618246/bca53a0e1da6/nanomaterials-11-02936-sch001.jpg

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