摘要
To enable real-time imaging of boron delivery with cellular resolution, a series of fluorescent [10B] compounds was developed via a one-step synthesis using cost-effective, scalable reagents. The tumor-targeting agent, [10B]-a11, allowed noninvasive monitoring to identify the optimal time point for boron neutron capture therapy (BNCT) based on peak tumor accumulation. Fluorescence imaging analysis revealed a heterogeneous intratumoral distribution of [10B]-a11, confirming that macroscopic accumulation does not equate to microscopic uniformity and emphasizing the need for improved tumor penetration in next-generation boron carriers. Furthermore, [10B]-a11 demonstrated efficacy for fluorescence-guided surgery in prostate cancer, suggesting a potential synergistic strategy to combine precise resection with BNCT for improved therapeutic outcomes.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 16964-16974 |
| 页数 | 11 |
| 期刊 | Journal of Medicinal Chemistry |
| 卷 | 69 |
| 期 | 14 |
| DOI | |
| 出版状态 | 已出版 - 23 7月 2026 |
| 已对外发布 | 是 |
联合国可持续发展目标
此成果有助于实现下列可持续发展目标:
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可持续发展目标 3 良好健康与福祉
学术指纹
探究 'The One-Step Incorporation of Boron-10 Atom into Prostate Cancer-Targeted Fluorophores for Visualizing In Vivo Boron-10 Delivery and Intratumoral Distribution with Cellular Resolution' 的科研主题。它们共同构成独一无二的学术指纹。引用此
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