内封底:具有高药物负载和EGFR、PI3K/AKT双重抑制特性的小分子纳米前药,用于膀胱癌症治疗(EXP2 5/2023)

Guoyin Li, Zewen Song, Yi Ru, Jing Zhang, Lianxiang Luo, Wei Yang, Hao Wu, Haibao Jin, Xuanwen Bao, Di Wei, Zhao Yan, Haijing Qu, Zheng Zhu, Gang Zhou
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引用次数: 0

摘要

在高达74%的膀胱癌症组织中发现EGFR的过度表达。发现的两种天然产物雷公藤甲素(以闪电为代表)和橙皮苷(以橙色为代表)可以抑制EGFR通路。它们连接在一起形成前药,可以形成纳米颗粒(以含有闪电的橙子为代表),这不仅显著提高了它们的生物利用度和治疗效果,还降低了它们的全身毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Inside Back Cover: Small-molecule nanoprodrug with high drug loading and EGFR, PI3K/AKT dual-inhibiting properties for bladder cancer treatment (EXP2 5/2023)

Inside Back Cover: Small-molecule nanoprodrug with high drug loading and EGFR, PI3K/AKT dual-inhibiting properties for bladder cancer treatment (EXP2 5/2023)

Overexpression of the EGFR is found in up to 74% of bladder cancer tissue. Two natural products that were found, triptolide (represented by lightning) and hesperidin (represented by orange), could inhibit EGFR pathways. They are linked together into a prodrug that can form nanoparticles (represented by oranges containing lightning), which not only remarkably improved their bioavailability and therapeutic but also reduced their systemic toxicity.

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