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通过基于重组蛋白的超分子纳米载体提高骨肿瘤治疗中疏水性前药的生物利用度。

Improving Bioavailability of Hydrophobic Prodrugs through Supramolecular Nanocarriers Based on Recombinant Proteins for Osteosarcoma Treatment.

机构信息

Musculoskeletal Tumor Center and Beijing Key Laboratory of Musculoskeletal Tumor, Peking University People's Hospital, Beijing, 100044, China.

State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, 130022, China.

出版信息

Angew Chem Int Ed Engl. 2021 May 10;60(20):11252-11256. doi: 10.1002/anie.202101938. Epub 2021 Apr 8.

Abstract

Supramolecular nanodrug assembly driven by supramolecular chemistry is becoming a powerful strategy for medication. The potential of engineered proteins as building blocks for nanoformulations is rarely investigated. Here, we developed a new generation of recombinant protein-based nanodrug carriers, which is very efficient for loading and delivering the hydrophobic prodrug aldoxorubicin. Significantly enhanced anti-tumor effects in osteosarcoma (OS) models were observed. The half-life of the nanodrug reached almost two days and the corresponding bioavailability increased by 17-fold. This is significantly superior to other drug counterparts, empowering long-acting OS treatment scenarios. Importantly, off-target side effects of the prodrug, including cardiotoxicity and lung-metastasis, were greatly mitigated with our medication. Thus, our assembly strategy enables the customized design of advanced nanodelivery systems employing broader biomaterial building blocks for cancer therapy.

摘要

超分子化学驱动的超分子纳米药物组装正在成为一种强大的药物治疗策略。然而,工程蛋白作为纳米制剂构建块的潜力很少被研究。在这里,我们开发了新一代基于重组蛋白的纳米药物载体,它非常有效地负载和递送疏水性前药阿霉素。在骨肉瘤(OS)模型中观察到显著增强的抗肿瘤效果。纳米药物的半衰期达到近两天,相应的生物利用度增加了 17 倍。这明显优于其他药物对照物,为长效 OS 治疗方案提供了可能。重要的是,我们的药物大大减轻了前药的脱靶副作用,包括心脏毒性和肺转移。因此,我们的组装策略为癌症治疗提供了一种新的方法,可以利用更广泛的生物材料构建块来定制先进的纳米递药系统。

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