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用于增强肿瘤靶向联合治疗及生物降解介导的转移抑制的多功能介孔黑磷基纳米片

Multifunctional mesoporous black phosphorus-based nanosheet for enhanced tumor-targeted combined therapy with biodegradation-mediated metastasis inhibition.

作者信息

Chen Leilei, Qian Min, Jiang Huiling, Zhou Yiwei, Du Yilin, Yang Yafeng, Huo Taotao, Huang Rongqin, Wang Yi

机构信息

Center for Advanced Low-dimension Materials, State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Chemistry, Chemical Engineering and Biotechnology, Donghua University, Shanghai, 201600, China.

Department of Pharmaceutics, School of Pharmacy, Key Laboratory of Smart Drug Delivery, Ministry of Education, Fudan University, Shanghai, 201203, China.

出版信息

Biomaterials. 2020 Apr;236:119770. doi: 10.1016/j.biomaterials.2020.119770. Epub 2020 Jan 10.

DOI:10.1016/j.biomaterials.2020.119770
PMID:32006702
Abstract

Functionalizing black phosphorus nanosheet (BP) with efficient drug loading and endowing mesoporous silica nanomaterials with appropriate biodegradation for controllable tumor-targeted chemo-photothermal therapy are still urgent challenges. Herein, an ordered mesoporous silica-sandwiched black phosphorus nanosheet (BP@MS) with the vertical pore coating was prepared. The strategy could not only enhance the BP's dispersity and improve its doxorubicin (DOX)-loading efficiency, but also facilitate post-modification such as PEGylation and conjugation of targeting ligand, TKD peptide, yielding BSPT. A DOX-loaded BSPT-based system (BSPTD) showed heat-stimulative, pH-responsive, and sustained release manners. In vitro and in vivo results demonstrated that BSPTD had a delayed but finally complete degradation in physiological medium, contributing to an optimal therapeutic window and good biosafety. As a result, BSPTD can achieve an effective chemo-photothermal synergistic targeted therapy of tumor. Moreover, treating by BSPTD was found to be capable of remarkably inhibiting the lung metastasis of tumor, attributing to the photothermal degradation-facilitated secondary drug delivery. Our study provided a robust strategy to functionalize BP nanosheet and biodegrade the mesoporous silica for extended biomedical applications.

摘要

实现高效药物负载的黑磷纳米片(BP)功能化以及赋予介孔二氧化硅纳米材料适当的生物降解性以用于可控的肿瘤靶向化学-光热疗法,仍然是亟待解决的挑战。在此,制备了一种具有垂直孔涂层的有序介孔二氧化硅夹心黑磷纳米片(BP@MS)。该策略不仅可以提高BP的分散性并提高其阿霉素(DOX)负载效率,还便于进行聚乙二醇化和靶向配体TKD肽偶联等后修饰,从而得到BSPT。基于负载DOX的BSPT系统(BSPTD)表现出热刺激、pH响应和缓释特性。体外和体内结果表明,BSPTD在生理介质中具有延迟但最终完全降解的特性,有助于实现最佳治疗窗口和良好的生物安全性。因此,BSPTD可以实现有效的肿瘤化学-光热协同靶向治疗。此外,发现用BSPTD治疗能够显著抑制肿瘤的肺转移,这归因于光热降解促进的二次药物递送。我们的研究为功能化BP纳米片和降解介孔二氧化硅以拓展生物医学应用提供了一种强有力的策略。

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