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贻贝启发的配体点击和离子配位在二维黑磷用于癌症多模态成像和治疗。

Mussel-Inspired Ligand Clicking and Ion Coordination on 2D Black Phosphorus for Cancer Multimodal Imaging and Therapy.

机构信息

Institute of Pharmaceutics, School of Pharmaceutical Sciences (Shenzhen), Sun Yat-sen University, Shenzhen, 518107, China.

Institute for Advanced Materials, School of Materials Science and Engineering, Jiangsu University, Zhenjiang, 212013, China.

出版信息

Small. 2022 Jul;18(26):e2201803. doi: 10.1002/smll.202201803. Epub 2022 May 26.

Abstract

As a promising 2D nanocarrier, the biggest challenge of bare black phosphorus nanosheets (BP NSs) lies in the inherent instability, while it can be improved by surface modification strategies to a great extent. Considering the existing infirm BP NSs surface modification strategies, A mussels-inspired strong adhesive biomimetic peptide with azide groups for surface modification to increase the stability of BP NSs is synthesized. The azide groups on the peptide can quickly and precisely bind to the targeting ligand through click chemistry, solving the problem of nonspecificity of secondary modification of other mussel-mimicking materials. Besides, a catechol-Gd coordination network is further constructed for magnetic resonance imaging (MRI) and inducing intracellular endo/lysosome escape. The fabricated BP-DOX@Gd/(DOPA) -PEG-TL nanoplatform exhibits enhanced antitumor abilities through synergetic chemo/photothermal effects both in vitro and in vivo.

摘要

作为一种很有前途的 2D 纳米载体,裸露黑磷纳米片(BP NSs)最大的挑战在于其内在的不稳定性,而通过表面修饰策略在很大程度上可以改善这一问题。考虑到现有的 BP NSs 表面修饰策略的不稳定性,我们合成了一种具有叠氮基团的贻贝启发型强粘附仿生肽用于表面修饰,以提高 BP NSs 的稳定性。肽上的叠氮基团可以通过点击化学快速、精确地与靶向配体结合,解决了其他贻贝模拟材料二次修饰非特异性的问题。此外,进一步构建了儿茶酚-Gd 配位网络,用于磁共振成像(MRI)和诱导细胞内内体/溶酶体逃逸。所制备的 BP-DOX@Gd/(DOPA)-PEG-TL 纳米平台通过协同化学/光热作用在体外和体内均表现出增强的抗肿瘤能力。

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