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黑磷通过晶格重构实现近红外二区响应的癌症治疗。

Transformation of Black Phosphorus through Lattice Reconstruction for NIR-II-Responsive Cancer Therapy.

机构信息

Shenzhen Key Laboratory of Micro/Nano Biosensing, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055, China.

出版信息

Adv Sci (Weinh). 2024 Jan;11(3):e2305762. doi: 10.1002/advs.202305762. Epub 2023 Dec 19.

Abstract

The photothermal performance of black phosphorus (BP) in the near infrared (NIR)-II bio-window (1000-1500 nm) is low, which limits its biomedical applications. Herein, ultrasmall nickel phosphide quantum dots (Ni P QDs) are synthesized with BP quantum dots (BPQDs) as the template by topochemical transformation. The size of Ni P QDs is ≈3.5 nm, similar to that of BPQDs, whereas the absorption and photothermal conversion efficiency of Ni P QDs at 1064 nm (43.5%) are significantly improved compared with those of BPQDs. To facilitate in vivo applications, an Ni P QDs-based liposomal nano-platform (Ni P-DOX@Lipo-cRGD) is designed by incorporation of Ni P QDs and doxorubicin (DOX) into liposomal bilayers and the interior, respectively. The encapsulated DOX is responsively released from liposomes upon 1064-nm laser irradiation owing to the photothermal effect of Ni P QDs, and the drug release rate and amount are controlled by the light intensity and exposure time. In vivo, experiments show that Ni P-DOX@Lipo-cRGD has excellent tumor target capability and biocompatibility, as well as complete tumor ablation through the combination of photothermal therapy and chemotherapy. The work provides a new paradigm for the NIR-II transformation of nano-materials and may shed light on the construction of multifunctional nano-platforms for cancer treatment.

摘要

黑磷(BP)在近红外(NIR)-II 生物窗口(1000-1500nm)的光热性能较低,限制了其在生物医学中的应用。在此,通过拓扑转化,以 BP 量子点(BPQDs)为模板合成了超小的磷化镍量子点(Ni P QDs)。Ni P QDs 的尺寸约为 3.5nm,与 BPQDs 的尺寸相似,而 Ni P QDs 在 1064nm 处的吸收和光热转换效率(43.5%)明显高于 BPQDs。为了便于体内应用,通过将 Ni P QDs 和阿霉素(DOX)分别掺入脂质体双层和内部,设计了基于 Ni P QDs 的脂质体纳米平台(Ni P-DOX@Lipo-cRGD)。由于 Ni P QDs 的光热效应,包封的 DOX 在 1064nm 激光照射下从脂质体中响应性释放,并且药物释放速率和量由光强度和暴露时间控制。在体内实验中,结果表明 Ni P-DOX@Lipo-cRGD 具有优异的肿瘤靶向能力和生物相容性,并通过光热疗法和化学疗法的结合实现了完全的肿瘤消融。这项工作为纳米材料的 NIR-II 转化提供了新的范例,并可能为癌症治疗的多功能纳米平台的构建提供思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd3b/10797469/7c4a247612d4/ADVS-11-2305762-g002.jpg

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