Curcumin-enhanced NIR-II-responsive gold nanobipyramids for targeted HSP 90 inhibition

IF 10.2 1区 医学 Q1 ENGINEERING, BIOMEDICAL Materials Today Bio Pub Date : 2025-04-01 Epub Date: 2025-02-01 DOI:10.1016/j.mtbio.2025.101541
Zhenying Diao , Youcheng Liang , Yong Liu , Dou Zhang , Long Qiu , Jianbo Sun , Qiaoyou Lu , Yanlei Liu , Daxiang Cui , Ting Yin
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Abstract

Blockade of heat shock protein 90 (HSP90) expression in multimodal synergistic therapy has a great prospect for cancer treatment. Nanomaterials combined with bioinformatic analysis provides accurate guidance for the design of anti-HSP90 nanomedicines. Herein, a NIR-II-responsive nanoplatform was developed under bioinformatics guided to effectly inhibit HSP90 for enhanced synergistic mild-photothermal chemotherapy without any notable tissue damage. The nanoplatforms were assembled from NIR-II-responsive gold nanobipyramids (GNBs) combined with curcumin (Cur) via hydrophobic-hydrophobic interactions and hydrogen bonds. On the basis of drug discovery and network pharmacology, we found that Cur has impressive anti-HSP90 capability and analyzed its therapeutic mechanism against NSCLC. Under the irradiation of NIR-II light, the obtained GNBs-Cur blocked the expression of HPS90 and inhibited related antiapoptotic pathways, thus enhancing the mild PTT of GNBs under 1064 nm laser irradiation. Meanwhile, Cur served as chemotherapeutic agents to induce apoptosis in tumor cells. In vivo photoacoustic imaging-guided, GNBs-Cur achieved effective tumor elimination through mild-photothermal chemotherapy without systemic toxicity. Overall, this work provides a new therapeutic modality paradigm for potential NSCLC treatment on the basis of synergistic therapies.

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姜黄素增强的nir - ii响应金纳米金字塔对hsp90的靶向抑制
阻断热休克蛋白90 (HSP90)在多模式协同治疗中的表达在癌症治疗中具有广阔的前景。纳米材料与生物信息学分析相结合,为抗hsp90纳米药物的设计提供了准确的指导。本研究在生物信息学的指导下,构建了nir - ii响应纳米平台,有效抑制HSP90,增强了温和光热化疗的协同作用,而没有明显的组织损伤。纳米平台是由nir - ii响应金纳米金字塔(GNBs)与姜黄素(Cur)通过疏水-疏水相互作用和氢键组合而成。在药物发现和网络药理学的基础上,我们发现Cur具有较强的抗hsp90能力,并分析了其治疗NSCLC的机制。在NIR-II光照射下,获得的GNBs- cur可阻断HPS90的表达,抑制相关抗凋亡通路,从而增强GNBs在1064 nm激光照射下的轻度PTT。同时,Cur作为化疗药物可诱导肿瘤细胞凋亡。在体内光声成像引导下,GNBs-Cur通过温和的光热化疗实现了有效的肿瘤消除,没有全身毒性。总之,本研究在协同治疗的基础上为潜在的非小细胞肺癌治疗提供了一种新的治疗模式范式。
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索莱宝
dimethylsulfoxide (DMSO)
阿拉丁
4′,6-Diamidino-2-phenylindole (DAPI)
阿拉丁
L-ascorbic acid (AA)
阿拉丁
silver nitrate (AgNO3)
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cetyltrimethylammonium chloride (CTAC)
阿拉丁
cetyltrimethylammonium bromide (CTAB)
阿拉丁
gold (III) chloride hydrate (HAuCl4·3H2O)
来源期刊
CiteScore
8.30
自引率
4.90%
发文量
303
审稿时长
30 days
期刊介绍: Materials Today Bio is a multidisciplinary journal that specializes in the intersection between biology and materials science, chemistry, physics, engineering, and medicine. It covers various aspects such as the design and assembly of new structures, their interaction with biological systems, functionalization, bioimaging, therapies, and diagnostics in healthcare. The journal aims to showcase the most significant advancements and discoveries in this field. As part of the Materials Today family, Materials Today Bio provides rigorous peer review, quick decision-making, and high visibility for authors. It is indexed in Scopus, PubMed Central, Emerging Sources, Citation Index (ESCI), and Directory of Open Access Journals (DOAJ).
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