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基于二酮吡咯并吡咯的一体化纳米平台用于肿瘤自增强温和光热治疗级联免疫治疗。

A Diketopyrrolopyrrole-Based All-in-One Nanoplatform for Self-Reinforcing Mild Photothermal Therapy Cascade Immunotherapy for Tumors.

机构信息

Key Laboratory for Advanced Materials, College of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai, 200237, China.

College of Chemistry and Chemical Engineering, Donghua University, Shanghai, 201620, China.

出版信息

Adv Healthc Mater. 2024 Oct;13(27):e2400766. doi: 10.1002/adhm.202400766. Epub 2024 Jul 15.

Abstract

Mild photothermal therapy (PTT) has attracted attention for effectively avoiding the severe side effects associated with high-temperature tumor ablation. However, its progress is hindered by the limited availability of high-performance photothermal agents (PTAs) and the thermoresistance of cancer cells induced by heat shock reactions. Herein, this work proposes a new strategy to expand the library of high-performance organic small-molecule PTAs and utilize it to construct a multifunctional nano-theranostic platform. By incorporating additional acceptors and appropriate π-bridges, a diketopyrrolopyrrole-based dye BDB is developed, which exhibits strong absorption and bright fluorescence emission in the near-infrared (NIR) region. Subsequently, BDB is co-coated with the heat shock protein (HSP) inhibitor tanespimycin (17-AAG) using the functional amphiphilic polymers DSPE-Hyd-PEG-cRGD to form an all-in-one nanoplatform BAG NPs. As a result, BAG NPs can precisely target tumor tissue, guide the treatment process in real-time through NIR-II fluorescence/photoacoustic/photothermal imaging, and release 17-AAG on demand to enhance mild PTT. Additionally, the mild PTT has been demonstrated to induce immunogenic cell death (ICD) and activate a systemic anti-tumor immune response, thereby suppressing both primary and distant tumors. Overall, this study presents a multifunctional nanoplatform designed for precise mild PTT combined with immunotherapy for effective tumor treatment.

摘要

轻度光热疗法 (PTT) 因其能有效避免高温肿瘤消融所带来的严重副作用而受到关注。然而,其发展受到高性能光热剂 (PTAs) 的有限可用性和热休克反应引起的癌细胞耐热性的限制。在此,本工作提出了一种扩展高性能有机小分子 PTA 库的新策略,并利用该策略构建了多功能纳米治疗平台。通过引入额外的受体和合适的π-桥,开发了基于二酮吡咯并吡咯的染料 BDB,它在近红外 (NIR) 区域表现出强吸收和明亮的荧光发射。随后,BDB 与热休克蛋白 (HSP) 抑制剂坦那西普米 (17-AAG) 一起使用功能两亲聚合物 DSPE-Hyd-PEG-cRGD 进行共包封,形成一体化纳米平台 BAG NPs。因此,BAG NPs 可以精确靶向肿瘤组织,通过近红外二区荧光/光声/光热成像实时指导治疗过程,并按需释放 17-AAG 以增强温和 PTT。此外,温和 PTT 已被证明可诱导免疫原性细胞死亡 (ICD) 并激活全身性抗肿瘤免疫反应,从而抑制原发和远处肿瘤。总的来说,本研究提出了一种用于精确温和 PTT 联合免疫治疗的多功能纳米平台,可有效治疗肿瘤。

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