Chiral‐induced highly efficient NIR–photothermal conversion of perylene diimide@silica nanocapsules for photothermal therapy

Aggregate Pub Date : 2024-07-03 DOI:10.1002/agt2.630
Yue Zhao, Fuhao An, Jichao Wu, Haining Li, Xueyu Wang, Lanya Jiao, Ying Kong, Jinghan Zhu, Xun Sun, Xu Li, Miao Wang, Yu Zhang, Xuan Sun
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Abstract

Photothermal agents (PTAs) with ultra‐high photothermal conversion efficiency (PCE) activated upon near‐infrared (NIR) laser irradiation can heat up and destroy tumor cells under low‐intensity laser excitation to allow safe and efficient tumor therapy. Herein, an organic PTA with an outstanding PCE of 89.6% is developed from rationally designed perylene diimide (PDI) with electron‐donating cyclohexylamine moiety at the bay‐positions of its skeleton and chiral phenethylamine (PEA) moiety at its N terminals, termed here PEAPDI. The strong intermolecular interaction between the PDI skeletons induced by PEA together with the intramolecular charge transfer from cyclohexylamine to PDI skeleton severely quenches the fluorescence emission from PEAPDI and significantly enhances its NIR absorption, resulting in super NIR–photothermal conversion. PEAPDI molecules are subsequently encapsulated within silica nanocapsules (SNCs), creating PEAPDI@SNC. Characterized by its small hydrodynamic diameter, monodispersity, high PDI encapsulation efficiency, colloidal stability, and biocompatibility, PEAPDI@SNC exhibits prolonged blood circulation and enhanced permeability and retention effect, enabling targeted accumulation at the tumor site. An in vivo study using a 4T1 tumor–bearing mice model illustrates the agent's potent tumor ablation capability without side effects at low dosage under NIR laser irradiation (808 nm). The findings demonstrate PEAPDI@SNC's significant potential as a PTA for tumor treatment.

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用于光热疗法的手性诱导高效近红外光热转换过二亚胺@二氧化硅纳米胶囊
具有超高光热转换效率(PCE)的光热制剂(PTAs)在近红外激光照射下被激活,可在低强度激光激发下加热并破坏肿瘤细胞,从而实现安全高效的肿瘤治疗。本文以合理设计的过二甲苯二亚胺(PDI)为基础,在其骨架的畦位上添加了电子捐赠的环己胺分子,并在其 N 端添加了手性苯乙胺分子(PEA),从而开发出一种 PCE 高达 89.6% 的有机 PTA,即 PEAPDI。PEA 诱导的 PDI 骨架之间强烈的分子间相互作用,以及环己胺到 PDI 骨架的分子内电荷转移,严重淬灭了 PEAPDI 的荧光发射,并显著增强了其近红外吸收,从而实现了超近红外-光热转换。PEAPDI 分子随后被封装在二氧化硅纳米胶囊(SNC)中,形成 PEAPDI@SNC。PEAPDI@SNC 具有流体力学直径小、单分散性、高 PDI 封装效率、胶体稳定性和生物相容性等特点,可延长血液循环,增强渗透性和滞留效应,实现肿瘤部位的靶向蓄积。利用 4T1 肿瘤小鼠模型进行的体内研究表明,在近红外激光(808 纳米)照射下,该制剂在低剂量下即可有效消融肿瘤,且无副作用。研究结果表明,PEAPDI@SNC 具有作为 PTA 治疗肿瘤的巨大潜力。
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