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细胞因子诱导的杀伤细胞介导的负载二氢卟吩 e6 的金纳米星用于肺癌靶向 NIR 成像和免疫-光动力联合治疗

英文原题:Cytokine-induced killer cells-mediated chlorin e6-loaded gold nanostars for targeted NIR imaging and immuno-photodynamic combination therapy for lung cancer.

查看英文原题

Cytokine-induced killer cells-mediated chlorin e6-loaded gold nanostars for targeted NIR imaging and immuno-photodynamic combination therapy for lung cancer.

PubMed 2024/06/25(内容时间) Biomed Mater Q2 · IF 3.9(JCR 2025)

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中文摘要

近年来,细胞因子诱导的杀伤(CIK)细胞因其独特的杀伤和靶向恶性肿瘤的特性,在肿瘤综合诊断和治疗中具有广阔的应用前景。在此,我们报道了一种简便的策略,基于PEG化合成单分散金纳米星(GNSs),并共载光敏剂二氢卟吩e6(Ce6)形成GNSs-PEG@Ce6 NPs。随后利用CIK细胞负载所制备的GNSs-PEG@Ce6 NPs,构建基于CIK细胞的药物递送系统(GNSs-PEG@Ce6-CIK)用于肺癌治疗。其中,GNSs作为运输介质,Ce6作为近红外(NIR)荧光成像剂和光动力治疗(PDT)剂,CIK细胞作为免疫治疗的靶向载体,可提高肿瘤富集效率和治疗效果。细胞实验结果表明,GNSs-PEG@Ce6 NPs在生理条件下具有良好的分散性、水溶性和低毒性,培养的CIK细胞具有强抗肿瘤特性。随后,GNSs-PEG@Ce6-CIK在633 nm激光照射下可有效抑制A549细胞生长,其杀伤效果强于GNSs-PEG@Ce6 NPs或CIK细胞。

此外,它们在体内表现出良好的肿瘤靶向性和肿瘤协同杀伤活性。因此,GNSs-PEG@Ce6-CIK被构建用于肺癌的靶向NIR荧光成像、增强PDT和免疫治疗。

展开英文摘要原文

Recently, cytokine-induced killer (CIK) cells have a broad application prospect in the comprehensive diagnosis and treatment of tumors owing to their unique characteristics of killing and targeting malignant tumors.

Herein, we report a facile strategy for synthesis of monodisperse gold nanostars (GNSs) based on PEGylation and co-loaded with the photosensitizer chlorin e6 (Ce6) to form GNSs-PEG@Ce6 NPs. Then employing CIK cells loading the as-prepared GNSs-PEG@Ce6 NPs to fabricate a CIK cells-based drug delivery system (GNSs-PEG@Ce6-CIK) for lung cancer. Among them, GNSs was functioned as transport media, Ce6 acted as the near-infrared (NIR) fluorescence imaging agent and photodynamic therapy (PDT), and CIK cells served as targeting vectors for immunotherapy, which can increase the efficiency of tumor enrichment and treatment effect.

The results of cellular experiments demonstrated that GNSs-PEG@Ce6 NPs had good dispersibility, water solubility and low toxicity under physiological conditions, and the cultured CIK cells had strong anti-tumor properties. Subsequently, GNSs-PEG@Ce6-CIK could effectively inhibit the growth of A549 cells under the exposure of 633 nm laser, which showed stronger killing effect than that of GNSs-PEG@Ce6 NPs or CIK cells.

In addition, they showed good tumor targeting and tumor synergistic killing activity in vivo .

Therefore, GNSs-PEG@Ce6-CIK was constructed for targeted NIR fluorescence imaging, enhanced PDT and immunotherapy of lung cancer.

论文信息

作者
Li C、Liu Z、Cheng Z、Gu S、Zhao W、Zhang Q、Feng Z
单位
Department of Gastroenterology, Xuhui District Central Hospital of Shanghai, Shanghai 200031, People's Republic of China.China
期刊
Biomedical materials (Bristol, England)2024 Jun 25
原文标识
PubMed 38870927 · DOI 10.1088/1748-605X/ad580c