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天然多酚-铂纳米复合物刺激免疫系统用于联合癌症治疗。

Natural Polyphenols-Platinum Nanocomplexes Stimulate Immune System for Combination Cancer Therapy.

作者信息

Xiang Jiajia, Zhang Yifan, Liu Xin, Zhou Quan, Piao Ying, Shao Shiqun, Tang Jianbin, Zhou Zhuxian, Xie Tao, Shen Youqing

机构信息

Zhejiang Key Laboratory of Smart BioMaterials and Center for Bionanoengineering, College of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310027, China.

ZJU-Hangzhou Global Scientific and Technological Innovation Center, Hangzhou 311215, China.

出版信息

Nano Lett. 2022 Jul 13;22(13):5615-5625. doi: 10.1021/acs.nanolett.2c02161. Epub 2022 Jun 24.

Abstract

Nanocarriers have been employed extensively to enhance drug delivery efficacy and reduce the side effect. However, carrier materials for drug delivery have challenging aspects, including safety concerns, low drug content, complexity in preparation, and low reproducibility. Herein, we propose a facile, universal, and green preparation way to use natural polyphenols to build platinum nanocomplex with stable structure, proper size, and high Pt content. The nanocomplexes are constructed by metal-polyphenol coordination using natural polyphenols and 1,2-diaminocyclohexane-Pt (II), enabling dual-responsive drug release behavior. For proof of concept, we demonstrate the antitumor activity of the Pt nanocomplex using a representative tannic acid-Pt nanocomplex (denoted as PTI). PTI can induce intensive tumor cell apoptosis, trigger immunogenic cell death (ICD), remarkably promote cytotoxic T lymphocytes (CTLs) infiltration in tumors, and significantly reduce immunosuppression of the tumor microenvironments, thus stimulating potent antitumor immune responses and showing effective antitumor activity by synergizing immune checkpoint blockade (ICB) therapy.

摘要

纳米载体已被广泛用于提高药物递送效率并降低副作用。然而,用于药物递送的载体材料存在诸多挑战,包括安全性问题、药物含量低、制备复杂以及重现性低。在此,我们提出一种简便、通用且绿色的制备方法,利用天然多酚构建具有稳定结构、合适尺寸和高铂含量的铂纳米复合物。这些纳米复合物通过使用天然多酚和1,2 - 二氨基环己烷 - 铂(II)进行金属 - 多酚配位构建而成,具有双响应药物释放行为。为了验证概念,我们使用代表性的单宁酸 - 铂纳米复合物(记为PTI)证明了铂纳米复合物的抗肿瘤活性。PTI可诱导强烈的肿瘤细胞凋亡,引发免疫原性细胞死亡(ICD),显著促进细胞毒性T淋巴细胞(CTLs)浸润肿瘤,并显著降低肿瘤微环境的免疫抑制作用,从而通过协同免疫检查点阻断(ICB)疗法刺激强大的抗肿瘤免疫反应并显示出有效的抗肿瘤活性。

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