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肿瘤微环境响应型靶向 SWCNT 递送来实现协同光热治疗和化学疗法。

Synergistic Photothermal Therapy and Chemotherapy Enabled by Tumor Microenvironment-Responsive Targeted SWCNT Delivery.

机构信息

School of Biological Engineering, Henan University of Technology, Zhengzhou 450001, China.

Institute for Complexity Science, Henan University of Technology, Zhengzhou 450001, China.

出版信息

Int J Mol Sci. 2024 Aug 23;25(17):9177. doi: 10.3390/ijms25179177.

Abstract

As a novel therapeutic approach, photothermal therapy (PTT) combined with chemotherapy can synergistically produce antitumor effects. Herein, dithiodipropionic acid (DTDP) was used as a donor of disulfide bonds sensitive to the tumor microenvironment for establishing chemical bonding between the photosensitizer indocyanine green amino (ICG-NH) and acidified single-walled carbon nanotubes (CNTs). The CNT surface was then coated with conjugates (HD) formed by the targeted modifier hyaluronic acid (HA) and 1,2-tetragacylphosphatidyl ethanolamine (DMPE). After doxorubicin hydrochloride (DOX), used as the model drug, was loaded by CNT carriers, functional nano-delivery systems (HD/CNTs-SS-ICG@DOX) were developed. Nanosystems can effectively induce tumor cell (MCF-7) death in vitro by accelerating cell apoptosis, affecting cell cycle distribution and reactive oxygen species (ROS) production. The in vivo antitumor activity results in tumor-bearing model mice, further verifying that HD/CNTs-SS-ICG@DOX inhibited tumor growth most significantly by mediating a synergistic effect between chemotherapy and PTT, while various functional nanosystems have shown good biological tissue safety. In conclusion, the composite CNT delivery systems developed in this study possess the features of high biocompatibility, targeted delivery, and responsive drug release, and can achieve the efficient coordination of chemotherapy and PTT, with broad application prospects in cancer treatment.

摘要

作为一种新型的治疗方法,光热治疗(PTT)与化疗相结合可以协同产生抗肿瘤作用。在此,二硫代二丙酸(DTDP)被用作对肿瘤微环境敏感的二硫键供体,以在光敏剂吲哚菁绿氨基(ICG-NH)和酸化的单壁碳纳米管(CNTs)之间建立化学键。然后,通过靶向修饰剂透明质酸(HA)和 1,2-四油酰基磷脂酰乙醇胺(DMPE)形成的缀合物(HD)对 CNT 表面进行涂层。盐酸阿霉素(DOX)作为模型药物被 CNT 载体负载后,开发了功能纳米递药系统(HD/CNTs-SS-ICG@DOX)。纳米系统可以通过加速细胞凋亡、影响细胞周期分布和产生活性氧(ROS)来有效诱导体外肿瘤细胞(MCF-7)死亡。荷瘤模型小鼠的体内抗肿瘤活性结果进一步验证了 HD/CNTs-SS-ICG@DOX 通过介导化疗和 PTT 的协同作用最显著地抑制肿瘤生长,而各种功能纳米系统表现出良好的生物组织安全性。总之,本研究开发的复合 CNT 递药系统具有高生物相容性、靶向递送和响应性药物释放的特点,可以实现化疗和 PTT 的高效协同,在癌症治疗中有广阔的应用前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eed/11394823/e98a1144f8d5/ijms-25-09177-sch001.jpg

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