转移素向级别纳米平台用于抑制转录因子 核因子 红状腺2-相关因子2和增强铁质灭 抗癌疗法
Wenjie Chen1, Li Xie1, Can Lv1
1Key Laboratory of Luminescence Analysis and Molecular Sensing, Ministry of Education, College of Pharmaceutical Sciences, Southwest University, 2 Tiansheng Road, Beibei District, Chongqing 400715, China.
ACS applied materials & interfaces
|May 30, 2023
概括
这项研究介绍了一种新的纳米平台,该纳米平台将铁灭症诱导剂与Nrf2抑制剂结合起来. 这种方法通过增加活性氧物种 (ROS) 来提高癌细胞死亡,以改善铁疗法.
科学领域:
- 生物医学工程 生物医学工程
- 纳米技术纳米技术
- 癌症治疗 癌症治疗
背景情况:
- 铁,一种依赖于铁的细胞死亡,是一个有前途的抗癌策略.
- 核素红细胞2-关联因子2 (Nrf2) 激活通过减少活性氧物种 (ROS) 来阻碍铁化.
研究的目的:
- 开发一个有针对性的纳米平台,以克服Nrf2介导的耐药性,并增强癌症治疗的铁化.
- 使用转移素向的中孔多多巴胺纳米平台 (TPM@AM) 同时提供铁亡诱导剂 (artsunate) 和Nrf2抑制剂 (ML385).
主要方法:
- 设计了一个转移素 (Tf) 向的半孔多多巴胺 (MPDA) 纳米平台 (TPM@AM).
- 同封装的阿尔特苏纳酸 (ART) 作为铁灭诱导剂和ML385作为Nrf2抑制剂.
- 利用瘤微环境的酸度和激光照射来触发药物释放和光热效应.
主要成果:
- 该纳米平台通过转移素受体 (TfR) 识别专门针对癌细胞.
- 控制释放的ART和ML385增强了细胞内ROS的积累.
- MPDA提供光热能力,有助于协同抑制瘤.
结论:
- TPM@AM纳米平台为精确的协同癌症治疗提供了一个空间时间控制的策略.
- 这种方法通过克服Nrf2介导的耐药性,有效地增强了铁疗法.
- 这项研究表明,通过向药物输送和组合疗法来提高抗癌疗效的有希望的方法.
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