含有塞拉斯特罗的双靶向混合胶束的开发及对三阴性乳腺癌治疗的评估

IF 4.9 3区 医学 Q1 PHARMACOLOGY & PHARMACY Pharmaceutics Pub Date : 2024-09-06 DOI:10.3390/pharmaceutics16091174
Siying Huang, Simeng Xiao, Xuehao Li, Ranran Tao, Zhangwei Yang, Ziwei Gao, Junjie Hu, Yan Meng, Guohua Zheng, Xinyan Chen
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引用次数: 0

摘要

考虑到将塞拉斯特罗(Cst)精确递送至线粒体以诱导线粒体功能障碍可能是改善塞拉斯特罗对TNBC治疗效果的一种潜在方法,研究人员通过自合成的三苯基膦修饰胆固醇(TPP-Chol)和透明质酸(HA)修饰胆固醇(HA-Chol)制备了一种新型肿瘤线粒体双靶向混合胶束纳米系统。Cst载药混合胶束(Cst@HA/TPP-M)具有粒径小、表面电位为负、载药率高达22.8%和持续释药等特点。与仅由 TPP-Chol 组装的 Cst 负载胶束(Cst@TPP-M)相比,Cst@HA/TPP-M 降低了溶血率,提高了体内稳定性和安全性。此外,以三阴性乳腺癌细胞株 MDA-MB-231 为细胞模型进行的一系列细胞实验证明,Cst@HA/TPP-M 通过 CD44 受体介导的内吞作用有效增加了细胞对药物的吸收,吸收量是游离 Cst 组的三倍。共聚焦研究结果表明,Cst@HA/TPP-M在内含溶酶体中降解HA后,其电荷反向作用引发了成功的内含溶酶体逃逸和有效的线粒体转运。与游离 Cst 组相比,Cst@HA/TPP-M 能显著提高 ROS 水平,降低线粒体膜电位,促进肿瘤细胞凋亡,对线粒体功能障碍有更好的诱导作用。基于MDA-MB-231肿瘤裸鼠的体内成像和抗肿瘤实验表明,与游离Cst相比,Cst@HA/TPP-M有利于药物在肿瘤部位的富集,减弱药物的全身分布,提高Cst的抗肿瘤疗效。总之,作为一种靶向给药系统,由TPP-Chol和HA-Chol共同构建的混合胶束可能会为改善Cst对TNBC的治疗效果提供一种有前景的策略。
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Development of Dual-Targeted Mixed Micelles Loaded with Celastrol and Evaluation on Triple-Negative Breast Cancer Therapy
Considering that the precise delivery of Celastrol (Cst) into mitochondria to induce mitochondrial dysfunction may be a potential approach to improve the therapeutic outcomes of Cst on TNBC, a novel tumor mitochondria dual-targeted mixed-micelle nano-system was fabricated via self-synthesized triphenylphosphonium-modified cholesterol (TPP-Chol) and hyaluronic acid (HA)-modified cholesterol (HA-Chol). The Cst-loaded mixed micelles (Cst@HA/TPP-M) exhibited the characteristics of a small particle size, negative surface potential, high drug loading of up to 22.8%, and sustained drug release behavior. Compared to Cst-loaded micelles assembled only by TPP-Chol (Cst@TPP-M), Cst@HA/TPP-M decreased the hemolysis rate and upgraded the in vivo stability and safety. In addition, a series of cell experiments using the triple-negative breast cancer cell line MDA-MB-231 as a cell model proved that Cst@HA/TPP-M effectively increased the cellular uptake of the drug through CD44-receptors-mediated endocytosis, and the uptake amount was three times that of the free Cst group. The confocal results demonstrated successful endo-lysosomal escape and effective mitochondrial transport triggered by the charge converse of Cst@HA/TPP-M after HA degradation in endo-lysosomes. Compared to the free Cst group, Cst@HA/TPP-M significantly elevated the ROS levels, reduced the mitochondrial membrane potential, and promoted tumor cell apoptosis, showing a better induction effect on mitochondrial dysfunction. In vivo imaging and antitumor experiments based on MDA-MB-231-tumor-bearing nude mice showed that Cst@HA/TPP-M facilitated drug enrichment at the tumor site, attenuated drug systemic distribution, and polished up the antitumor efficacy of Cst compared with free Cst. In general, as a target drug delivery system, mixed micelles co-constructed by TPP-Chol and HA-Chol might provide a promising strategy to ameliorate the therapeutic outcomes of Cst on TNBC.
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来源期刊
Pharmaceutics
Pharmaceutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.90
自引率
11.10%
发文量
2379
审稿时长
16.41 days
期刊介绍: Pharmaceutics (ISSN 1999-4923) is an open access journal which provides an advanced forum for the science and technology of pharmaceutics and biopharmaceutics. It publishes reviews, regular research papers, communications,  and short notes. Covered topics include pharmacokinetics, toxicokinetics, pharmacodynamics, pharmacogenetics and pharmacogenomics, and pharmaceutical formulation. Our aim is to encourage scientists to publish their experimental and theoretical details in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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