Huang Siying, Xiao Simeng, Li Xuehao, Tao Ranran, Yang Zhangwei, Gao Ziwei, Hu Junjie, Meng Yan, Zheng Guohua, Chen Xinyan
Pharmacy Faculty, Hubei University of Chinese Medicine, Wuhan 430065, China.
Hubei Shizhen Laboratory, Wuhan 430065, China.
Pharmaceutics. 2024 Sep 6;16(9):1174. doi: 10.3390/pharmaceutics16091174.
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.
鉴于将雷公藤红素(Cst)精确递送至线粒体以诱导线粒体功能障碍可能是提高Cst对三阴性乳腺癌(TNBC)治疗效果的一种潜在方法,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)制备了一种新型的肿瘤线粒体双靶向混合胶束纳米系统。负载Cst的混合胶束(Cst@HA/TPP-M)具有粒径小、表面电位为负、高达22.8%的高载药量以及药物缓释行为等特点。与仅由TPP-Chol组装的负载Cst的胶束(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,一系列以三阴性乳腺癌细胞系MDA-MB-231为细胞模型的细胞实验证明,Cst@HA/TPP-M通过CD44受体介导的内吞作用有效增加了药物的细胞摄取,摄取量是游离Cst组的三倍。共聚焦结果表明,Cst@HA/TPP-M在内吞溶酶体中HA降解后,通过电荷反转触发了成功的内吞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显著提高了活性氧(ROS)水平,降低了线粒体膜电位,并促进了肿瘤细胞凋亡,对线粒体功能障碍表现出更好的诱导作用。基于携带MDA-MB-231肿瘤的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促进了药物在肿瘤部位的富集,减弱了药物的全身分布,并提高了Cst的抗肿瘤疗效。总体而言,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为改善Cst对TNBC的治疗效果提供一种有前景的策略。