Arvejeh Pooria Mohammadi, Chermahini Fatemeh Amini, Marincola Francesco, Taheri Fatemeh, Mirzaei Seyed Abbas, Alizadeh Akram, Deris Fatemeh, Jafari Raziyeh, Amiri Niloufar, Soltani Amin, Bijad Elham, Dehkordi Ebrahim Soleiman, Khosravian Pegah
Cellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran.
Student Research Committee, Shahrekord University of Medical Sciences, Shahrekord, Iran.
J Transl Med. 2025 Mar 31;23(1):382. doi: 10.1186/s12967-025-06396-4.
Breast cancer remains one of the leading causes of death among women globally, with traditional therapies often limited by challenges such as drug resistance and significant side effects. Combination therapies, coupled with nanotechnology-based co-delivery systems, offer enhanced efficacy by targeting multiple pathways in cancer progression. In this study, we developed an injectable, stimuli-responsive nanosystem using a chitosan hydrogel embedded with mesoporous silica nanoparticles for the co-administration of 5-fluorouracil and everolimus. This approach aims to optimize controlled drug release, enhance the synergistic anticancer effect, and overcome challenges associated with co-loading different therapeutic agents.
Various techniques were employed to characterize the nanoparticles and the hydrogel. Cell uptake, apoptosis, and proliferation of 4T1 breast cancer cells were evaluated by flow cytometry and Resazurin assay, respectively. The Balb/C mice model of breast cancer, which received the therapeutical nanoplatforms subcutaneously near the tumoral region was used to examine tumor size and lung metastases.
The results revealed that the nanoparticles had a suitable loading capacity and high cellular uptake. The drug release was pH-sensitive and synergistic. By incorporating nanoparticles into the hydrogel, the cell death rate and apoptosis of 4T1 breast cancer cells increased significantly, due to the synergistic effects of co-delivered drugs. Additionally, the combination treatment groups showed a significant reduction in tumor size and lung metastasis compared to the monotherapy and control groups.
These findings underscore the potential of the nanocomposite used to develop a novel co-delivery system to enhance therapeutic outcomes, reduce side effects, and provide a promising new strategy for future cancer treatments.
乳腺癌仍然是全球女性主要死因之一,传统疗法常常受到耐药性和严重副作用等挑战的限制。联合疗法以及基于纳米技术的共递送系统,通过靶向癌症进展中的多个途径,可提高疗效。在本研究中,我们开发了一种可注射的、刺激响应性纳米系统,该系统使用嵌入介孔二氧化硅纳米颗粒的壳聚糖水凝胶来共同给药5-氟尿嘧啶和依维莫司。这种方法旨在优化药物的控释,增强协同抗癌效果,并克服与共同负载不同治疗剂相关的挑战。
采用各种技术对纳米颗粒和水凝胶进行表征。分别通过流式细胞术和刃天青测定法评估4T1乳腺癌细胞的细胞摄取、凋亡和增殖情况。使用在肿瘤区域附近皮下注射治疗性纳米平台的Balb/C乳腺癌小鼠模型来检测肿瘤大小和肺转移情况。
结果显示,纳米颗粒具有合适的负载能力和高细胞摄取率。药物释放具有pH敏感性且具有协同作用。通过将纳米颗粒掺入水凝胶中,由于共同递送药物的协同作用,4T1乳腺癌细胞的细胞死亡率和凋亡率显著增加。此外,与单一疗法和对照组相比,联合治疗组的肿瘤大小和肺转移明显减少。
这些发现强调了用于开发新型共递送系统的纳米复合材料在提高治疗效果、减少副作用以及为未来癌症治疗提供有前景的新策略方面的潜力。