Maghsoudian Samane, Yektakasmaei Mohaddese Pourashory, Shaabani Alireza, Perseh Sahra, Fatahi Yousef, Nouri Zeinab, Gholami Mahdi, Sayyari Nastaran, Hoseinzadeh Hesam Aldin, Motasadizadeh Hamidreza, Dinarvand Rassoul
Department of Pharmaceutical Nanotechnology, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran; Nanotechnology Research Centre, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Faculty of Veterinary Medicine, Islamic Azad University, Garmsar Branch, Garmsar, Iran.
Int J Biol Macromol. 2025 Feb;289:138910. doi: 10.1016/j.ijbiomac.2024.138910. Epub 2024 Dec 17.
A promising new approach to mitigate the adverse effects of chemotherapeutic drugs on healthy tissues involves combining sonodynamic therapy with topical chemotherapy to enhance the therapeutic efficacy of anticancer drugs. In this study, we introduce a multi-functional in situ chitosan hydrogel (CS) containing silk fibroin nanoparticles (SFNPs) loaded with doxorubicin (DOXSFNPs) and CuO/TiO nanoparticles (CTNPs) for combination therapy. The developed DOXSFNPs exhibited a size of 257 ± 6 nm, a zeta potential of -14.3 ± 1.8 mV, and a high loading capacity of 12.38 ± 1.73 %. The pH-dependent controlled release of DOX from DOXSF2/CS2 was observed to be more pronounced than that from DOX/CS2. MTT results indicated dose-dependent toxicity of CT/CS2 in response to ultrasaound radiation (US). Our findings revealed a 1.83-fold increase in reactive oxygen species (ROS) production with therapy, with the IC of CT3-DOXSF2/CS2-US showing a 58 % reduction compared to CT3/DOXSF2/CS2. In vivo outcomes and histopathological staining demonstrated that the CT3/DOXSF2/CS2-US treatment group exhibited the highest tumor growth inhibition rate, reaching approximately 83.65 %. These findings underscore the potential of this approach in minimizing the adverse effects of chemotherapy while maximizing therapeutic outcomes, offering a valuable contribution to the field of cancer therapy.
一种减轻化疗药物对健康组织不良影响的有前景的新方法是将声动力疗法与局部化疗相结合,以提高抗癌药物的治疗效果。在本研究中,我们引入了一种多功能原位壳聚糖水凝胶(CS),其包含负载阿霉素的丝素蛋白纳米颗粒(SFNPs)(DOXSFNPs)和用于联合治疗的CuO/TiO纳米颗粒(CTNPs)。所制备的DOXSFNPs粒径为257±6nm,zeta电位为-14.3±1.8mV,载药量高达12.38±1.73%。观察到DOX从DOXSF2/CS2中的pH依赖性控释比从DOX/CS2中更明显。MTT结果表明CT/CS2对超声辐射(US)具有剂量依赖性毒性。我们的研究结果显示,治疗后活性氧(ROS)生成增加了1.83倍,CT3-DOXSF2/CS2-US的半数抑制浓度(IC)相比CT3/DOXSF2/CS2降低了58%。体内实验结果和组织病理学染色表明,CT3/DOXSF2/CS2-US治疗组表现出最高的肿瘤生长抑制率,达到约83.65%。这些发现强调了该方法在最小化化疗不良反应同时最大化治疗效果方面的潜力,为癌症治疗领域做出了有价值的贡献。