Enhancing ovarian cancer treatment: Synergistic effects of methotrexate (Methotrexate)- and quercetin-loaded chitosan nanoparticles

IF 6.5 Q1 CHEMISTRY, APPLIED Carbohydrate Polymer Technologies and Applications Pub Date : 2024-12-01 Epub Date: 2024-11-28 DOI:10.1016/j.carpta.2024.100619
Hamed Dadashi , Amir Reza Nazemiyeh , Alireza Karimian-Shaddel , Milad mashinchian , Aria Mohabbat , Shahrbano Karamnejad Faragheh , Somayeh Vandghanooni , Morteza Eskandani
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Abstract

Ovarian cancer, a leading cause of cancer-related deaths in women, is often diagnosed at advanced stages and exhibits treatment resistance. This study investigates chitosan-based nanoparticles (Cs NPs) as a drug delivery system to enhance the efficacy of methotrexate (MTX) and quercetin (Que) in ovarian cancer therapy. Cs NPs were synthesized for drug delivery, and their physicochemical properties, in vitro release profiles, and cytotoxicity against OVCAR-3 cells were evaluated. The study found high encapsulation efficiencies of 97.92 % for MTX and 76.23 % for Que, with controlled release demonstrated at pH 5.7 over 50 h. Cytotoxicity assays revealed IC50 values of 57.23 ng/mL for MTX-Cs NPs and 13.22 ng/mL for Que-Cs NPs, indicating superior effectiveness compared to plain drugs. The combination treatment showed a synergistic effect (CI of 0.266), significantly enhancing apoptosis and reducing OVCAR-3 mammosphere size by 25 %. Cell migration assays indicated a reduction to 25.02 % compared to controls. The CAM assay confirmed anti-angiogenic activity, while Western blot analysis showed reduced E2F-1 and increased BAX expression. These findings suggest that MTX/Que-loaded Cs NPs could significantly improve ovarian cancer treatment outcomes.

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增强卵巢癌治疗:甲氨蝶呤(甲氨蝶呤)和槲皮素负载壳聚糖纳米颗粒的协同作用
卵巢癌是妇女癌症相关死亡的主要原因,通常在晚期才被诊断出来,并表现出治疗耐药性。本研究研究了壳聚糖纳米颗粒(Cs NPs)作为一种药物传递系统,以提高甲氨蝶呤(MTX)和槲皮素(Que)在卵巢癌治疗中的疗效。合成Cs NPs用于给药,并评价其理化性质、体外释放谱及对OVCAR-3细胞的细胞毒性。研究发现,MTX的包封率为97.92%,Que的包封率为76.23%,在pH为5.7的条件下控释50小时。细胞毒性实验显示,MTX- cs NPs的IC50值为57.23 ng/mL, Que- cs NPs的IC50值为13.22 ng/mL,表明与普通药物相比,MTX- cs NPs的效果更好。联合治疗显示出协同效应(CI为0.266),显著促进细胞凋亡,使OVCAR-3乳腺球大小减少25%。细胞迁移试验表明,与对照组相比,减少了25.02%。CAM实验证实了抗血管生成活性,而Western blot分析显示E2F-1表达减少,BAX表达增加。这些发现表明MTX/ queue -loaded Cs NPs可以显著改善卵巢癌的治疗结果。
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