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Anti-tumor efficacy of folate modified PLGA-based nanoparticles for the co-delivery of drugs in ovarian cancer

机译:叶酸修饰的基于PLGA的纳米颗粒在卵巢癌中共同递送药物的抗肿瘤功效

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摘要

>Background: Ovarian cancer is a leading cause of death in gynecologic malignancies. The high mortality is mainly caused by advanced stage at presentation in most patients. Even after the combination of cytoreductive surgery and systemic platinum and taxane treatment, most patients relapse and eventually succumb to the disease. Therefore, there is an urgent need for new treatments. >Purpose: A novel folate (FA)-targeted co-delivery of docetaxel (DTX) and gemcitabine (GEM) nanoparticles (NPs) was developed to overcome ovarian cancer. >Materials and methods: Physicochemical characteristics of NPs such as size, morphology, and release profiles were explored. In vitro and in vivo studies were carried out to assess the efficacy of their antitumor activity in target cells. >Results: FA modified DTX and GEM co-loaded NPs were prepared using the solvent evaporation method. The NPs with a particle size of ~120nm were stable in the observation period. The hemolysis results indicated that FA-PEG2000-PLGA was potentially feasible for targeted antitumor drug delivery through blood circulation. In vitro release study suggested that in comparison with the free drug, PLGA-DTX/GEM NPs and FA-PEG2000-PLGA-DTX/GEM NPs had sustained-release properties. However, there was no obvious difference between the two NPs with the same drug in the release profile. Ovarian cancer cells in vitro efficiently took up the non-targeted and FA-targeted NPs; improved cytotoxicity was observed in the FA-targeted NPs, showing a 3.59- fold drop in the IC50 in SKOV-3 cells as compared to DTX/GEM alone. Cellular uptake showed that through surface modification, more drugs entered the cell successfully. Pharmacodynamics results showed a statistically significant effect on the rate of reduction of tumor volume for FA-PEG2000-PLGA-DTX/GEM NPs than other groups and no toxicity of organs.>Conclusion: The present study indicates that the FA-PEG2000-PLGA-DTX/GEM NPs provides a promising platform for the treatment of ovarian cancer.
机译:>背景:卵巢癌是妇科恶性肿瘤的主要死亡原因。高死亡率主要是由大多数患者的晚期就诊引起的。即使在细胞减灭术以及全身性铂和紫杉烷治疗相结合后,大多数患者仍会复发并最终死于该疾病。因此,迫切需要新的治疗方法。 >目的:开发了靶向叶酸(FA)的多西他赛(DTX)和吉西他滨(GEM)纳米颗粒(NPs)共同给药以克服卵巢癌。 >材料和方法:探讨了NP的理化特性,例如大小,形态和释放曲线。进行了体外和体内研究以评估其在靶细胞中抗肿瘤活性的功效。 >结果:使用溶剂蒸发法制备了FA修饰的DTX和GEM共载NP。粒径约为120nm的NP在观察期内是稳定的。溶血结果表明,FA-PEG2000-PLGA对于通过血液循环靶向靶向抗肿瘤药物可能是可行的。体外释放研究表明,与游离药物相比,PLGA-DTX / GEM NP和FA-PEG2000-PLGA-DTX / GEM NP具有缓释特性。然而,具有相同药物的两个NP之间的释放曲线没有明显差异。体外卵巢癌细胞可有效吸收非靶向和FA靶向的NP;与单独使用DTX / GEM相比,在以FA为目标的NP中观察到改善的细胞毒性,显示SKOV-3细胞中IC50下降了3.59倍。细胞吸收表明,通过表面修饰,更多的药物成功进入细胞。药效学结果显示FA-PEG2000-PLGA-DTX / GEM NPs的肿瘤缩小率比其他组有统计学意义,并且没有器官毒性。>结论:本研究表明FA-PEG2000-PLGA-DTX / GEM NP为卵巢癌的治疗提供了有希望的平台。

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