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Nanomedicine-Assisted Combination Therapy of NSCLC: New Platinum-Based Anticancer Drug Synergizes the Therapeutic Efficacy of Ganetespib

机译:纳米药物辅助的NSCLC联合治疗:新的基于铂的抗癌药物协同Ganetespib的治疗功效

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摘要

>Purpose: K-RAS is the most common mutated oncogene associated with Non-Small-Cell Lung Cancer (NSCLC). So far, there are no promising chemotherapies for the direct inhibition of K-RAS, and considered to be undruggable. In this work, we have introduced a new platinum-based cyanoximate complex, Pt(MCO)2, as an anti-cancer drug to enhance the therapeutic efficacy of Hsp90 inhibitor drug, ganetespib for the combination therapy of NSCLC.>Methods: We have synthesized polyacrylic acid (PAA)-coated magnetic nanoparticles (MNPs) and used as drug delivery system. These MNPs were decorated with folic acid in order to target folate receptor-expressing NSCLC. The individual and combination of drugs as well as an optical dye DiI were co-encapsulated successfully inside the PAA-coating of MNPs to evaluate synergistic treatment option for NSCLC. The magnetic resonance (MR) and optical imaging modalities assisted for the monitoring drug loading and NSCLC treatment.>Results: To evaluate the therapeutic efficacy of these customized MNPs, various cell-based assays including cell viability, apoptosis and necrosis, cell migration, comet and ROS experiments were performed. Results showed minimal toxicity for functional MNPs with no therapeutic drug and more than 60% cell death within 48 h of treatment, when single drug was encapsulated. Importantly, more than 90% cells were dead when both drugs were delivered. Overall, the results indicated that the Pt(MCO)2 drug enhances the therapeutic efficacy of ganetespib by more than 30% toxicity towards the targeted treatment of NSCLC, while showed minimal toxicity to the normal healthy tissues.>Conclusion: We successfully developed new dual-modal magnetic nanomedicines for the rapid and controlled release of combination of drugs for the effective treatment of NSCLC. The MR and fluorescence modalities help monitoring the delivery of drugs, where the new platinum-based drug Pt(MCO)2 synergizes the therapeutic efficacy of ganetespib.
机译:>目的:K-RAS是与非小细胞肺癌(NSCLC)相关的最常见的突变癌基因。迄今为止,尚无用于直接抑制K-RAS的有前途的化学疗法,被认为是不可药物的。在这项工作中,我们引入了一种新的铂基氰基肟酸酯复合物Pt(MCO)2作为抗癌药物,以增强Hsp90抑制剂药物ganetespib对NSCLC的联合治疗的疗效。>方法: 我们已经合成了涂覆有聚丙烯酸(PAA)的磁性纳米颗粒(MNP),并已用作药物递送系统。用叶酸修饰这些MNP,以靶向表达叶酸受体的NSCLC。药物的个体和组合以及光学染料DiI已成功地共封装在MNP的PAA涂层内,以评估NSCLC的协同治疗选择。磁共振(MR)和光学成像方法有助于监测药物装载和NSCLC治疗。>结果:要评估这些定制的MNP的治疗效果,需要进行各种基于细胞的测定,包括细胞存活率,凋亡和进行了坏死,细胞迁移,彗星和ROS实验。结果显示,当封装单一药物时,对于无治疗药物的功能性MNP毒性最小,并且在治疗后48小时内细胞死亡超过60%。重要的是,两种药物均交付时,有90%以上的细胞死亡。总体而言,该结果表明,Pt(MCO)2药物对ganetespib的靶向NSCLC治疗毒性提高30%以上,而对正常健康组织的毒性却最小。>结论:我们成功开发了新型双峰磁性纳米药物,用于快速有效地控制NSCLC药物组合的释放。 MR和荧光模式有助于监测药物的递送,其中新的基于铂的药物Pt(MCO)2可以增强ganetespib的疗效。

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