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Co-delivery of paclitaxel and cisplatin with biocompatible PLGA-PEG nanoparticles enhances chemoradiotherapy in non-small cell lung cancer models

机译:紫杉醇和顺铂与生物相容性PLGA-PEG纳米颗粒的共同给药可增强非小细胞肺癌模型的放化疗

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摘要

Chemoradiotherapy (CRT) with paclitaxel (PTX) and cisplatin (CP) is part of the standard of care for patients with locally advanced non-small cell lung cancer (NSCLC). Despite the high treatment intensity, many patients still develop local recurrence after treatment. Thus, there is a strong need to further improve CRT for lung cancer. One strategy is to co-deliver cytotoxic chemotherapy agents using biocompatible nanoparticles (NPs) which can limit off-target tissue toxicity and improve therapeutic efficacy. Herein, we report the development of dual-drug loaded nanoformulations that improve the efficacy of CRT for NSCLC by co-encapsulation of cisplatin (CP) and PTX in PLGA-PEG NPs. Mice bearing NSCLC xenografts given the dual-drug loaded NPs during CRT showed greater inhibition of tumor growth than free drug combinations or combinations of single-drug loaded NPs. These results indicate that using a NP co-delivery strategy for this common CRT regimen may improve clinical responses in NSCLC patients.
机译:紫杉醇(PTX)和顺铂(CP)的放化疗(CRT)是局部晚期非小细胞肺癌(NSCLC)患者治疗标准的一部分。尽管治疗强度高,许多患者在治疗后仍会出现局部复发。因此,强烈需要进一步改善肺癌的CRT。一种策略是使用生物相容性纳米颗粒(NPs)共同递送细胞毒性化疗药物,这可以限制脱靶组织的毒性并提高治疗效果。在本文中,我们报道了通过在PLGA-PEG NP中共包裹顺铂(CP)和PTX来改善NSCLC的CRT疗效的双药物纳米制剂的开发。在CRT期间给予双药物负荷NP的带有NSCLC异种移植物的小鼠对肿瘤生长的抑制作用比游离药物组合或单药物负荷NP的组合更大。这些结果表明,对于这种常见的CRT方案使用NP共递送策略可能会改善NSCLC患者的临床反应。

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