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用于肺癌治疗的谷胱甘肽响应型生物可降解聚氨酯纳米颗粒。

Glutathione-responsive biodegradable polyurethane nanoparticles for lung cancer treatment.

机构信息

Department of Bioengineering, University of Texas at Arlington, Arlington, TX 76019, USA.

Department of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.

出版信息

J Control Release. 2020 May 10;321:363-371. doi: 10.1016/j.jconrel.2020.02.021. Epub 2020 Feb 12.

Abstract

Lung cancer is one of the major causes of cancer-related deaths worldwide. Stimuli-responsive polymers and nanoparticles, which respond to exogenous or endogenous stimuli in the tumor microenvironment, have been widely investigated for spatiotemporal chemotherapeutic drug release applications for cancer chemotherapy. We developed glutathione (GSH)-responsive polyurethane nanoparticles (GPUs) using a GSH-cleavable disulfide bond containing polyurethane that responds to elevated levels of GSH within lung cancer cells. The polyurethane nanoparticles were fabricated using a single emulsion and mixed organic solvent method. Cisplatin-loaded GSH-sensitive nanoparticles (CGPU) displayed a GSH-dose dependent release of cisplatin. In addition, a significant reduction in in vitro survival fraction of A549 lung cancer cells was observed compared to free cisplatin of equivalent concentration (survival fraction of 0.5 and ~0.7, respectively). The in vivo biodistribution studies showed localization of fluorescently labeled GPUs (7% of total injected dose per gram tissue) in the lung tumor regions after mouse-tail IV injections in xenograft A549 lung tumor models. The animals exposed to CGPUs also exhibited the inhibition of lung tumor growth compared to animals administered with saline (tumor growth rate of 1.5 vs. 13 in saline) and free cisplatin (tumor growth rate of 5.9) in mouse xenograft A549 lung tumor models within 14 days. These nanoparticles have potential to be used for on-demand drug release for an enhanced chemotherapy to effectively treat lung cancer.

摘要

肺癌是全球癌症相关死亡的主要原因之一。刺激响应性聚合物和纳米颗粒能够对外源性或内源性刺激做出响应,这些聚合物和纳米颗粒在肿瘤微环境中已被广泛研究,用于实现化疗药物的时空控制释放。我们使用含有可被谷胱甘肽(GSH)裂解的二硫键的可被 GSH 响应的聚氨酯,开发了谷胱甘肽响应型聚氨酯纳米颗粒(GPUs),这种聚氨酯对肺癌细胞中升高的 GSH 水平做出响应。采用单乳液和混合有机溶剂法制备了聚氨酯纳米颗粒。载顺铂的 GSH 敏感纳米颗粒(CGPU)表现出顺铂的 GSH 剂量依赖性释放。此外,与同等浓度的游离顺铂相比,A549 肺癌细胞的体外存活分数显著降低(分别为0.5 和0.7)。体内生物分布研究表明,在荷瘤 A549 肺癌模型中,经小鼠尾静脉注射后,荧光标记的 GPUs 主要定位于肺部肿瘤区域(注射后每克组织约有 7%的标记纳米颗粒)。与生理盐水(生理盐水组肿瘤生长速率为 1.5,而生理盐水组为 13)和游离顺铂(顺铂组肿瘤生长速率为 5.9)相比,接受 CGPUs 治疗的动物在荷瘤 A549 肺癌模型中也表现出抑制肺部肿瘤生长的作用,在 14 天内。这些纳米颗粒具有按需释放药物的潜力,可增强化疗效果,有效治疗肺癌。

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