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Preparation and properties of inhalable nanocomposite particles for treatment of lung cancer

机译:可吸入性纳米复合颗粒治疗肺癌的制备及性能

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Nanoparticles have widely been studied in drug delivery research for targeting and controlled release. The aim of this article is application of nanoparticles as an inhalable agent for treatment of lung cancer. To deposit effectively deep the particles in the lungs, the PLGA nanoparticles loaded with the anticancer drug 6-{[2-(dimethylamino)ethyl]amino}-3-hydroxyl-7H-indeno[2,1-c]quinolin-7- one dihydrochloride (TAS-103) were prepared in the form of nanocomposite particles. The nanocomposite particles consist of the complex of drug-loaded nanoparticles and excipients. in this study, the anticancer effects of the nanocomposite particles against the lung cancer cell line A549. Also, the concentration of TAS-103 in blood and lungs were determined after administration of the nanocomposite particles by inhalation to rats. TAS-103-loaded PLGA nanoparticles were prepared with 5% and 10% of loading ratio by spray drying method with trehalose as an excipient. The 5% drug-loaded nanocomposite particles were more suitable for inhalable agent because of the sustained release of TAS-103 and higher FPF value. Cytotoxicity of nanocomposite particles against A549 cells was higher than that of free drug. When the nanocomposite particles were administered in rats by inhalation, drug concentration in lung was much higher than that in plasma. Furthermore, drug concentration in lungs administered by inhalation of nanocomposite particles was much higher than that after intravenous administration of free drug. From these results, the nanocomposite particle systems could be promising for treatment of lung cancer.
机译:纳米颗粒已经在药物递送研究中针对靶向和控释进行了广泛研究。本文的目的是将纳米颗粒用作可吸入剂治疗肺癌。为了有效地将微粒深深地沉积在肺中,负载了抗癌药6-{[[((2-(二甲基氨基)乙基]氨基} -3-羟基l-7H-茚并[2,1-c]喹啉-7-以纳米复合颗粒的形式制备了一种二盐酸盐(TAS-103)。纳米复合颗粒由载药纳米颗粒和赋形剂的复合物组成。在这项研究中,纳米复合颗粒对肺癌细胞A549的抗癌作用。而且,在通过向大鼠吸入施用纳米复合颗粒之后,确定了血液和肺中TAS-103的浓度。以海藻糖为赋形剂,通过喷雾干燥法制备了负载率为5%和10%的TAS-103负载的PLGA纳米颗粒。由于TAS-103的持续释放和较高的FPF值,5%载药量的纳米复合颗粒更适合吸入剂。纳米复合颗粒对A549细胞的细胞毒性高于游离药物。当通过吸入将纳米复合颗粒给药于大鼠时,肺中的药物浓度远高于血浆中的药物浓度。此外,通过吸入纳米复合颗粒给药的肺部药物浓度远高于静脉注射游离药物后的浓度。从这些结果来看,纳米复合颗粒系统有望用于治疗肺癌。

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