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首页> 外文期刊>Materials science & engineering, C. Materials for Biogical applications >Genistein-loaded nanoparticles of star-shaped diblock copolymer mannitol-core PLGA-TPGS for the treatment of liver cancer
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Genistein-loaded nanoparticles of star-shaped diblock copolymer mannitol-core PLGA-TPGS for the treatment of liver cancer

机译:染料木素负载的星形二嵌段共聚物甘露醇核心PLGA-TPGS纳米颗粒用于治疗肝癌

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The purpose of this research is to develop nanoparticles (NPs) of star-shaped copolymer mannitol-functionalized PLGA-TPGS for Genistein delivery for liver cancer treatment, and evaluate their therapeutic effects in liver cancer cell line and hepatoma-tumor-bearing nude mice in comparison with the linear PLGA nanoparticles and PLGA-TAGS nanoparticles. The Genistein-loaded M-PLGA-TPGS nanoparticles (MPTN), prepared by a modified nanoprecipitation method, were observed by FESEM and TEM to be near-spherical shape with narrow size distribution. The nanoparticles were further characterized in terms of their size, size distribution, surface charge, drug-loading content, encapsulation efficiency and in vitro drug release profiles. The data showed that the M-PLGA-TPGS nanoparticles were found to be stable, showing almost no change in particle size and surface charge during 3-month storage of their aqueous solution. In vitro Genistein release from the nanoparticles exhibited biphasic pattern with burst release at the initial 4 days and sustained release afterwards. The cellular uptake efficiency of fluorescent M-PLGA-TPGS nanoparticles was 1.25-, 122-, and 1.29-fold higher than that of the PLGA-TPGS nanoparticles at the nanoparticle concentrations of 100, 250, and 500 [ig/mL, respectively. In the MPTN group, the ratio of apoptotic cells increased with the drug dose increased, which exhibited dosedependent effect and a significant difference compared with.Genistein solution group (p < 0.05). The data also showed that the Genistein-loaded M-PLGA-TPGS nanoparticles have higher antitumor efficacy than that of linear PLGA-TPGS nanoparticles and PLGA nanopartides in vitro and in vivo. In conclusion, the star-shaped copolymer M-PLGA-TPGS could be used as a potential and promising bioactive material for nanomedicine development for liver cancer treatment. (C) 2015 Elsevier B.V. All rights reserved.
机译:这项研究的目的是开发星形共聚物甘露醇官能化的PLGA-TPGS的纳米颗粒(NPs),用于Genistein传递以治疗肝癌,并评估它们在肝癌细胞系和荷瘤肝癌裸鼠中的治疗效果。与线性PLGA纳米颗粒和PLGA-TAGS纳米颗粒进行比较。通过改进的纳米沉淀法制备的染料木黄酮负载的M-PLGA-TPGS纳米颗粒(MPTN)通过FESEM和TEM观察到呈近球形,尺寸分布狭窄。根据其尺寸,尺寸分布,表面电荷,载药量,包封效率和体外药物释放曲线进一步表征了纳米颗粒。数据显示,发现M-PLGA-TPGS纳米颗粒稳定,在水溶液保存3个月期间,粒径和表面电荷几乎没有变化。体外金雀异黄素从纳米颗粒的释放表现出双相模式,在最初的4天突然释放,然后持续释放。荧光M-PLGA-TPGS纳米粒子的细胞吸收效率分别是100、250和500 [ig / mL]纳米粒子时PLGA-TPGS纳米粒子的1.25、122和1.29倍。 MPTN组凋亡细胞的比例随药物剂量的增加而增加,与Genistein溶液组相比,具有剂量依赖性,差异有统计学意义(p <0.05)。数据还表明,在体外和体内,染料木黄酮负载的M-PLGA-TPGS纳米粒子比线性PLGA-TPGS纳米粒子和PLGA纳米粒子具有更高的抗肿瘤功效。总之,星形共聚物M-PLGA-TPGS可以用作潜在且有前途的生物活性材料,用于肝癌治疗的纳米药物开发。 (C)2015 Elsevier B.V.保留所有权利。

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