载姜黄素壳聚糖/聚(丁基氰基丙烯酸酯)纳米粒的合成及体内外抗肿瘤活性评价。

Synthesis and in vitro/in vivo anti-cancer evaluation of curcumin-loaded chitosan/poly(butyl cyanoacrylate) nanoparticles.

机构信息

Key Laboratory of Nanobiological Technology, Ministry of Health National Hepatobiliary and Enteric Surgery Research Center, Central South University, Changsha, Hunan 410008, PR China.

出版信息

Int J Pharm. 2010 Nov 15;400(1-2):211-20. doi: 10.1016/j.ijpharm.2010.08.033. Epub 2010 Sep 8.

Abstract

We have synthesized novel cationic poly(butyl) cyanoacrylate (PBCA) nanoparticles coated with chitosan, formulation of curcumin nanoparticles. The size and zeta potential of prepared curcumin nanoparticles were about 200 nm and +29.11 mV, respectively with 90.04% encapsulation efficiency. The transmission electron microscopy (TEM) study revealed the spherical nature of the prepared nanoparticles along with confirmation of particle size. Curcumin nanoparticles demonstrate comparable in vitro therapeutic efficacy to free curcumin against a panel of human hepatocellular cancer cell lines, as assessed by cell viability (3-[4,5-dimethylthiazol-2-yl]2,5-diphenyltetrazolium bromide assay [MTT assay]) and proapoptotic effects (annexin V/propidium iodide staining). In vivo, curcumin nanoparticles suppressed hepatocellular carcinoma growth in murine xenograft models and inhibited tumor angiogenesis. The curcumin nanoparticles' mechanism of action on hepatocellular carcinoma cells is a mirror that of free curcumin.

摘要

我们合成了新型阳离子聚(丁基)氰基丙烯酸酯(PBCA)纳米粒子,其表面覆盖壳聚糖,可用于包载姜黄素纳米粒子。制备的姜黄素纳米粒子的粒径和 zeta 电位分别约为 200nm 和+29.11mV,包封率为 90.04%。透射电子显微镜(TEM)研究表明,所制备的纳米粒子具有球形性质,并证实了粒径。通过细胞活力(3-[4,5-二甲基噻唑-2-基]-2,5-二苯基四氮唑溴化物(MTT 测定)和促凋亡作用( Annexin V/碘化丙啶染色)评估,姜黄素纳米粒子对一系列人肝癌细胞系的体外治疗效果与游离姜黄素相当。在体内,姜黄素纳米粒子抑制了小鼠异种移植模型中的肝癌生长并抑制了肿瘤血管生成。姜黄素纳米粒子对肝癌细胞的作用机制与游离姜黄素相似。

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