RGD肽修饰的异长春花碱-粉防己碱脂质体的制备及体外抑瘤作用研究
x

请在关注微信后,向客服人员索取文件

篇名: RGD肽修饰的异长春花碱-粉防己碱脂质体的制备及体外抑瘤作用研究
TITLE:
摘要: 目的:制备RGD肽修饰的异长春花碱(VRB)-粉防己碱(TET)脂质体,研究其对脑胶质瘤C6细胞的抑制作用。方法:采用薄膜分散法和硫酸铵梯度法制备RGD肽修饰的VRB-TET脂质体,观察其形态和粒径分布,测定其中VRB的含量;以磺酰罗丹明B法分别测定空白靶向脂质体、VRB普通脂质体和RGD肽修饰的VRB-TET脂质体对C6细胞的抑制作用。结果:所制RGD肽修饰的VRB-TET脂质体呈圆球状或类圆球状,表面光滑,粒径为120 nm左右,其中VRB的平均含量为28.27 μg/mL(RSD=0.38%,n=3)。空白靶向脂质体对C6细胞生长无显著影响;RGD肽修饰的VRB-TET脂质体能明显抑制C6细胞生长,其作用后细胞存活率明显低于VRB普通脂质体(P<0.05)。结论:成功制得RGD肽修饰的VRB-TET脂质体,其具有明显的抑制C6细胞生长的作用。
ABSTRACT: OBJECTIVE: To prepare the vinorelbine-tetrandrine liposomes modified with RGD, and study the inhibitory effect on glioma C6 cells. METHODS: Film dispersion method and ammonium sulfate gradient method were used to prepare the vinorelbine-tetrandrine liposomes modified with RGD, and the morphology and particle size distribution were observed. The vinorelbine content was determined, and sulforhodamine B method was used to respectively determine the inhibitory effects of blank targeting liposomes, normal vinorelbine liposomes and vinorelbine-tetrandrine liposomes modified with RGD on C6 cells. RESULTS: The prepared vinorelbine-tetrandrine liposomes modified with RGD were spherical or almost spherical with smooth surface, and particle size was about 120 nm. The average content of vinorelbine was 28.27 μg/mL (RSD=0.38%, n=3). Blank targeting liposomes had no significant effect on the growth of C6 cells; vinorelbine-tetrandrine liposomes modified with RGD can obviously inhibit the growth of C6 cells, and cell viability after its effect was significantly lower than normal vinorelbine liposomes (P<0.05). CONCLUSIONS: Vinorelbine-tetrandrine liposomes modified with RGD are successfully prepared, and they show obvious inhibitory effects on the growth of C6 cells.
期刊: 2017年第28卷第25期
作者: 居瑞军,王晓敏,晁建平,程岚,李学涛
AUTHORS: JU Ruijun,WANG Xiaomin,CHAO Jianping,CHENG Lan,LI Xuetao
关键字: RGD肽;异长春花碱;粉防己碱;脂质体;体外抑瘤作用
KEYWORDS: RGD; Vinorelbine; Tetrandrine; Liposomes; in vitro antitumor effect
阅读数: 336 次
本月下载数: 3 次

* 注:未经本站明确许可,任何网站不得非法盗链资源下载连接及抄袭本站原创内容资源!在此感谢您的支持与合作!