基础医学与临床 ›› 2014, Vol. 34 ›› Issue (11): 1548-1552.

• 研究论文 • 上一篇    下一篇

转铁蛋白修饰共载阿霉素与蒽贝素脂质体的构建及其体外评价

权毅   

  1. 泸州医学院 附属医院
  • 收稿日期:2014-03-31 修回日期:2014-05-30 出版日期:2014-11-05 发布日期:2014-11-03
  • 通讯作者: 权毅 E-mail:1187718581@qq.com

Preparation and in vitro Anti-tumor Activity of doxorubicin and embelin co-loaded Liposomes Decorated with transferrin

  • Received:2014-03-31 Revised:2014-05-30 Online:2014-11-05 Published:2014-11-03

摘要: 目的 研究转铁蛋白修饰共载阿霉素(DOX)和蒽贝素的脂质体(TFLP-DOX/EB)与乳腺癌细胞的亲和力和增殖抑制作用。方法 后插入法制备转铁蛋白修饰共载阿霉素和蒽贝素脂质体(TFLP-DOX/EB)。细胞摄取法检测细胞对普通脂质体(LP)和转铁蛋白修饰脂质体(TFLP)的摄取。将MCF-7细胞分为TFLP-DOX/EB组、TFLP-DOX组、TFLP-EB组、LP-DOX/EB组和PBS组,MTT检测细胞的增殖。构建乳腺癌MCF-7细胞肿瘤球模型,激光共聚焦显微镜检测脂质体的肿瘤球穿透能力和肿瘤球的生长。结果 MCF-7细胞对TFLP的摄取效率是LP的3.2倍(P<0.01);给药48 h后,TFLP-DOX/EB 对MCF-3细胞的抑制率分别是TFLP-DOX、TFLP-EB和LP-DOX/EB、的1.95倍、2.43倍和2.75倍(P<0.01)。TFLP-DOX/EB具有良好的肿瘤球穿透作用和肿瘤球生长抑制作用(P<0.01)。结论 铁蛋白修饰共载阿霉素和蒽贝素脂质体是一种潜在高效的乳腺癌靶向给药系统。

关键词: 转铁蛋白, 阿霉素, 蒽贝素, 肿瘤靶向

Abstract: Objective To prepare TF conjugated doxorubicin and embelin loaded liposome and evaluate their properties and effect on the treatment of breast cancer. Methods The liposomes were prepared by thin film hydration method. The efficiency of cellular uptake on MCF-7 cells in vitro was evaluated. The anti-proliferation efficiency of TFLP-DOX/EB was evaluated by MTT assay. Tumor spheroids were used to evaluate anti-tumor ability of TF-LP-DOX/EB. Results The result demonstrated that TFLP uptaken by MCF-7 were 3.2 times higher than that of LP(P<0.01). The MTT assay and the inhibition of tumor spheroids in vitro confirmed strong inhibitory effect of TFLP-DOX/EB. Conclusion TFLP-DOX/EB were easy to prepare and it is a potential delivery system for the treatment of breast cancer.

Key words: transferrin, doxorubicin, embelin, tumor targeting