李娜梅,杨飒,宁倩,黄灿,黄文,贺子宁,贺冬秀,喻翠云.半乳糖化壳聚糖—氟尿嘧啶偶合物纳米给药体系的制备、表征及体外性能研究[J].南华大学学报(自然科学版),2015,29(3):82~86, 91.[LI Na-mei,YANG Sa,NING Qian,HUANG Can,HUANG Wen,HE Zi-ning,HE Dong-xiu,YU Cui-yun.Fabrication,Characterization and in Vitro Performance Evaluation of GC-FUA Based Nanoparticles Delivery System[J].Journal of University of South China(Science and Technology),2015,29(3):82~86, 91.]
半乳糖化壳聚糖—氟尿嘧啶偶合物纳米给药体系的制备、表征及体外性能研究
Fabrication,Characterization and in Vitro Performance Evaluation of GC-FUA Based Nanoparticles Delivery System
投稿时间:2015-03-10  
DOI:
中文关键词:  GC-FUA纳米给药体系  5-Fu  缓释  HepG2
英文关键词:GC-FUA nano-delivery systems  5-Fu  sustained release  HepG2
基金项目:国家自然科学基金资助项目(81471177);湖南省科学技术厅基金资助项目(2014GK3082);南华大学抗肿瘤药物创新团队;南华大学青年英才计划
作者单位
李娜梅 南华大学 药物药理研究所,湖南 衡阳 421001 
杨飒 南华大学 药物药理研究所,湖南 衡阳 421001 
宁倩 南华大学 药物药理研究所,湖南 衡阳 421001 
黄灿 南华大学 药物药理研究所,湖南 衡阳 421001 
黄文 南华大学 药物药理研究所,湖南 衡阳 421001 
贺子宁 南华大学 药物药理研究所,湖南 衡阳 421001 
贺冬秀 南华大学 药物药理研究所,湖南 衡阳 421001 
喻翠云 南华大学 药物药理研究所,湖南 衡阳 421001 
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中文摘要:
      以预先合成的半乳糖化壳聚糖—氟尿嘧啶偶合物(GC-FUA)为原料,采用离子交联法制备出了GC-FUA纳米给药体系,并结合单因素分析法筛选出其最佳制备条件为GC-FUA浓度2.0 mg/mL,TPP浓度1.0 mg/mL,pH值4.5,GC-FUA/TPP质量比12∶1.应用SEM、UV等表征该纳米给药体系多呈球形,大小较均一,且具有缓释性能;采用 MTT 法观察 5-Fu、物理包封5-Fu GC纳米粒子、GC-FUA纳米粒子对HepG2细胞的增殖抑制作用.结果表明三者对 HepG2细胞的增殖具有明显抑制作用,且呈剂量依赖性,GC-FUA纳米粒子作用较 5-Fu和物理包封5-Fu GC纳米粒子明显增强.
英文摘要:
      In this experiment,N-galactosylated-chitosan-5-fluorouracil acetic acid conjugate (GC- FUA) which we previously synthesized nanoparticles,were produced by ionic crosslinking method based on modified ionic gelation of tripolyphosphate (TPP) with GC-FUA.The effects of GC-FUA concerntration,TPP concerntration,pH value,etc.on the preparation of GC-FUA nanoparticles were evaluated.And results were when GC-FUA concerntration was 2.0 mg/mL,TPP concerntration was 1.0 mg/mL,pH value was 4.5,GC-FUA/TPP mass ratio was 12∶1,opalescent solution of stable GC-FUA nanoparticles could be easily obtained.GC-FUA nanoparticles exhibited regularly spherical shapes,with a smooth surface and uniform size,and has a slow release properties which were confirmed by SEM and Nano ZS.Cytotoxicity study (MTT) in HepG2 cell lines demonstrated that the resulting GC-FUA nanoparticles were more potent in killing cancer cells,compared to free 5-fluorouracil (5-Fu) and 5-Fu-loaded GC nanoparticles.
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