期刊文献+

水飞蓟宾自乳化制剂对CCl_4所致肝损伤的保护作用 被引量:5

Protective Effects of Silybin Self-emulsifying Drug Delivery Systems on Acute Liver Injury Induced by CCl_4
原文传递
导出
摘要 目的探讨水飞蓟宾自乳化制剂对CCl4所致急性肝损伤的保护作用。方法以CCl4所致小鼠急性肝损伤为模型,以生理盐水为阴性对照,以联苯双酯为阳性对照,以水飞蓟宾混悬剂为参比,以血清中谷丙转氨酶(ALT)、谷草转氨酶(AST)和肝脏中谷胱甘肽过氧化物酶(GSH-PX)活性及肝脏病理组织切片检查为指标,对比研究水飞蓟宾自乳化制剂对CCl4所致急性肝损伤的保护作用。结果水飞蓟宾自乳化制剂能显著的抑制CCl4所致的血清ALT和AST活性升高,使肝脏中的GSH-PX维持在正常水平,保护肝脏并避免其发生严重病变。结论水飞蓟宾自乳化制剂对CCl4所致急性肝损伤有保护作用。 OBJECTIVE To explore the protective effects of silybin self-emulsifying drug delivery systems on acute liver injury induced by CCl4. METHODS Saline and bifendate were selected as negative and positive control, respectively. The protective effects of silybin self-emulsifying drug delivery systems on acute liver injury induced by CCl4 was evaluated by the levels of ALT and AST in plasma, glutathione peroxidase in liver and liver histopathology, and compared with silybin suspension. RESULTS Silybin self-emulsifying drug delivery systems inhibited the increase of the ALT and AST in serum markedly, maintained the normal level of GSH-PX in liver and protect liver from lesion. CONCLUSION Silybin self-emulsifying drug delivery system has protectived effect on acute liver injury induced by CCl4.
出处 《中国现代应用药学》 CAS CSCD 2016年第8期1006-1009,共4页 Chinese Journal of Modern Applied Pharmacy
关键词 水飞蓟宾 自乳化 四氯化碳 急性肝损伤 silybin self-emulsifying drug delivery systems CCl4 acute liver injury
  • 相关文献

参考文献1

二级参考文献22

  • 1Sallee VL, Dietschy JM. Determinants of intestinal mucosal uptake of medium-chain fatty acids and alcohols. J Lipid Res 1973; 14: 475- 84.
  • 2Westergaard H, Dietschy JM. The mechanism whereby bile acid micelles increase the rate of fatty acid and cholesterol uptake into the intestinal mucosal cell. J Clin Invest 1976; 58: 97-108.
  • 3Wilson, FA. Intestinal transport of bile acids. Am J Physiol 1981; 241: G83-G92.
  • 4O'Reilly JR, Corrigan OI, O'Driscoll CM. The effect of mixed micellar systems, bile acid/fatty acids, on the solubility and intestinal absorption of clofazimine (B663) in the anesthetized rat. Int J Pharm 1994; 109: 147-94.
  • 5Garidel P, Hildebrand A, BlumeA. Membranolytic activity of bile salts: Influence of biological membrane properties and composition. Molecules 2007; 12: 2292-326.
  • 6Dangi JS, Vyas SP, Dixit VK. Effect of various lipid-bile salt mixed micelles on transfer of amphotericin-B across the everted rat intestine. Drug Dev Ind Pharm 1995; 21: 2021-7.
  • 7Wiedmann TS, Kamel L. Examination of the solubilization of drugs by bile salt micelles. J Pharm Sci 2002; 91: 1743-64.
  • 8Wiedmann TS, Liang W, Kamel L. Solubilization of drugs by physiological mixtures of bile salts. Pharm Res 2002; 19: 1203-8.
  • 9Hammad MA, Muller BW. Increasing drug solubility by means of bile salt-phosphatidylcholine-based mixed micelles, Eur J Pharm Biopharm 1998; 46: 361-7.
  • 10Dongowski G, Fritzsch B, Giessler J, Hartl A, Kuhlmann O, Neubert RHH. The influence of bile salts and mixed micelles on the pharmacokinetics of quinine in rabbits. Eur J Pharm Biopharm 2005; 60: 147-51.

共引文献11

同被引文献54

引证文献5

二级引证文献43

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部