期刊文献+

脂/水分配预测10-羟基喜树碱在大鼠小肠中的吸收

Prediction of absorption of 10-hydroxycamptothecin in small intestines of rats with its partition coefficients in phases of liposomes and water
原文传递
导出
摘要 目的:探讨脂质体/水(脂/水)相中的分配,预测10-羟基喜树碱(HCPT)在大鼠小肠中吸收的可行性。方法:采取在体小肠吸收模型,研究不同pH条件下HCPT在大鼠小肠中的吸收;采取平衡透析法检测不同pH条件下药物在脂质体/水相中分配系数;探讨HCPT在脂质体/水相中分配与药物的在体吸收的相关性。结果:HCPT在脂质体/水相中的分配及在体小肠吸收随外界环境pH的不同而改变,两者相关性良好。结论:用脂质体/水相中的分配可以预测HCPT在大鼠小肠中的吸收。 This paper explore the possibility of using the partition of 10-hydroxycamptothecin in the phases of lipesome and water to predict the absorption of the drug in small intestine of rats. In order to certify this theory, the in vivo absorption model have been used to study the absorption of 10-hydroxycamptothecin in the small intestine of rats while altering the pH of the medium. The correlation has been explored between the partition of drug in the phases of liposome and water and the absorption of drug in the small intestines of rats. And it was found that the partition of 10-hydroxycamptothecin in the phases of liposome and water and the absorption of the drug in small intestines of rats altered with the changes of pH, and there existed a good relative coefficient between them. All of these indicated that partition of 10-hydroxycamptothecin in phases of lipesome and water can be used to predict its absorption in small intestines of rats.
出处 《中国中药杂志》 CAS CSCD 北大核心 2010年第3期378-380,共3页 China Journal of Chinese Materia Medica
基金 广东药学院"重点培养青年教师"基金项目(200809052)
关键词 10-羟基喜树碱 脂质体/水相 小肠吸收 10-hydroxycamptothecin phases of liposome/water absorption in small intestines
  • 相关文献

参考文献9

  • 1Beigi F, Cottschalk I, Lagerguist H, et al. Immobilized liposome and biomembrane partitioning chromatography of drugs for prediction of drug transport [J]. Int J Pharm, 1998, 164: 129.
  • 2Ong S, Liu H, Pedgeon C. Immobilized-artificial-membrane chromatography measurement of membrane partition coefficient and predicting drug membrane permeability[J ]. J Chromatogr A, 1996, 728: 113.
  • 3Balon K, Riebesehl B U, Muller B W. Drug liposome partitioning as a tool for the prediction of human passive intestinal absorption [J]. Pharm Res, 1999, 16(6) : 882.
  • 4王安训,李苏,丁学强,陈宇,陈丹.开环及闭环羟基喜树碱对口腔鳞癌细胞株抗癌作用的研究[J].癌症,2005,24(8):970-974. 被引量:4
  • 5Pauletti G M, Wunderli-Allenspach H. Partition coefficients in vitro: Artificial membranes as a standardized distribution model [J]. EurJ Pharm Sci, 1994, 1: 273.
  • 6Huang C, Mason J T. Geometric packing constraints in egg phosphatidylcholine vesicles[ J]. Proc Natl Acad Sci, 1978, 75 : 308.
  • 7张徐宁,丁建花,刘苏怡,刘强,范益,胡刚.高效液相色谱法测定犬全血中两种基喜树碱活性成份[J].中国临床药理学与治疗学,2004,9(10):1179-1182. 被引量:7
  • 8王淑丽,陈济民.苏子油乳剂小肠吸收动力学研究[J].沈阳药科大学学报,2000,17(1):1-4. 被引量:10
  • 9刘璐,崔景斌,方洪壮.替硝唑大鼠小肠吸收的研究[J].中国医院药学杂志,2003,23(1):4-6. 被引量:21

二级参考文献41

  • 1储晓岩,陈济民.γ-亚麻酸甲酯乳剂小肠吸收动力学研究[J].沈阳药学院学报,1994,11(1):5-11. 被引量:4
  • 2崔景斌,吴文惠,胡晋.拉马宁碱大鼠小肠吸收的研究[J].沈阳药学院学报,1994,11(2):79-82. 被引量:12
  • 3王淑丽,陈济民.苏子油与a-亚麻酸[J].沈阳药科大学学报,1995,12(3):228-233. 被引量:45
  • 4姚崇舜 张汝华.鸦胆子油静脉乳剂的研究[J].沈阳药学院学报,1979,11:1-6.
  • 5毛凤斐 屠锡德.贡苓甙大鼠小肠吸收研究[J].南京药学院学报,1984,15(1):61-69.
  • 6孟娟如.大白鼠颈静脉及肝门静脉持久性导管术及其应用[J].药学学报,1987,22(5):326-329.
  • 7蒋雪涛.生物药剂学[M].北京:解放军出版社,1985.472-508.
  • 8Wilsion TH 王复周(译).小肠的吸收[M].北京:科学出版社,1973.176-183.
  • 9陆彬.药剂学试验[M].北京:人民卫生出版社,1997.132.
  • 10[2]Christian B. Homocamptothecins:potent topoisomerase I inhibitors and promising anticancer drugs[J]. Crit Rev Oncol Hematol, 2003 ;45( 1 ) :91 - 108

共引文献37

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