期刊文献+

利多卡因脂质体的初步研制及其质量评价 被引量:2

Preparation of Liposomal Lidocaine and It's Quality Evaluation
下载PDF
导出
摘要 目的研制利多卡因的一种缓释长效制剂—利多卡因脂质体,并对其制备工艺进行研究,且评价其质量。方法以磷脂、胆固醇为膜材,采用乙醚注入法和薄膜分散法制备利多卡因脂质体并对制剂的形态学、载药量及包封率等进行研究。结果利多卡因脂质体为乳白色、近透明的胶体溶液。光镜下呈双同心球体满视野。测得其包封率分别为22.7%和21.6%,结论乙醚注入法和薄膜分散法两种制备工艺所得的利多卡因脂质体无明显区别。 Objective To prepare a sustained-release formulalion of lidocaine-liposomal lidocaine, study the formulation and preparation of liposonmal lidocaine, and evaluate its qualily. Methods Soy phosphalidylcholine and cholesterol were used as liposome malerials. Liposomes were prepared through ether injeetion method and film dispersion method. The morphology of liposomal lidocaine, the drug loading and the entrapment efficiency were studied. Results Liposomes were microscopie spheres that consis of a phospholipid bilaver that encapsulates an aqueous core. The pereentage of apparently entrapped lidocaine were 22.7% and 21.6% respectivcly. Conclusion There were no ohvious differences between liposomes prepared through the two methods.
出处 《潍坊医学院学报》 2005年第5期339-341,i0001,共4页 Acta Academiae Medicinae Weifang
关键词 利多卡因 脂质体 缓释 质量评价 Lidoeaine Liposomes Sustained-release Quality evaluation
  • 相关文献

参考文献5

  • 1国家药典委员会.中华人民共和国药典[S]第2部[M].北京:化学工业出版社,2000.附录26-27.
  • 2Dyhre H,Wallin R,Bjorkman S,et al.Inclusion of lignocaine base into a polar lipid formulation-in vitro release,duration of peripheral nerve block and arterial blood concentrations in the rat[J].Acta Anaesthesiol Scand,2001,45(6):583~589.
  • 3赵建华,肖常思.丁哌卡因甘油溶液和水溶液在大鼠硬膜外腔的镇痛效应比较[J].中华麻醉学杂志,1996,16(3):129-130. 被引量:1
  • 4Mashimo T,Uchidal I,Pak M,et al.Prolongation of canine epidural anesthesia by liposome encapsulation of lidocaine[J].Anesth and Analg,1992,74(9):827~834.
  • 5张光杰.药物辅料应用技术[M].北京:中国医药科技出版社,1991.408-410.

二级参考文献2

  • 1刘俊杰,现代麻醉学,1987年
  • 2鲁纯新,中级医刊,1986年,5卷,21期,43页

共引文献4

同被引文献13

  • 1杨建平,蒋豪,吴珏.吗啡或苯哌利定和可乐定镇痛的相互加强作用[J].中华麻醉学杂志,1994,14(5):375-377. 被引量:4
  • 2王晓梅,唐星,何海冰.多囊脂质体的研究进展[J].中国新药杂志,2006,15(15):1243-1246. 被引量:17
  • 3Zhong H,Deng Y,Wang X,et al.Multivesicular liposome for-mulation for the sustained delivery of breviscapine[J].Int JPharm,2005,301(1-2):15-24.
  • 4Katre N V,Asherman J,Schaefer H,et al.Multivesicular lipo-some(DepoFoam)technology for the sustained delivery ofinsulin-like growth factor-Ⅰ(IGF-Ⅰ)[J].J Pharm Sci,1998,87(11):1341-1346.
  • 5Mantripragada S.A lipid based depot(DepoFoam-technology)for sustained release drug delivery[J].Prog Lipid Res,2002,41(5):392-406.
  • 6张光杰,主编.药物辅料应用技术.第1版.北京:中国医药科技出版社.1991.408.
  • 7Malinovsky JM, Benhamou D, Alafandy M , et al. Neurotoxicological assessment after intracistemal injection of liposomal bupivaeaine in rabbits. Anesth Analg, 1997,85: 1331-1336.
  • 8Mashimo T, Uchida I, Pak M, et al. Prolongation of canine epidural anesthesia by lipesome encapsulation of lidocaine. Anesth Analg, 1992,74: 827-834.
  • 9Vogel HC,Vogel WH,主编,杜冠华,译.药理学实验指南.第1版.北京:科学出版社,2001.471-472.
  • 10Mowat JJ, Mok MJ, MacLeod BA, et al. Lipesomal bupivacaine extended duration nerve blockade using large unilamellar vesicles that exhibit a proton gradient. Anesthesiology, 1996,85: 635 -643.

引证文献2

二级引证文献9

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