期刊文献+

盐酸丁卡因离子导入凝胶的研究 被引量:3

Influence of current on tetracaine hydrochloride jel transdermal iontophoresis
下载PDF
导出
摘要 目的研究电流强度对盐酸丁卡因离子导入凝胶的渗透速率的影响。方法以盐酸丁卡因为模型药物,采用离子导入作为促透方法,分别测定不同电流强度下的盐酸丁卡因离子导入凝胶在离子导入后接受室溶液的吸收度,计算它们的稳态透皮速率。结果电流强度为0.05,0.1,0.15,0.2和0.25mA时,稳态透皮速率分别为10.18,22.94,34.62,41.60和51.35μg/cm2×h。结论在一定的电流强度下,漏槽条件下,盐酸丁卡因离子导入凝胶渗透速率与电流强度有较好的线性关系。 OBJECTIVE To investigate the effect of current on drug transdermal iontophoresis flux of jel. METHODS Tetracaine hydrochloride was employed as model drug, The iontophorefie flux of tetracaine hydroehloride jel through rat skin was investigated using modified Franz one-chamber diffusion ceils. RESULTS When the current strength of iontophoresis was 0.05mA,0.1mA,0. 15 mA, 0.2mA and 0.25 mA, the iontophoretic flux of tetracaine hydrochloride jel were 10.18,22.94,34.62,41.60 and 51.35 ( g/cm^2 × h respectively. CONCLUSION The iontophoretic flux of jel is proportional to the applied current density.
作者 胡珏 许东航
出处 《中国现代应用药学》 CAS CSCD 北大核心 2006年第4期307-308,共2页 Chinese Journal of Modern Applied Pharmacy
基金 浙江省药剂专业委员会医院药学基金资助
关键词 盐酸丁卡因 离子导入 凝胶 电流强度 渗透速率 tetracaine hydrochloride iontophoresis jel current iontophoretic flux
  • 相关文献

参考文献7

二级参考文献12

共引文献38

同被引文献29

  • 1朱姚亮,刘卫,陈华兵,杨祥良.多肽蛋白质类药物离子导入经皮给药的研究进展[J].中国新药杂志,2005,14(12):1394-1400. 被引量:4
  • 2高见曙,高建青,张丽菊.药物经皮离子电渗的影响因素[J].中国药学杂志,1996,31(1):6-9. 被引量:19
  • 3黄磊.促进药物透皮吸收的方法及应用前景[J].中国药业,2006,15(21):62-63. 被引量:4
  • 4Shoji T, Emoto M, Tabata T. Advanced atherosclerosis in pred- ialysis patients with chronic renal failure [J ]. Kidney Int, 2002, 61(6): 2187-2192.
  • 5Karande P, Mitragotri S. Enhancement of transdermal drug deliv- ery via synergistic action of chemicals[J ]. Biochim Biophys A cta, 2009, 1788( 11 ) : 2362-2373.
  • 6Babu RJ, Pandit JK. Effect of penetration enhancers on the rele- ase and skin permeation of bupranolol from reservoir-type transd- ermal delivery systems [J]. Int JPharrn, 2005, 288(2) : 325-334.
  • 7Dubey V, Mishra D, Asthana A, et all. Transdermal delivery of a pineal hormone: melatonin via elastic liposomes [J]. B/ornat, 2006, 27(18) : 3491-3496.
  • 8Maghraby GME. Transdermal delivery of hydroeortisone from euc- alyptus oil microemulsion: effects of cosurfactants[J]. lnt J Pharm, 2008, 355(1/2) : 285-292.
  • 9Cevc G, Vierl U. Nanotechnology and the transdermal route: a state of the art review and critical appraisal [J]. J Control Release, 2010, 141(3): 277-299.
  • 10Zhang L, Li L, An Z, et al. In vivo transderrnal delivery of large molecules by pressure-mediated electroincorporation and electrop- oration: a novel method for drug and gene delivery [J]. Bioele- ctrochem Bioenerg, 1997, 42( l ) : 283-292.

引证文献3

二级引证文献7

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