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角质层与真皮层对氟尿嘧啶贴剂经皮吸收的影响 被引量:3

Influence of the stratum corneum and dermis of the skin on the percutaneous absorption of fluorouracil delivered through skin patch
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摘要 目的 比较皮肤角质层和真皮层及促透剂对药物经皮吸收的影响。方法 制备氟尿嘧啶(5-FU)贴剂为模型药剂,以肉豆蔻酸异丙酯(TPM)为促透剂,采用Franz扩散池法,用高效液相色谱法和气相色谱法分别检测5-FU和IPM浓度,计算5-FU在各种皮肤状态下的透皮能力(Kp)。结果剥离角质层后,5-FU的Kp是经完整皮肤的2.3倍;在IPM作用下5-FU的Kp为原来的1.8倍(经完整皮肤)和2.4倍(经剥离角质层皮肤)。结论剥离角质层能增加5-FU的吸收;IPM主要降低角质层对5-FU的屏障作用,在剥离角质层后其对5-FU的吸收也没有增加作用。 Objective To investigate the respective influence of skin layers, specifically the stratum corneum (SC) and the viable layer, and isopropyl myristate (IPM), an absorption enhancer, on the permeability (Kp) of drug. Methods Patches saturated with fluorouracil (5-FU), which was used as a test drug, were prepared. The Franz diffusion experiment via different rat skin layers was carried out, and high-performance liquid chromatography (HPLC) or gas chromatography (GC) was employed to determine the contents of 5-FU and IPM. Kp of 5-FU in various conditions was calculated. Results The Kp of 5-FU via SC -stripped skin was 2.3 times that via intact skin, and in the presence of IPM, Kp was 1.8 times that via intact skin and 2.4 times that via SC-stripped skin. Conclusion The permeability of 5-FU is enhanced after the SC is stripped, and IPM can overcome the barrier of SC in intact skin to facilitate 5-FU absorption, but can not enhance the Kp of 5-FU via SC-stripped skin.
出处 《第一军医大学学报》 CSCD 北大核心 2002年第9期800-802,共3页 Journal of First Military Medical University
关键词 角质层 真皮层 氟尿嘧啶 肉豆蔻酸异丙酸 药物吸收 促透剂 Franz扩散池法 高效液相色谱法 气相色谱法 fluorouracil isopropyl myristate pharmacon absorption, percutaneous absorption enhancer
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  • 1Adrian C. Williams,Brian W. Barry. Terpenes and the Lipid–Protein–Partitioning Theory of Skin Penetration Enhancement[J] 1991,Pharmaceutical Research(1):17~24 被引量:1

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  • 1匡秀华,苑丽,司红彬,胡功政.中药透皮吸收的研究进展[J].中国兽药杂志,2005,39(7):51-54. 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陈培丰.清洗型护发素研制探讨[J].福建轻纺,2007(4):1-4. 被引量:3
  • 4[4]Barry BW.Lipid-protein-partitioning theory of skin penetration enhancement[J].J Controlled Release, 1991,15(2):237. 被引量:1
  • 5[5]Michniak BB,Player MR,Godwin DA,et al.A study of enhancer structure activity relationships in a series of 2-oxopiperidine-l-acetic acid esters[J].Pharm Res, 1995,13(9):S268. 被引量:1
  • 6[6]Michniak BB,Player MR,Jett PE,et al. Topical delivery enhancement of hydrocortisone in hairless mouse skin using N-ycloheptyl amides[J].Pharm Res, 1995,13(9):S267. 被引量:1
  • 7[7]Michniak BB,Player MR,Godwin DA,et al. Investigation of miscellaneous Azone analagues as novel dermal penetration enhancers[J].Pharm Res, 1995,13(9):S268. 被引量:1
  • 8[8]Pfister WR,Rajadhyaksha VJ.Oxazolidinones:a new class of cyclic urethane transdermal enhancers (cute)[J].Pharm Res,1995,13(9):S280. 被引量:1
  • 9[13]Kunta JR,Khan MA,Reddy IK.Effect of menthol on permeability of an optically active and racemic propranolol across guinea pig skin[J].J Pharm Sci,1997,86(12):1369. 被引量:1
  • 10[15]Michniak BB,Player MR,Godwin DA,et al. Skin permeation kinetics of hydrocortisone 2.dermal enhancer/vehicle synergism effects[J].Pharm Res, 1995,13(9):S268. 被引量:1

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