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齐多夫定在大鼠和人体皮肤中的经皮给药增强

Enhanced transdermal delivery of zidovudine in rats and human skin.

作者信息

Seki T, Toeda C, Kawaguchi T, Juni K, Sugibayashi K, Morimoto Y

机构信息

Faculty of Pharmaceutical Sciences, Josai University, Saitama, Japan.

出版信息

Chem Pharm Bull (Tokyo). 1990 Nov;38(11):3086-9. doi: 10.1248/cpb.38.3086.

Abstract

Zidovudine (azidothymidine, AZT), a potent antiviral agent acting on acquired immunodeficiency syndrome virus, was examined with regard to permeation through rat and human skin. A steady state plasma concentration of AZT after transdermal application in rats estimated from both pharmacokinetics data after i.v. administration and penetration rate through excised rat skin from 10% oleic acid (OA) aqueous solution shows penetration about 85 times higher compared to that from 10% OA would be needed for therapeutic efficacy. A mixed-solvent system consisted of 5% Sefsol-318 (S-318), 10% OA, 10% N-methyl-2-pyrrolidone (MP), 20% propylene glycol (PG) and water showed promising characteristics as a vehicle in terms of permeability of AZT through excised rat skin. The maximum flux of 0.41 mumol/cm2/h was observed in excised human skin after application of a gel formulation including S-318, OA, MP and PG. The result suggests a possible use of the gel formulation to gain an effective plasma concentration in humans.

摘要

齐多夫定(叠氮胸苷,AZT)是一种作用于获得性免疫缺陷综合征病毒的强效抗病毒药物,我们对其透过大鼠和人类皮肤的渗透情况进行了研究。根据静脉注射给药后的药代动力学数据以及从10%油酸(OA)水溶液透过切除的大鼠皮肤的渗透率估算,大鼠经皮给药后AZT的稳态血浆浓度显示,其渗透率比治疗效果所需的10%OA溶液高出约85倍。由5%司氟舒318(S-318)、10%OA、10%N-甲基-2-吡咯烷酮(MP)、20%丙二醇(PG)和水组成的混合溶剂系统,就AZT透过切除的大鼠皮肤的渗透性而言,显示出作为载体的良好特性。在应用包含S-318、OA、MP和PG的凝胶制剂后,在切除的人类皮肤中观察到最大通量为0.41μmol/cm²/h。结果表明,该凝胶制剂有可能用于在人体中获得有效的血浆浓度。

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