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局部用类固醇生物利用度的优化:封闭条件下的渗透促进剂

Optimization of bioavailability of topical steroids: penetration enhancers under occlusion.

作者信息

Barry B W, Southwell D, Woodford R

出版信息

J Invest Dermatol. 1984 Jan;82(1):49-52. doi: 10.1111/1523-1747.ep12259101.

Abstract

The occluded vasoconstrictor assay was used to assess the effect of penetration enhancers on the topical bioavailability of a representative steroid, betamethasone 17-benzoate, with dimethylisosorbide (DMI) as a reference solvent. In the initial test, only N-methyl-2-pyrrolidone (NMP) increased the steroid bioavailability; acetone, dimethylformamide (DMF), 2-pyrrolidone (2-P), and 1-ethyl-2-pyrrolidone (EP) were equal to DMI, while propylene glycol (PG) and N,N-diethyl-m-toluamide (DEET) were poorer. Reocclusion showed that NMP and acetone established superior stratum corneum reservoirs; DMF, 2-P, EP, and PG were as effective as DMI but DEET was less effective. It was concluded that occlusive hydration and lack of thermodynamic control may have obscured the enhancing abilities of the solvents, 2-P, NMP, EP, DMF, and DEET induced erythema in some volunteers, although this was usually short-lived.

摘要

采用闭塞血管收缩测定法,以二甲基异山梨醇(DMI)作为参比溶剂,评估渗透促进剂对代表性甾体药物17 - 苯甲酸倍他米松经皮生物利用度的影响。在初始试验中,只有N - 甲基 - 2 - 吡咯烷酮(NMP)提高了甾体药物的生物利用度;丙酮、二甲基甲酰胺(DMF)、2 - 吡咯烷酮(2 - P)和1 - 乙基 - 2 - 吡咯烷酮(EP)与DMI相当,而丙二醇(PG)和N,N - 二乙基间甲苯甲酰胺(DEET)则较差。再次闭塞显示,NMP和丙酮形成了更好的角质层储库;DMF、2 - P、EP和PG与DMI效果相当,但DEET效果较差。得出的结论是,闭塞性水合作用和缺乏热力学控制可能掩盖了溶剂的增强能力,2 - P、NMP、EP、DMF和DEET在一些志愿者中引起了红斑,不过这种情况通常持续时间较短。

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