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硝酸异山梨酯浓度对其从黏附基质制剂透皮性能的影响。

Influence of isosorbide dinitrate concentration on its skin permeability from adhesive matrix devices.

作者信息

Hatanaka T, Oguchi M, Sugibayashi K, Morimoto Y

机构信息

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

出版信息

Chem Pharm Bull (Tokyo). 1991 Jul;39(7):1802-5. doi: 10.1248/cpb.39.1802.

Abstract

Adhesive matrix devices containing a model drug, isosorbide dinitrate (ISDN), were prepared with three different types of pressure sensitive adhesives (PSAs). ISDN permeation through excised hairless rat skin from the different devices was measured in vitro. For each PSA type, the steady state permeation rate of ISDN increased proportionally with an increase of ISDN concentration in the PSA and reached a maximum level at a certain concentration. Although the concentrations reaching the maximum skin permeation level varied among PSA types, the maximum rate for each PSA type was largely similar to that for ISDN aqueous suspension. The release rate of ISDN from devices was too fast to influence the skin permeation rate for all devices. In the PSA of devices showing maximum skin permeability, ISDN crystalline was observed by polarizing microscopy and differential scanning calorimetry. These results suggest that the skin permeation of ISDN from adhesive matrix devices was controlled by the thermodynamic activity of the drug in the PSAs.

摘要

使用三种不同类型的压敏胶(PSA)制备了含有模型药物硝酸异山梨酯(ISDN)的黏附基质装置。在体外测量了不同装置中ISDN透过切除的无毛大鼠皮肤的渗透情况。对于每种PSA类型,ISDN的稳态渗透速率随PSA中ISDN浓度的增加而呈比例增加,并在一定浓度下达到最大值。尽管达到最大皮肤渗透水平的浓度因PSA类型而异,但每种PSA类型的最大速率与ISDN水悬浮液的最大速率大致相似。所有装置中ISDN从装置的释放速率都太快,以至于不会影响皮肤渗透速率。在显示出最大皮肤渗透性的装置的PSA中,通过偏光显微镜和差示扫描量热法观察到了ISDN晶体。这些结果表明,黏附基质装置中ISDN的皮肤渗透受药物在PSA中的热力学活性控制。

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