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使用体外扩散模型比较无毛大鼠和马阴茎黏膜中胸腺氧胺的渗透情况。

Comparison of thymoxamine permeation between hairless rat and horse penile mucous membrane using an in vitro diffusion model.

作者信息

Neau B, Lozano P, Gomond P, Roux J, Grislain L, Lambrey B

机构信息

Sarget Laboratories, Mérignac, France.

出版信息

Skin Pharmacol. 1994;7(3):121-9. doi: 10.1159/000211286.

Abstract

Moxisylyte (or thymoxamine) administered intracavernously is known to improve erection in organically impotent patients. Prior to drug administration by percutaneous route, we have to define its in vitro permeation parameters after application of thymoxamine on both rat skin and horse penile mucous membrane. 24 h after drug application, the percentages of thymoxamine which diffused through the penile mucous and the rat skin were 88 and 75%, respectively. Thymoxamine flux varied according to the biological membrane tested. With regard to the penile mucous membrane, a maximal flux (1,774 nmol.h-1.cm-2) was observed 2.5 h after drug application, whereas for the rat skin a maximal flux (657 nmol.h-1.cm-2) was noted at 3.5 h. Thymoxamine flux decreased rapidly in the penile mucous membrane. This decrease was slower when thymoxamine penetrated the rat skin; the difference could be due to a different morphology of the tested biological membranes. In contrast to the rat skin, the external keratinized layer was absent in the penile mucous membrane. In conclusion, the ability of thymoxamine to penetrate easily and rapidly the biological membrane, and particularly the penile mucous membrane, suggests that thymoxamine could reach the pharmacological target represented by the corpus cavernosum of the penis.

摘要

已知海绵体内注射莫西赛利(或百里胺)可改善器质性阳痿患者的勃起功能。在经皮给药之前,我们必须确定将百里胺应用于大鼠皮肤和马阴茎黏膜后其体外渗透参数。给药24小时后,透过阴茎黏膜和大鼠皮肤扩散的百里胺百分比分别为88%和75%。百里胺通量根据所测试的生物膜而有所不同。对于阴茎黏膜,给药2.5小时后观察到最大通量(1774 nmol·h-1·cm-2),而对于大鼠皮肤,在3.5小时时记录到最大通量(657 nmol·h-1·cm-2)。百里胺通量在阴茎黏膜中迅速下降。当百里胺渗透大鼠皮肤时,这种下降较慢;差异可能归因于所测试生物膜的不同形态。与大鼠皮肤不同,阴茎黏膜中不存在外部角质化层。总之,百里胺易于快速穿透生物膜,尤其是阴茎黏膜的能力表明,百里胺可能到达以阴茎海绵体为代表的药理学靶点。

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