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多次表皮给药后双氯芬酸的透皮渗透情况。

Transdermal penetration of diclofenac after multiple epicutaneous administration.

作者信息

Müller M, Rastelli C, Ferri P, Jansen B, Breiteneder H, Eichler H G

机构信息

Department of Clinical Pharmacology, University of Vienna, Austria.

出版信息

J Rheumatol. 1998 Sep;25(9):1833-6.

PMID:9733468
Abstract

OBJECTIVE

To test whether therapeutic diclofenac concentrations are attained in skeletal muscle tissue beneath the application site of an epicutaneously administered diclofenac foam formulation.

METHODS

Diclofenac foam (5%) was administered epicutaneously at the thigh 80 mg/200 cm2 twice daily for a period of 7 days in healthy volunteers (n=12). On Day 8, 2 microdialysis probes were inserted into skeletal muscle tissue beneath the application site and an 80 mg dose was administered epicutaneously. Concentration versus time profiles in plasma and skeletal muscle were followed for 10 hours.

RESULTS

Concentration versus time profiles were obtained for plasma and interstitial muscle fluid in all experiments. Mean Cmax in plasma was 18.75+/-4.97 ng/ml. Corresponding interstitial concentrations in skeletal muscle were significantly higher, 219.68+/-66.36 ng/ml (p=0.01). Plasma concentrations were not correlated to tissue concentrations (r=-0.08).

CONCLUSION

There is significant direct penetration of diclofenac into skeletal muscle following multiple epicutaneous administration. However, the concentration attained in individual subjects is not predictable and may be strongly influenced by individual skin properties.

摘要

目的

测试经皮给药双氯芬酸泡沫制剂应用部位下方的骨骼肌组织中是否能达到治疗性双氯芬酸浓度。

方法

在12名健康志愿者的大腿处经皮给予双氯芬酸泡沫(5%),剂量为80mg/200cm²,每日两次,持续7天。在第8天,将2个微透析探头插入应用部位下方的骨骼肌组织,并经皮给予80mg剂量。监测血浆和骨骼肌中浓度随时间的变化情况,持续10小时。

结果

在所有实验中均获得了血浆和肌间质液的浓度-时间曲线。血浆中的平均Cmax为18.75±4.97ng/ml。骨骼肌中相应的间质浓度显著更高,为219.68±66.36ng/ml(p=0.01)。血浆浓度与组织浓度不相关(r=-0.08)。

结论

多次经皮给药后,双氯芬酸可显著直接渗透到骨骼肌中。然而,个体受试者中达到的浓度不可预测,可能会受到个体皮肤特性的强烈影响。

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