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首页> 外文期刊>International journal of clinical pharmacology and therapeutics >In vitro investigations of drug release and penetration--enhancing effect of ultrasound on transmembrane transport of flufenamic acid.
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In vitro investigations of drug release and penetration--enhancing effect of ultrasound on transmembrane transport of flufenamic acid.

机译:药物释放和渗透的体外研究-超声波对氟芬那酸跨膜转运的增强作用。

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摘要

Although topical drugs are usually applied at a convenient site, the target for the drug interaction may be systemic. Phonophoresis is the use of ultrasound to enhance the delivery of topical applied drugs. The purposes of our study were to investigate the in vitro penetration and the in vivo transport of flufenamic acid in dependence of ultrasound. Percutaneous absorption studies are performed in various in vitro models to determine the rate of drug absorption via the skin. We designed a phonophoretic drug delivery system to investigate the influence of ultrasound on transmembrane transport of different drugs. We investigated the absorption of flufenamic acid in a buffer medium in dependence of ultrasound energy and application time. For evaluating membrane penetration of flufenamic acid, the concentration range of buffer solution was measured. Ultrasound energy was supplied for between 5 and 30 min at a range of intensities up to 1.5 W/cm2, energy levels commonly used for therapeutic purpose. The pronounced effect of ultrasound on the transmembrane absorption of the drug was observed at all ultrasound energy levels studied. The time of application was found to play an important role in delivery and transport of drug. Dependent on time, we observed a rise of temperature up to 4.5 degrees C. It appears that there was no difference between an intensity of 0.3 and 1.5 W/cm2 and the measured drug concentrations in solution. The highest penetration was observed at an intensity of 1.0 W/cm2 after 30 min. These results were not significantly different from concentration measurements after 30 min and 0.5 and 1.5 W/cm2. It seems that the arise of drug concentration is caused by effects of temperature and by variation of membrane delivery in dependence of temperature. Using this in vitro model we note it is possible to compare the transdermal penetration and absorption of commercial flufenamic ointment in volunteers.
机译:尽管局部用药通常在方便的地方使用,但药物相互作用的目标可能是全身性的。发声疗法是使用超声来增强局部应用药物的递送。我们研究的目的是研究氟苯那酸在超声中的体外渗透和体内转运。在各种体外模型中进行经皮吸收研究,以确定药物通过皮肤的吸收速率。我们设计了一种语音药物递送系统,以研究超声对不同药物跨膜转运的影响。我们研究了取决于超声能量和应用时间的缓冲液中氟虫酰胺酸的吸收。为了评估氟芬那酸的膜渗透性,测量了缓冲溶液的浓度范围。超声波能量以高达1.5 W / cm2的强度范围提供5至30分钟,这通常用于治疗目的。在研究的所有超声能量水平下,均观察到超声对药物跨膜吸收的明显影响。发现施用时间在药物的递送和运输中起重要作用。取决于时间,我们观察到温度升高到4.5摄氏度。似乎在0.3和1.5 W / cm2的强度与溶液中测得的药物浓度之间没有差异。 30分钟后观察到最高穿透强度为1.0 W / cm2。这些结果与30分钟,0.5和1.5 W / cm2后的浓度测量值没有显着差异。似乎药物浓度的升高是由于温度的影响以及取决于温度的膜递送的变化所引起的。使用该体外模型,我们注意到可以比较志愿者中商业氟苯胺软膏的透皮渗透和吸收。

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