Chiang C H, Chen J L, Liu Y T, Wang D P
School of Pharmacy, National Defense Medical Center, Taipei, Taiwan.
Drug Dev Ind Pharm. 1998 Mar;24(3):213-7. doi: 10.3109/03639049809085612.
Ketotifen transdermal delivery systems were prepared using polyisobutylene, liquid paraffin, and fatty acid. In vitro skin penetration studies were conducted in Franz diffusion cells using excised porcine skin to determine the skin permeation rates of ketotifen patches. A trend of increased skin penetration of ketotifen was observed as the amount of liquid paraffin in the patch was increased. In addition, we found that lauric acid was a suitable enhancer for percutaneous absorption of ketotifen. Challenge tests were performed in guinea pigs to determine the therapeutic effect of the delivery systems for the inhibition of anaphylactic shock using varied concentrations of chicken ovum albumin as sensitizer. Our results showed that compared with the treatment of intramuscular administration, the skin patch was more effective and produced higher survival rates. The pharmacokinetics of the ketotifen patch were determined by applying the skin patch to the dorsal skin of rabbits. The plasma levels were maintained constant (42.5-36.4 ng/ml) from 9 to 30 hr. From our study, the prepared ketotifen patch may further be developed for the treatment or prevention of allergic asthma.
使用聚异丁烯、液体石蜡和脂肪酸制备了酮替芬透皮给药系统。在Franz扩散池中使用切除的猪皮进行体外皮肤渗透研究,以确定酮替芬贴片的皮肤渗透速率。随着贴片中液体石蜡量的增加,观察到酮替芬皮肤渗透增加的趋势。此外,我们发现月桂酸是酮替芬经皮吸收的合适促进剂。在豚鼠中进行激发试验,以确定使用不同浓度的鸡卵白蛋白作为致敏剂的给药系统对抑制过敏性休克的治疗效果。我们的结果表明,与肌肉注射治疗相比,皮肤贴片更有效且生存率更高。通过将皮肤贴片应用于兔背部皮肤来确定酮替芬贴片的药代动力学。血浆水平在9至30小时内保持恒定(42.5 - 36.4 ng/ml)。根据我们的研究,制备的酮替芬贴片可能会进一步开发用于治疗或预防过敏性哮喘。