케토프로펜의 경피전달 및 전기삼투압의 영향Transdermal Delivery of Ketoprofen and the Effect of Electroosmosis
- Other Titles
- Transdermal Delivery of Ketoprofen and the Effect of Electroosmosis
- Authors
- 오승열
- Issue Date
- Dec-2004
- Publisher
- 한국약제학회
- Keywords
- Ketoprofen; pH; poly (L-lysin); Electroosmotic flow
- Citation
- Journal of Pharmaceutical Investigation, v.34, no.6, pp 491 - 497
- Pages
- 7
- Journal Title
- Journal of Pharmaceutical Investigation
- Volume
- 34
- Number
- 6
- Start Page
- 491
- End Page
- 497
- URI
- https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/9296
- ISSN
- 2093-5552
2093-6214
- Abstract
- We investigated some important factors which affect the transdermal flux of ketoprofen, a nonsteroidal anti-inflammatory agent, as a first step to provide some basic knowledge for the development of a iontophoretic transdermal patch system. Factors such as current density, polarity, buffer (HEPES) and electrolyte concentration and pH were studied using hairless mouse skin. The effect of poly(L-lysin), which is known to affect the electro-osmotic flow through skin, on flux was also studied. Passive flux was about 20mg/cm2hr at pH 4.0, but was negligible at pH 7.4 where all ketoprofen molecules dissolved are ionized (ketoprofen pKa=5.94). At pH 4.0, application of anodal current increased the flux further above the passive level, however anodal flux at pH 7.4 was much smaller than passive flux at pH 4.0. The application of cathodal current at pH 4.0 increased the average flux to 30-40mg/cm2hr, depending on the current density applied. At pH 7.4, cathodal flux was only about 5mg/cm2hr. Decrease in buffer and electrolyte concentration increased this cathodal flux about 10 fold. However decrease in HEPES buffer concentration 100 fold did not affect the flux. Anodal flux of acetaminophen was much larger than cathodal flux, indicating that electroosmotic flow can be playing an important role in the flux. Poly(L-lysin) increased the cathodal flux at pH 7.4. These results provide some important insights into the mechanism of transdermal flux of ketoprofen and the role of electroosmotic flow.
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