Korean J Dermatol.
1997 Aug;35(4):702-711.
The Changes in the Skin Permeability Barrier and Epidermais of Hairless Mouse on Oleic Acid Treatment
- Affiliations
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- 1Department of Dermatology, Yonsei University, Wonju College of Medicine, Wonju, Korea.
- 2Department of Dermatology, Yonsei University, College of Medicine, Seoul, Korea.
Abstract
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BACKGROUND: The stratum corneum(SC) inhibits t,ransepidermal water loss and makes a permeability barrier against foreign materials, so strategies to overcome relative impermeability of the SC is very important in transdermal drug delivery. This includes occlusion, hydration, chemical permeation enhancers, iontophoresis and sonophoresis, Oleic acid, which is one of the cis-unsaturated fatty acid and chemical permeation enhancers, increases the permeability of the lipophilic molecules and polar miolecules through the SC. By spectrometry, calorimetry and the flux technique, the hypothesis that oleic acid does exist as a liquid within the SC lipids and enhances the transport of polar molecules across the SC by the formation of permeable interfacial defects within the SC lipid bilayers was suggested. Also, repeated application of oleic acid induces epidermal proliferation, hyperkeratosis and sebaceous gland hyperplasia', However the exact pathomechanism was not reported.
OBJECTIVE
We carried out some research to observe the mechanism by which oleic acid in creases transdermal drug delivery and the effect to the skin permeability barrier and epidermis by repeated application.
METHODS
In the repeated treatment group, hairless mice(6 to 8 weeks) were treated with oleic acid once a day for 7 days unilaterally, and in the single treatment group, only one time, Transepidermal water loss(TEWL) was checked at 24hour after 1, 3 and 7 days of treatment and at, 1 hour, 6 hours, 24 hours, 72 hours after single treatment. Biopsies were taken from treated and controlateral(control) sides immediately after the TEWL checks at each time for light microscopic(H & E stain) and electron microscopic studies.
RESULTS
In the repeated treatment group, TEWL was increased by day and epidermal proliferation and hyperkeratosis were also increased. In the single treatment group, TEWL was highly increased in the treated site at 1 hour after treatment and decreased with time. By electronmicroscope, we observed dilated lacunae, intrcellular lipid structural abnormalities and loss of normal calcium gradient.
CONCLUSION
The possible domains of the epidermis interacting with oleic acid as a penetration enhancer are the lacunae and liipid bilayer by EM. The suggested pathomechanism of the epidermal changes, epidermal proliferation and hyperkeratosis was increased DNA synthesis of epidermal cells by the loss of epidermal calcium gradient in chronic barrier impairment.