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Journal of veterinary pharmacology and therapeutics2006; 29(1); 25-30; doi: 10.1111/j.1365-2885.2006.00705.x

Regional differences in the in vitro penetration of hydrocortisone through equine skin.

Abstract: Little is known about the transdermal penetration of hydrocortisone in the horse and, although commercial formulations containing hydrocortisone are registered for topical use in the horse, there have been no studies investigating the movement of this glucocorticoid through different regions of equine skin. Skin was harvested from the thorax, groin and leg (dorsal metacarpal) regions of five Thoroughbred geldings and frozen (-20 degrees C) until required. Defrosted skin was placed in Franz-type diffusion cells and the amount of radiolabelled ((3)H) hydrocortisone, in a saturated solution of unlabelled hydrocortisone in 50% ethanol (w/w), which penetrated through and remained within skin samples was measured over 24 h. Significantly higher (P < 0.001) maximum flux (J(max); mol/cm(2)/h) was measured when hydrocortisone was applied to skin from the leg, compared to thorax and groin, although significantly less hydrocortisone (P < 0.001) was retained within skin from the leg at 24 h. Topical application of hydrocortisone in a vehicle containing ethanol would penetrate faster through leg skin from the lower leg when compared with the thorax or groin, which depending on cutaneous blood flow, may result in higher systemic drug concentrations or greater efficiency in treating local inflamed tissue.
Publication Date: 2006-01-20 PubMed ID: 16420298DOI: 10.1111/j.1365-2885.2006.00705.xGoogle Scholar: Lookup
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  • Comparative Study
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This research investigates how the drug hydrocortisone penetrates the skin of horses in different body regions. The researchers found that the drug penetrates faster through skin on the leg but is retained less at this site compared to the thorax and groin areas.

Objective and Methodology

  • The study set out to address the lack of knowledge about the absorption and retention of the steroid hydrocortisone through different regions of horse skin. Commercial formulations of the drug are available for horses, but their absorption and retention have not been previously assessed. The researchers specifically looked at the thorax, groin, and leg regions.
  • To conduct the study, skin was taken from the aforementioned regions from five Thoroughbred geldings. The skin was then frozen until needed for the experiment.
  • The experiment used Franz-type diffusion cells to study the absorption and retention of the drug. The skin samples were placed in these cells with a saturated solution of hydrocortisone. The solution also contained radiolabeled hydrocortisone, which allowed the researchers to track and measure it as it moved through and remained within the skin samples over a 24-hour period.

Results

  • The study found significant regional differences in the penetration and retention of hydrocortisone in horse skin. When the drug was applied to the leg, the maximum flux (rate of movement) was significantly higher than when applied to the skin from the thorax or groin.
  • At the same time, whereas the hydrocortisone penetrated more quickly on the leg, significantly less of it was retained within the leg skin after 24 hours compared with the other regions. This suggests that while the drug might absorb faster through the skin at the leg, it might not be retained long enough at the site to have its full effect.

Implication

  • These results provide practical insights for the application of topical hydrocortisone to horses. If the aim is to achieve higher systemic drug concentrations quickly, then the leg may be the best application site. However, in the case of treating local inflamed tissue, applying the drug to the thorax or groin might result in greater efficacy due to the longer retention of the drug within the skin at these sites.

Cite This Article

APA
Mills PC, Cross SE. (2006). Regional differences in the in vitro penetration of hydrocortisone through equine skin. J Vet Pharmacol Ther, 29(1), 25-30. https://doi.org/10.1111/j.1365-2885.2006.00705.x

Publication

ISSN: 0140-7783
NlmUniqueID: 7910920
Country: England
Language: English
Volume: 29
Issue: 1
Pages: 25-30

Researcher Affiliations

Mills, P C
  • School of Veterinary Science, University of Queensland, Brisbane, Qld, Australia. p.mills@uq.edu.au
Cross, S E

    MeSH Terms

    • Administration, Topical
    • Animals
    • Anti-Inflammatory Agents / administration & dosage
    • Anti-Inflammatory Agents / pharmacokinetics
    • Cell Membrane Permeability / drug effects
    • Ethanol / pharmacology
    • Horses
    • Hydrocortisone / administration & dosage
    • Hydrocortisone / pharmacokinetics
    • In Vitro Techniques
    • Male
    • Skin Absorption / drug effects

    Citations

    This article has been cited 4 times.
    1. Slovak JE, Costa AP. A pilot study of transdermal gabapentin in cats.. J Vet Intern Med 2021 Jul;35(4):1981-1987.
      doi: 10.1111/jvim.16137pubmed: 34060655google scholar: lookup
    2. Weber LA, Funtan A, Paschke R, Delarocque J, Kalbitz J, Meißner J, Feige K, Kietzmann M, Cavalleri JV. In vitro assessment of triterpenoids NVX-207 and betulinyl-bis-sulfamate as a topical treatment for equine skin cancer.. PLoS One 2020;15(11):e0241448.
      doi: 10.1371/journal.pone.0241448pubmed: 33151949google scholar: lookup
    3. Weber LA, Meißner J, Delarocque J, Kalbitz J, Feige K, Kietzmann M, Michaelis A, Paschke R, Michael J, Pratscher B, Cavalleri JV. Betulinic acid shows anticancer activity against equine melanoma cells and permeates isolated equine skin in vitro.. BMC Vet Res 2020 Feb 5;16(1):44.
      doi: 10.1186/s12917-020-2262-5pubmed: 32024502google scholar: lookup
    4. Zhang YT, Shen LN, Zhao JH, Feng NP. Evaluation of psoralen ethosomes for topical delivery in rats by using in vivo microdialysis.. Int J Nanomedicine 2014;9:669-78.
      doi: 10.2147/IJN.S57314pubmed: 24489470google scholar: lookup