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Related Experiment Videos

Transdermal-controlled administration of oxycodone.

J H Tien1

  • 1Medical Laboratories, National Defense Medical Center, Taipei, Taiwan, Republic of China.

Journal of Pharmaceutical Sciences
|August 1, 1991
PubMed
Summary
This summary is machine-generated.

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Oxycodone permeability through mouse skin is significantly higher for its non-ionized form. Silicone elastomer formulations show release rates proportional to drug loading, impacting skin permeation.

Area of Science:

  • Pharmacokinetics and Drug Delivery
  • Dermal Permeation Studies
  • Materials Science

Background:

  • Oxycodone, a weak base analgesic, exhibits pH-dependent solubility and skin permeability.
  • Understanding drug behavior in transdermal systems is crucial for effective drug delivery.

Purpose of the Study:

  • To investigate the permeability of hairless mouse skin to oxycodone.
  • To evaluate the impact of pH on oxycodone solubility and skin permeation.
  • To assess the release and skin permeation characteristics of oxycodone incorporated in a silicone elastomer.

Main Methods:

  • In vitro skin permeation studies using hairless mouse skin.
  • Solubility and permeation rate measurements at varying pH.
  • Formulation of oxycodone in silicone elastomer with different drug loadings.

Related Experiment Videos

  • Analysis of release kinetics using Higuchi's equation.
  • Main Results:

    • Permeability of oxycodone base was approximately 7.4 times higher than protonated oxycodone.
    • Release rate from silicone elastomer followed Higuchi's equation (Q/t1/2 proportional to sqrt(drug loading)).
    • Skin permeation rate increased with drug loading, plateauing at 60 mg/cm3.

    Conclusions:

    • The non-ionic form of oxycodone is key for enhanced skin penetration.
    • Silicone elastomer formulations offer controlled release, with loading dose influencing permeation.
    • Findings inform the development of oxycodone transdermal delivery systems.