Biopharmaceutics of topical and transdermal formulations

Hannah Batchelor*

*Corresponding author for this work

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Topical pharmaceutical products are usually liquids or semisolids, whereas transdermal products are often formulated as patches that deliver drugs to or through the skin to provide therapy. The pharmacokinetic response to a topical/transdermal formulation depends on the drug release, then penetration of the drug through the skin then distribution to the site of action. The relative efficiency of the processes will determine the exposure of the drug at the site of action, hence the biopharmaceutics. The rate of drug release can depend upon several factors including active pharmaceutical ingredient particle size. Drug release from topical and transdermal products is measured using a modified dissolution apparatus. Tape stripping is also used as a tool to measure the concentration of drug in the stratum corneum over time, often termed dermatopharmacokinetic methods. Dermal microdialysis enables in situ measurement of drug concentration in the dermis using an extremely thin dialysis probe that is located within the dermal layer.

Original languageEnglish
Title of host publicationBiopharmaceutics
Subtitle of host publicationFrom Fundamentals to Industrial Practice
Place of PublicationChichester
Chapter16
Pages265-276
Number of pages12
ISBN (Electronic)9781119678366
DOIs
Publication statusPublished - 28 Jan 2022

Keywords

  • active pharmaceutical ingredient
  • biopharmaceutics
  • dermal microdialysis
  • dermatopharmacokinetic methods
  • drug concentrations
  • drug release
  • topical formulation
  • transdermal formulation

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