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Decreasing systemic toxicity via transdermal delivery of anticancer drugs

  • Jia You Fang
  • , Pei Feng Liu
  • , Chun Ming Huang*
  • *Corresponding author for this work
  • Department of Veterans Affairs
  • University of California at San Diego

Research output: Contribution to journalReview articlepeer-review

23 Scopus citations

Abstract

When used at a high dose, many anticancer drugs produce undesirable side effects including hepatotoxicity. Transdermal delivery bypasses first-pass metabolism, allowing the use of a lower dose of drug while decreasing systemic toxicity. In this review, we summarize various advanced technologies for improving anticancer drug delivery via the skin. This technology is discussed in the context of three anticancer drugs, 5-fluorouracil (5-FU), methotrexate (MTX) and 5-aminolevulinic acid (5-ALA). The use of a erbium:YAG (Er:YAG) laser for transdermal delivery of anticancer drugs is specifically highlighted in this review.

Original languageEnglish
Pages (from-to)592-597
Number of pages6
JournalCurrent Drug Metabolism
Volume9
Issue number7
DOIs
StatePublished - 2008

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Anticancer drugs
  • Laser
  • Toxicity
  • Transdermal delivery

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