AAPS PharmSciTech

, Volume 5, Issue 3, pp 82–89 | Cite as

Transdermal delivery of zidovudine (AZT): The effects of vehicles, enhancers, and polymer membranes on permeation across cadaver pig skin

  • Nuntakan Suwanpidokkul
  • Phensri Thongnopnua
  • Kaisri Umprayn


The purpose of this study was to investigate the effects of vehicles, enhancers, and polymer membranes on 3-azido-3-deoxythymidine (AZT) permeation across cadaver pig skin. Four binary vehicles (ethanol/water, isopropyl alcohol/water, polyethylene glycol 400/water, and ethanol/isopropyl myristate [IPM] were tested for AZT solubility and permeability across pig skin; ethanol/IPM (50/50, vol/vol) demonstrated the highest AZT flux (185.23 μ/cm2/h). Next, the addition of various concentrations of different enhancers (N-methyl-2-pyrrolidone [NMP], oleic acid, and lauric acid) to different volume ratios of ethanol/IPM was investigated for their effect on AZT solubility and permeability across pig skin. The use of 2 conbinations (ethanol/IPM [20/80] plus 10% NMP and ethanol/IPM [30/70] plus 10% NMP) resulted in increased AZT solubility (42.6 and 56.27 mg/mL, respectively) and also high AZT flux values (284.92 and 460.34 μg/cm2/h, respectively) without appreciable changes in lag times (6.25 and 7.49 hours, respectively) when compared with formulations using only ethanol/IPM at 20/80 and 30/70 volume ratios without addition of the enhancer NMP. Finally, AZT permeation across pig skin covered with a microporous polyethylene (PE) membrane was investigated. The addition of the PE membrane to the pig skin reduced AZT flux values to ∼50% of that seen with pig skin alone. However, the AZT flux value attained with ethanol/IPM (30/70) plus 10% NMP was 215.30 μg/cm2/h, which was greater than the target flux (208 μg/cm2/h) needed to maintain the steady-state plasma concentration in humans. The results obtained from this study will be helpful in the development of an AZT transdermal drug delivery system.


Zidovudine permeation enhancer binary vehicles polymer membrane transdermal delivery system 


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Copyright information

© American Association of Pharmaceutical Scientists 2004

Authors and Affiliations

  • Nuntakan Suwanpidokkul
    • 1
  • Phensri Thongnopnua
    • 2
  • Kaisri Umprayn
    • 3
  1. 1.The Government Pharmaceutical OrganizationBangkokThailand
  2. 2.Department of Pharmaceutical Chemistry, Faculty of Pharmaceutical SciencesChulalongkorn UniversityBangkokThailand
  3. 3.Department of Manufacturing Pharmacy, Faculty of Pharmaceutical SciencesChulalongkorn UniversityBangkokThailand

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