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Human epidermal in vitro permeation test (IVPT) analyses of alcohols and steroids.
Alinaghi, Azadeh; Macedo, Ana; Cheruvu, Hanumanth S; Holmes, Amy; Roberts, Michael S.
Affiliation
  • Alinaghi A; Clinical and Medical Sciences, University of South Australia, Adelaide, Australia and The Basil Hetzel Institute for Translational Health Research, Adelaide, Australia.
  • Macedo A; Clinical and Medical Sciences, University of South Australia, Adelaide, Australia and The Basil Hetzel Institute for Translational Health Research, Adelaide, Australia.
  • Cheruvu HS; Diamantina Research Institute, The University of Queensland, Translational Research Institute, Brisbane, Australia.
  • Holmes A; Clinical and Medical Sciences, University of South Australia, Adelaide, Australia and The Basil Hetzel Institute for Translational Health Research, Adelaide, Australia.
  • Roberts MS; Clinical and Medical Sciences, University of South Australia, Adelaide, Australia and The Basil Hetzel Institute for Translational Health Research, Adelaide, Australia; Diamantina Research Institute, The University of Queensland, Translational Research Institute, Brisbane, Australia. Electronic addr
Int J Pharm ; 627: 122114, 2022 Nov 05.
Article in En | MEDLINE | ID: mdl-35973591
This study examined a number of factors that can impact the outcomes of in vitro human epidermal permeation coefficients for aliphatic alcohols and steroids, including receptor phase composition and study conditions. We determined experimentally the solubilities and IVPT permeation of a homologous series of 14C labeled aliphatic alcohols (ethanol, propanol, pentanol, heptanol, octanol and decanol) in different receptor fluids as recommended by Organisation Economic Co-operation and Development (OECD). We used human epidermal membranes at 25 °C and phosphate-buffered saline (PBS), 2 %w/v bovine serum albumin (2 %w/v BSA), 50 %w/v ethanol and 0.1, 2 and 6 %w/v Oleth-20 receptor phases. We also explored and confirmed the discrepancies between in vitro human epidermal permeability coefficients (kp) and diffusion lag times for steroids from Scheuplein's group with our own work and that of others. The main reason for the observed differences is not clear but is likely to be multifactorial, including the effects of diffusion cell design, receptor phase solubility, unstirred receptor phase effects, epidermal membrane hydration, diffusion cell configuration, transport through appendageal pathways and steroid lipophilicity. We conclude with a summary of experimental conditions that should be considered in undertaking IVPT studies.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Alcohols / Pentanols Limits: Humans Language: En Journal: Int J Pharm Year: 2022 Document type: Article Affiliation country: Australia Country of publication: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Alcohols / Pentanols Limits: Humans Language: En Journal: Int J Pharm Year: 2022 Document type: Article Affiliation country: Australia Country of publication: Netherlands