Literature DB >> 11205736

Does epidermal turnover reduce percutaneous penetration?

M B Reddy1, R H Guy, A L Bunge.   

Abstract

PURPOSE: After its removal from the skin surface, chemical remaining within the skin can become systemically available. The fraction of chemical in the skin that eventually enters the body depends on the relative rates of percutaneous transport and epidermal turnover (i.e., stratum corneum desquamation). Indeed, some investigators have claimed that desquamation is an efficient mechanism for eliminating dermally absorbed chemical from the skin.
METHODS: The fate of chemical within the skin following chemical contact was examined using a mathematical model representing turnover of and absorption into the stratum corneum and viable epidermis. The effects of turnover rate, exposure duration, penetrant lipophilicity, and lag time for chemical diffusion were explored.
RESULTS: These calculations show that significant amounts of chemical can be removed from skin by desquamation if epidermal turnover is fast relative to chemical diffusion through the stratum corneum. However, except for highly lipophilic and/or high molecular weight (>350 Da) chemicals, the normal epidermal turnover rate is not fast enough and most of the chemical in the skin at the end of an exposure will enter the body.
CONCLUSIONS: Epidermal turnover can significantly reduce subsequent chemical absorption into the systemic circulation only for highly lipophilic or high molecular weight chemicals.

Mesh:

Year:  2000        PMID: 11205736     DOI: 10.1023/a:1007522200422

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  19 in total

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Authors:  P R Bergstresser; J R Taylor
Journal:  Br J Dermatol       Date:  1977-05       Impact factor: 9.302

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Authors:  F Pirot; Y N Kalia; A L Stinchcomb; G Keating; A Bunge; R H Guy
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3.  Utility of real time breath analysis and physiologically based pharmacokinetic modeling to determine the percutaneous absorption of methyl chloroform in rats and humans.

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Journal:  Toxicol Sci       Date:  2000-03       Impact factor: 4.849

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Journal:  Dermatol Clin       Date:  1986-07       Impact factor: 3.478

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Journal:  Pharm Res       Date:  1993-04       Impact factor: 4.200

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Journal:  J Invest Dermatol       Date:  1980-01       Impact factor: 8.551

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Journal:  Hum Exp Toxicol       Date:  1994-01       Impact factor: 2.903

9.  Percutaneous absorption of benzoic acid across human skin. II. Prediction of an in vivo, skin-flap system using in vitro parameters.

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Journal:  Pharm Res       Date:  1990-04       Impact factor: 4.200

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  3 in total

1.  Dermal absorption of chlorpyrifos in human volunteers.

Authors:  Wim J A Meuling; Luco C Ravensberg; Len Roza; Joop J van Hemmen
Journal:  Int Arch Occup Environ Health       Date:  2004-12-31       Impact factor: 3.015

2.  The transient dermal exposure II: post-exposure absorption and evaporation of volatile compounds.

Authors:  H Frederick Frasch; Annette L Bunge
Journal:  J Pharm Sci       Date:  2015-01-21       Impact factor: 3.534

Review 3.  Nanotechnology for the treatment of melanoma skin cancer.

Authors:  Lucas B Naves; Chetna Dhand; Jayarama Reddy Venugopal; Lakshminarayanan Rajamani; Seeram Ramakrishna; Luis Almeida
Journal:  Prog Biomater       Date:  2017-03-16
  3 in total

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