Publication: Evaluation of skin permeation of β-blockers for topical drug delivery
Issued Date
2013-03-01
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ISSN
1573904X
07248741
07248741
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2-s2.0-84878875115
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Mahidol University
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SCOPUS
Bibliographic Citation
Pharmaceutical Research. Vol.30, No.3 (2013), 866-877
Suggested Citation
Doungdaw Chantasart, Jinsong Hao, S. Kevin Li Evaluation of skin permeation of β-blockers for topical drug delivery. Pharmaceutical Research. Vol.30, No.3 (2013), 866-877. doi:10.1007/s11095-012-0928-9 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/31353
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Title
Evaluation of skin permeation of β-blockers for topical drug delivery
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Abstract
Purpose: β-Blockers have recently become the main form of treatment of infantile hemangiomas. Due to the potential systemic adverse effects of β-blockers, topical skin treatment of the drugs is preferred. However, the effect and mechanism of dosage form pH upon skin permeation of these weak bases is not well understood. To develop an effective topical skin delivery system for the β-blockers, the present study evaluated skin permeation of β-blockers propranolol, betaxolol, timolol, and atenolol. Methods: Experiments were performed in side-by-side diffusion cells with human epidermal membrane (HEM) in vitro to determine the effect of donor solution pH upon the permeation of the β-blockers across HEM. Results: The apparent permeability coefficients of HEM for the β-blockers increased with their lipophilicity, suggesting the HEM lipoidal pathway as the main permeation mechanism of the β-blockers. The pH in the donor solution was a major factor influencing HEM permeation for the β-blockers with a 2- to 4-fold increase in the permeability coefficient per pH unit increase. This permeability versus pH relationship was found to deviate from theoretical predictions, possibly due to the effective stratum corneum pH being different from the pH in the donor solution. Conclusions: The present results suggest the possibility of topical treatment of hemangioma using β-blockers. © 2012 Springer Science+Business Media New York.