Literature DB >> 15704860

Evaluation of the physicochemical stability and skin permeation of glucosamine sulfate.

Marion Kanwischer1, Seok-Yong Kim, Jung Sun Kim, Shengjie Bian, Kyoung Ae Kwon, Dae-Duk Kim.   

Abstract

Glucosamine sulfate (GS) is known to stop the degenerative process of osteoarthritis. Because most of the GS formulation on the market is in the oral form, an alternative formulation such as a transdermal delivery system (TDS) is necessary in order to increase patient compliance. As the initial step to develop a TDS of GS, the physicochemical stability and permeation study in rat skin were examined. Evaluation of the stability of GS at different pHs showed the compound to be most stable at pH 5.0. The degradation rate constant at 25 degrees C was estimated to be 5.93 x 10(-6) hr(-1) (t90 approximately 2.03 years) in a pH 5 buffer solution. Due to its hydrophilic characteristic, low skin permeability was expected of GS. However, the skin permeation rate was determined to be 13.27 microg/cm2/hr at 5% concentration. Results of this study suggest the possibility of developing GS into a transdermal delivery system.

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Year:  2005        PMID: 15704860     DOI: 10.1081/ddc-44181

Source DB:  PubMed          Journal:  Drug Dev Ind Pharm        ISSN: 0363-9045            Impact factor:   3.225


  2 in total

1.  Niosome as a drug carrier for topical delivery of N-acetyl glucosamine.

Authors:  M A Shatalebi; S A Mostafavi; A Moghaddas
Journal:  Res Pharm Sci       Date:  2010-07

2.  A randomised pilot equivalence trial to evaluate diamagnetically enhanced transdermal delivery of key ground substance components in comparison to an established transdermal non-steroidal anti-inflammatory formulation in males with prior knee injury.

Authors:  Bill Vicenzino; Peter Lawrenson; Asaduzzaman Khan; Aiofe Stephenson; Luke Heales; Heather A E Benson; Anthony Wright
Journal:  PLoS One       Date:  2019-02-22       Impact factor: 3.240

  2 in total

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