Article ID Journal Published Year Pages File Type
2484918 Journal of Pharmaceutical Sciences 2010 8 Pages PDF
Abstract
A feather degrading strain of Bacillus licheniformis ER-15 was isolated which also degraded α-keratin of hooves. A detailed analysis revealed that a novel monomeric γ-glutamyl transpeptidase (GGT30), a proteolytic product of heterodimeric 67 kDa γ-glutamyl transpeptidase (GGT67), assists subtilisin during its action on α keratin. An equimolar combination of subtilisin and GGT30 was designated as KerN and was used as ungual enhancer for topical application. KerN was effective in releasing proteins from nail plate surface and 300 μg of enzyme could release 41 μg protein/ μg of nail after 24 h treatment. Scanning electron micrograph (SEM) revealed loosening of nail matrix confirming the action of KerN on nail keratin. Drug permeation studies revealed permeation of clotrimazole through both enzymatically pretreated nail plates and also through nail plates in presence of KerN. Nearly 58% drug could be retained by nail plates after 24 h of 300 μg/mL KerN which further enhanced up to 97% by prolonging the enzyme application. The enzyme was found to be stable in presence of drug even after 72 h. Thus, KerN can be used as an additive in formulation of topical drug for onchomycosis. © 2010 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 99:4866-4873, 2010
Related Topics
Health Sciences Pharmacology, Toxicology and Pharmaceutical Science Drug Discovery
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