Hydration and N-acetyl-l-cysteine alter the microstructure of human nail and bovine hoof: Implications for drug delivery

JOURNAL OF CONTROLLED RELEASE

卷:156

Article

Nogueiras-Nieto, L.²  Gomez-Amoza, J. L.²  Delgado-Charro, M. B.¹  Otero-Espinar, F. J.² 

[1] Univ Bath, Dept Pharm & Pharmacol, Bath BA2 7AY, Avon, England

[2] Univ Santiago de Compostela, Dept Farm & Tecnol Farmaceut, Santiago De Compostela 15782, Spain

关键词: Nail;    Hydration;    N-acetyl-l-cysteine;    Microstructure;    Porosity;    Intrusion porosimetry;   

DOI  :  10.1016/j.jconrel.2011.08.021

来源: Elsevier

【 摘 要 】

This work aimed to (a) characterize the microstructure and porosity of human nail and bovine hoof by mercury intrusion porosimetry and SEM image analysis, (b) study the effects of hydration and of N-acetyl-l-cysteine treatment on the microstructure of both membranes, and (c) determine whether the microstructural modifications were associated with changes in drug penetration measured by standard diffusion studies. Bovine hoof surface is more porous than nail surface although there were no differences between the mean surface pore sizes. Hydration and N-acetyl-l-cysteine increased the roughness and apparent surface porosity, and the porosity determined by mercury intrusion porosimetry of both membranes. Pore-Cor (TM) was used to generate tridimensional structures having percolation characteristics comparable to nail and hooves. The modeled structures were horizontally banded having an inner less-porous area which disappeared upon treatment. Treatment increased the predicted permeability of the simulated structures. Triamcinolone permeation increased significantly for hooves treated N-acetyl-l-cysteine, i.e., the membranes for which microstructural and permeability changes were the largest. Thus, microstructural changes determined via mercury intrusion porosimetry and subsequently modeled by Pore-Cor (TM) were related to drug diffusion. Further refinement of the technique will allow fast screening of penetration enhancers to be used in ungual drug delivery. (C) 2011 Elsevier B.V. All rights reserved.

【 授权许可】

Free