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Development of terbinafine solid lipid nanoparticles as a topical delivery system

Authors Chen Y, Liu D, Liu, Chang T, Ho H , Sheu M 

Received 8 May 2012

Accepted for publication 31 May 2012

Published 15 August 2012 Volume 2012:7 Pages 4409—4418


Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 4

Ying-Chen Chen,1* Der-Zen Liu,2* Jun-Jen Liu,3 Tsung-Wei Chang,1 Hsiu-O Ho,1 Ming-Thau Sheu,1,4

1School of Pharmacy, College of Pharmacy, 2Graduate Institute of Biomedical Materials and Engineering, 3School of Medical Laboratory Science and Biotechnology, 4Clinical Research Center and Traditional Herbal Medicine Research Center, Taipei Medical University Hospital, Taipei, Taiwan

*Ying-Chen Chen and Der-Zen Liu contributed equally in the preparation of this manuscript.

Abstract: To resolve problems of long treatment durations and frequent administration of the antifungal agent terbinafine (TB), solid lipid nanoparticles (SLNs) with the ability to load lipophilic drugs and nanosize were developed. The SLNs were manufactured by a microemulsion technique in which glyceryl monostearate (GMS), glyceryl behenate (Compritol® 888; Gattefossé), and glyceryl palmitostearate (Precirol® ATO 5; Gattefossé) were used as the solid lipid phases, Tween® and Cremophor® series as the surfactants, and propylene glycol as the cosurfactant to construct ternary phase diagrams. The skin of nude mice was used as a barrier membrane, and penetration levels of TB of the designed formulations and a commercial product, Lamisil® OnceTM (Novartis Pharmaceuticals), in the stratum corneum (SC), viable epidermis, and dermis were measured; particle sizes were determined as an indicator of stability. The optimal SLN system contained a <5% lipid phase and >50% water phase. The addition of ethanol or etchants had no significant effect on enhancing the amount of TB that penetrated the skin layers, but it was enhanced by increasing the percentage of the lipid phase. Furthermore, the combination of GMS and Compritol® 888 was able to increase the stable amount of TB that penetrated all skin layers. For the ACP1-GM1 (4% lipid phase; Compritol® 888: GMS of 1:1) formulation, the amount of TB that penetrated the SC was similar to that of Lamisil® OnceTM, whereas the amount of TB of the dermis was higher than that of Lamisil® OnceTM at 12 hours, and it was almost the same as that of Lamisil® OnceTM at 24 hours. It was concluded that the application of ACP1-GM1 for 12 hours might have an efficacy comparable to that of Lamisil® OnceTM for 24 hours, which would resolve the practical problem of the longer administration period that is necessary for Lamisil® OnceTM.

Keywords: terbinafine, solid lipid nanoparticle, topical delivery system

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