噻吗洛尔
肺表面活性物质
挤压
渗透
材料科学
药物输送
色谱法
Zeta电位
分散性
生物利用度
化学
生物医学工程
膜
纳米技术
青光眼
复合材料
药理学
眼科
工程类
纳米颗粒
医学
高分子化学
生物化学
作者
Marı́a Luisa González-Rodrı́guez,Carmen Martina Arroyo García,Mj Cózar-Bernal,Pedro L. González‐R,Jm León,Marcos Calle Suárez,David Canca,A. M. Rabasco
标识
DOI:10.3109/03639045.2016.1165691
摘要
The purpose of this work was to analyze the deformability properties of different timolol maleate (TM)-loaded transfersomes by extrusion. This was performed because elastic liposomes may contribute to the elevation of amount and rate of drug permeation through the corneal membrane. This paper describes the optimization of a transfersome formulation by use of Taguchi orthogonal experimental design and two different statistical analysis approaches were utilized. The amount of cholesterol (F1), the amount of edge-activator (F2), the distribution of the drug into the vesicle (F3), the addition of stearylamine (F4) and the type of edge-activator (F5) were selected as causal factors. The deformability index, the phosphorous recovery, the vesicle size, the polydispersity index, the zeta potential and percentage of drug entrapped were fixed as the dependent variables and these responses were evaluated for each formulation. Two different statistical analysis approaches were applied. The better statistical approach was determined by comparing their prediction errors, where regression analysis provided better optimized responses than marginal means. From the study, an optimized formulation of TM-loaded transfersomes was prepared and obtained for the proposed ophthalmic delivery for the treatment of open angle glaucoma. It was found that the lipid to surfactant ratio and type of surfactant are the main key factors for determining the flexibility of the bilayer of transfersomes. From in vitro permeation studies, we can conclude that TM-loaded transfersomes may enhance the corneal transmittance and improve the bioavailability of conventional TM delivery.
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