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首页> 外文期刊>Pharmaceutical development and technology >Using principal component analysis in studying the transdermal delivery of a lipophilic drug from soft nano-colloidal carriers to develop a quantitative composition effect permeability relationship
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Using principal component analysis in studying the transdermal delivery of a lipophilic drug from soft nano-colloidal carriers to develop a quantitative composition effect permeability relationship

机译:使用主成分分析研究亲脂性药物从软纳米胶体载体的透皮递送,以建立定量的成分效应渗透率关系

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The aim of principal component analysis is to reduce the dimensionality of the data while retaining its variation. Obtaining a vector component representing the most important variation amongst the data and summarizing the factors are usually needed to achieve a new descriptor for the system. This can be used to elaborate certain properties related to the components used in formulating drug delivery systems. To this end, it is possible to develop what exclusively can be called quantitative composition effect permeability relationship. In this study, fundamental features of the Fourier transform infrared spectroscopy together with the degree of saturation of a model drug, testosterone hormone, were used as initial dimensions and their extent of change were utilized as original variables to generate a correlation matrix. The principal component (PC) with the largest eigen value was selected for regression analysis to provide a quantitative model relating the effects of different compositions with the enhanced penetration of the model lipophilic drug from microemulsions. A strong correlation (r = 0.90) was obtained between the main PC derived data and the observed permeability coefficient results which warrants the use of this analyzing method in optimizing different drug delivery systems.
机译:主成分分析的目的是减少数据的维数,同时保留其变化。通常需要获取代表数据中最重要变化的矢量分量,并对这些因素进行汇总,以实现系统的新描述符。这可以用来阐述与配制药物输送系统中使用的组分有关的某些特性。为此,有可能开发专门称为定量组成效应渗透率关系的物质。在这项研究中,傅里叶变换红外光谱的基本特征以及模型药物睾丸激素的饱和度被用作初始尺寸,其变化程度被用作原始变量以生成相关矩阵。选择具有最大特征值的主成分(PC)进行回归分析,以提供一个定量模型,该模型将不同组合物的作用与微乳状模型亲脂性药物的渗透性提高联系起来。在主要的PC衍生数据和观察到的渗透系数结果之间获得了很强的相关性(r = 0.90),这有必要在优化不同的药物输送系统中使用这种分析方法。

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