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The Effect of Molecular Properties on Active Ingredient Release from Electrospun Eudragit Fibers

机译:分子性质对静电纺制Eudragit纤维中活性成分释放的影响

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摘要

The formation of nanoscale fibers from pH-sensitive polymers is a route which has been widely explored for targeted drug delivery. In particular, the Eudragit L100 and S100 families of polymers have received significant attention for this purpose. However, while in some cases it is shown that making drug-loaded Eudragit polymers effectively prevents drug release in low-pH media where the polymer is insoluble, this is not always the case, and other studies have reported significant amounts of drug release at acidic pHs. In this study, we sought to gain insight into the factors influencing the release of active ingredients from Eudragit S100 (ES100) fibers. A family of materials was prepared loaded with the model active ingredients (AIs) benzoic acid, 1-naphthoic acid, 1-naphthylamine, and 9-anthracene carboxylic acid. Analogous systems were prepared with an AI-loaded core and an ES100 sheath. The resultant fibers were smooth and cylindrical in the majority of cases, and X-ray diffraction and differential scanning calorimetry showed them to comprise amorphous solid dispersions. When AI release from the monolithic fibers was probed, it was found that there was significant release at pH 1 in all cases except with 9-anthracene carboxylic acid. Analysis of the results indicated that both the molecular weight of the AI and its acidity/basicity are important in controlling release, with lower molecular weight AIs and basic species released more quickly. The same release trends are seen with the core/shell fibers, but AI release at pH 1 is attenuated. The most significant change between the monolithic and core/shell systems was observed in the case of 1-naphthylamine. Mathematical equations were devised to connect molecular properties and AI release under acidic conditions.
机译:由pH敏感的聚合物形成纳米级纤维是针对靶向药物输送进行了广泛探索的途径。尤其是,Eudragit L100和S100聚合物家族为此目的受到了极大的关注。然而,尽管在某些情况下已表明,制备载有药物的Eudragit聚合物可有效防止在聚合物不溶的低pH介质中释放药物,但情况并非总是如此,其他研究也报告了在酸性条件下有大量药物释放pH值。在这项研究中,我们寻求深入了解影响Eudragit S100(ES100)纤维中活性成分释放的因素。制备了一系列材料,其中装有模型活性成分(AIs)苯甲酸,1-萘甲酸,1-萘胺和9-蒽羧酸。准备了带有AI加载芯和ES100护套的类似系统。所得纤维在大多数情况下是光滑且呈圆柱形的,并且X射线衍射和差示扫描量热法显示它们包含无定形固体分散体。当探测从单块纤维中释放出AI时,发现在所有情况下,除9-蒽羧酸外,在所有pH值下都有明显的释放。结果分析表明,AI的分子量及其酸度/碱度对控制释放都很重要,较低分子量的AI和碱性物质释放速度更快。核/壳纤维的释放趋势相同,但pH 1时AI的释放减弱。在1-萘胺的情况下,在整体式系统和核/壳系统之间观察到了最显着的变化。设计了数学方程式以连接酸性条件下的分子特性和AI释放。

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