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Prediction of Drug Solubility in Adhesive Matrix for Transdermal Drug Delivery Based on a Solvation Parameter Model

机译:基于溶剂化参数模型的透皮药物递送药物溶解度预测

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The work presented here establishes the relationship between drug solubility in two acrylate adhesives with a previously defined drug-polymer interaction parameter and drug solubility in acetonitrile. The drug solvation parameter model decomposes a hard-to-measure quantity into two easily measurable parameters. It is concluded that there is an excellent linear relationship for the parameters involved. Thus, the model can be used to compute the solubility in the polymer for new drug candidates. Moreover, the two parameters in the ralationship can be either easily measured or computed based on their molecular properties by the solvation parameter model. The methodologies presented can be applied to other adhesives.
机译:本文提出的作品在两个丙烯酸酯粘合剂中具有先前定义的药物 - 聚合物相互作用参数和乙腈中的药物溶解度的药物溶解度之间的关系。药物溶剂化参数模型将难以测量的数量分解成两个易于测量的参数。得出结论是,对于所涉及的参数存在出色的线性关系。因此,该模型可用于计算用于新药候选物的聚合物中的溶解度。此外,ralationHip中的两个参数可以基于溶剂化参数模型的分子特性容易地测量或计算。呈现的方法可以应用于其他粘合剂。

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