Department of Pharmaceutical Chemistry, The University of Kansas, Lawrence, KS, 66047, USA.
Adv Healthc Mater. 2021 Jun;10(12):e2100015. doi: 10.1002/adhm.202100015. Epub 2021 May 14.
Controlling drug release kinetics within a desired therapeutic window is the central task when designing polymeric drug delivery systems. Complex polymer chemistries have often been explored to control water penetration, polymer degradation rate, or the mesh network size of delivery systems. Here, a simple parameter for controlling the release rate and duration of nondegradable hydrophobic polymers is discovered. A systematic study involving 59 polymers and multiple drugs demonstrates that the glass transition temperature, T , is a critical factor that dictates drug release kinetics from nondegradable hydrophobic polymers. Drug release rate exhibits a unique and simple linear correlation of (T - T ) despite variability of polymer structure and type. An empirical model established based on the special correlation can accurately simulate and predict drug release kinetics from polymers saving substantial time typically required to test long-acting drug delivery systems.
控制药物释放动力学在期望的治疗窗口内是设计聚合物药物传递系统的核心任务。为了控制水的渗透、聚合物的降解速率或传递系统的网格网络尺寸,通常会探索复杂的聚合物化学。在这里,发现了一个控制不可降解疏水性聚合物释放速率和持续时间的简单参数。一项涉及 59 种聚合物和多种药物的系统研究表明,玻璃化转变温度 T 是决定不可降解疏水性聚合物药物释放动力学的关键因素。尽管聚合物结构和类型存在差异,但药物释放速率表现出独特且简单的线性相关性(T - T )。基于该特殊相关性建立的经验模型可以准确地模拟和预测聚合物中的药物释放动力学,从而节省通常需要测试长效药物传递系统的大量时间。