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Evaluation of the recrystallization kinetics of hot-melt extruded polymeric solid dispersions using an improved Avrami equation

机译:使用改进的Avrami方程评估热熔挤出聚合物固体分散体的重结晶动力学

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摘要

The recrystallization of an amorphous drug in a solid dispersion system could lead to a loss in the drug solubility and bioavailability. The primary objective of the current research was to use an improved kinetic model to evaluate the recrystallization kinetics of amorphous structures and to further understand the factors influencing the physical stability of amorphous solid dispersions. Amorphous solid dispersions of fenofibrate with different molecular weights of hydroxypropylcellulose, HPC (Klucel™ LF, EF, ELF) were prepared utilizing hot-melt extrusion technology. Differential scanning calorimetry was utilized to quantitatively analyze the extent of recrystallization in the samples stored at different temperatures and relative humidity (RH) conditions. The experimental data were fitted into the improved kinetics model of a modified Avrami equation to calculate the recrystallization rate constants. Klucel LF, the largest molecular weight among the HPCs used, demonstrated the greatest inhibition of fenofibrate recrystallization. Additionally, the recrystallization rate (k) decreased with increasing polymer content, however exponentially increased with higher temperature. Also k increased linearly rather than exponentially over the range of RH studied.
机译:固体分散系统中无定形药物的重结晶可能会导致药物溶解度和生物利用度下降。当前研究的主要目的是使用改进的动力学模型来评估非晶态结构的重结晶动力学,并进一步了解影响非晶态固体分散体物理稳定性的因素。利用热熔挤出技术制备了具有不同分子量羟丙基纤维素HPC(非诺贝特)的非晶态固体分散体,即HPC(Klucel™LF,EF,ELF)。差示扫描量热法用于定量分析在不同温度和相对湿度(RH)条件下存储的样品中的重结晶程度。将实验数据拟合到改进的Avrami方程的​​改进动力学模型中,以计算重结晶速率常数。所使用的HPC中分子量最大的Klucel LF对非诺贝特重结晶的抑制作用最大。另外,重结晶速率(k)随聚合物含量的增加而降低,但随温度升高呈指数增长。在研究的RH范围内,k也呈线性增长,而不是呈指数增长。

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