Effects of the Molecular Weight and Concentration of Polymer Additives, and Temperature on the Melt Crystallization Kinetics of a Small Drug Molecule

非洛地平 结晶 聚合物 Crystal(编程语言) 动力学 化学 氢键 分子 晶体生长 分析化学(期刊) 材料科学 高分子化学 化学工程 结晶学 有机化学 物理 放射科 工程类 血压 医学 程序设计语言 量子力学 计算机科学
作者
Umesh S. Kestur,Hoyoung Lee,Darlene Santiago,Carlos Rinaldi,You‐Yeon Won,Lynne S. Taylor
出处
期刊:Crystal Growth & Design [American Chemical Society]
卷期号:10 (8): 3585-3595 被引量:76
标识
DOI:10.1021/cg1004853
摘要

The purpose of the present study was to investigate the effect of molecular weight (MW) and concentration of a polymeric additive, poly(vinyl pyrrolidone) (PVP), on the crystal growth rate of a small molecule drug, felodipine. PVP samples with three different molecular weights (2−3 × 103 g/mol for PVP K-12, 4−5 × 104 g/mol for PVP K-29/32, and 1−1.5 × 106 g/mol for PVP K-90) were used to study the effect of molecular weight. Optical microscopy was used to measure the growth rates at various temperatures in the range of 70−110 °C. While PVP was found to reduce the crystal growth rate at all temperatures, the inhibitory effect was much greater at lower temperatures. The inhibiting effect of PVP on the crystal growth rate of felodipine increased as a function of polymer molecular weight. The effect of polymer concentration on the crystal growth rate was investigated with varying concentrations of PVP K-29/32 (0.5−4.5 wt %), and a log linear relationship between crystal growth rate and concentration was observed. The calorimetric glass transition temperatures (Tg) of the solid dispersions were not significantly different from the Tg of pure felodipine. IR spectroscopy results indicate that among the PVP polymers of three different MWs, there is no difference in their hydrogen-bonding interactions with felodipine molecules. We present discussions of these experimental results with reference to established thermodynamic theories of crystallization kinetics and mass transfer models.
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