高于重叠浓度 (c*) 的聚合物对分子液体结晶的抑制作用:延迟首次成核事件。

IF 3.7 3区 医学 Q2 CHEMISTRY, MEDICINAL
Journal of pharmaceutical sciences Pub Date : 2025-01-01 Epub Date: 2024-02-17 DOI:10.1016/j.xphs.2024.02.011
Sichen Song, Shuquan Cui, Changquan Calvin Sun, Timothy P Lodge, Ronald A Siegel
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引用次数: 0

摘要

低浓度聚合物添加剂可显著改变分子液体和玻璃的晶体生长动力学。然而,人们对聚合物浓度对成核动力学的影响仍然知之甚少。根据实验测定的首次成核时间(形成第一个临界晶核的时间,t0),我们发现聚合物重叠浓度 c* 是有效抑制分子液体结晶的临界聚合物浓度。当聚合物浓度 c 低于 c* 时,t0 值大致等于纯分子液体的 t0 值,但当 c > c* 时,t0 值会显著增加。这一发现对于有效筛选聚合物和预测工程多组分非晶材料(尤其是药用非晶固体分散体)的性能具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Crystallization inhibition in molecular liquids by polymers above the overlap concentration (c*): Delay of the first nucleation event.

Low concentration polymer additives can significantly alter crystal growth kinetics of molecular liquids and glasses. However, the effect of polymer concentration on nucleation kinetics remains poorly understood. Based on an experimentally determined first nucleation time (time to form the first critical nucleus, t0), we show that the polymer overlap concentration, c*, where polymer coils in the molecular liquid start to overlap with each other, is a critical polymer concentration for efficient inhibition of crystallization of a molecular liquid. The value of t0 is approximately equal to that of the neat molecular liquid when the polymer concentration, c, is below c*, but increases significantly when c > c*. This finding is relevant for effective polymer screening and performance prediction of engineered multicomponent amorphous materials, particularly pharmaceutical amorphous solid dispersions.

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来源期刊
CiteScore
7.30
自引率
13.20%
发文量
367
审稿时长
33 days
期刊介绍: The Journal of Pharmaceutical Sciences will publish original research papers, original research notes, invited topical reviews (including Minireviews), and editorial commentary and news. The area of focus shall be concepts in basic pharmaceutical science and such topics as chemical processing of pharmaceuticals, including crystallization, lyophilization, chemical stability of drugs, pharmacokinetics, biopharmaceutics, pharmacodynamics, pro-drug developments, metabolic disposition of bioactive agents, dosage form design, protein-peptide chemistry and biotechnology specifically as these relate to pharmaceutical technology, and targeted drug delivery.
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