通过热熔反应挤压在聚合物基质中形成原位共晶以及使用偏最小二乘法回归模型确定反应产量

IF 4.5 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Gavin P. Andrews, Alice Culkin, David S. Jones and Shu Li*, 
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引用次数: 0

摘要

通过研究互补官能团,这些官能团可以通过形成氢键(H 键)等非共价键可靠地相互作用,从而设计和合成新的结晶多组分系统,这方面的研究工作已经取得了很大进展。利用这种方法形成的结晶多组分分子加合物(如共晶体、盐和共晶)已成为药物产品的中间体,可有效改变药物特性。最近,这些多组分分子加合物的生产技术已经从依赖大量使用溶剂的间歇式技术转变为无溶剂、连续式和工业化生产的技术,如反应挤压技术。在本研究中,我们发现了一种新型共晶体系,该体系是以 1:2 的摩尔比处理阿苯达唑和马来酸,并采用机械化学方法(包括液体辅助研磨和热熔反应挤压)成功制备。与原生药物化合物相比,所制备的共晶体的熔化温度降低了 100 °C,溶解性能也有所提高(在 2 小时内溶解度提高了 12 倍)。为了避免将共晶作为制剂中间体进行处理,采用了端到端连续生产就绪工艺,可以将原始母体试剂以各自的天然形式与所选的聚合物赋形剂 Eudragit EPO 一起投入生产。经证实,共晶的形成是在聚合物存在的情况下就地进行的,反应产率是通过光谱分析与偏最小二乘回归模型相结合的多元校准模型确定的。三元挤出物的溶解曲线与 1:2 制备的共晶类似,表明原位合成的共晶内容物在聚合物基质中的物理分布(或悬浮)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

In Situ Eutectic Formation in a Polymeric Matrix via Hot-Melt Reactive Extrusion and the Use of Partial Least Squares Regression Modeling for Reaction Yield Determination

In Situ Eutectic Formation in a Polymeric Matrix via Hot-Melt Reactive Extrusion and the Use of Partial Least Squares Regression Modeling for Reaction Yield Determination

There has been a significant volume of work investigating the design and synthesis of new crystalline multicomponent systems via examining complementary functional groups that can reliably interact through the formation of noncovalent bonds, such as hydrogen bonds (H-bonds). Crystalline multicomponent molecular adducts formed using this approach, such as cocrystals, salts, and eutectics, have emerged as drug product intermediates that can lead to effective drug property modifications. Recent advancement in the production for these multicomponent molecular adducts has moved from batch techniques that rely upon intensive solvent use to those that are solvent-free, continuous, and industry-ready, such as reactive extrusion. In this study, a novel eutectic system was found when processing albendazole and maleic acid at a 1:2 molar ratio and successfully prepared using mechanochemical methods including liquid-assisted grinding and hot-melt reactive extrusion. The produced eutectic was characterized to exhibit a 100 °C reduction in melting temperature and enhanced dissolution performance (>12-fold increase at 2 h point), when compared to the native drug compound. To remove handling of the eutectic as a formulation intermediate, an end-to-end continuous-manufacturing-ready process enables feeding of the raw parent reagents in their respective natural forms along with a chosen polymeric excipient, Eudragit EPO. The formation of the eutectic was confirmed to have taken place in situ in the presence of the polymer, with the reaction yield determined using a multivariate calibration model constructed by combining spectroscopic analysis with partial least-squares regression modeling. The ternary extrudates exhibited a dissolution profile similar to that of the 1:2 prepared eutectic, suggesting a physical distribution (or suspension) of the in situ synthesized eutectic contents within the polymeric matrix.

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来源期刊
Molecular Pharmaceutics
Molecular Pharmaceutics 医学-药学
CiteScore
8.00
自引率
6.10%
发文量
391
审稿时长
2 months
期刊介绍: Molecular Pharmaceutics publishes the results of original research that contributes significantly to the molecular mechanistic understanding of drug delivery and drug delivery systems. The journal encourages contributions describing research at the interface of drug discovery and drug development. Scientific areas within the scope of the journal include physical and pharmaceutical chemistry, biochemistry and biophysics, molecular and cellular biology, and polymer and materials science as they relate to drug and drug delivery system efficacy. Mechanistic Drug Delivery and Drug Targeting research on modulating activity and efficacy of a drug or drug product is within the scope of Molecular Pharmaceutics. Theoretical and experimental peer-reviewed research articles, communications, reviews, and perspectives are welcomed.
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