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苯甲酰胺:二苄基砜共晶的特征、溶解度和本征溶出行为。

Characterisation, solubility and intrinsic dissolution behaviour of benzamide: dibenzyl sulfoxide cocrystal.

机构信息

School of Pharmacy and Pharmaceutical Sciences, Trinity College Dublin, Dublin 2, Ireland.

出版信息

Int J Pharm. 2012 Jan 17;422(1-2):24-32. doi: 10.1016/j.ijpharm.2011.10.016. Epub 2011 Oct 13.

DOI:10.1016/j.ijpharm.2011.10.016
PMID:22020274
Abstract

This study examined the 1:1 cocrystal benzamide:dibenzyl sulfoxide, comprising the poorly water soluble dibenzyl sulfoxide (DBSO) and the more soluble benzamide (BA), to establish if this cocrystal shows advantages in terms of solubility and dissolution in comparison to its pure components and to a physical mixture. Solubility studies were performed by measuring DBSO solubility as a function of BA concentration, and a ternary phase diagram was constructed. Dissolution was examined through intrinsic dissolution studies. Solid-state characterisation was carried out by powder X-ray diffraction (PXRD), energy-dispersive X-ray diffraction (EDX), infra-red spectroscopy (ATR-FTIR) and thermal analysis. DBSO solubility was increased by means of complexation with BA. For the cocrystal, the solubility of both components was decreased in comparison to pure components. The cocrystal was identified as metastable and incongruently saturating. Dissolution studies revealed that dissolution of DBSO from the cocrystal was not enhanced in comparison to the pure compound or a physical mix, while BA release was retarded and followed square root of time kinetics. At the disk surface a layer of DBSO was found. The extent of complexation in solution can change the stability of the complex substantially. Incongruent solubility and dissolution behaviour of a cocrystal can result in no enhancement in the dissolution of the less soluble component and retardation of release of the more soluble component.

摘要

本研究考察了 1:1 的苯甲酰胺-二苄基砜共晶,其包含难溶于水的二苄基砜(DBSO)和更易溶于水的苯甲酰胺(BA),以确定与纯组分和物理混合物相比,该共晶在溶解度和溶解方面是否具有优势。通过测量 BA 浓度对 DBSO 溶解度的影响来进行溶解度研究,并构建三元相图。通过内在溶解研究来考察溶解。通过粉末 X 射线衍射(PXRD)、能量分散 X 射线衍射(EDX)、红外光谱(ATR-FTIR)和热分析进行固态特性研究。通过与 BA 络合增加了 DBSO 的溶解度。与纯组分相比,共晶中两种组分的溶解度均降低。共晶被鉴定为亚稳和非一致饱和。溶解研究表明,与纯化合物或物理混合物相比,共晶中 DBSO 的溶解没有得到增强,而 BA 的释放受到延迟并遵循平方根时间动力学。在磁盘表面发现了一层 DBSO。溶液中络合的程度可以大大改变络合物的稳定性。共晶的不一致溶解度和溶解行为可能导致较难溶组分的溶解没有得到增强,而较易溶组分的释放受到延迟。

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