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新型自组装美沙拉嗪-硫糖铝复合物:制备、表征及制剂方面

Novel self-assembled mesalamine-sucralfate complexes: preparation, characterization, and formulation aspects.

作者信息

Ispas-Szabo Pompilia, Friciu Mihaela Maria, Nguyen Phuong, Dumoulin Yves, Mateescu Mircea Alexandru

机构信息

a Department of Chemistry and Center Pharmaqam , Université du Québec à Montréal , Montréal , Québec , Canada.

出版信息

Drug Dev Ind Pharm. 2016;42(7):1183-93. doi: 10.3109/03639045.2015.1118493. Epub 2015 Dec 15.

Abstract

Two well-known active agents, mesalamine (MES) and sucralfate (SUC), were investigated for possible utilization as fixed-dose combination product. The anti-inflammatory action of MES in association with bioadhesiveness and mucosal healing properties of SUC were considered promising for the development of a new compound containing both molecules, aimed as an improved treatment of ulcerative colitis. The present study investigates the capacity of the two active agents to interact and generate a new and stable entity via self-assembling. Spray-drying was used to co-process the two active principles from an aqueous mixture where the ratio MES:SUC was in the range 25:75, 50:50, and 75:25. The structural data (X-Ray, FTIR, SEM, DSC, and (1)H NMR) have shown that MES and SUC are interacting leading to complexes with properties differing from those of each separate active agent and from their physical blends. (1)H NMR results indicated that complexation occurred when the aqueous suspensions of drugs were mixed, prior to spray-drying. Drug-drug self-assembling was the driving mechanism in the formation of the new entity. Based on the structural data, a hypothetical structure of the complex was proposed. Co-processing of MES and SUC represents a simple and useful procedure to prepare new self-assembled compounds by valorizing the ionic interactions between the two entities. Preliminary studies with oral solid dosage forms based on MES-SUC complexes tested in vitro have shown a controlled MES release, opening the perspective of a new colon-targeted delivery system and a novel class of compounds with therapeutic application in inflammatory bowel diseases.

摘要

研究了两种著名的活性药物美沙拉嗪(MES)和硫糖铝(SUC)作为固定剂量复方制剂的潜在用途。MES的抗炎作用与SUC的生物黏附性和黏膜愈合特性相结合,有望开发出一种包含这两种分子的新化合物,旨在改善溃疡性结肠炎的治疗。本研究考察了这两种活性药物通过自组装相互作用并生成新的稳定实体的能力。采用喷雾干燥法从MES:SUC比例为25:75、50:50和75:25的水性混合物中共处理这两种活性成分。结构数据(X射线、傅里叶变换红外光谱、扫描电子显微镜、差示扫描量热法和氢核磁共振)表明,MES和SUC相互作用形成了性质不同于各单一活性成分及其物理混合物的复合物。氢核磁共振结果表明,在喷雾干燥之前,当药物的水性悬浮液混合时就发生了络合作用。药物-药物自组装是形成新实体的驱动机制。基于结构数据,提出了复合物的假设结构。MES和SUC的共处理是一种简单且有用的方法,通过利用两种实体之间的离子相互作用来制备新的自组装化合物。基于MES-SUC复合物的口服固体剂型的体外初步研究表明,MES的释放得到了控制,为新型结肠靶向给药系统和一类在炎症性肠病中有治疗应用的新型化合物开辟了前景。

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