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长效稳定且高溶解性的苯扎贝特-格列齐特共无定形二元体系。

Long-Term Stabilized and Highly Soluble Bezafibrate-Gliclazide Co-Amorphous Binary System.

作者信息

Cruz-Angeles Jorge, Martínez Luz María, López López Alice M, Cabada-Aguirre Paulina, Videa Marcelo, Flores Alejandra

机构信息

School of Engineering and Sciences, Tecnologico de Monterrey, Campus Monterrey, Ave. Eugenio Garza Sada 2501 Sur, C.P. 64849, Monterrey, N.L., Mexico.

出版信息

AAPS PharmSciTech. 2025 Jan 30;26(1):48. doi: 10.1208/s12249-025-03045-3.

Abstract

Metabolic syndrome (MS) has a high prevalence, with an estimated one-quarter of the world population affected by this pathological condition. Among the diseases of this syndrome are dysregulation of lipids, hypertension, and insulin resistance. Unfortunately, available drugs in the market used for treating MS, as almost 75% of all drugs, are highly insoluble, presenting a significant demand for strategies to increase their solubility. Taking advantage of the fact that drugs in the amorphous state can provide a solubility enhancement, a new drug-drug co-amorphous (CoA) formulation to potentially simultaneously treat two or more MS conditions was explored, combining the co-formers Bezafibrate (BZT) a lipid-regulating drug, and Gliclazide (GZD) a hypoglycemic agent. A phase diagram was constructed to characterize the binary system's thermal properties, including glass transition temperatures of all compositions studied. The formulations were characterized by FTIR; redshifts of IR bands from 1547 to 1538 cm and 1717 to 1609 cm were observed due to the formation of intermolecular interactions, such as hydrogen bonds. The co-amorphous binary systems lead to an increase in the solubility of both BZT and GZD; specifically, for the composition x = 0.5, the increase was 2.1× for BZT and 1.5 times for GZD while for x = 0.7 an increase of 4× of BZT was achieved. The structural stability of the samples was verified by XRD and DSC, showing long-term stability retention of the amorphous state for more than eight years. The enhanced solubility and stability of the co-amorphous systems make them potential formulations for regulating lipids and lowering glycemia.

摘要

代谢综合征(MS)的患病率很高,估计全球有四分之一的人口受此病理状况影响。该综合征的疾病包括脂质代谢失调、高血压和胰岛素抵抗。不幸的是,市场上用于治疗MS的现有药物,几乎与所有药物的75%一样,高度不溶,因此对提高其溶解度的策略有很大需求。利用无定形状态的药物可提高溶解度这一事实,探索了一种新型药物 - 药物共无定形(CoA)制剂,以潜在地同时治疗两种或更多种MS病症,该制剂将共形成物——降脂药物苯扎贝特(BZT)和降糖药格列齐特(GZD)结合在一起。构建了相图以表征二元体系的热性质,包括所研究的所有组合物的玻璃化转变温度。通过傅里叶变换红外光谱(FTIR)对制剂进行表征;由于形成了分子间相互作用,如氢键,观察到红外波段从1547 cm至1538 cm以及从1717 cm至1609 cm出现红移。共无定形二元体系导致BZT和GZD的溶解度均增加;具体而言,对于组成x = 0.5,BZT的溶解度增加了2.1倍,GZD增加了1.5倍,而对于x = 0.7,BZT的溶解度增加了4倍。通过X射线衍射(XRD)和差示扫描量热法(DSC)验证了样品的结构稳定性,结果表明无定形状态在八年多时间内保持长期稳定性。共无定形体系增强的溶解度和稳定性使其成为调节脂质和降低血糖的潜在制剂。

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