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新型戊内酰胺-芬苯达唑纳米晶的体外溶出性能得到改善。

Nanocrystals of Novel Valerolactam-Fenbendazole Hybrid with Improved in vitro Dissolution Performance.

机构信息

Área de Farmacología, CIENFAR, Facultad de Química, Universidad de la República (Udelar), General Flores 2124, 11800, Montevideo, Uruguay.

Unidad de Investigación y Desarrollo en Tecnología Farmacéutica (UNITEFA), CONICET and Departamento de Ciencias Farmacéuticas, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Córdoba, Argentina.

出版信息

AAPS PharmSciTech. 2020 Aug 17;21(7):237. doi: 10.1208/s12249-020-01777-y.

Abstract

Valero-fenbendazole (VAL-FBZ) is a novel hybrid compound with in vitro anthelmintic activity, designed and synthesized to address the global problem of resistance to anthelmintic compounds. This new molecule derives from fenbendazole (FBZ), a well-known commercially available benzimidazole used in veterinary medicine despite its poor water solubility. In this work, we report for the first time a strategy to solve the solubility problems of FBZ and VAL-FBZ by means of self-dispersible nanocrystals (SDNC). Nanocrystals were prepared by media milling followed by a spray-drying step, and a comprehensive and exhaustive structural and physicochemical characterization was carried out, in order to understand the systems and their behavior. The formulation poloxamer 188 (P188):FBZ 1:1 turned out with the best process yield (53%) and re-dispersability properties, particle size average of 258 nm, and polydispersity index of 0.2 after redispersion in water. The dissolution profile showed a markedly increased dissolution rate compared with the simple mixture of the components (80% FBZ dissolved in 15 min from the SDNC vs 14% from the control formulation). FTIR spectroscopy, thermal analysis, and X-Ray Powder Diffraction (XRPD) studies showed no chemical interactions between components and an extensive confocal Raman microscopy analysis of the formulations showed very homogeneous spatial distribution of components in the SDNC samples. This manufacturing process was then successfully transferred for preparing and characterizing VAL-FBZ:P188 (1:1) SDNC with similar results, suggesting the promising interest of a novel anthelmintic with improved biopharmaceutical behavior. In conclusion, new FBZ and VAL-FBZ SDNC with improved dissolution rate were successfully prepared and characterized. Graphical abstract.

摘要

伐伦硝唑-芬苯达唑(VAL-FBZ)是一种具有体外驱虫活性的新型杂合化合物,旨在解决抗寄生虫化合物耐药性这一全球性问题。该新型分子源自芬苯达唑(FBZ),后者是一种广为人知的兽医用苯并咪唑类驱虫药物,但水溶性较差。本研究首次报道了一种通过自分散纳米晶体(SDNC)解决 FBZ 和 VAL-FBZ 溶解度问题的策略。纳米晶体是通过介质研磨随后喷雾干燥制备的,并对其进行了全面详尽的结构和物理化学特性研究,以了解系统及其行为。泊洛沙姆 188(P188):FBZ 1:1 的配方表现出最佳的工艺收率(53%)和再分散性,重分散后粒径平均为 258nm,多分散指数为 0.2。与简单的组分混合物相比,溶解曲线显示出明显的溶解速率提高(80%的 FBZ 在 15 分钟内从 SDNC 溶解,而对照配方为 14%)。傅里叶变换红外光谱、热分析和 X 射线粉末衍射(XRPD)研究表明,各组分之间没有发生化学相互作用,对制剂进行广泛的共聚焦拉曼显微镜分析表明,SDNC 样品中各组分具有非常均匀的空间分布。然后成功地将该制造工艺转移到制备和表征 VAL-FBZ:P188(1:1)SDNC,得到了类似的结果,这表明具有改善的生物制药特性的新型驱虫剂具有广阔的应用前景。总之,成功制备和表征了具有改善溶解速率的新型 FBZ 和 VAL-FBZ SDNC。

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