Jug Mario, Mura Paola Angela
Department of Pharmaceutical Technology, Faculty of Pharmacy and Biochemistry, University of Zagreb, A. Kovačića 1, 10000 Zagreb, Croatia.
Department of Chemistry 'Ugo Schiff', School of Human Health Sciences, University of Florence, Via Schiff 6, Sesto Fiorentino, 50019 Florence, Italy.
Pharmaceutics. 2018 Oct 16;10(4):189. doi: 10.3390/pharmaceutics10040189.
Among the different techniques proposed for preparing cyclodextrin inclusion complex in the solid state, mechanochemical activation by grinding appears as a fast, highly efficient, convenient, versatile, sustainable, and eco-friendly solvent-free method. This review is intended to give a systematic overview of the currently available data in this field, highlighting both the advantages as well as the shortcomings of such an approach. The possible mechanisms involved in the inclusion complex formation in the solid state, by grinding, have been illustrated. For each type of applied milling device, the respective process variables have been examined and discussed, together with the characteristics of the obtained products, also in relation with the physicochemical characteristics of both the drug and cyclodextrin subjected to grinding. The critical process parameters were evidenced in order to provide a useful guide for a rational selection of the most suitable conditions for an efficient inclusion complex preparation by grinding, with the final purpose of promoting a wider use of this effective solvent-free cyclodextrin inclusion complex preparation method in the solid state.
在为制备固态环糊精包合物而提出的不同技术中,研磨法进行的机械化学活化似乎是一种快速、高效、便捷、通用、可持续且环保的无溶剂方法。本综述旨在对该领域目前可用的数据进行系统概述,突出这种方法的优点和缺点。文中阐述了通过研磨在固态中形成包合物可能涉及的机制。对于每种应用的研磨设备,研究并讨论了各自的工艺变量,以及所得产品的特性,同时还涉及了研磨的药物和环糊精的物理化学特性。确定了关键工艺参数,以便为合理选择最适合的条件以通过研磨高效制备包合物提供有用的指导,最终目的是促进这种有效的无溶剂固态环糊精包合物制备方法得到更广泛的应用。