Chavan Dhanashri D, Thorat Vandana M, Shete Amol S, Bhosale Rohit R, Patil Sarika J, Tiwari Devkumar D
Department of Pharmacology, Krishna Institute of Medical Sciences, Krishna Vishwa Vidyapeeth (Deemed to be University), Karad, IND.
Department of Pharmaceutics, Krishna Institute of Pharmacy, Krishna Vishwa Vidyapeeth (Deemed to be University), Karad, IND.
Cureus. 2024 Sep 27;16(9):e70328. doi: 10.7759/cureus.70328. eCollection 2024 Sep.
In recent years, the design of pharmaceutical cocrystals has garnered significant attention. The process of cocrystallization offers a remarkable opportunity to develop drug products with enhanced properties such as improved stability, solubility, hygroscopicity, dissolution rate, and bioavailability. This detailed review delves into this evolving area, thereby exploring its relevance in pharmaceutical formulation by defining cocrystals and their practical applications and also by discussing methods for their preparation as well as characterization. It also contrasts traditional and innovative techniques for cocrystal formation. Historically, cocrystals have been synthesized using methods like solvent evaporation, grinding, and slurry techniques; however, each has its own set of limitations under specific conditions. The latest trends in cocrystal formation lean toward more advanced approaches such as spray-drying, hot melt extrusion, and supercritical fluid technology, as well as the cutting-edge technique of laser irradiation. The aim behind developing new methods is not just to address the limitations of traditional cocrystallization techniques but also to streamline the process by introducing simpler steps and enabling a continuous production workflow for cocrystal products. In general, this full-length review article offers a report on various techniques available for the creation of pharmaceutical cocrystals, along with the methods for their evaluation. Moreover, it includes reporting developments and diverse applications of cocrystals along with the commercially available cocrystals in the pharmaceutical as well as medical domains.
近年来,药物共晶的设计备受关注。共结晶过程为开发具有增强性质(如提高稳定性、溶解度、吸湿性、溶解速率和生物利用度)的药物产品提供了绝佳机会。这篇详细的综述深入探讨了这个不断发展的领域,通过定义共晶及其实际应用,以及讨论其制备和表征方法,探索其在药物制剂中的相关性。它还对比了共晶形成的传统技术和创新技术。从历史上看,共晶是通过溶剂蒸发、研磨和浆体技术等方法合成的;然而,每种方法在特定条件下都有其自身的局限性。共晶形成的最新趋势倾向于更先进的方法,如喷雾干燥、热熔挤出和超临界流体技术,以及激光辐照这一前沿技术。开发新方法的目的不仅是为了解决传统共结晶技术的局限性,还在于通过引入更简单的步骤并实现共晶产品的连续生产流程来简化工艺。总体而言,这篇长篇综述文章提供了关于用于制备药物共晶的各种技术及其评估方法的报告。此外,它还包括共晶的发展和多样应用以及药物和医疗领域中已上市的共晶产品的报道。