Hot Melt Extrusion Technique for Developing Pharmaceutical Co-crystals: A Review

Q2 Pharmacology, Toxicology and Pharmaceutics
Ritu Rathi, Sanshita, Inderbir Singh
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引用次数: 0

Abstract

In the era of pharmaceutical research and development, the most challenging aspect is to enhance the physicochemical properties of drugs. Hot Melt Extrusion (HME) is a solvent-free, one-step, continuous, scalable, and industrially feasible method for developing pharmaceutical co-crystals. Co-crystallization, as a technique, has gained significant attention for its potential to modify various physicochemical properties of drugs like solubility, stability, compressibility, permeability, taste masking, and therapeutic efficacy. We determine the characteristic features of HME and explore published literature using the keywords, HME, co-crystals, and PAT, in databases, such as PubMed, Google Scholar, ScienceDirect, and Research Gate. The present review embarks on a detailed journey through the multifaceted domain of HME and its pivotal role in co-crystal development. The process parameters, such as temperature, extruder type, screw configuration, screw speed, and feed rate, are involved in determining the characteristics of the co-crystals produced. Additionally, the review explores the role of materials, including Active Pharmaceutical Ingredients (APIs), plasticizers, polymers, and other pharmaceutical aids, underlining their impact on co-crystal development. The existing literature on HME and its application for pharmaceutical co-crystal production is comprehensively surveyed. The review highlights the utility of Process Analytical Technology (PAT) in realtime process control. The role of HME in the future of pharmaceutical co-crystal development is discussed, making this review essential for researchers and industry professionals alike.
开发药用共晶体的热熔挤压技术:综述
在药物研发时代,最具挑战性的问题是如何提高药物的理化特性。热熔挤压(HME)是一种无溶剂、一步法、连续、可扩展且在工业上可行的药物共晶体开发方法。我们确定了 HME 的特征,并在 PubMed、Google Scholar、ScienceDirect 和 Research Gate 等数据库中使用 HME、共晶体和 PAT 等关键词搜索了已发表的文献。温度、挤出机类型、螺杆配置、螺杆速度和喂料速率等工艺参数决定了所生产共晶体的特性。此外,该综述还探讨了材料的作用,包括活性药物成分(API)、增塑剂、聚合物和其他制药助剂,强调了它们对共晶体开发的影响。综述强调了过程分析技术(PAT)在实时过程控制中的作用。此外,还讨论了 HME 在未来药用共晶体开发中的作用,因此本综述对研究人员和行业专业人士都非常重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Drug Delivery Letters
Drug Delivery Letters Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
CiteScore
1.70
自引率
0.00%
发文量
30
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