{"title":"Cutting-Edge Approaches in the Co-Amorphization Process.","authors":"Azza A K Mahmoud, Géza Regdon, Katalin Kristó","doi":"10.3390/pharmaceutics17070850","DOIUrl":null,"url":null,"abstract":"<p><p><b>Background:</b> Recently, the co-amorphization method has been widely used to refine the bioavailability characteristics of poorly soluble drugs in addition to overcoming the drawbacks of other traditional amorphization techniques. <b>Objectives:</b> The main aim of this systematic review is to present an extensive outline of different co-former classes, co-former selection, and evaluation of produced co-amorphous systems. Methods: The systematic research was carried out based on three different databases, including PubMed, Scopus, and Web of Science time using co-amorphous, co-former, and drug as keywords. The selected papers were written in the English language and published between 2016 and 2024, and they focused on the co-amorphous systems, while articles discussing other amorphization techniques and crystallization processes were excluded. <b>Results:</b> 127 peer-reviewed articles were selected and summarized. <b>Conclusions:</b> This paper revealed that amino acid is the most commonly used co-former, specifically arginine with acidic drugs and tryptophan with acidic and basic drugs, and it reported other co-formers that were used and different co-amorphous systems with their dissolution behaviour and stabilities, and different computational tools that were applied in the selection of co-former and process result evaluation.</p>","PeriodicalId":19894,"journal":{"name":"Pharmaceutics","volume":"17 7","pages":""},"PeriodicalIF":5.5000,"publicationDate":"2025-06-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12297907/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmaceutics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3390/pharmaceutics17070850","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Recently, the co-amorphization method has been widely used to refine the bioavailability characteristics of poorly soluble drugs in addition to overcoming the drawbacks of other traditional amorphization techniques. Objectives: The main aim of this systematic review is to present an extensive outline of different co-former classes, co-former selection, and evaluation of produced co-amorphous systems. Methods: The systematic research was carried out based on three different databases, including PubMed, Scopus, and Web of Science time using co-amorphous, co-former, and drug as keywords. The selected papers were written in the English language and published between 2016 and 2024, and they focused on the co-amorphous systems, while articles discussing other amorphization techniques and crystallization processes were excluded. Results: 127 peer-reviewed articles were selected and summarized. Conclusions: This paper revealed that amino acid is the most commonly used co-former, specifically arginine with acidic drugs and tryptophan with acidic and basic drugs, and it reported other co-formers that were used and different co-amorphous systems with their dissolution behaviour and stabilities, and different computational tools that were applied in the selection of co-former and process result evaluation.
背景:近年来,共非晶化方法被广泛用于改善难溶性药物的生物利用度特征,同时克服了其他传统非晶化技术的缺点。目的:这篇系统综述的主要目的是对不同的共成型物类别、共成型物的选择和生产的共非晶体系的评估进行广泛的概述。方法:基于PubMed、Scopus和Web of Science time 3个不同的数据库,以co-amorphous、co-former和drug为关键词进行系统研究。入选论文均为英文,发表时间在2016年至2024年之间,主要集中在共非晶体系,而讨论其他非晶化技术和结晶过程的文章被排除在外。结果:选取并总结同行评议文章127篇。结论:氨基酸是最常用的共成体,特别是精氨酸与酸性药物和色氨酸与酸性和碱性药物的共成体,并报道了所使用的其他共成体和不同的共晶体系的溶解行为和稳定性,以及不同的计算工具在共成体的选择和工艺结果评价中的应用。
PharmaceuticsPharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.90
自引率
11.10%
发文量
2379
审稿时长
16.41 days
期刊介绍:
Pharmaceutics (ISSN 1999-4923) is an open access journal which provides an advanced forum for the science and technology of pharmaceutics and biopharmaceutics. It publishes reviews, regular research papers, communications, and short notes. Covered topics include pharmacokinetics, toxicokinetics, pharmacodynamics, pharmacogenetics and pharmacogenomics, and pharmaceutical formulation. Our aim is to encourage scientists to publish their experimental and theoretical details in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.