{"title":"Modulating Milling-Induced Amorphization Propensity of Drug Crystals by Cocrystallization","authors":"Sayantan Chattoraj, and , Changquan Calvin Sun*, ","doi":"10.1021/acs.cgd.5c0016310.1021/acs.cgd.5c00163","DOIUrl":null,"url":null,"abstract":"<p >Amorphization is a common phase transformation that occurs during stress-intensive processes, such as milling. This study aims to evaluate the impact of cocrystallization on the amorphization behavior of sulfamethazine (SMT) during cryo-milling using two SMT cocrystals: one with <i>p</i>-hydroxybenzoic acid (SMT-HBA) and the other with benzamide (SMT-BNZ). At short milling durations (<i>t</i> < 30 min), the rank order of amorphous generation was SMT-BNZ > SMT ≫ SMT-HBA. However, after 2 h of cryo-milling, this order shifted to SMT-HBA > SMT-BNZ > SMT. Both SMT and SMT-BNZ exhibited an earlier onset of amorphization than SMT-HBA. The delayed amorphization onset of SMT-HBA is attributed to its higher crystal lattice strength. The rank order of amorphization extent over longer milling (up to 2 h) aligns with the physical stability of the generated amorphous phase, as assessed using configurational entropy and structural relaxation times based on the Adam–Gibbs equation. The combination of a slow onset of amorphization and the slow crystallization of the generated amorphous phase in SMT-HBA explains the shift in the rank order of amorphization extent over the entire milling duration. Understanding the interplay between crystal lattice strength and amorphous stability in stress-induced amorphization offers valuable guidance for mitigating the stress sensitivity of certain drugs through cocrystallization.</p>","PeriodicalId":34,"journal":{"name":"Crystal Growth & Design","volume":"25 9","pages":"3128–3136 3128–3136"},"PeriodicalIF":3.2000,"publicationDate":"2025-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Crystal Growth & Design","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.cgd.5c00163","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Amorphization is a common phase transformation that occurs during stress-intensive processes, such as milling. This study aims to evaluate the impact of cocrystallization on the amorphization behavior of sulfamethazine (SMT) during cryo-milling using two SMT cocrystals: one with p-hydroxybenzoic acid (SMT-HBA) and the other with benzamide (SMT-BNZ). At short milling durations (t < 30 min), the rank order of amorphous generation was SMT-BNZ > SMT ≫ SMT-HBA. However, after 2 h of cryo-milling, this order shifted to SMT-HBA > SMT-BNZ > SMT. Both SMT and SMT-BNZ exhibited an earlier onset of amorphization than SMT-HBA. The delayed amorphization onset of SMT-HBA is attributed to its higher crystal lattice strength. The rank order of amorphization extent over longer milling (up to 2 h) aligns with the physical stability of the generated amorphous phase, as assessed using configurational entropy and structural relaxation times based on the Adam–Gibbs equation. The combination of a slow onset of amorphization and the slow crystallization of the generated amorphous phase in SMT-HBA explains the shift in the rank order of amorphization extent over the entire milling duration. Understanding the interplay between crystal lattice strength and amorphous stability in stress-induced amorphization offers valuable guidance for mitigating the stress sensitivity of certain drugs through cocrystallization.
期刊介绍:
The aim of Crystal Growth & Design is to stimulate crossfertilization of knowledge among scientists and engineers working in the fields of crystal growth, crystal engineering, and the industrial application of crystalline materials.
Crystal Growth & Design publishes theoretical and experimental studies of the physical, chemical, and biological phenomena and processes related to the design, growth, and application of crystalline materials. Synergistic approaches originating from different disciplines and technologies and integrating the fields of crystal growth, crystal engineering, intermolecular interactions, and industrial application are encouraged.