{"title":"Crosslink Dynamics Control Injection Force and Flow Profiles of Non-Covalent Gels","authors":"Noah Eckman, Eric A. Appel","doi":"10.1021/acs.macromol.5c00854","DOIUrl":null,"url":null,"abstract":"Dynamically cross-linked hydrogels have found remarkable utility in 3D bioprinting and injectable slow-release delivery of pharmaceutics and vaccines, applications which take advantage of their ability to flow through needles or extrusion devices with relative ease. Predicting the force required to inject or extrude dynamic hydrogel materials is paramount to their application. Here, we report an injectable dynamic hydrogel with facile tunability of the cross-link exchange rate using a small-molecule surfactant. We found surprising nonmonotonic trends in injection force with respect to cross-link dynamics, not explained by traditional flow rheology measurements. By using an optical in situ capillary rheometer, we found that wall slip is the dominant mechanism influencing flow profiles, rather than shear banding, as has been reported in previous studies of dynamically cross-linked hydrogels. We hypothesize that the main driver of flow rheology and injection force for these materials is the combination of a lower slip distance and bulk stiffness with increasing dynamicity, balancing the bulk cohesive force with adhesive forces to the wall. Finally, by developing new models which describe the flow behavior of noncovalent gels, we present new criteria for extrudability, enabling better predictions for operating conditions of downstream applications of dynamic hydrogels.","PeriodicalId":51,"journal":{"name":"Macromolecules","volume":"9 1","pages":""},"PeriodicalIF":5.1000,"publicationDate":"2025-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Macromolecules","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.macromol.5c00854","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
Dynamically cross-linked hydrogels have found remarkable utility in 3D bioprinting and injectable slow-release delivery of pharmaceutics and vaccines, applications which take advantage of their ability to flow through needles or extrusion devices with relative ease. Predicting the force required to inject or extrude dynamic hydrogel materials is paramount to their application. Here, we report an injectable dynamic hydrogel with facile tunability of the cross-link exchange rate using a small-molecule surfactant. We found surprising nonmonotonic trends in injection force with respect to cross-link dynamics, not explained by traditional flow rheology measurements. By using an optical in situ capillary rheometer, we found that wall slip is the dominant mechanism influencing flow profiles, rather than shear banding, as has been reported in previous studies of dynamically cross-linked hydrogels. We hypothesize that the main driver of flow rheology and injection force for these materials is the combination of a lower slip distance and bulk stiffness with increasing dynamicity, balancing the bulk cohesive force with adhesive forces to the wall. Finally, by developing new models which describe the flow behavior of noncovalent gels, we present new criteria for extrudability, enabling better predictions for operating conditions of downstream applications of dynamic hydrogels.
期刊介绍:
Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.