{"id":{"repo_id":"uiuc","oai_identifier":"oai:www.ideals.illinois.edu:2142/108254"},"canonical_url":"https://search.dev.ndltd.org/etd/uiuc/oai:www.ideals.illinois.edu:2142/108254","repository":{"repo_id":"uiuc","name":"University of Illinois - Urbana-Champaign","base_url":"https://www.ideals.illinois.edu/oai-pmh"},"display":{"title":"Engineering tough, hygroscopic, and active hydrogels for surgical simulation and anti-biofouling","abstract":"Hydrogels have emerged as a class of materials useful for a variety of contexts, including tissue engineering, anti-fouling, drug release, medical devices, and flexible electronics. The usefulness of hydrogels in these contexts stems from their structure, consisting of a 3D cross-linked polymer network containing mostly water. This structure leads to a material with tunable, tissue-like softness and water content, biocompatibility, resistance to biological fouling, high porosity, and transparency. However, the utility of these numerous properties is often offset by hydrogel brittleness and, if exposed directly to air, eventual drying. Therefore, hydrogels are difficult to use for applications involving puncture or high shear forces, such as surgical simulation, as well as open-air environments. The goal of my thesis research is to bridge this technological gap by engineering hydrogels that are both tough and non-drying so that new applications may be opened for this unique material. Chapter 2 discusses a general strategy to improve hydrogel toughness by forming a highly concentrated polyacrylamide hydrogel with a low number of cross-links, thereby increasing the polymer entanglements that may form between cross-linking junctions. Chapter 3 demonstrates that the drying of hydrogels exposed to air can be prevented by incorporating glycerol within the gel network, leading to a hygroscopic material that draws humidity from the surrounding ambient air. Both of these properties of toughness and non-drying are combined in Chapter 4 to demonstrate the 3D printing of suturable organ mimics for preoperative planning and surgical training. Further applications of the tough hydrogel in drug release are shown in Chapter 5. In this study, drug-binding cyclodextrin linked within the tough polyacrylamide hydrogel releases its molecular cargo in response to tensile stretching. The tough hydrogels also exhibited anti-fouling properties due to the high water content in the gel. Therefore, they were used for anti-fouling in contexts where physical forces are present. Chapter 6 demonstrates the anti-fouling capabilities of the tough hydrogel by layering it on top of a vibrating dielectric actuator to actively remove pre-formed biofilms. Finally, in Chapter 7, the anti-fouling property of the hydrogel is enhanced by interpenetrating the network with polyvinylpyrrolidone complexed with anti-bacterial iodine to prevent corrosion of stainless steel by sulfate-reducing bacteria. Overall, tough and non-drying hydrogels were successfully engineered and then used for a variety of applications, including model organs for surgical simulation, flexible electronics, drug release, and anti-biofouling.","abstract_html":"Hydrogels have emerged as a class of materials useful for a variety of contexts, including tissue engineering, anti-fouling, drug release, medical devices, and flexible electronics. The usefulness of hydrogels in these contexts stems from their structure, consisting of a 3D cross-linked polymer network containing mostly water. This structure leads to a material with tunable, tissue-like softness and water content, biocompatibility, resistance to biological fouling, high porosity, and transparency. However, the utility of these numerous properties is often offset by hydrogel brittleness and, if exposed directly to air, eventual drying. Therefore, hydrogels are difficult to use for applications involving puncture or high shear forces, such as surgical simulation, as well as open-air environments. The goal of my thesis research is to bridge this technological gap by engineering hydrogels that are both tough and non-drying so that new applications may be opened for this unique material. Chapter 2 discusses a general strategy to improve hydrogel toughness by forming a highly concentrated polyacrylamide hydrogel with a low number of cross-links, thereby increasing the polymer entanglements that may form between cross-linking junctions. Chapter 3 demonstrates that the drying of hydrogels exposed to air can be prevented by incorporating glycerol within the gel network, leading to a hygroscopic material that draws humidity from the surrounding ambient air. Both of these properties of toughness and non-drying are combined in Chapter 4 to demonstrate the 3D printing of suturable organ mimics for preoperative planning and surgical training. Further applications of the tough hydrogel in drug release are shown in Chapter 5. In this study, drug-binding cyclodextrin linked within the tough polyacrylamide hydrogel releases its molecular cargo in response to tensile stretching. The tough hydrogels also exhibited anti-fouling properties due to the high water content in the gel. Therefore, they were used for anti-fouling in contexts where physical forces are present. Chapter 6 demonstrates the anti-fouling capabilities of the tough hydrogel by layering it on top of a vibrating dielectric actuator to actively remove pre-formed biofilms. Finally, in Chapter 7, the anti-fouling property of the hydrogel is enhanced by interpenetrating the network with polyvinylpyrrolidone complexed with anti-bacterial iodine to prevent corrosion of stainless steel by sulfate-reducing bacteria. Overall, tough and non-drying hydrogels were successfully engineered and then used for a variety of applications, including model organs for surgical simulation, flexible electronics, drug release, and anti-biofouling.","abstract_has_math":false,"creators":["Ballance, William C"],"institution":"University of Illinois at Urbana-Champaign","degree_name":"Ph.D.","degree_level":"Dissertation","degree_discipline":"Chemical Engineering","degree_department":null,"school":null,"contributors":["Kong, Hyunjoon","Sing, Charles","Rogers, Simon","Phillips, Heidi"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2020,"date_issued":"2020-08-27T00:49:56Z","date_published":"2020-08-27T00:49:56Z","updated_at":"2026-07-22T22:24:48Z","subjects":["hydrogel","toughness","anti-fouling","hygroscopic","polyacrylamide","3D printing","drug release","cyclodextrin"],"languages":["en"],"rights":["Copyright 2020 William C. Ballance"],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"http://hdl.handle.net/2142/108254","outbound_label":"Handle","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Kong, Hyunjoon","Sing, Charles","Rogers, Simon","Phillips, Heidi"]},{"key":"dc:creator","label":"Author","values":["Ballance, William C"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2020-08-27T00:49:56Z","2022-08-27T00:51:40Z","2020-04-20","2020-05"]},{"key":"dc:type","label":"Dc Type","values":["text","Thesis"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Chemical Engineering"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Dissertation"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Ph.D."]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["University of Illinois at Urbana-Champaign"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["hydrogel","toughness","anti-fouling","hygroscopic","polyacrylamide","3D printing","drug release","cyclodextrin"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["en"]},{"key":"dc:rights","label":"Dc Rights","values":["Copyright 2020 William C. 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Therefore, hydrogels are difficult to use for applications involving puncture or high shear forces, such as surgical simulation, as well as open-air environments. The goal of my thesis research is to bridge this technological gap by engineering hydrogels that are both tough and non-drying so that new applications may be opened for this unique material. Chapter 2 discusses a general strategy to improve hydrogel toughness by forming a highly concentrated polyacrylamide hydrogel with a low number of cross-links, thereby increasing the polymer entanglements that may form between cross-linking junctions. Chapter 3 demonstrates that the drying of hydrogels exposed to air can be prevented by incorporating glycerol within the gel network, leading to a hygroscopic material that draws humidity from the surrounding ambient air. Both of these properties of toughness and non-drying are combined in Chapter 4 to demonstrate the 3D printing of suturable organ mimics for preoperative planning and surgical training. Further applications of the tough hydrogel in drug release are shown in Chapter 5. In this study, drug-binding cyclodextrin linked within the tough polyacrylamide hydrogel releases its molecular cargo in response to tensile stretching. The tough hydrogels also exhibited anti-fouling properties due to the high water content in the gel. Therefore, they were used for anti-fouling in contexts where physical forces are present. Chapter 6 demonstrates the anti-fouling capabilities of the tough hydrogel by layering it on top of a vibrating dielectric actuator to actively remove pre-formed biofilms. Finally, in Chapter 7, the anti-fouling property of the hydrogel is enhanced by interpenetrating the network with polyvinylpyrrolidone complexed with anti-bacterial iodine to prevent corrosion of stainless steel by sulfate-reducing bacteria. Overall, tough and non-drying hydrogels were successfully engineered and then used for a variety of applications, including model organs for surgical simulation, flexible electronics, drug release, and anti-biofouling.","Submission published under a 24 month embargo labeled 'Closed Access', the embargo will last until 2022-05-01","The student, William Ballance, accepted the attached license on 2020-04-17 at 13:35.","The student, William Ballance, submitted this Dissertation for approval on 2020-04-17 at 13:51.","This Dissertation was approved for publication on 2020-04-20 at 09:55.","DSpace SAF Submission Ingestion Package generated from Vireo submission #14995 on 2020-08-25 at 17:40:21","Made available in DSpace on 2020-08-27T00:49:56Z (GMT). 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The usefulness of hydrogels in these contexts stems from their structure, consisting of a 3D cross-linked polymer network containing mostly water. This structure leads to a material with tunable, tissue-like softness and water content, biocompatibility, resistance to biological fouling, high porosity, and transparency. However, the utility of these numerous properties is often offset by hydrogel brittleness and, if exposed directly to air, eventual drying. Therefore, hydrogels are difficult to use for applications involving puncture or high shear forces, such as surgical simulation, as well as open-air environments. The goal of my thesis research is to bridge this technological gap by engineering hydrogels that are both tough and non-drying so that new applications may be opened for this unique material. Chapter 2 discusses a general strategy to improve hydrogel toughness by forming a highly concentrated polyacrylamide hydrogel with a low number of cross-links, thereby increasing the polymer entanglements that may form between cross-linking junctions. Chapter 3 demonstrates that the drying of hydrogels exposed to air can be prevented by incorporating glycerol within the gel network, leading to a hygroscopic material that draws humidity from the surrounding ambient air. Both of these properties of toughness and non-drying are combined in Chapter 4 to demonstrate the 3D printing of suturable organ mimics for preoperative planning and surgical training. Further applications of the tough hydrogel in drug release are shown in Chapter 5. In this study, drug-binding cyclodextrin linked within the tough polyacrylamide hydrogel releases its molecular cargo in response to tensile stretching. The tough hydrogels also exhibited anti-fouling properties due to the high water content in the gel. Therefore, they were used for anti-fouling in contexts where physical forces are present. Chapter 6 demonstrates the anti-fouling capabilities of the tough hydrogel by layering it on top of a vibrating dielectric actuator to actively remove pre-formed biofilms. Finally, in Chapter 7, the anti-fouling property of the hydrogel is enhanced by interpenetrating the network with polyvinylpyrrolidone complexed with anti-bacterial iodine to prevent corrosion of stainless steel by sulfate-reducing bacteria. Overall, tough and non-drying hydrogels were successfully engineered and then used for a variety of applications, including model organs for surgical simulation, flexible electronics, drug release, and anti-biofouling.","Submission published under a 24 month embargo labeled 'Closed Access', the embargo will last until 2022-05-01","The student, William Ballance, accepted the attached license on 2020-04-17 at 13:35.","The student, William Ballance, submitted this Dissertation for approval on 2020-04-17 at 13:51.","This Dissertation was approved for publication on 2020-04-20 at 09:55.","DSpace SAF Submission Ingestion Package generated from Vireo submission #14995 on 2020-08-25 at 17:40:21","Made available in DSpace on 2020-08-27T00:49:56Z (GMT). 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