{"title":"通过亲水性网络中两亲共聚物的原位自组装的仿生坚韧和消肿水凝胶","authors":"Changzhi Xu, Mengyu Li, Yi Wang, Yujiao Jiang, Jiahui Yin, Wenjie Ma, Xuelan Hu, Wanqing Zeng, Yanfei Ma, Shuwang Wu, Mingyuan Gao","doi":"10.1021/acsmacrolett.5c00188","DOIUrl":null,"url":null,"abstract":"Inspired by tropoelastin coacervation, a process in elastic fiber formation driven by hydrophobic interactions, we developed a tough, antiswelling hydrogel, PHEA-(PVA-<i>co</i>-PE), by incorporating amphiphilic poly(vinyl alcohol-<i>co</i>-ethylene) (PVA-<i>co</i>-PE) into a hydrophilic poly(2-hydroxyethyl acrylate) (PHEA) network. The PHEA-(PVA-<i>co</i>-PE) hydrogel was prepared by UV-induced polymerization of a PHEA precursor dimethyl sulfoxide (DMSO) solution containing PVA-<i>co</i>-PE, followed by immersion in water. During solvent exchange, PVA-<i>co</i>-PE self-assembled into micellar structures within the PHEA matrix, mimicking the coacervation of tropoelastin. Compared with PHEA and PVA-<i>co</i>-PE hydrogels, the strength of PHEA-(PVA-<i>co</i>-PE) increased by 83 and 7 times, while the toughness increased by 145 and 97 times. This strategy can be further extended to a variety of amphiphilic copolymers, demonstrating the universality. In vitro and in vivo tests demonstrated that the hydrogel possesses excellent biocompatibility and antiswelling capability. This study provides a simple method for developing a tough, biocompatible, and antiswelling hydrogel.","PeriodicalId":18,"journal":{"name":"ACS Macro Letters","volume":"29 1","pages":""},"PeriodicalIF":5.1000,"publicationDate":"2025-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bioinspired Tough and Antiswelling Hydrogel via in Situ Self-Assembly of Amphiphilic Copolymers within a Hydrophilic Network\",\"authors\":\"Changzhi Xu, Mengyu Li, Yi Wang, Yujiao Jiang, Jiahui Yin, Wenjie Ma, Xuelan Hu, Wanqing Zeng, Yanfei Ma, Shuwang Wu, Mingyuan Gao\",\"doi\":\"10.1021/acsmacrolett.5c00188\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Inspired by tropoelastin coacervation, a process in elastic fiber formation driven by hydrophobic interactions, we developed a tough, antiswelling hydrogel, PHEA-(PVA-<i>co</i>-PE), by incorporating amphiphilic poly(vinyl alcohol-<i>co</i>-ethylene) (PVA-<i>co</i>-PE) into a hydrophilic poly(2-hydroxyethyl acrylate) (PHEA) network. The PHEA-(PVA-<i>co</i>-PE) hydrogel was prepared by UV-induced polymerization of a PHEA precursor dimethyl sulfoxide (DMSO) solution containing PVA-<i>co</i>-PE, followed by immersion in water. During solvent exchange, PVA-<i>co</i>-PE self-assembled into micellar structures within the PHEA matrix, mimicking the coacervation of tropoelastin. Compared with PHEA and PVA-<i>co</i>-PE hydrogels, the strength of PHEA-(PVA-<i>co</i>-PE) increased by 83 and 7 times, while the toughness increased by 145 and 97 times. This strategy can be further extended to a variety of amphiphilic copolymers, demonstrating the universality. In vitro and in vivo tests demonstrated that the hydrogel possesses excellent biocompatibility and antiswelling capability. This study provides a simple method for developing a tough, biocompatible, and antiswelling hydrogel.\",\"PeriodicalId\":18,\"journal\":{\"name\":\"ACS Macro Letters\",\"volume\":\"29 1\",\"pages\":\"\"},\"PeriodicalIF\":5.1000,\"publicationDate\":\"2025-05-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Macro Letters\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acsmacrolett.5c00188\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Macro Letters","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acsmacrolett.5c00188","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
Bioinspired Tough and Antiswelling Hydrogel via in Situ Self-Assembly of Amphiphilic Copolymers within a Hydrophilic Network
Inspired by tropoelastin coacervation, a process in elastic fiber formation driven by hydrophobic interactions, we developed a tough, antiswelling hydrogel, PHEA-(PVA-co-PE), by incorporating amphiphilic poly(vinyl alcohol-co-ethylene) (PVA-co-PE) into a hydrophilic poly(2-hydroxyethyl acrylate) (PHEA) network. The PHEA-(PVA-co-PE) hydrogel was prepared by UV-induced polymerization of a PHEA precursor dimethyl sulfoxide (DMSO) solution containing PVA-co-PE, followed by immersion in water. During solvent exchange, PVA-co-PE self-assembled into micellar structures within the PHEA matrix, mimicking the coacervation of tropoelastin. Compared with PHEA and PVA-co-PE hydrogels, the strength of PHEA-(PVA-co-PE) increased by 83 and 7 times, while the toughness increased by 145 and 97 times. This strategy can be further extended to a variety of amphiphilic copolymers, demonstrating the universality. In vitro and in vivo tests demonstrated that the hydrogel possesses excellent biocompatibility and antiswelling capability. This study provides a simple method for developing a tough, biocompatible, and antiswelling hydrogel.
期刊介绍:
ACS Macro Letters publishes research in all areas of contemporary soft matter science in which macromolecules play a key role, including nanotechnology, self-assembly, supramolecular chemistry, biomaterials, energy generation and storage, and renewable/sustainable materials. Submissions to ACS Macro Letters should justify clearly the rapid disclosure of the key elements of the study. The scope of the journal includes high-impact research of broad interest in all areas of polymer science and engineering, including cross-disciplinary research that interfaces with polymer science.
With the launch of ACS Macro Letters, all Communications that were formerly published in Macromolecules and Biomacromolecules will be published as Letters in ACS Macro Letters.