{"title":"聚合诱导热响应胶束的自组装及其润滑适应性","authors":"Linjie Yang, Hanfeng Liu, Pengrui Cao, Junhui Gong, Xinrui Zhang, Tingmei Wang, Liming Tao, Xianqiang Pei, Qihua Wang, Jianqiang Zhang, Yaoming Zhang","doi":"10.1038/s41428-025-01057-1","DOIUrl":null,"url":null,"abstract":"Responsive materials have significant application value because of their ability to actively adjust their structure or properties in response to external stimuli. Poly(N-isopropylacrylamide) (PNIPAM) is widely used to form micelles, particularly for drug delivery, because its lower critical solution temperature (LCST) is close to body temperature. However, the preparation of micelles based on PNIPAM block copolymers often involves complex processes, which limit their broader application. Here, we employed polymerization-induced self-assembly (PISA) combined with in situ crosslinking to synthesize stabilized thermoresponsive micelles, such as poly(glycerol methacrylate)-b-poly(N-isopropylacrylamide)-B (PGMAx-b-PNIPAMy-B), which are spherical micelles with a thermoresponsive core of PNIPAM and a crosslinked shell of PGMA formed by sodium tetraborate decahydrate. The micelles exhibited rapid and reversible self-assembly and collapsed at 31 °C, enabling temperature regulation through light transmittance, which makes them suitable for smart window applications. Furthermore, these micelles demonstrated excellent friction-reducing and wear-resistant properties at various temperatures (25–36 °C) and under various loads (20–70 N), indicating their adaptive lubrication as additives. This work presents the facile fabrication of thermoresponsive micelles and expands the application of PISA technology in the tribological field. Responsive materials have significant application value because of their ability to actively adjust their structure or properties in response to external stimuli. We employed polymerization-induced self-assembly combined with in situ crosslinking to synthesize stabilized thermoresponsive micelles, such as poly(glycerol methacrylate)-b-poly(N-isopropylacrylamide)-B, which exhibited rapid and reversible self-assembly. Furthermore, these micelles demonstrated excellent friction-reducing and wear-resistant properties showcasing their adaptive lubrication as additives. This work presents the facile fabrication of thermoresponsive micelles and expands the application of PISA technology in the tribological field.","PeriodicalId":20302,"journal":{"name":"Polymer Journal","volume":"57 10","pages":"1115-1125"},"PeriodicalIF":2.7000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Polymerization-induced self-assembly of thermoresponsive micelles and their lubrication adaptivity\",\"authors\":\"Linjie Yang, Hanfeng Liu, Pengrui Cao, Junhui Gong, Xinrui Zhang, Tingmei Wang, Liming Tao, Xianqiang Pei, Qihua Wang, Jianqiang Zhang, Yaoming Zhang\",\"doi\":\"10.1038/s41428-025-01057-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Responsive materials have significant application value because of their ability to actively adjust their structure or properties in response to external stimuli. Poly(N-isopropylacrylamide) (PNIPAM) is widely used to form micelles, particularly for drug delivery, because its lower critical solution temperature (LCST) is close to body temperature. However, the preparation of micelles based on PNIPAM block copolymers often involves complex processes, which limit their broader application. Here, we employed polymerization-induced self-assembly (PISA) combined with in situ crosslinking to synthesize stabilized thermoresponsive micelles, such as poly(glycerol methacrylate)-b-poly(N-isopropylacrylamide)-B (PGMAx-b-PNIPAMy-B), which are spherical micelles with a thermoresponsive core of PNIPAM and a crosslinked shell of PGMA formed by sodium tetraborate decahydrate. The micelles exhibited rapid and reversible self-assembly and collapsed at 31 °C, enabling temperature regulation through light transmittance, which makes them suitable for smart window applications. Furthermore, these micelles demonstrated excellent friction-reducing and wear-resistant properties at various temperatures (25–36 °C) and under various loads (20–70 N), indicating their adaptive lubrication as additives. This work presents the facile fabrication of thermoresponsive micelles and expands the application of PISA technology in the tribological field. Responsive materials have significant application value because of their ability to actively adjust their structure or properties in response to external stimuli. We employed polymerization-induced self-assembly combined with in situ crosslinking to synthesize stabilized thermoresponsive micelles, such as poly(glycerol methacrylate)-b-poly(N-isopropylacrylamide)-B, which exhibited rapid and reversible self-assembly. Furthermore, these micelles demonstrated excellent friction-reducing and wear-resistant properties showcasing their adaptive lubrication as additives. This work presents the facile fabrication of thermoresponsive micelles and expands the application of PISA technology in the tribological field.\",\"PeriodicalId\":20302,\"journal\":{\"name\":\"Polymer Journal\",\"volume\":\"57 10\",\"pages\":\"1115-1125\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Polymer Journal\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.nature.com/articles/s41428-025-01057-1\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer Journal","FirstCategoryId":"92","ListUrlMain":"https://www.nature.com/articles/s41428-025-01057-1","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
Polymerization-induced self-assembly of thermoresponsive micelles and their lubrication adaptivity
Responsive materials have significant application value because of their ability to actively adjust their structure or properties in response to external stimuli. Poly(N-isopropylacrylamide) (PNIPAM) is widely used to form micelles, particularly for drug delivery, because its lower critical solution temperature (LCST) is close to body temperature. However, the preparation of micelles based on PNIPAM block copolymers often involves complex processes, which limit their broader application. Here, we employed polymerization-induced self-assembly (PISA) combined with in situ crosslinking to synthesize stabilized thermoresponsive micelles, such as poly(glycerol methacrylate)-b-poly(N-isopropylacrylamide)-B (PGMAx-b-PNIPAMy-B), which are spherical micelles with a thermoresponsive core of PNIPAM and a crosslinked shell of PGMA formed by sodium tetraborate decahydrate. The micelles exhibited rapid and reversible self-assembly and collapsed at 31 °C, enabling temperature regulation through light transmittance, which makes them suitable for smart window applications. Furthermore, these micelles demonstrated excellent friction-reducing and wear-resistant properties at various temperatures (25–36 °C) and under various loads (20–70 N), indicating their adaptive lubrication as additives. This work presents the facile fabrication of thermoresponsive micelles and expands the application of PISA technology in the tribological field. Responsive materials have significant application value because of their ability to actively adjust their structure or properties in response to external stimuli. We employed polymerization-induced self-assembly combined with in situ crosslinking to synthesize stabilized thermoresponsive micelles, such as poly(glycerol methacrylate)-b-poly(N-isopropylacrylamide)-B, which exhibited rapid and reversible self-assembly. Furthermore, these micelles demonstrated excellent friction-reducing and wear-resistant properties showcasing their adaptive lubrication as additives. This work presents the facile fabrication of thermoresponsive micelles and expands the application of PISA technology in the tribological field.
期刊介绍:
Polymer Journal promotes research from all aspects of polymer science from anywhere in the world and aims to provide an integrated platform for scientific communication that assists the advancement of polymer science and related fields. The journal publishes Original Articles, Notes, Short Communications and Reviews.
Subject areas and topics of particular interest within the journal''s scope include, but are not limited to, those listed below:
Polymer synthesis and reactions
Polymer structures
Physical properties of polymers
Polymer surface and interfaces
Functional polymers
Supramolecular polymers
Self-assembled materials
Biopolymers and bio-related polymer materials
Polymer engineering.