{"title":"Tailoring Protein Adsorption at the Solid–Liquid Interface for Long-Term Superhemophobicity","authors":"Huali Yu, Dehui Wang, Xijing Yang, Xianchun Jin, Shengjun Cheng, Yijia Zhu, Bingyang Lu, Jiaxin Liu, Luohuizi Li, Jing Luo, Xu Deng","doi":"10.1002/adma.202502388","DOIUrl":null,"url":null,"abstract":"Super-repellent surfaces with micro/nanoscale roughness can sustain blood in the Cassie–Baxter state and minimize the solid–liquid contact area, exhibiting potential for biomedical applications. Conventional superhydrophobic surfaces with hydrophobic solid–liquid interface are susceptible to protein adsorption under blood flow, leading to a transition to the Wenzel state and increasing the risk of thrombosis. Inspired by <i>Salvinia</i>, hydrophilic molecules are incorporated at the solid–liquid contact area based on the interaction between blood and the surface topography as well as chemistry, thereby engineering a chemically heterogeneous superhemophobic surface which effectively prevents protein adsorption and maintains a long-term Cassie–Baxter state. The blood-repellent time of the heterogeneous surface is greater than tenfold those of conventional superhydrophobic surfaces. In vivo rabbit blood circulation confirms sustained hemocompatibility and effective thrombosis resistance, demonstrating prolonged superhemophobicity for over 55 h. The heterogeneous design ensures extended resistance to complex biological fluids and is promising for the development of blood-contacting devices, such as the gas-permeable blood-repellent membranes for extracorporeal membrane oxygenators.","PeriodicalId":114,"journal":{"name":"Advanced Materials","volume":"121 1","pages":"e2502388"},"PeriodicalIF":27.4000,"publicationDate":"2025-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/adma.202502388","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Super-repellent surfaces with micro/nanoscale roughness can sustain blood in the Cassie–Baxter state and minimize the solid–liquid contact area, exhibiting potential for biomedical applications. Conventional superhydrophobic surfaces with hydrophobic solid–liquid interface are susceptible to protein adsorption under blood flow, leading to a transition to the Wenzel state and increasing the risk of thrombosis. Inspired by Salvinia, hydrophilic molecules are incorporated at the solid–liquid contact area based on the interaction between blood and the surface topography as well as chemistry, thereby engineering a chemically heterogeneous superhemophobic surface which effectively prevents protein adsorption and maintains a long-term Cassie–Baxter state. The blood-repellent time of the heterogeneous surface is greater than tenfold those of conventional superhydrophobic surfaces. In vivo rabbit blood circulation confirms sustained hemocompatibility and effective thrombosis resistance, demonstrating prolonged superhemophobicity for over 55 h. The heterogeneous design ensures extended resistance to complex biological fluids and is promising for the development of blood-contacting devices, such as the gas-permeable blood-repellent membranes for extracorporeal membrane oxygenators.
期刊介绍:
Advanced Materials, one of the world's most prestigious journals and the foundation of the Advanced portfolio, is the home of choice for best-in-class materials science for more than 30 years. Following this fast-growing and interdisciplinary field, we are considering and publishing the most important discoveries on any and all materials from materials scientists, chemists, physicists, engineers as well as health and life scientists and bringing you the latest results and trends in modern materials-related research every week.