Yan Du, Xuehui Duan, Hanxiao Liu, Zhongjie Tang, Xu Li, Tianying Ren, Xinlei Chu, Yunsai Wang, Wei Xu, Hongliang Wang*, Yingyi Wang* and Yixuan Tang*,
{"title":"协同氨基和羟基增强姜黄素碳点的sod样活性,改善结肠炎治疗。","authors":"Yan Du, Xuehui Duan, Hanxiao Liu, Zhongjie Tang, Xu Li, Tianying Ren, Xinlei Chu, Yunsai Wang, Wei Xu, Hongliang Wang*, Yingyi Wang* and Yixuan Tang*, ","doi":"10.1021/acsami.5c11952","DOIUrl":null,"url":null,"abstract":"<p >Inflammatory bowel disease (IBD) is a globally prevalent inflammatory disorder with limited therapeutic options due to efficacy-safety trade-offs. Herein, we rationally designed polyethylenimine (PEI)-functionalized curcumin-derived carbon dots (cu@CDs-po) as a multifunctional nanotherapeutic agent for colitis management. Combined experimental and computational analyses revealed that the synergistic interplay between surface-engineered amino and hydroxyl groups significantly enhanced the superoxide dismutase (SOD)-like activity of cu@CDs-po by 5.51-fold compared to unmodified cu@CDs, enabling efficient reactive oxygen species (ROS) scavenging and anti-inflammatory effects. PEI modification further improved cellular uptake and intestinal targeting. In a murine dextran sulfate sodium (DSS)-induced colitis model, cu@CDs-po effectively alleviated colon injury, restored intestinal barrier integrity, suppressed pro-inflammatory cytokines, and remodeled the immune microenvironment through T-cell suppression and M2 macrophage/Treg polarization. Critically, 16S rDNA sequencing revealed that cu@CDs-po induced targeted gut microbiota remodeling by restoring the Firmicutes/Bacteroidota ratio, suppressing pro-inflammatory Proteobacteria, enriching beneficial taxa such as <i>Lachnospiraceae</i>, and normalizing key commensals such as <i>Lachnospiraceae_NK4A136_group</i>. Functional analysis links these microbial shifts to enhanced metabolic and immune-related pathways. This study establishes a surface-chemistry-guided strategy for engineering catalytic carbon dots capable of simultaneously modulating oxidative stress, immune responses, and gut microbiota homeostasis, offering a promising and translatable paradigm for IBD nanomedicine.</p>","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":"17 34","pages":"48075–48093"},"PeriodicalIF":8.2000,"publicationDate":"2025-08-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synergistic Amino and Hydroxyl Groups That Enhance SOD-Like Activity in Curcumin Carbon Dots for Improved Colitis Treatment\",\"authors\":\"Yan Du, Xuehui Duan, Hanxiao Liu, Zhongjie Tang, Xu Li, Tianying Ren, Xinlei Chu, Yunsai Wang, Wei Xu, Hongliang Wang*, Yingyi Wang* and Yixuan Tang*, \",\"doi\":\"10.1021/acsami.5c11952\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Inflammatory bowel disease (IBD) is a globally prevalent inflammatory disorder with limited therapeutic options due to efficacy-safety trade-offs. Herein, we rationally designed polyethylenimine (PEI)-functionalized curcumin-derived carbon dots (cu@CDs-po) as a multifunctional nanotherapeutic agent for colitis management. Combined experimental and computational analyses revealed that the synergistic interplay between surface-engineered amino and hydroxyl groups significantly enhanced the superoxide dismutase (SOD)-like activity of cu@CDs-po by 5.51-fold compared to unmodified cu@CDs, enabling efficient reactive oxygen species (ROS) scavenging and anti-inflammatory effects. PEI modification further improved cellular uptake and intestinal targeting. In a murine dextran sulfate sodium (DSS)-induced colitis model, cu@CDs-po effectively alleviated colon injury, restored intestinal barrier integrity, suppressed pro-inflammatory cytokines, and remodeled the immune microenvironment through T-cell suppression and M2 macrophage/Treg polarization. Critically, 16S rDNA sequencing revealed that cu@CDs-po induced targeted gut microbiota remodeling by restoring the Firmicutes/Bacteroidota ratio, suppressing pro-inflammatory Proteobacteria, enriching beneficial taxa such as <i>Lachnospiraceae</i>, and normalizing key commensals such as <i>Lachnospiraceae_NK4A136_group</i>. Functional analysis links these microbial shifts to enhanced metabolic and immune-related pathways. This study establishes a surface-chemistry-guided strategy for engineering catalytic carbon dots capable of simultaneously modulating oxidative stress, immune responses, and gut microbiota homeostasis, offering a promising and translatable paradigm for IBD nanomedicine.</p>\",\"PeriodicalId\":5,\"journal\":{\"name\":\"ACS Applied Materials & Interfaces\",\"volume\":\"17 34\",\"pages\":\"48075–48093\"},\"PeriodicalIF\":8.2000,\"publicationDate\":\"2025-08-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Materials & Interfaces\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acsami.5c11952\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Materials & Interfaces","FirstCategoryId":"88","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsami.5c11952","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
Synergistic Amino and Hydroxyl Groups That Enhance SOD-Like Activity in Curcumin Carbon Dots for Improved Colitis Treatment
Inflammatory bowel disease (IBD) is a globally prevalent inflammatory disorder with limited therapeutic options due to efficacy-safety trade-offs. Herein, we rationally designed polyethylenimine (PEI)-functionalized curcumin-derived carbon dots (cu@CDs-po) as a multifunctional nanotherapeutic agent for colitis management. Combined experimental and computational analyses revealed that the synergistic interplay between surface-engineered amino and hydroxyl groups significantly enhanced the superoxide dismutase (SOD)-like activity of cu@CDs-po by 5.51-fold compared to unmodified cu@CDs, enabling efficient reactive oxygen species (ROS) scavenging and anti-inflammatory effects. PEI modification further improved cellular uptake and intestinal targeting. In a murine dextran sulfate sodium (DSS)-induced colitis model, cu@CDs-po effectively alleviated colon injury, restored intestinal barrier integrity, suppressed pro-inflammatory cytokines, and remodeled the immune microenvironment through T-cell suppression and M2 macrophage/Treg polarization. Critically, 16S rDNA sequencing revealed that cu@CDs-po induced targeted gut microbiota remodeling by restoring the Firmicutes/Bacteroidota ratio, suppressing pro-inflammatory Proteobacteria, enriching beneficial taxa such as Lachnospiraceae, and normalizing key commensals such as Lachnospiraceae_NK4A136_group. Functional analysis links these microbial shifts to enhanced metabolic and immune-related pathways. This study establishes a surface-chemistry-guided strategy for engineering catalytic carbon dots capable of simultaneously modulating oxidative stress, immune responses, and gut microbiota homeostasis, offering a promising and translatable paradigm for IBD nanomedicine.
期刊介绍:
ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.