{"title":"全活性纳米平台恢复ROS稳态,通过内源性和外源性双重途径协同治疗脂肪肝。","authors":"Ziyi Lin,Peng Xu,Yuehai Xu,Yixin Zheng,Huimin Li,Zixin Chen,Zhe Wang,Shaochen Song,Yuhao Liu,Zhao Yang,Ju Cui,Heyun Shen","doi":"10.1021/acsami.5c15203","DOIUrl":null,"url":null,"abstract":"The therapeutic potential of nanomaterials in metabolic dysfunction-associated steatohepatitis (MASH) management remains limited by suboptimal drug loading efficiency and insufficient modulation of the disease's multifactorial pathogenesis. To address these issues, we developed a fully active pharmaceutical ingredient (API)-based nanodrug designed for synergistic MASH therapy through three integrated mechanisms: dual modulation of reactive oxygen species (ROS) homeostasis via endogenous and exogenous pathways, mitigation of pathological lipid accumulation, and suppression of inflammatory cascades. The nanodrug (QRDP) system utilizes arginine-modified polydopamine as both a nanocarrier and intrinsic antioxidant and codelivery of quercetin and the mitochondrial uncoupler 2,4-dinitrophenol. QRDP eliminates more than 80% of ROS and increases hepatic glutathione levels by 1.5-fold through exogenous antioxidant delivery and endogenous ROS suppression via regulating mitochondrial proton channels. Additionally, QRDP-mediated mitochondrial uncoupling reduced intracellular lipid overload by 90% through inhibition of ATP synthesis, accompanied by significant decreases in serum total cholesterol (39%), triglycerides (30%), and free fatty acids (59%). Furthermore, QRDP significantly downregulated pro-inflammatory cytokines (TNF-α, IL-6, and IL-1β) in vitro and in vivo, while restoring anti-inflammatory markers (Arg-1 and IL-10) to over 78% of baseline levels. In high-fat diet (HFD)-induced MASH mice, QRDP treatment not only attenuated hepatic fibrosis and normalized liver function but also provided substantial protection against lipotoxicity. This full-API nanotherapeutic platform represents a safe and effective multitarget strategy for comprehensive MASH intervention.","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":"69 1","pages":""},"PeriodicalIF":8.2000,"publicationDate":"2025-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Full Active Nanoplatform Restores ROS Homeostasis for Synergistic Therapy of Fatty Liver Disease via Dual Endogenous-Exogenous Pathways.\",\"authors\":\"Ziyi Lin,Peng Xu,Yuehai Xu,Yixin Zheng,Huimin Li,Zixin Chen,Zhe Wang,Shaochen Song,Yuhao Liu,Zhao Yang,Ju Cui,Heyun Shen\",\"doi\":\"10.1021/acsami.5c15203\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The therapeutic potential of nanomaterials in metabolic dysfunction-associated steatohepatitis (MASH) management remains limited by suboptimal drug loading efficiency and insufficient modulation of the disease's multifactorial pathogenesis. To address these issues, we developed a fully active pharmaceutical ingredient (API)-based nanodrug designed for synergistic MASH therapy through three integrated mechanisms: dual modulation of reactive oxygen species (ROS) homeostasis via endogenous and exogenous pathways, mitigation of pathological lipid accumulation, and suppression of inflammatory cascades. The nanodrug (QRDP) system utilizes arginine-modified polydopamine as both a nanocarrier and intrinsic antioxidant and codelivery of quercetin and the mitochondrial uncoupler 2,4-dinitrophenol. QRDP eliminates more than 80% of ROS and increases hepatic glutathione levels by 1.5-fold through exogenous antioxidant delivery and endogenous ROS suppression via regulating mitochondrial proton channels. Additionally, QRDP-mediated mitochondrial uncoupling reduced intracellular lipid overload by 90% through inhibition of ATP synthesis, accompanied by significant decreases in serum total cholesterol (39%), triglycerides (30%), and free fatty acids (59%). Furthermore, QRDP significantly downregulated pro-inflammatory cytokines (TNF-α, IL-6, and IL-1β) in vitro and in vivo, while restoring anti-inflammatory markers (Arg-1 and IL-10) to over 78% of baseline levels. In high-fat diet (HFD)-induced MASH mice, QRDP treatment not only attenuated hepatic fibrosis and normalized liver function but also provided substantial protection against lipotoxicity. This full-API nanotherapeutic platform represents a safe and effective multitarget strategy for comprehensive MASH intervention.\",\"PeriodicalId\":5,\"journal\":{\"name\":\"ACS Applied Materials & Interfaces\",\"volume\":\"69 1\",\"pages\":\"\"},\"PeriodicalIF\":8.2000,\"publicationDate\":\"2025-10-12\",\"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://doi.org/10.1021/acsami.5c15203\",\"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://doi.org/10.1021/acsami.5c15203","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}
Full Active Nanoplatform Restores ROS Homeostasis for Synergistic Therapy of Fatty Liver Disease via Dual Endogenous-Exogenous Pathways.
The therapeutic potential of nanomaterials in metabolic dysfunction-associated steatohepatitis (MASH) management remains limited by suboptimal drug loading efficiency and insufficient modulation of the disease's multifactorial pathogenesis. To address these issues, we developed a fully active pharmaceutical ingredient (API)-based nanodrug designed for synergistic MASH therapy through three integrated mechanisms: dual modulation of reactive oxygen species (ROS) homeostasis via endogenous and exogenous pathways, mitigation of pathological lipid accumulation, and suppression of inflammatory cascades. The nanodrug (QRDP) system utilizes arginine-modified polydopamine as both a nanocarrier and intrinsic antioxidant and codelivery of quercetin and the mitochondrial uncoupler 2,4-dinitrophenol. QRDP eliminates more than 80% of ROS and increases hepatic glutathione levels by 1.5-fold through exogenous antioxidant delivery and endogenous ROS suppression via regulating mitochondrial proton channels. Additionally, QRDP-mediated mitochondrial uncoupling reduced intracellular lipid overload by 90% through inhibition of ATP synthesis, accompanied by significant decreases in serum total cholesterol (39%), triglycerides (30%), and free fatty acids (59%). Furthermore, QRDP significantly downregulated pro-inflammatory cytokines (TNF-α, IL-6, and IL-1β) in vitro and in vivo, while restoring anti-inflammatory markers (Arg-1 and IL-10) to over 78% of baseline levels. In high-fat diet (HFD)-induced MASH mice, QRDP treatment not only attenuated hepatic fibrosis and normalized liver function but also provided substantial protection against lipotoxicity. This full-API nanotherapeutic platform represents a safe and effective multitarget strategy for comprehensive MASH intervention.
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.