{"title":"细胞器靶向光触发乙酰过氧自由基递送,调节氧化还原平衡","authors":"Mengqi Liu, Yijie Wang, Youjun Yang*, Xuhong Qian* and Xiao Luo*, ","doi":"10.1021/acs.analchem.4c0643510.1021/acs.analchem.4c06435","DOIUrl":null,"url":null,"abstract":"<p >Dysfunction of subcellular organelles initiates complex pathophysiological cascades and underlies numerous diseases, underscoring the need for organelle-specific therapeutic interventions. Precise spatiotemporal control of reactive oxygen species (ROS) generation within organelles offers a promising intervention approach. Herein, we report the design and synthesis of a novel series of organelle-targeted, photoactivatable acetylperoxyl radical donors (<b>ACR575s</b>) based on an acetyl-caged rhodamine scaffold. Blue light irradiation triggered the release of highly oxidative acetylperoxyl radicals, concomitantly generating a rhodamine dye for real-time monitoring. In vitro studies demonstrated the organelle-specific delivery of acetylperoxyl radicals, which subsequently induced concentration-dependent oxidative stress within specific subcellular compartments. Notably, this resulted in membrane damage and the modulation of macrophage polarization, providing clear evidence of the therapeutic potential of acetylperoxyl radicals in regulating redox balance and inflammatory responses. The <b>ACR575</b> series provides a novel toolset for acetylperoxyl radical biology and subcellular redox regulation, enabling precise spatiotemporal control of acetylperoxyl radical-mediated oxidative stress and showing potential for applications in precise cancer therapy.</p>","PeriodicalId":27,"journal":{"name":"Analytical Chemistry","volume":"97 10","pages":"5653–5660 5653–5660"},"PeriodicalIF":6.7000,"publicationDate":"2025-03-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Organelle-Targeted Photo-triggered Delivery of Acetylperoxyl Radicals for Redox Homeostasis Modulation\",\"authors\":\"Mengqi Liu, Yijie Wang, Youjun Yang*, Xuhong Qian* and Xiao Luo*, \",\"doi\":\"10.1021/acs.analchem.4c0643510.1021/acs.analchem.4c06435\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Dysfunction of subcellular organelles initiates complex pathophysiological cascades and underlies numerous diseases, underscoring the need for organelle-specific therapeutic interventions. Precise spatiotemporal control of reactive oxygen species (ROS) generation within organelles offers a promising intervention approach. Herein, we report the design and synthesis of a novel series of organelle-targeted, photoactivatable acetylperoxyl radical donors (<b>ACR575s</b>) based on an acetyl-caged rhodamine scaffold. Blue light irradiation triggered the release of highly oxidative acetylperoxyl radicals, concomitantly generating a rhodamine dye for real-time monitoring. In vitro studies demonstrated the organelle-specific delivery of acetylperoxyl radicals, which subsequently induced concentration-dependent oxidative stress within specific subcellular compartments. Notably, this resulted in membrane damage and the modulation of macrophage polarization, providing clear evidence of the therapeutic potential of acetylperoxyl radicals in regulating redox balance and inflammatory responses. The <b>ACR575</b> series provides a novel toolset for acetylperoxyl radical biology and subcellular redox regulation, enabling precise spatiotemporal control of acetylperoxyl radical-mediated oxidative stress and showing potential for applications in precise cancer therapy.</p>\",\"PeriodicalId\":27,\"journal\":{\"name\":\"Analytical Chemistry\",\"volume\":\"97 10\",\"pages\":\"5653–5660 5653–5660\"},\"PeriodicalIF\":6.7000,\"publicationDate\":\"2025-03-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Analytical Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.analchem.4c06435\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analytical Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.analchem.4c06435","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
Organelle-Targeted Photo-triggered Delivery of Acetylperoxyl Radicals for Redox Homeostasis Modulation
Dysfunction of subcellular organelles initiates complex pathophysiological cascades and underlies numerous diseases, underscoring the need for organelle-specific therapeutic interventions. Precise spatiotemporal control of reactive oxygen species (ROS) generation within organelles offers a promising intervention approach. Herein, we report the design and synthesis of a novel series of organelle-targeted, photoactivatable acetylperoxyl radical donors (ACR575s) based on an acetyl-caged rhodamine scaffold. Blue light irradiation triggered the release of highly oxidative acetylperoxyl radicals, concomitantly generating a rhodamine dye for real-time monitoring. In vitro studies demonstrated the organelle-specific delivery of acetylperoxyl radicals, which subsequently induced concentration-dependent oxidative stress within specific subcellular compartments. Notably, this resulted in membrane damage and the modulation of macrophage polarization, providing clear evidence of the therapeutic potential of acetylperoxyl radicals in regulating redox balance and inflammatory responses. The ACR575 series provides a novel toolset for acetylperoxyl radical biology and subcellular redox regulation, enabling precise spatiotemporal control of acetylperoxyl radical-mediated oxidative stress and showing potential for applications in precise cancer therapy.
期刊介绍:
Analytical Chemistry, a peer-reviewed research journal, focuses on disseminating new and original knowledge across all branches of analytical chemistry. Fundamental articles may explore general principles of chemical measurement science and need not directly address existing or potential analytical methodology. They can be entirely theoretical or report experimental results. Contributions may cover various phases of analytical operations, including sampling, bioanalysis, electrochemistry, mass spectrometry, microscale and nanoscale systems, environmental analysis, separations, spectroscopy, chemical reactions and selectivity, instrumentation, imaging, surface analysis, and data processing. Papers discussing known analytical methods should present a significant, original application of the method, a notable improvement, or results on an important analyte.