Protein‐Interference‐Free and Kidney‐Targeting NIR Fluorophores for Accurate in Vivo Imaging of H2S2 during Kidney Ferroptosis

体内 荧光 肾脏疾病 肾毒性 肾功能 材料科学 生物医学工程 医学 化学 生物 生物化学 内科学 光学 物理 生物技术
作者
Zhangkang Lv,Jing Wang,Jinyuan Xu,Xiaoshan Chen,Dongxue Lu,Jingting Huang,Xing‐Can Shen,Hua Chen
出处
期刊:Advanced Healthcare Materials [Wiley]
卷期号:14 (12): e2500273-e2500273 被引量:5
标识
DOI:10.1002/adhm.202500273
摘要

Abstract High‐fidelity kidney function imaging is important for assessing the nephrotoxicity of drugs and diagnosing renal diseases. However, the current challenges in achieving accurate kidney imaging include unspecific signal enhancement due to albumin binding and relatively low distribution of imaging agents in kidneys. Here, for the first time, a side‐chain engineering strategy that incorporates hydrophilic six‐membered heterocycles into aza‐hemicyanine for generating high‐performance kidney imaging agents with protein‐interference‐free and kidney‐targeting features is proposed. Based on these unique aza‐hemicyanine dyes, the first kidney‐targeting and albumin‐insensitive H 2 S 2 near‐infrared (NIR) fluorescent probe NA‐H 2 S 2 is designed, which demonstrates effective kidney distribution following intravenous injection and is specifically activated by H 2 S 2 . The designed probe presents a highly rapid, selective and sensitive response to H 2 S 2 with a detection limit as low as 24.21 n m . Additionally, it successfully achieves real‐time in vivo NIR fluorescence imaging of H 2 S 2 during erastin/cisplatin induced renal ferroptosis. Moreover, it also enables rapid detection of H 2 S 2 through in vitro optical urinalysis, offering significant diagnostic value for renal ferroptosis. Overall, this study not only presents a practical kidney‐targeting H 2 S 2 fluorescent probe NA‐H 2 S 2 with increased imaging accuracy but also provides promising kidney‐targeting and albumin‐insensitive aza‐hemicyanine dyes for further development of kidney disease‐related probes.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
量子星尘发布了新的文献求助10
1秒前
2秒前
浮游应助科研通管家采纳,获得10
2秒前
CipherSage应助科研通管家采纳,获得10
2秒前
Lucas应助科研通管家采纳,获得10
2秒前
浮游应助科研通管家采纳,获得10
2秒前
ccm应助科研通管家采纳,获得10
2秒前
英俊的铭应助科研通管家采纳,获得10
2秒前
科研通AI6应助科研通管家采纳,获得10
2秒前
2秒前
英俊的铭应助科研通管家采纳,获得30
2秒前
李爱国应助科研通管家采纳,获得10
2秒前
天天快乐应助科研通管家采纳,获得10
3秒前
小蘑菇应助科研通管家采纳,获得10
3秒前
wanci应助科研通管家采纳,获得10
3秒前
3秒前
科研通AI2S应助科研通管家采纳,获得10
3秒前
浮游应助科研通管家采纳,获得10
3秒前
浮游应助科研通管家采纳,获得10
3秒前
Yun yun发布了新的文献求助20
3秒前
科研通AI6应助科研通管家采纳,获得10
3秒前
科研通AI2S应助科研通管家采纳,获得10
3秒前
orixero应助科研通管家采纳,获得10
3秒前
ccm应助科研通管家采纳,获得10
3秒前
3秒前
指南针指北完成签到 ,获得积分10
4秒前
DD发布了新的文献求助10
4秒前
4秒前
陈晶发布了新的文献求助10
4秒前
金金发布了新的文献求助10
5秒前
6秒前
羊羊完成签到,获得积分10
7秒前
7秒前
7秒前
泡泡发布了新的文献求助20
8秒前
Kimber完成签到,获得积分10
8秒前
8秒前
所所应助争取少吃点采纳,获得10
9秒前
9秒前
jinzhao发布了新的文献求助10
9秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Binary Alloy Phase Diagrams, 2nd Edition 8000
Comprehensive Methanol Science Production, Applications, and Emerging Technologies 2000
Research Handbook on Social Interaction 1000
Building Quantum Computers 800
Translanguaging in Action in English-Medium Classrooms: A Resource Book for Teachers 700
二氧化碳加氢催化剂——结构设计与反应机制研究 660
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 计算机科学 有机化学 物理 生物化学 纳米技术 复合材料 内科学 化学工程 人工智能 催化作用 遗传学 数学 基因 量子力学 物理化学
热门帖子
关注 科研通微信公众号,转发送积分 5656742
求助须知:如何正确求助?哪些是违规求助? 4805800
关于积分的说明 15077356
捐赠科研通 4814948
什么是DOI,文献DOI怎么找? 2576219
邀请新用户注册赠送积分活动 1531465
关于科研通互助平台的介绍 1490025