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240528s2024 xx |||||o 00| ||eng c |
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|a 10.1002/adma.202310731
|2 doi
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|a pubmed25n1242.xml
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|a (NLM)38805174
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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|a Kong, Ying
|e verfasserin
|4 aut
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|a Ultrasmall Polyphenol-NAD+ Nanoparticle-Mediated Renal Delivery for Mitochondrial Repair and Anti-Inflammatory Treatment of AKI-to-CKD Progression
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|c 2024
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
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|2 rdacarrier
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|a Date Completed 25.07.2024
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|a Date Revised 25.07.2024
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a © 2024 Wiley‐VCH GmbH.
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|a As a central metabolic molecule, nicotinamide adenine dinucleotide (NAD+) can potentially treat acute kidney injury (AKI) and chronic kidney disease (CKD); however, its bioavailability is poor due to short half-life, instability, the deficiency of targeting, and difficulties in transmembrane transport. Here a physiologically adaptive gallic acid-NAD+ nanoparticle is designed, which has ultrasmall size and pH-responsiveness, passes through the glomerular filtration membrane to reach injured renal tubules, and efficiently delivers NAD+ into the kidneys. With an effective accumulation in the kidneys, it restores renal function, immune microenvironment homeostasis, and mitochondrial homeostasis of AKI mice via the NAD+-Sirtuin-1 axis, and exerts strong antifibrotic effects on the AKI-to-CKD transition by inhibiting TGF-β signaling. It also exhibits excellent stability, biodegradable, and biocompatible properties, ensuring its long-term safety, practicality, and clinical translational feasibility. The present study shows a potential modality of mitochondrial repair and immunomodulation through nanoagents for the efficient and safe treatment of AKI and CKD
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|a Journal Article
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|a acute kidney injury
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|a chronic kidney disease
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|a inflammation
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|a mitochondria
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|a nanoparticle
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|a nicotinamide adenine dinucleotide
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|a NAD
|2 NLM
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|a 0U46U6E8UK
|2 NLM
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|a Polyphenols
|2 NLM
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|a Anti-Inflammatory Agents
|2 NLM
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|a Gallic Acid
|2 NLM
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|a 632XD903SP
|2 NLM
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1 |
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|a Chen, Xu
|e verfasserin
|4 aut
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1 |
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|a Liu, Feng
|e verfasserin
|4 aut
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|a Tang, Jiageng
|e verfasserin
|4 aut
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1 |
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|a Zhang, Yijing
|e verfasserin
|4 aut
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|a Zhang, Xiangxiang
|e verfasserin
|4 aut
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|a Zhang, Luyao
|e verfasserin
|4 aut
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1 |
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|a Zhang, Tong
|e verfasserin
|4 aut
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1 |
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|a Wang, Yaqi
|e verfasserin
|4 aut
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1 |
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|a Su, Mengxiao
|e verfasserin
|4 aut
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1 |
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|a Zhang, Qixin
|e verfasserin
|4 aut
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1 |
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|a Chen, Hanxiang
|e verfasserin
|4 aut
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1 |
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|a Zhou, Di
|e verfasserin
|4 aut
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1 |
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|a Yi, Fan
|e verfasserin
|4 aut
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1 |
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|a Liu, Hong
|e verfasserin
|4 aut
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|a Fu, Yi
|e verfasserin
|4 aut
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|i Enthalten in
|t Advanced materials (Deerfield Beach, Fla.)
|d 1998
|g 36(2024), 30 vom: 31. Juli, Seite e2310731
|w (DE-627)NLM098206397
|x 1521-4095
|7 nnas
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|g volume:36
|g year:2024
|g number:30
|g day:31
|g month:07
|g pages:e2310731
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|u http://dx.doi.org/10.1002/adma.202310731
|3 Volltext
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|d 36
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|h e2310731
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