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Prussian blue-based theranostics for ameliorating acute kidney injury

BACKGROUND: Acute kidney injury (AKI) with high mortality rates is associated with an excess of reactive oxygen/nitrogen species (RONS) within kidney tissues. Recently, nanomedicine antioxidant therapy has been used to alleviate AKI. Herein, we synthesized ultrasmall Prussian blue nanozymes (PB NZs,...

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Autores principales: Zhang, Dong-Yang, Liu, Hengke, Zhu, Kathy S., He, Ting, Younis, Muhammad Rizwan, Yang, Chen, Lei, Shan, Wu, Jiayingzi, Lin, Jing, Qu, Junle, Huang, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419910/
https://www.ncbi.nlm.nih.gov/pubmed/34488789
http://dx.doi.org/10.1186/s12951-021-01006-z
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author Zhang, Dong-Yang
Liu, Hengke
Zhu, Kathy S.
He, Ting
Younis, Muhammad Rizwan
Yang, Chen
Lei, Shan
Wu, Jiayingzi
Lin, Jing
Qu, Junle
Huang, Peng
author_facet Zhang, Dong-Yang
Liu, Hengke
Zhu, Kathy S.
He, Ting
Younis, Muhammad Rizwan
Yang, Chen
Lei, Shan
Wu, Jiayingzi
Lin, Jing
Qu, Junle
Huang, Peng
author_sort Zhang, Dong-Yang
collection PubMed
description BACKGROUND: Acute kidney injury (AKI) with high mortality rates is associated with an excess of reactive oxygen/nitrogen species (RONS) within kidney tissues. Recently, nanomedicine antioxidant therapy has been used to alleviate AKI. Herein, we synthesized ultrasmall Prussian blue nanozymes (PB NZs, 4.5 nm) as theranostic agents for magnetic resonance (MR)/photoacoustic (PA) dual-modal imaging guided AKI treatment. RESULTS: PB NZs exhibited multi-enzyme mimetic abilities, promoting the effective elimination of RONS both in vitro and in vivo. Moreover, benefiting from their imaging contrast properties, the rapid renal accumulation of PB NZs was verified by in vivo PA/MR dual-modal imaging. Due to their excellent enrichment in the kidney and unique multi-enzyme mimetic abilities, ultrasmall PB NZs displayed superior AKI treatment efficacy compared with that of amifostine in two clinically relevant types of AKI induced murine models (either by rhabdomyolysis or cisplatin). CONCLUSION: Our findings suggested ultrasmall PB NZs, as nanozyme theranostics, have great potential for AKI management. GRAPHIC ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-021-01006-z.
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spelling pubmed-84199102021-09-09 Prussian blue-based theranostics for ameliorating acute kidney injury Zhang, Dong-Yang Liu, Hengke Zhu, Kathy S. He, Ting Younis, Muhammad Rizwan Yang, Chen Lei, Shan Wu, Jiayingzi Lin, Jing Qu, Junle Huang, Peng J Nanobiotechnology Research BACKGROUND: Acute kidney injury (AKI) with high mortality rates is associated with an excess of reactive oxygen/nitrogen species (RONS) within kidney tissues. Recently, nanomedicine antioxidant therapy has been used to alleviate AKI. Herein, we synthesized ultrasmall Prussian blue nanozymes (PB NZs, 4.5 nm) as theranostic agents for magnetic resonance (MR)/photoacoustic (PA) dual-modal imaging guided AKI treatment. RESULTS: PB NZs exhibited multi-enzyme mimetic abilities, promoting the effective elimination of RONS both in vitro and in vivo. Moreover, benefiting from their imaging contrast properties, the rapid renal accumulation of PB NZs was verified by in vivo PA/MR dual-modal imaging. Due to their excellent enrichment in the kidney and unique multi-enzyme mimetic abilities, ultrasmall PB NZs displayed superior AKI treatment efficacy compared with that of amifostine in two clinically relevant types of AKI induced murine models (either by rhabdomyolysis or cisplatin). CONCLUSION: Our findings suggested ultrasmall PB NZs, as nanozyme theranostics, have great potential for AKI management. GRAPHIC ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-021-01006-z. BioMed Central 2021-09-06 /pmc/articles/PMC8419910/ /pubmed/34488789 http://dx.doi.org/10.1186/s12951-021-01006-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Zhang, Dong-Yang
Liu, Hengke
Zhu, Kathy S.
He, Ting
Younis, Muhammad Rizwan
Yang, Chen
Lei, Shan
Wu, Jiayingzi
Lin, Jing
Qu, Junle
Huang, Peng
Prussian blue-based theranostics for ameliorating acute kidney injury
title Prussian blue-based theranostics for ameliorating acute kidney injury
title_full Prussian blue-based theranostics for ameliorating acute kidney injury
title_fullStr Prussian blue-based theranostics for ameliorating acute kidney injury
title_full_unstemmed Prussian blue-based theranostics for ameliorating acute kidney injury
title_short Prussian blue-based theranostics for ameliorating acute kidney injury
title_sort prussian blue-based theranostics for ameliorating acute kidney injury
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419910/
https://www.ncbi.nlm.nih.gov/pubmed/34488789
http://dx.doi.org/10.1186/s12951-021-01006-z
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