Cargando…

A Cyclodextrin‐Hosted Ir(III) Complex for Ratiometric Mapping of Tumor Hypoxia In Vivo

Hypoxia is considered as a key microenvironmental feature of solid tumors. Luminescent transition metal complexes particularly those based on iridium and ruthenium have shown remarkable potentials for constructing sensitive oxygen‐sensing probes due to their unique oxygen quenching pathway. However,...

Descripción completa

Detalles Bibliográficos
Autores principales: Xiao, Peng, Liu, Chunyan, Ma, Tiancong, Lu, Xiuhong, Jing, Lihong, Hou, Yi, Zhang, Peisen, Huang, Gang, Gao, Mingyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8061356/
https://www.ncbi.nlm.nih.gov/pubmed/33898188
http://dx.doi.org/10.1002/advs.202004044
_version_ 1783681549723500544
author Xiao, Peng
Liu, Chunyan
Ma, Tiancong
Lu, Xiuhong
Jing, Lihong
Hou, Yi
Zhang, Peisen
Huang, Gang
Gao, Mingyuan
author_facet Xiao, Peng
Liu, Chunyan
Ma, Tiancong
Lu, Xiuhong
Jing, Lihong
Hou, Yi
Zhang, Peisen
Huang, Gang
Gao, Mingyuan
author_sort Xiao, Peng
collection PubMed
description Hypoxia is considered as a key microenvironmental feature of solid tumors. Luminescent transition metal complexes particularly those based on iridium and ruthenium have shown remarkable potentials for constructing sensitive oxygen‐sensing probes due to their unique oxygen quenching pathway. However, the low aqueous solubility of these complexes largely retards their sensing applications in biological media. Moreover, it remains difficult so far to use the existing complexes typically possessing only one luminescent domain to quantitatively detect the intratumoral hypoxia degree. Herein, an Ir(III) complex showing red emissions is designed and synthesized, and innovatively encapsulated within a hydrophobic pocket of Cyanine7‐modified cyclodextrin. The Ir(III) complex enables the oxygen detection, while the cyclodextrin is used not only for improving the water solubility and suppressing the luminescence quenching effect of the surrounding aqueous media, but also for carrying Cyanine7 to establish a ratiometric oxygen fluorescence probe. 2D nuclear magnetic resonance is carried out to confirm the host–guest structure. The oxygen‐responsive ability of the resulting ratiometric probe is evaluated through in vitro cell and multicellular experiments. Further animal studies about tumor oxygen level mapping demonstrate that the probe can be successfully used for quantitatively visualizing tumor hypoxia in vivo.
format Online
Article
Text
id pubmed-8061356
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-80613562021-04-23 A Cyclodextrin‐Hosted Ir(III) Complex for Ratiometric Mapping of Tumor Hypoxia In Vivo Xiao, Peng Liu, Chunyan Ma, Tiancong Lu, Xiuhong Jing, Lihong Hou, Yi Zhang, Peisen Huang, Gang Gao, Mingyuan Adv Sci (Weinh) Full Papers Hypoxia is considered as a key microenvironmental feature of solid tumors. Luminescent transition metal complexes particularly those based on iridium and ruthenium have shown remarkable potentials for constructing sensitive oxygen‐sensing probes due to their unique oxygen quenching pathway. However, the low aqueous solubility of these complexes largely retards their sensing applications in biological media. Moreover, it remains difficult so far to use the existing complexes typically possessing only one luminescent domain to quantitatively detect the intratumoral hypoxia degree. Herein, an Ir(III) complex showing red emissions is designed and synthesized, and innovatively encapsulated within a hydrophobic pocket of Cyanine7‐modified cyclodextrin. The Ir(III) complex enables the oxygen detection, while the cyclodextrin is used not only for improving the water solubility and suppressing the luminescence quenching effect of the surrounding aqueous media, but also for carrying Cyanine7 to establish a ratiometric oxygen fluorescence probe. 2D nuclear magnetic resonance is carried out to confirm the host–guest structure. The oxygen‐responsive ability of the resulting ratiometric probe is evaluated through in vitro cell and multicellular experiments. Further animal studies about tumor oxygen level mapping demonstrate that the probe can be successfully used for quantitatively visualizing tumor hypoxia in vivo. John Wiley and Sons Inc. 2021-02-05 /pmc/articles/PMC8061356/ /pubmed/33898188 http://dx.doi.org/10.1002/advs.202004044 Text en © 2021 The Authors. Published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Xiao, Peng
Liu, Chunyan
Ma, Tiancong
Lu, Xiuhong
Jing, Lihong
Hou, Yi
Zhang, Peisen
Huang, Gang
Gao, Mingyuan
A Cyclodextrin‐Hosted Ir(III) Complex for Ratiometric Mapping of Tumor Hypoxia In Vivo
title A Cyclodextrin‐Hosted Ir(III) Complex for Ratiometric Mapping of Tumor Hypoxia In Vivo
title_full A Cyclodextrin‐Hosted Ir(III) Complex for Ratiometric Mapping of Tumor Hypoxia In Vivo
title_fullStr A Cyclodextrin‐Hosted Ir(III) Complex for Ratiometric Mapping of Tumor Hypoxia In Vivo
title_full_unstemmed A Cyclodextrin‐Hosted Ir(III) Complex for Ratiometric Mapping of Tumor Hypoxia In Vivo
title_short A Cyclodextrin‐Hosted Ir(III) Complex for Ratiometric Mapping of Tumor Hypoxia In Vivo
title_sort cyclodextrin‐hosted ir(iii) complex for ratiometric mapping of tumor hypoxia in vivo
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8061356/
https://www.ncbi.nlm.nih.gov/pubmed/33898188
http://dx.doi.org/10.1002/advs.202004044
work_keys_str_mv AT xiaopeng acyclodextrinhostediriiicomplexforratiometricmappingoftumorhypoxiainvivo
AT liuchunyan acyclodextrinhostediriiicomplexforratiometricmappingoftumorhypoxiainvivo
AT matiancong acyclodextrinhostediriiicomplexforratiometricmappingoftumorhypoxiainvivo
AT luxiuhong acyclodextrinhostediriiicomplexforratiometricmappingoftumorhypoxiainvivo
AT jinglihong acyclodextrinhostediriiicomplexforratiometricmappingoftumorhypoxiainvivo
AT houyi acyclodextrinhostediriiicomplexforratiometricmappingoftumorhypoxiainvivo
AT zhangpeisen acyclodextrinhostediriiicomplexforratiometricmappingoftumorhypoxiainvivo
AT huanggang acyclodextrinhostediriiicomplexforratiometricmappingoftumorhypoxiainvivo
AT gaomingyuan acyclodextrinhostediriiicomplexforratiometricmappingoftumorhypoxiainvivo
AT xiaopeng cyclodextrinhostediriiicomplexforratiometricmappingoftumorhypoxiainvivo
AT liuchunyan cyclodextrinhostediriiicomplexforratiometricmappingoftumorhypoxiainvivo
AT matiancong cyclodextrinhostediriiicomplexforratiometricmappingoftumorhypoxiainvivo
AT luxiuhong cyclodextrinhostediriiicomplexforratiometricmappingoftumorhypoxiainvivo
AT jinglihong cyclodextrinhostediriiicomplexforratiometricmappingoftumorhypoxiainvivo
AT houyi cyclodextrinhostediriiicomplexforratiometricmappingoftumorhypoxiainvivo
AT zhangpeisen cyclodextrinhostediriiicomplexforratiometricmappingoftumorhypoxiainvivo
AT huanggang cyclodextrinhostediriiicomplexforratiometricmappingoftumorhypoxiainvivo
AT gaomingyuan cyclodextrinhostediriiicomplexforratiometricmappingoftumorhypoxiainvivo