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Near-infrared light-triggered theranostics for tumor-specific enhanced multimodal imaging and photothermal therapy

The major challenge in current clinic contrast agents (CAs) and chemotherapy is the poor tumor selectivity and response. Based on the self-quench property of IR820 at high concentrations, and different contrast effect ability of Gd-DOTA between inner and outer of liposome, we developed “bomb-like” l...

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Autores principales: Wu, Bo, Wan, Bing, Lu, Shu-Ting, Deng, Kai, Li, Xiao-Qi, Wu, Bao-Lin, Li, Yu-Shuang, Liao, Ru-Fang, Huang, Shi-Wen, Xu, Hai-Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5481284/
https://www.ncbi.nlm.nih.gov/pubmed/28670120
http://dx.doi.org/10.2147/IJN.S137835
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author Wu, Bo
Wan, Bing
Lu, Shu-Ting
Deng, Kai
Li, Xiao-Qi
Wu, Bao-Lin
Li, Yu-Shuang
Liao, Ru-Fang
Huang, Shi-Wen
Xu, Hai-Bo
author_facet Wu, Bo
Wan, Bing
Lu, Shu-Ting
Deng, Kai
Li, Xiao-Qi
Wu, Bao-Lin
Li, Yu-Shuang
Liao, Ru-Fang
Huang, Shi-Wen
Xu, Hai-Bo
author_sort Wu, Bo
collection PubMed
description The major challenge in current clinic contrast agents (CAs) and chemotherapy is the poor tumor selectivity and response. Based on the self-quench property of IR820 at high concentrations, and different contrast effect ability of Gd-DOTA between inner and outer of liposome, we developed “bomb-like” light-triggered CAs (LTCAs) for enhanced CT/MRI/FI multimodal imaging, which can improve the signal-to-noise ratio of tumor tissue specifically. IR820, Iohexol and Gd-chelates were firstly encapsulated into the thermal-sensitive nanocarrier with a high concentration. This will result in protection and fluorescence quenching. Then, the release of CAs was triggered by near-infrared (NIR) light laser irradiation, which will lead to fluorescence and MRI activation and enable imaging of inflammation. In vitro and in vivo experiments demonstrated that LTCAs with 808 nm laser irradiation have shorter T(1) relaxation time in MRI and stronger intensity in FI compared to those without irradiation. Additionally, due to the high photothermal conversion efficiency of IR820, the injection of LTCAs was demonstrated to completely inhibit C6 tumor growth in nude mice up to 17 days after NIR laser irradiation. The results indicate that the LTCAs can serve as a promising platform for NIR-activated multimodal imaging and photothermal therapy.
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spelling pubmed-54812842017-06-30 Near-infrared light-triggered theranostics for tumor-specific enhanced multimodal imaging and photothermal therapy Wu, Bo Wan, Bing Lu, Shu-Ting Deng, Kai Li, Xiao-Qi Wu, Bao-Lin Li, Yu-Shuang Liao, Ru-Fang Huang, Shi-Wen Xu, Hai-Bo Int J Nanomedicine Original Research The major challenge in current clinic contrast agents (CAs) and chemotherapy is the poor tumor selectivity and response. Based on the self-quench property of IR820 at high concentrations, and different contrast effect ability of Gd-DOTA between inner and outer of liposome, we developed “bomb-like” light-triggered CAs (LTCAs) for enhanced CT/MRI/FI multimodal imaging, which can improve the signal-to-noise ratio of tumor tissue specifically. IR820, Iohexol and Gd-chelates were firstly encapsulated into the thermal-sensitive nanocarrier with a high concentration. This will result in protection and fluorescence quenching. Then, the release of CAs was triggered by near-infrared (NIR) light laser irradiation, which will lead to fluorescence and MRI activation and enable imaging of inflammation. In vitro and in vivo experiments demonstrated that LTCAs with 808 nm laser irradiation have shorter T(1) relaxation time in MRI and stronger intensity in FI compared to those without irradiation. Additionally, due to the high photothermal conversion efficiency of IR820, the injection of LTCAs was demonstrated to completely inhibit C6 tumor growth in nude mice up to 17 days after NIR laser irradiation. The results indicate that the LTCAs can serve as a promising platform for NIR-activated multimodal imaging and photothermal therapy. Dove Medical Press 2017-06-16 /pmc/articles/PMC5481284/ /pubmed/28670120 http://dx.doi.org/10.2147/IJN.S137835 Text en © 2017 Wu et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Wu, Bo
Wan, Bing
Lu, Shu-Ting
Deng, Kai
Li, Xiao-Qi
Wu, Bao-Lin
Li, Yu-Shuang
Liao, Ru-Fang
Huang, Shi-Wen
Xu, Hai-Bo
Near-infrared light-triggered theranostics for tumor-specific enhanced multimodal imaging and photothermal therapy
title Near-infrared light-triggered theranostics for tumor-specific enhanced multimodal imaging and photothermal therapy
title_full Near-infrared light-triggered theranostics for tumor-specific enhanced multimodal imaging and photothermal therapy
title_fullStr Near-infrared light-triggered theranostics for tumor-specific enhanced multimodal imaging and photothermal therapy
title_full_unstemmed Near-infrared light-triggered theranostics for tumor-specific enhanced multimodal imaging and photothermal therapy
title_short Near-infrared light-triggered theranostics for tumor-specific enhanced multimodal imaging and photothermal therapy
title_sort near-infrared light-triggered theranostics for tumor-specific enhanced multimodal imaging and photothermal therapy
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5481284/
https://www.ncbi.nlm.nih.gov/pubmed/28670120
http://dx.doi.org/10.2147/IJN.S137835
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