Molecular radio afterglow probes for cancer radiodynamic theranostics

X-ray-induced afterglow and radiodynamic therapy tackle the tissue penetration issue of optical imaging and phototherapy. However, inorganic nanophosphors used in this therapy have their radio afterglow dynamic function as always on, limiting the detection specificity and treatment efficacy. Here we...

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Main Authors: Huang, Jingsheng, Su, Lichao, Xu, Cheng, Ge, Xiaoguang, Zhang, Ruiping, Song, Jibin, Pu, Kanyi
Other Authors: Lee Kong Chian School of Medicine (LKCMedicine)
Format: Journal Article
Language:English
Published: 2023
Subjects:
Online Access:https://hdl.handle.net/10356/171019
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author Huang, Jingsheng
Su, Lichao
Xu, Cheng
Ge, Xiaoguang
Zhang, Ruiping
Song, Jibin
Pu, Kanyi
author2 Lee Kong Chian School of Medicine (LKCMedicine)
author_facet Lee Kong Chian School of Medicine (LKCMedicine)
Huang, Jingsheng
Su, Lichao
Xu, Cheng
Ge, Xiaoguang
Zhang, Ruiping
Song, Jibin
Pu, Kanyi
author_sort Huang, Jingsheng
collection NTU
description X-ray-induced afterglow and radiodynamic therapy tackle the tissue penetration issue of optical imaging and phototherapy. However, inorganic nanophosphors used in this therapy have their radio afterglow dynamic function as always on, limiting the detection specificity and treatment efficacy. Here we report organic luminophores (IDPAs) with near-infrared afterglow and 1O2 production after X-ray irradiation for cancer theranostics. The in vivo radio afterglow of IDPAs is >25.0 times brighter than reported inorganic nanophosphors, whereas the radiodynamic production of 1O2 is >5.7 times higher than commercially available radio sensitizers. The modular structure of IDPAs permits the development of a smart molecular probe that only triggers its radio afterglow dynamic function in the presence of a cancer biomarker. Thus, the probe enables the ultrasensitive detection of a diminutive tumour (0.64 mm) with superb contrast (tumour-to-background ratio of 234) and tumour-specific radiotherapy for brain tumour with molecular precision at low dosage. Our work reveals the molecular guidelines towards organic radio afterglow agents and highlights new opportunities for cancer radio theranostics.
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spelling ntu-10356/1710192023-10-15T15:38:33Z Molecular radio afterglow probes for cancer radiodynamic theranostics Huang, Jingsheng Su, Lichao Xu, Cheng Ge, Xiaoguang Zhang, Ruiping Song, Jibin Pu, Kanyi Lee Kong Chian School of Medicine (LKCMedicine) School of Chemistry, Chemical Engineering and Biotechnology Science::Medicine Diseases Infrared Devices X-ray-induced afterglow and radiodynamic therapy tackle the tissue penetration issue of optical imaging and phototherapy. However, inorganic nanophosphors used in this therapy have their radio afterglow dynamic function as always on, limiting the detection specificity and treatment efficacy. Here we report organic luminophores (IDPAs) with near-infrared afterglow and 1O2 production after X-ray irradiation for cancer theranostics. The in vivo radio afterglow of IDPAs is >25.0 times brighter than reported inorganic nanophosphors, whereas the radiodynamic production of 1O2 is >5.7 times higher than commercially available radio sensitizers. The modular structure of IDPAs permits the development of a smart molecular probe that only triggers its radio afterglow dynamic function in the presence of a cancer biomarker. Thus, the probe enables the ultrasensitive detection of a diminutive tumour (0.64 mm) with superb contrast (tumour-to-background ratio of 234) and tumour-specific radiotherapy for brain tumour with molecular precision at low dosage. Our work reveals the molecular guidelines towards organic radio afterglow agents and highlights new opportunities for cancer radio theranostics. Ministry of Education (MOE) National Research Foundation (NRF) Submitted/Accepted version K.P. thanks Singapore National Research Foundation (NRF) (NRF-NRFI07-2021-0005) and the Singapore Ministry of Education, Academic Research Fund Tier 1 (2019-T1-002-045, RG125/19, RT05/20) and Academic Research Fund Tier 2 (MOE-T2EP30220-0010, MOE-T2EP30221-0004) for financial support. R.Z. thanks the Nature Materials Article https://doi.org/10.1038/s41563-023-01659-1 National Natural Science Foundation of China (nos. 82120108016 and 82071987) for financial support. J.S. thanks the National Natural Science Foundation of China (No. U22A20348, U21A20377) and the Natural Science Foundation of Fujian Province (No. 2020J02012). 2023-10-10T05:39:10Z 2023-10-10T05:39:10Z 2023 Journal Article Huang, J., Su, L., Xu, C., Ge, X., Zhang, R., Song, J. & Pu, K. (2023). Molecular radio afterglow probes for cancer radiodynamic theranostics. Nature Materials. https://dx.doi.org/10.1038/s41563-023-01659-1 1476-1122 https://hdl.handle.net/10356/171019 10.1038/s41563-023-01659-1 37667071 2-s2.0-85169824401 en NRF-NRFI07-2021-0005 2019-T1-002-045 RG125/19 RT05/20 MOE-T2EP30220-0010 MOE-T2EP30221-0004 Nature Materials © 2023 The Author(s), under exclusive licence to Springer Nature Limited. All rights reserved. This article may be downloaded for personal use only. Any other use requires prior permission of the copyright holder. The Version of Record is available online at http://doi.org/10.1038/s41563-023-01659-1. application/pdf
spellingShingle Science::Medicine
Diseases
Infrared Devices
Huang, Jingsheng
Su, Lichao
Xu, Cheng
Ge, Xiaoguang
Zhang, Ruiping
Song, Jibin
Pu, Kanyi
Molecular radio afterglow probes for cancer radiodynamic theranostics
title Molecular radio afterglow probes for cancer radiodynamic theranostics
title_full Molecular radio afterglow probes for cancer radiodynamic theranostics
title_fullStr Molecular radio afterglow probes for cancer radiodynamic theranostics
title_full_unstemmed Molecular radio afterglow probes for cancer radiodynamic theranostics
title_short Molecular radio afterglow probes for cancer radiodynamic theranostics
title_sort molecular radio afterglow probes for cancer radiodynamic theranostics
topic Science::Medicine
Diseases
Infrared Devices
url https://hdl.handle.net/10356/171019
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