Protein sulfenic acid-mediated anchoring of gold nanoparticles for enhanced CT imaging and radiotherapy of tumors in vivo
Jianan Ding
1, 2, 3, 4, 5, 6
,
Qiulian Mao
1, 2, 3, 4, 5, 6
,
Meng Zhao
1
,
Yinjia Gao
1, 2, 3, 4, 5, 6
,
Anna Wang
1, 2, 3, 4, 5, 6
,
Shuyue Ye
1, 2, 3, 4, 5, 6
,
Xiaoyan Wang
6, 7, 8, 9, 10
,
Wei Xie
6, 11, 12, 13, 14
,
Haibin Shi
1, 2, 3, 4, 5, 6
2
State Key Laboratory of Radiation Medicine and Protection
3
School for Radiological and Interdisciplinary Sciences (RAD-X) and Collaborative Innovation Center of Radiation Medicine of Jiangsu Higher Education Institutions
4
SooChow University
5
Suzhou 215123
|
6
P. R. China
|
8
Department of Ultrasound
10
Changzhi 046000
|
12
Shanghai Key Laboratory for Molecular Imaging
|
14
Shanghai 201318
|
Publication type: Journal Article
Publication date: 2020-11-06
scimago Q1
wos Q1
SJR: 1.245
CiteScore: 9.9
Impact factor: 5.1
ISSN: 20403364, 20403372
PubMed ID:
33206090
General Materials Science
Abstract
Radiotherapy (RT) has become one of the most widely used treatments for malignant tumors in clinics. Developing a novel radiosensitizer for the integration of precise diagnosis and effective radiotherapy against hypoxic tumors is desirable but remains a great challenge. Herein, protein sulfenic acid reactive gold nanoparticles as effective radiosensitizers were for the first time reported for enhanced X-ray computed tomography (CT) imaging and radiotherapy of tumors in vivo. The gold nanoparticles were decorated with biocompatible poly(ethylene glycol), folic acid (FA), and sulfenic acid reactive groups 1,3-cyclohexanedione (CHD). Such a nanostructure enables on-site immobilization within tumors under oxidative stress through the specific reaction between CHD and endogenous protein sulfenic acids resulting in enhanced accumulation and retention of gold nanoparticles within tumors, which remarkably improves the sensitivity of CT imaging and the radiotherapeutic efficacy of tumors in living mice. This study thus is the first to demonstrate that protein sulfenic acid reactive gold nanoparticles with a tumor anchoring function may serve as effective radiosensitizers for clinical X-ray theranostic application in the future.
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Total citations:
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Citations from 2024:
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(47.37%)
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GOST
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Ding J. et al. Protein sulfenic acid-mediated anchoring of gold nanoparticles for enhanced CT imaging and radiotherapy of tumors in vivo // Nanoscale. 2020. Vol. 12. No. 45. pp. 22963-22969.
GOST all authors (up to 50)
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Ding J., Mao Q., Zhao M., Gao Y., Wang A., Ye S., Wang X., Xie W., Shi H. Protein sulfenic acid-mediated anchoring of gold nanoparticles for enhanced CT imaging and radiotherapy of tumors in vivo // Nanoscale. 2020. Vol. 12. No. 45. pp. 22963-22969.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1039/d0nr06440h
UR - https://xlink.rsc.org/?DOI=D0NR06440H
TI - Protein sulfenic acid-mediated anchoring of gold nanoparticles for enhanced CT imaging and radiotherapy of tumors in vivo
T2 - Nanoscale
AU - Ding, Jianan
AU - Mao, Qiulian
AU - Zhao, Meng
AU - Gao, Yinjia
AU - Wang, Anna
AU - Ye, Shuyue
AU - Wang, Xiaoyan
AU - Xie, Wei
AU - Shi, Haibin
PY - 2020
DA - 2020/11/06
PB - Royal Society of Chemistry (RSC)
SP - 22963-22969
IS - 45
VL - 12
PMID - 33206090
SN - 2040-3364
SN - 2040-3372
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2020_Ding,
author = {Jianan Ding and Qiulian Mao and Meng Zhao and Yinjia Gao and Anna Wang and Shuyue Ye and Xiaoyan Wang and Wei Xie and Haibin Shi},
title = {Protein sulfenic acid-mediated anchoring of gold nanoparticles for enhanced CT imaging and radiotherapy of tumors in vivo},
journal = {Nanoscale},
year = {2020},
volume = {12},
publisher = {Royal Society of Chemistry (RSC)},
month = {nov},
url = {https://xlink.rsc.org/?DOI=D0NR06440H},
number = {45},
pages = {22963--22969},
doi = {10.1039/d0nr06440h}
}
Cite this
MLA
Copy
Ding, Jianan, et al. “Protein sulfenic acid-mediated anchoring of gold nanoparticles for enhanced CT imaging and radiotherapy of tumors in vivo.” Nanoscale, vol. 12, no. 45, Nov. 2020, pp. 22963-22969. https://xlink.rsc.org/?DOI=D0NR06440H.
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