Metalloporphyrin-Encapsulated Biodegradable Nanosystems for Highly Efficient Magnetic Resonance Imaging-Guided Sonodynamic Cancer Therapy.
Ping Huang
1
,
Xiaoqin Qian
2
,
Yu Chen
3
,
Luodan Yu
3
,
Hui Lin
3
,
Liying Wang
3
,
Yufang Zhu
1
,
Publication type: Journal Article
Publication date: 2017-01-11
scimago Q1
wos Q1
SJR: 5.554
CiteScore: 22.5
Impact factor: 15.6
ISSN: 00027863, 15205126
PubMed ID:
28024395
General Chemistry
Catalysis
Biochemistry
Colloid and Surface Chemistry
Abstract
Traditional photodynamic therapy (PDT) suffers from the critical issues of low tissue-penetrating depth of light and potential phototoxicity, which are expected to be solved by developing new dynamic therapy-based therapeutic modalities such as sonodynamic therapy (SDT). In this work, we report on the design/fabrication of a high-performance multifunctional nanoparticulate sonosensitizer for efficient in vivo magnetic resonance imaging (MRI)-guided SDT against cancer. The developed approach takes the structural and compositional features of mesoporous organosilica-based nanosystems for the fabrication of sonosensitizers with intriguing theranostic performance. The well-defined mesoporosity facilitates the high loading of organic sonosensitizers (protoporphyrin, PpIX) and further chelating of paramagnetic transitional metal Mn ions based on metalloporphyrin chemistry (MnPpIX). The mesoporous structure of large surface area also maximizes the accessibility of water molecules to the encapsulated paramagnetic Mn ions, endowing the composite sonosensitizers with markedly high MRI performance (r1 = 9.43 mM-1 s-2) for SDT guidance and monitoring. Importantly, the developed multifunctional sonosensitizers (HMONs-MnPpIX-PEG) with controllable biodegradation behavior and high biocompatibility show distinctively high SDT efficiency for inducing the cancer-cell death in vitro and suppressing the tumor growth in vivo. This report provides a paradigm that nanotechnology-enhanced SDT based on elaborately designed high-performance multifunctional sonosensitizers will pave a new way for efficient cancer treatment by fully taking the advantages (noninvasiveness, convenience, cost-effectiveness, etc.) of ultrasound therapy and quickly developing nanomedicine.
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Huang P. et al. Metalloporphyrin-Encapsulated Biodegradable Nanosystems for Highly Efficient Magnetic Resonance Imaging-Guided Sonodynamic Cancer Therapy. // Journal of the American Chemical Society. 2017. Vol. 139. No. 3. pp. 1275-1284.
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Huang P., Qian X., Chen Yu., Yu L., Lin H., Wang L., Zhu Y., Shi J. Metalloporphyrin-Encapsulated Biodegradable Nanosystems for Highly Efficient Magnetic Resonance Imaging-Guided Sonodynamic Cancer Therapy. // Journal of the American Chemical Society. 2017. Vol. 139. No. 3. pp. 1275-1284.
Cite this
RIS
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TY - JOUR
DO - 10.1021/jacs.6b11846
UR - https://doi.org/10.1021/jacs.6b11846
TI - Metalloporphyrin-Encapsulated Biodegradable Nanosystems for Highly Efficient Magnetic Resonance Imaging-Guided Sonodynamic Cancer Therapy.
T2 - Journal of the American Chemical Society
AU - Huang, Ping
AU - Qian, Xiaoqin
AU - Chen, Yu
AU - Yu, Luodan
AU - Lin, Hui
AU - Wang, Liying
AU - Zhu, Yufang
AU - Shi, Jianlin
PY - 2017
DA - 2017/01/11
PB - American Chemical Society (ACS)
SP - 1275-1284
IS - 3
VL - 139
PMID - 28024395
SN - 0002-7863
SN - 1520-5126
ER -
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@article{2017_Huang,
author = {Ping Huang and Xiaoqin Qian and Yu Chen and Luodan Yu and Hui Lin and Liying Wang and Yufang Zhu and Jianlin Shi},
title = {Metalloporphyrin-Encapsulated Biodegradable Nanosystems for Highly Efficient Magnetic Resonance Imaging-Guided Sonodynamic Cancer Therapy.},
journal = {Journal of the American Chemical Society},
year = {2017},
volume = {139},
publisher = {American Chemical Society (ACS)},
month = {jan},
url = {https://doi.org/10.1021/jacs.6b11846},
number = {3},
pages = {1275--1284},
doi = {10.1021/jacs.6b11846}
}
Cite this
MLA
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Huang, Ping, et al. “Metalloporphyrin-Encapsulated Biodegradable Nanosystems for Highly Efficient Magnetic Resonance Imaging-Guided Sonodynamic Cancer Therapy..” Journal of the American Chemical Society, vol. 139, no. 3, Jan. 2017, pp. 1275-1284. https://doi.org/10.1021/jacs.6b11846.
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