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Stimuli-Responsive Polymeric Nanoplatforms for Cancer Therapy.

作者信息

Chang Di, Ma Yuanyuan, Xu Xiaoxuan, Xie Jinbing, Ju Shenghong

机构信息

Jiangsu Key Laboratory of Molecular and Functional Imaging, Department of Radiology, Zhongda Hospital, Medical School of Southeast University, Nanjing, China.

出版信息

Front Bioeng Biotechnol. 2021 Jun 25;9:707319. doi: 10.3389/fbioe.2021.707319. eCollection 2021.


DOI:10.3389/fbioe.2021.707319
PMID:34249894
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8267819/
Abstract

Polymeric nanoparticles have been widely used as carriers of drugs and bioimaging agents due to their excellent biocompatibility, biodegradability, and structural versatility. The principal application of polymeric nanoparticles in medicine is for cancer therapy, with increased tumor accumulation, precision delivery of anticancer drugs to target sites, higher solubility of pharmaceutical properties and lower systemic toxicity. Recently, the stimuli-responsive polymeric nanoplatforms attracted more and more attention because they can change their physicochemical properties responding to the stimuli conditions, such as low pH, enzyme, redox agents, hypoxia, light, temperature, magnetic field, ultrasound, and so on. Moreover, the unique properties of stimuli-responsive polymeric nanocarriers in target tissues may significantly improve the bioactivity of delivered agents for cancer treatment. This review introduces stimuli-responsive polymeric nanoparticles and their applications in tumor theranostics with the loading of chemical drugs, nucleic drugs and imaging molecules. In addition, we discuss the strategy for designing multifunctional polymeric nanocarriers and provide the perspective for the clinical applications of these stimuli-responsive polymeric nanoplatforms.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ea/8267819/60c10e86105d/fbioe-09-707319-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ea/8267819/631155138915/fbioe-09-707319-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ea/8267819/df9684674251/fbioe-09-707319-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ea/8267819/64dae74ee9fe/fbioe-09-707319-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ea/8267819/084f24e74b84/fbioe-09-707319-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ea/8267819/4f4d872aef72/fbioe-09-707319-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ea/8267819/e3472b860826/fbioe-09-707319-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ea/8267819/4504dcb3e1c2/fbioe-09-707319-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ea/8267819/de7bc7305c03/fbioe-09-707319-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ea/8267819/46f9cc1d9b8e/fbioe-09-707319-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ea/8267819/60c10e86105d/fbioe-09-707319-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ea/8267819/631155138915/fbioe-09-707319-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ea/8267819/df9684674251/fbioe-09-707319-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ea/8267819/64dae74ee9fe/fbioe-09-707319-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ea/8267819/084f24e74b84/fbioe-09-707319-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ea/8267819/4f4d872aef72/fbioe-09-707319-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ea/8267819/e3472b860826/fbioe-09-707319-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ea/8267819/4504dcb3e1c2/fbioe-09-707319-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ea/8267819/de7bc7305c03/fbioe-09-707319-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ea/8267819/46f9cc1d9b8e/fbioe-09-707319-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ea/8267819/60c10e86105d/fbioe-09-707319-g010.jpg

相似文献

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[2]
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[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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Pharmaceutics. 2024-7-31

[9]
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[10]
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本文引用的文献

[1]
Polymeric Nanocarriers: A Transformation in Doxorubicin Therapies.

Materials (Basel). 2021-4-22

[2]
Apigenin-loaded galactose tailored PLGA nanoparticles: A possible strategy for liver targeting to treat hepatocellular carcinoma.

Colloids Surf B Biointerfaces. 2021-8

[3]
Redox-responsive hyaluronic acid-based nanoparticles for targeted photodynamic therapy/chemotherapy against breast cancer.

J Colloid Interface Sci. 2021-9-15

[4]
Therapeutic Targeting of the Tumor Microenvironment.

Cancer Discov. 2021-4

[5]
The 35th Anniversary of the Discovery of EPR Effect: A New Wave of Nanomedicines for Tumor-Targeted Drug Delivery-Personal Remarks and Future Prospects.

J Pers Med. 2021-3-22

[6]
PLGA Based Nanospheres as a Potent Macrophage-Specific Drug Delivery System.

Nanomaterials (Basel). 2021-3-16

[7]
Nanodrug Delivery Systems Modulate Tumor Vessels to Increase the Enhanced Permeability and Retention Effect.

J Pers Med. 2021-2-14

[8]
Manganese-Dioxide-Coating-Instructed Plasmonic Modulation of Gold Nanorods for Activatable Duplex-Imaging-Guided NIR-II Photothermal-Chemodynamic Therapy.

Adv Mater. 2021-4

[9]
A Polymer Multicellular Nanoengager for Synergistic NIR-II Photothermal Immunotherapy.

Adv Mater. 2021-4

[10]
Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries.

CA Cancer J Clin. 2021-5

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