Low-intensity focused ultrasound-augmented Cascade chemodynamic therapy via boosting ROS generation. (April 2021)
- Record Type:
- Journal Article
- Title:
- Low-intensity focused ultrasound-augmented Cascade chemodynamic therapy via boosting ROS generation. (April 2021)
- Main Title:
- Low-intensity focused ultrasound-augmented Cascade chemodynamic therapy via boosting ROS generation
- Authors:
- Deng, Liming
Liu, Mingzhu
Sheng, Danli
Luo, Yuanli
Wang, Dong
Yu, Xian
Wang, Zhigang
Ran, Haitao
Li, Pan - Abstract:
- Abstract: Fenton reaction-mediated chemodynamic therapy (CDT), which destroys tumor cells by converting H2 O2 into cytotoxic hydroxyl radical (OH) and singlet oxygen ( 1 O2 ) species, is a promising field. However, Fenton-based CDT is severely impaired by the inappropriate tumor environment associated with undesirable intratumoral acidity and insufficient H2 O2 supply in tumor microenvironment (TME). Therefore, a strategy that can address these concerns is highly desired and beneficial for boosting such treatment. Herein, a magnetic nanoreactor system (denoted as poly (lactic-co-glycolic acid) (PLGA)–superparamagnetic iron oxide (SPIO)&vitamin C (Vc) was constructed with Vc in the core, SPIO on the shell, and PLGA as the building carrier. Upon low-intensity focused ultrasound irradiation, on-demand Vc release can locally decompose into H2 O2, which can generate a favorable condition for facilitating SPIO-based Fenton-like reaction and result in continuous O2 and OH/ 1 O2 generation. The TME modulation-augmented CDT by this nanoreactor based on the reinforced Fenton reaction tremendously improved the antitumor outcomes, especially under increased accumulation contributed by magnetic targeting combined with enhanced permeability and retention effect. Moreover, the explosive production of oxygen can be monitored by real-time photoacoustic imaging, offering a noninvasive means to forecast the treatment efficacy. Therefore, this established microenvironment modulation strategyAbstract: Fenton reaction-mediated chemodynamic therapy (CDT), which destroys tumor cells by converting H2 O2 into cytotoxic hydroxyl radical (OH) and singlet oxygen ( 1 O2 ) species, is a promising field. However, Fenton-based CDT is severely impaired by the inappropriate tumor environment associated with undesirable intratumoral acidity and insufficient H2 O2 supply in tumor microenvironment (TME). Therefore, a strategy that can address these concerns is highly desired and beneficial for boosting such treatment. Herein, a magnetic nanoreactor system (denoted as poly (lactic-co-glycolic acid) (PLGA)–superparamagnetic iron oxide (SPIO)&vitamin C (Vc) was constructed with Vc in the core, SPIO on the shell, and PLGA as the building carrier. Upon low-intensity focused ultrasound irradiation, on-demand Vc release can locally decompose into H2 O2, which can generate a favorable condition for facilitating SPIO-based Fenton-like reaction and result in continuous O2 and OH/ 1 O2 generation. The TME modulation-augmented CDT by this nanoreactor based on the reinforced Fenton reaction tremendously improved the antitumor outcomes, especially under increased accumulation contributed by magnetic targeting combined with enhanced permeability and retention effect. Moreover, the explosive production of oxygen can be monitored by real-time photoacoustic imaging, offering a noninvasive means to forecast the treatment efficacy. Therefore, this established microenvironment modulation strategy for augmenting Fenton reaction-based CDT paves a new avenue to realize highly efficient cancer theranostics. … (more)
- Is Part Of:
- Biomaterials. Volume 271(2021)
- Journal:
- Biomaterials
- Issue:
- Volume 271(2021)
- Issue Display:
- Volume 271, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 271
- Issue:
- 2021
- Issue Sort Value:
- 2021-0271-2021-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-04
- Subjects:
- Low-intensity focused ultrasound -- Chemodynamic therapy -- Fenton reaction -- Vitamin C -- Real-time monitoring
Biomedical materials -- Periodicals
Biocompatible Materials -- Periodicals
Biomatériaux -- Périodiques
610.28 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01429612 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/01429612 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/01429612 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.biomaterials.2021.120710 ↗
- Languages:
- English
- ISSNs:
- 0142-9612
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2087.715000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 23393.xml