H2O2-activated oxidative stress amplifier capable of GSH scavenging for enhancing tumor photodynamic therapy. (17th October 2019)
- Record Type:
- Journal Article
- Title:
- H2O2-activated oxidative stress amplifier capable of GSH scavenging for enhancing tumor photodynamic therapy. (17th October 2019)
- Main Title:
- H2O2-activated oxidative stress amplifier capable of GSH scavenging for enhancing tumor photodynamic therapy
- Authors:
- Liu, Yadong
Zhou, Zhanwei
Liu, Yidi
Li, Yanhui
Huang, Xinzhi
Qian, Chenggen
Sun, Minjie - Abstract:
- Abstract : An oxidative stress amplifier (OSA) capable of GSH scavenging and accelerated release by positive feedback was fabricated for enhancing the efficacy of tumor photodynamic therapy (PDT). Abstract : Photodynamic therapy (PDT) is a clinically approved cancer treatment approach that relies on the generation of excess reactive oxygen species (ROS) to eradicate tumor cells by inducing oxidative stress. Unfortunately, if the tumor's endogenous glutathione (GSH) is overexpressed, it will eliminate the ROS and restrict the therapeutic efficacy of PDT. Herein, we report a H2 O2 -activated oxidative stress amplifier (OSA) for enhancing the ROS generation for PDT via GSH scavenging. Cinnamaldehyde (Cin) and chlorin e6 (Ce6) were applied as the GSH scavenger and photosensitizer, respectively, which were assembled with the ROS-responsive amphipathic polymer (DPL) to form DPL@CC micelles as the OSA. In the circulation of blood, the OSA can effectively protect the Cin from albumin binding to retain its GSH depletion ability. Once the OSA reached the tumor site, the high level of H2 O2 triggered the degradation of DPL and led to the release of Cin and Ce6. Subsequently, the released Cin reacted with the intracellular GSH by Michael Addition and downregulated the GSH level to about 18.9%, versus untreated cells, to weaken the anti-oxidation ability of tumor cells. Thus, it provided a suitable environment for PDT to obtain an amplifying effect on oxidative stress and superiorAbstract : An oxidative stress amplifier (OSA) capable of GSH scavenging and accelerated release by positive feedback was fabricated for enhancing the efficacy of tumor photodynamic therapy (PDT). Abstract : Photodynamic therapy (PDT) is a clinically approved cancer treatment approach that relies on the generation of excess reactive oxygen species (ROS) to eradicate tumor cells by inducing oxidative stress. Unfortunately, if the tumor's endogenous glutathione (GSH) is overexpressed, it will eliminate the ROS and restrict the therapeutic efficacy of PDT. Herein, we report a H2 O2 -activated oxidative stress amplifier (OSA) for enhancing the ROS generation for PDT via GSH scavenging. Cinnamaldehyde (Cin) and chlorin e6 (Ce6) were applied as the GSH scavenger and photosensitizer, respectively, which were assembled with the ROS-responsive amphipathic polymer (DPL) to form DPL@CC micelles as the OSA. In the circulation of blood, the OSA can effectively protect the Cin from albumin binding to retain its GSH depletion ability. Once the OSA reached the tumor site, the high level of H2 O2 triggered the degradation of DPL and led to the release of Cin and Ce6. Subsequently, the released Cin reacted with the intracellular GSH by Michael Addition and downregulated the GSH level to about 18.9%, versus untreated cells, to weaken the anti-oxidation ability of tumor cells. Thus, it provided a suitable environment for PDT to obtain an amplifying effect on oxidative stress and superior anti-cancer efficacy of 94% growth inhibition. The preparation of the H2 O2 -activated oxidative stress amplifier is a convincing strategy for promoting intracellular ROS generation and enhancing the tumor PDT efficacy, which could also augment the clinical application of PDT. … (more)
- Is Part Of:
- Biomaterials science. Volume 7:Number 12(2019)
- Journal:
- Biomaterials science
- Issue:
- Volume 7:Number 12(2019)
- Issue Display:
- Volume 7, Issue 12 (2019)
- Year:
- 2019
- Volume:
- 7
- Issue:
- 12
- Issue Sort Value:
- 2019-0007-0012-0000
- Page Start:
- 5359
- Page End:
- 5368
- Publication Date:
- 2019-10-17
- Subjects:
- Biomedical materials -- Periodicals
610.28 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/bm ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9bm01354g ↗
- Languages:
- English
- ISSNs:
- 2047-4830
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2087.724000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 12145.xml