A glutathione-depleted prodrug platform of MnO2-coated hollow polydopamine nanospheres for effective cancer diagnosis and therapy. (4th May 2020)
- Record Type:
- Journal Article
- Title:
- A glutathione-depleted prodrug platform of MnO2-coated hollow polydopamine nanospheres for effective cancer diagnosis and therapy. (4th May 2020)
- Main Title:
- A glutathione-depleted prodrug platform of MnO2-coated hollow polydopamine nanospheres for effective cancer diagnosis and therapy
- Authors:
- Dong, Liang
Xu, Zhiai
An, Shangjie
Jia, Xiaodan
Zhang, Wen
Jiang, Xiue - Abstract:
- Abstract : A biocompatible and efficient nanoplatform for tumor diagnosis and treatment was fabricated based on manganese oxide-coated hollow polydopamine loaded with dihydroartemisinin. Abstract : Currently, cancer is regarded as one of the most life-threatening diseases worldwide. To date, much attention has been paid to treating this serious disease. Among various cancer therapies, chemotherapy has been used in the clinic for more than sixty years and is regarded as an ideal choice because of its high efficiency. Herein, a biocompatible and efficient nanoplatform for tumor treatment was fabricated based on manganese oxide-coated hollow polydopamine (HPDA@MnO2 ). Dihydroartemisinin (DHA), a derivative of the Chinese traditional anti-malarial medicine artemisinin, was selected to be loaded into the cavity of HPDA@MnO2 to form the final nanodrug DHA@HPDA@MnO2 . As a unique nanoplatform, DHA@HPDA@MnO2 showed biodegradable and controllable release of DHA and Mn ions upon reaching the tumor sites. It is worth mentioning that the reduced Mn 2+ interacts with DHA to generate cytotoxic reactive oxygen species (ROS) which effectively damage proteins and nucleic acids, thereby inducing the death of tumor cells. More importantly, the Mn ions reduced from MnO2 showed selective in vivo magnetic resonance imaging capability in response to the tumor microenvironment. In vitro and in vivo therapy experiments showed that the tumor inhibition of DHA@HPDA@MnO2 was more efficient than that ofAbstract : A biocompatible and efficient nanoplatform for tumor diagnosis and treatment was fabricated based on manganese oxide-coated hollow polydopamine loaded with dihydroartemisinin. Abstract : Currently, cancer is regarded as one of the most life-threatening diseases worldwide. To date, much attention has been paid to treating this serious disease. Among various cancer therapies, chemotherapy has been used in the clinic for more than sixty years and is regarded as an ideal choice because of its high efficiency. Herein, a biocompatible and efficient nanoplatform for tumor treatment was fabricated based on manganese oxide-coated hollow polydopamine (HPDA@MnO2 ). Dihydroartemisinin (DHA), a derivative of the Chinese traditional anti-malarial medicine artemisinin, was selected to be loaded into the cavity of HPDA@MnO2 to form the final nanodrug DHA@HPDA@MnO2 . As a unique nanoplatform, DHA@HPDA@MnO2 showed biodegradable and controllable release of DHA and Mn ions upon reaching the tumor sites. It is worth mentioning that the reduced Mn 2+ interacts with DHA to generate cytotoxic reactive oxygen species (ROS) which effectively damage proteins and nucleic acids, thereby inducing the death of tumor cells. More importantly, the Mn ions reduced from MnO2 showed selective in vivo magnetic resonance imaging capability in response to the tumor microenvironment. In vitro and in vivo therapy experiments showed that the tumor inhibition of DHA@HPDA@MnO2 was more efficient than that of free DHA, accompanied by negligible side effects; thus, the proposed nanomedicine platform is promising for application in tumor chemotherapy. … (more)
- Is Part Of:
- New journal of chemistry. Volume 44:Number 19(2020)
- Journal:
- New journal of chemistry
- Issue:
- Volume 44:Number 19(2020)
- Issue Display:
- Volume 44, Issue 19 (2020)
- Year:
- 2020
- Volume:
- 44
- Issue:
- 19
- Issue Sort Value:
- 2020-0044-0019-0000
- Page Start:
- 7838
- Page End:
- 7848
- Publication Date:
- 2020-05-04
- Subjects:
- Chemistry -- Periodicals
Chimie -- Périodiques
540 - Journal URLs:
- http://www.rsc.org/ ↗
http://www.rsc.org/is/journals/current/newjchem/njc.htm ↗ - DOI:
- 10.1039/d0nj01211d ↗
- Languages:
- English
- ISSNs:
- 1144-0546
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6084.319900
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 13868.xml