A glutathione-depleted prodrug platform of MnO 2 -coated hollow polydopamine nanospheres for effective cancer diagnosis and therapy
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...
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Veröffentlicht in: | New journal of chemistry 2020-05, Vol.44 (19), p.7838-7848 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | 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@MnO
2
). Dihydroartemisinin (DHA), a derivative of the Chinese traditional anti-malarial medicine artemisinin, was selected to be loaded into the cavity of HPDA@MnO
2
to form the final nanodrug DHA@HPDA@MnO
2
. As a unique nanoplatform, DHA@HPDA@MnO
2
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 MnO
2
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@MnO
2
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. |
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ISSN: | 1144-0546 1369-9261 |
DOI: | 10.1039/D0NJ01211D |