H 2 O 2 /O 2 self-supply and Ca 2+ overloading MOF-based nanoplatform for cascade-amplified chemodynamic and photodynamic therapy
Reactive oxygen species (ROS)-mediated therapies have typically been considered as noninvasive tumor treatments owing to their high selectivity and efficiency. However, the harsh tumor microenvironment severely impairs their efficiency. Herein, the biodegradable Cu-doped zeolitic imidazolate framewo...
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Published in | Frontiers in bioengineering and biotechnology Vol. 11; p. 1196839 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
2023
|
Subjects | |
Online Access | Get full text |
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Summary: | Reactive oxygen species (ROS)-mediated therapies have typically been considered as noninvasive tumor treatments owing to their high selectivity and efficiency. However, the harsh tumor microenvironment severely impairs their efficiency.
Herein, the biodegradable Cu-doped zeolitic imidazolate framework-8 (ZIF-8) was synthesized for loading photosensitizer Chlorin e6 (Ce6) and CaO
nanoparticles, followed by surface decoration by hyaluronic acid (HA), obtaining HA/CaO
-Ce6@Cu-ZIF nano platform.
Once HA/CaO
-Ce6@Cu-ZIF targets tumor sites, the degradation of Ce6 and CaO
release from the HA/CaO
-Ce6@Cu-ZIF in response to the acid environment, while the Cu
active sites on Cu-ZIF are exposed. The released CaO
decompose to generate hydrogen peroxide (H
O
) and oxygen (O
), which alleviate the insufficiency of intracellular H
O
and hypoxia in tumor microenvironment (TME), effectively enhancing the production of hydroxyl radical (•OH) and singlet oxygen (
O
) in Cu
-mediated chemodynamic therapy (CDT) and Ce6-induced photodynamic therapy (PDT), respectively. Importantly, Ca
originating from CaO
could further enhance oxidative stress and result in mitochondrial dysfunction induced by Ca
overloading.
Thus, the H
O
/O
self-supplying and Ca
overloading ZIF-based nanoplatform for cascade-amplified CDT/PDT synergistic strategy is promising for highly efficient anticancer therapy. |
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ISSN: | 2296-4185 2296-4185 |