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 inFrontiers in bioengineering and biotechnology Vol. 11; p. 1196839
Main Authors Liang, Yujia, Cai, Zhengmin, Tang, Yamei, Su, Chenglin, Xie, Liye, Li, Yan, Liang, Xinqiang
Format Journal Article
LanguageEnglish
Published Switzerland 2023
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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.
ISSN:2296-4185
2296-4185