Controlled Deliveryof Cytarabine in Sodium CarboxymethylCellulose/Copper-Doped Prussian Blue Hydrogels for Chemotherapy andChemodynamic Therapy

To improve the therapy of chemotherapy for cancer treatment, hydrogels of sodium carboxymethyl cellulose (CMC)/copper-doped Prussian blue (CDPB) are synthesized for the controlled delivery of cytarabine (Cyt). CMC is connected to 3-aminophenylboronic acid (PBA) and dopamine (DA), respectively, by amidation reactions, and the obtained CMC-PBA and CMC-DA are cross-linked through boronate affinity for the encapsulation of CDPB and Cyt. The resultant CMC/CDPB/Cyt hydrogels can, respectively, respond to pH and H<sub>2</sub>O<sub>2</sub>, and thus, pH- and H<sub>2</sub>O<sub>2</sub>-responsive delivery of Cyt from the hydrogels is successfully achieved. More importantly, the overexpressed H<sub>2</sub>O<sub>2</sub> in cancer cells can be converted to hydroxyl radicals (<sup>•</sup>OH) by the CDPB in the hydrogels through Fenton-like reactions, and the generated <sup>•</sup>OH can participate in the chemodynamic therapy (CDT) of cancers. Due to the combination treatment of chemotherapy and CDT, enhanced anticancer effects are obtained by using human acute promyelocytic leukemia (HL-60) cell lines as the model target.

Publication Details

Journal
Figshare
Published
2025-02-07
DOI
https://doi.org/10.1021/acsanm.5c00483.s001
Primary Topic
Nanoplatforms for cancer theranostics
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article
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article

Controlled Deliveryof Cytarabine in Sodium CarboxymethylCellulose/Copper-Doped Prussian Blue Hydrogels for Chemotherapy andChemodynamic Therapy

Figshare
Nanoplatforms for cancer theranostics
article

Controlled Deliveryof Cytarabine in Sodium CarboxymethylCellulose/Copper-Doped Prussian Blue Hydrogels for Chemotherapy andChemodynamic Therapy

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Abstract

To improve the therapy of chemotherapy for cancer treatment, hydrogels of sodium carboxymethyl cellulose (CMC)/copper-doped Prussian blue (CDPB) are synthesized for the controlled delivery of cytarabine (Cyt). CMC is connected to 3-aminophenylboronic acid (PBA) and dopamine (DA), respectively, by amidation reactions, and the obtained CMC-PBA and CMC-DA are cross-linked through boronate affinity for the encapsulation of CDPB and Cyt. The resultant CMC/CDPB/Cyt hydrogels can, respectively, respond to pH and H<sub>2</sub>O<sub>2</sub>, and thus, pH- and H<sub>2</sub>O<sub>2</sub>-responsive delivery of Cyt from the hydrogels is successfully achieved. More importantly, the overexpressed H<sub>2</sub>O<sub>2</sub> in cancer cells can be converted to hydroxyl radicals (<sup>•</sup>OH) by the CDPB in the hydrogels through Fenton-like reactions, and the generated <sup>•</sup>OH can participate in the chemodynamic therapy (CDT) of cancers. Due to the combination treatment of chemotherapy and CDT, enhanced anticancer effects are obtained by using human acute promyelocytic leukemia (HL-60) cell lines as the model target.

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