Synthesis of Amphiphilic pH-Responsive Doxorubicin and Ferrocene-containing Copolyprodrug as Drug Self-delivery System and Its In Vitro Synergistic Apoptosis and Ferroptosis Tumor Therapy
RESEARCH ARTICLE|Updated:2025-03-13
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Synthesis of Amphiphilic pH-Responsive Doxorubicin and Ferrocene-containing Copolyprodrug as Drug Self-delivery System and Its In Vitro Synergistic Apoptosis and Ferroptosis Tumor Therapy
Chinese Journal of Polymer ScienceVol. 43, Pages: 1-8(2025)
Affiliations:
State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, China
Zhao, X. M.; Liu, P. Synthesis of amphiphilic pH-responsive doxorubicin and ferrocene-containing copolyprodrug as drug self-delivery system and its in vitro synergistic apoptosis and ferroptosis tumor therapy. Chinese J. Polym. Sci. https://doi.org/10.1007/s10118-025-3316-8
Xiao-Mei Zhao, Peng Liu. Synthesis of Amphiphilic pH-Responsive Doxorubicin and Ferrocene-containing Copolyprodrug as Drug Self-delivery System and Its In Vitro Synergistic Apoptosis and Ferroptosis Tumor Therapy[J/OL]. Chinese journal of polymer science, 2025, 431-8.
Zhao, X. M.; Liu, P. Synthesis of amphiphilic pH-responsive doxorubicin and ferrocene-containing copolyprodrug as drug self-delivery system and its in vitro synergistic apoptosis and ferroptosis tumor therapy. Chinese J. Polym. Sci. https://doi.org/10.1007/s10118-025-3316-8DOI:
Xiao-Mei Zhao, Peng Liu. Synthesis of Amphiphilic pH-Responsive Doxorubicin and Ferrocene-containing Copolyprodrug as Drug Self-delivery System and Its In Vitro Synergistic Apoptosis and Ferroptosis Tumor Therapy[J/OL]. Chinese journal of polymer science, 2025, 431-8. DOI: 10.1007/s10118-025-3316-8.
Synthesis of Amphiphilic pH-Responsive Doxorubicin and Ferrocene-containing Copolyprodrug as Drug Self-delivery System and Its In Vitro Synergistic Apoptosis and Ferroptosis Tumor Therapy
and drug resistance of tumors make it challenging to meet the clinical needs of a single apoptosis-inducing chemotherapy. The combination of apoptosis and ferroptosis is expected to address the side effects of chemotherapy and enhance therapeutic efficacy. Here
an amphiphilic pH-responsive doxorubicin (DOX) and ferrocene (Fc)-containing copolyprodrug (P(ADH-DOX-Fc)-PEG) was designed with high DOX and Fc content of 66.5% and 0.58 mmol/g by a facile polycondensation for combining chemotherapy with ferroptosis in cancer treatment. A drug self-delivery system (DSDS) with an average hydrodynamic diameter (
D
h
) of 135 nm can be easily obtained
via
self-assembly with the polyprodrug blocks as the hydrophobic core and PEG as the hydrophilic brush. The cumulative DOX release reached 72.7% in the simulated tumor intracellular acidic microenvironment within 56 h
whereas the premature drug leakage was only 6.2% in the simulated normal physiological medium. The 3-(4
5-dimethylthiazol-2-yl)-2
5-diphenyltetrazolium bromide (MTT) assay results indicated an IC
50
of 8.2 μg/mL
exhibiting enhanced anti-tumor efficacy and a successful combination of apoptosis and ferroptosis
with a combination index (CI) of 0.88.
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