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Hypoxia-alleviating hemoglobin nanoclusters for sensitizing chemo-photodynamic therapy of cervical cancer

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Authors

Lee, Han Sol; Yoo, So-Yeol; Lee, Sang Min; Kang, Nae-Won; Kim, Sang Kyum; Song, Gyu Yong; Kim, Dae-Duk; Lee, Jae-Young

Issue Date
2023-02
Publisher
Elsevier B.V.
Citation
Chemical Engineering Journal, Vol.457
Abstract
© 2022 The Author(s)Hypoxia-alleviating hemoglobin (Hb) nanoclusters (NCs) have been developed for sensitizing combined chemo-photodynamic therapy (chemo-PDT) of cervical cancer. Hb was conjugated with chlorin e6 and biotinylated polyethylene glycol and adsorbed with doxorubicin (DOX), resulting in the self-assembly of 220 nm diameter protein NCs. These oxygen-carrying NCs, namely DOX@HPBC, exhibited improved colloidal stability in the serum compared to that of native Hb and pH-responsive drug release favorable for cancer treatment. DOX@HPBC alleviated hypoxia by 64.8% in HeLa cells cultured under hypoxia and normalized the levels of related biomarkers, HIF-1α and MDR1, with enhanced cellular uptake via biotin–receptor interactions. Moreover, antitumor efficacy tests performed in HeLa monolayer and spheroid cultures revealed that DOX@HPBC possessed 3.8-fold improved therapeutic efficacy compared to DOX and chlorin e6 physical mixture, showing synergism between chemotherapy and PDT. DOX@HPBC-mediated chemo-PDT significantly suppressed tumor growth in heterotopic (96.6% reduction in tumor volume compared to no-intervention) and orthotopic (comparable uterus weight to the normal group) HeLa-xenografted mice with no significant toxicity. These results showed the hypoxia amelioration effect, which lowered HIF-1α and MDR1 levels in tumor tissues, and efficient DOX distribution to hypoxic regions of the tumor, suggesting that DOX@HPBC could be a promising chemo-PDT strategy for cervical cancer treatment.
ISSN
1385-8947
URI
https://hdl.handle.net/10371/199461
DOI
https://doi.org/10.1016/j.cej.2022.141224
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  • College of Pharmacy
  • Department of Pharmacy
Research Area Biomaterial-based nano-platforms for cancer drug delivery and imaging, Formulation design and development, Functional protein expression and evaluation for drug delivery and therapy applications

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