To address the inherent limitations of single-mode cancer therapy—such as low efficacy, high susceptibility to drug resistance, and the inability to completely eliminate residual tumor cells—this study innovatively adopted an ion-doping strategy to successfully fabricate Co2+-doped ZIF-8 small nanocrystal carriers under mild room temperature conditions, avoiding harsh reaction environments that may impair material performance. Endowed with a unique porous structure and large specific surface area, the as-prepared carrier exhibited excellent drug-loading performance, achieving a maximum loading capacity of 84.4% for the widely used chemotherapeutic agent doxorubicin (DOX). Thus, a synergistic nanotherapeutic system (CFD) integrating chemodynamic therapy and chemotherapy was rationally constructed to leverage the complementary advantages of both modalities. In vitro cell experimental results demonstrated that after 24 hours of incubation, the chemo/chemodynamic synergistic nanosystem exerted a lethality rate of up to 87.1% against HeLa cervical cancer cells, which was significantly superior to that of either monotherapy (single chemotherapy or chemodynamic therapy alone). This finding fully confirms that the CFD nanotherapeutic system possesses potent in vitro anticancer activity, as it can synergistically leverage the merits of both treatment modalities to enhance therapeutic efficacy and effectively overcome the limitations of single-mode therapy. Collectively, this work provides a reliable experimental foundation and promising application prospects for subsequent in-depth in vivo tumor therapy research and potential clinical translation.
| Published in | Science Discovery (Volume 13, Issue 6) |
| DOI | 10.11648/j.sd.20251306.14 |
| Page(s) | 125-130 |
| Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
| Copyright |
Copyright © The Author(s), 2025. Published by Science Publishing Group |
Co/ZIF-8 Nanomaterials, DOX, Anti-cancer
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APA Style
Yu-fei, C., Bo-hua, F., Hui-yuan, C. (2025). Preparation of Novel Co/ZIF-8 Nanocomposites and Evaluation of Their Anticancer Cell Performance in Vitro. Science Discovery, 13(6), 125-130. https://doi.org/10.11648/j.sd.20251306.14
ACS Style
Yu-fei, C.; Bo-hua, F.; Hui-yuan, C. Preparation of Novel Co/ZIF-8 Nanocomposites and Evaluation of Their Anticancer Cell Performance in Vitro. Sci. Discov. 2025, 13(6), 125-130. doi: 10.11648/j.sd.20251306.14
@article{10.11648/j.sd.20251306.14,
author = {Chen Yu-fei and Fan Bo-hua and Chu Hui-yuan},
title = {Preparation of Novel Co/ZIF-8 Nanocomposites and Evaluation of Their Anticancer Cell Performance in Vitro
},
journal = {Science Discovery},
volume = {13},
number = {6},
pages = {125-130},
doi = {10.11648/j.sd.20251306.14},
url = {https://doi.org/10.11648/j.sd.20251306.14},
eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.sd.20251306.14},
abstract = {To address the inherent limitations of single-mode cancer therapy—such as low efficacy, high susceptibility to drug resistance, and the inability to completely eliminate residual tumor cells—this study innovatively adopted an ion-doping strategy to successfully fabricate Co2+-doped ZIF-8 small nanocrystal carriers under mild room temperature conditions, avoiding harsh reaction environments that may impair material performance. Endowed with a unique porous structure and large specific surface area, the as-prepared carrier exhibited excellent drug-loading performance, achieving a maximum loading capacity of 84.4% for the widely used chemotherapeutic agent doxorubicin (DOX). Thus, a synergistic nanotherapeutic system (CFD) integrating chemodynamic therapy and chemotherapy was rationally constructed to leverage the complementary advantages of both modalities. In vitro cell experimental results demonstrated that after 24 hours of incubation, the chemo/chemodynamic synergistic nanosystem exerted a lethality rate of up to 87.1% against HeLa cervical cancer cells, which was significantly superior to that of either monotherapy (single chemotherapy or chemodynamic therapy alone). This finding fully confirms that the CFD nanotherapeutic system possesses potent in vitro anticancer activity, as it can synergistically leverage the merits of both treatment modalities to enhance therapeutic efficacy and effectively overcome the limitations of single-mode therapy. Collectively, this work provides a reliable experimental foundation and promising application prospects for subsequent in-depth in vivo tumor therapy research and potential clinical translation.
},
year = {2025}
}
TY - JOUR T1 - Preparation of Novel Co/ZIF-8 Nanocomposites and Evaluation of Their Anticancer Cell Performance in Vitro AU - Chen Yu-fei AU - Fan Bo-hua AU - Chu Hui-yuan Y1 - 2025/12/10 PY - 2025 N1 - https://doi.org/10.11648/j.sd.20251306.14 DO - 10.11648/j.sd.20251306.14 T2 - Science Discovery JF - Science Discovery JO - Science Discovery SP - 125 EP - 130 PB - Science Publishing Group SN - 2331-0650 UR - https://doi.org/10.11648/j.sd.20251306.14 AB - To address the inherent limitations of single-mode cancer therapy—such as low efficacy, high susceptibility to drug resistance, and the inability to completely eliminate residual tumor cells—this study innovatively adopted an ion-doping strategy to successfully fabricate Co2+-doped ZIF-8 small nanocrystal carriers under mild room temperature conditions, avoiding harsh reaction environments that may impair material performance. Endowed with a unique porous structure and large specific surface area, the as-prepared carrier exhibited excellent drug-loading performance, achieving a maximum loading capacity of 84.4% for the widely used chemotherapeutic agent doxorubicin (DOX). Thus, a synergistic nanotherapeutic system (CFD) integrating chemodynamic therapy and chemotherapy was rationally constructed to leverage the complementary advantages of both modalities. In vitro cell experimental results demonstrated that after 24 hours of incubation, the chemo/chemodynamic synergistic nanosystem exerted a lethality rate of up to 87.1% against HeLa cervical cancer cells, which was significantly superior to that of either monotherapy (single chemotherapy or chemodynamic therapy alone). This finding fully confirms that the CFD nanotherapeutic system possesses potent in vitro anticancer activity, as it can synergistically leverage the merits of both treatment modalities to enhance therapeutic efficacy and effectively overcome the limitations of single-mode therapy. Collectively, this work provides a reliable experimental foundation and promising application prospects for subsequent in-depth in vivo tumor therapy research and potential clinical translation. VL - 13 IS - 6 ER -