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An intelligent responsive ZIF-8 co-delivery nanoplatform with multimodal synergistic technologies for closed-loop
Siqi Chen1, Yizhen Yan1, Jiayi Zou1
1School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, Liaoning 110016, China.
Abstract:
Multi-modal combination therapy for tumors can overcome the limitations of single-modal therapy and bring new opportunities for high-efficient tumor treatment. Nevertheless, how to ingeniously design functionalized nanocarriers to mediate the synergistict effects among various therapeutic approaches remains a core challenge. In this study, we developed a polydopamine (PDA) coated outside and glucose oxidase (GOx) adsorbed inside copper-doped zeolitic imidazolate framework-8 (CZ8) with metformin hydrochloride (MET) / doxorubicin (DOX) as a multifunctional nano-codelivery system, abbreviated as PMDGCZ8, which could focus more on the synergy and continuity of multiple therapies including photothermal therapy (PTT), chemodynamic therapy (CDT), starving tumor therapy (STT) and chemotherapy (CT). Herein, PMDGCZ8 innovatively combined the gating effect of PDA membrane with the pH sensitivity of CZ8 skeleton to form a dual-responsive bomb that could trigger release on demand and significantly improve the accuracy of tumor localization. Furthermore, we also incorporated the strategies of reshaping the tumor hypoxia and immunosuppressive microenvironment into the synergistic treatment process in order to achieve a comprehensive anti-tumor ecological network. Both in vitro and in vivo experiments suggested that PMDGCZ8 significantly enhanced drug accumulation on tumors, reduced systemic toxicity, activated anti-tumor immune response, further inhibited the recurrence and metastasis, and consequently was expected to become a new type of nano-delivery platform with great development potential.
Insights
This study introduces a novel nanodelivery system (PMDGCZ8) for multi-modal cancer therapy. It combines photothermal, chemodynamic, starving tumor, and chemotherapy to enhance efficacy and reduce toxicity.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Oncology
Background:
- Single-modal cancer therapies face limitations.
- Developing effective nanocarriers for synergistic multi-modal therapy is challenging.
Purpose of the Study:
- To develop a multifunctional nanocarrier (PMDGCZ8) for synergistic multi-modal cancer therapy.
- To combine photothermal therapy (PTT), chemodynamic therapy (CDT), starving tumor therapy (STT), and chemotherapy (CT).
Main Methods:
- Fabrication of polydopamine (PDA) coated, glucose oxidase (GOx) adsorbed copper-doped zeolitic imidazolate framework-8 (CZ8) nanocarrier.
- Co-delivery of metformin hydrochloride (MET) and doxorubicin (DOX) via the PMDGCZ8 system.
- Utilizing PDA's gating effect and CZ8's pH sensitivity for dual-responsive drug release.
- Investigating strategies to reshape the tumor microenvironment (hypoxia and immunosuppression).
Main Results:
- PMDGCZ8 demonstrated enhanced drug accumulation in tumors and reduced systemic toxicity.
- The system activated anti-tumor immune responses.
- Inhibition of tumor recurrence and metastasis was observed.
- Dual-responsive drug release improved tumor localization accuracy.
Conclusions:
- PMDGCZ8 shows significant potential as a nano-delivery platform for comprehensive anti-tumor treatment.
- The developed system effectively integrates multiple therapeutic modalities for enhanced cancer therapy.
- This approach offers a promising strategy for overcoming tumor recurrence and metastasis.
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