The Construction of a Multifunctional Nanoscale Porous Coordination Network-222 Nanodrug for Imaging-Guided Chemotherapy-Photodynamic Therapy.
Nanoscale metal-organic frameworks have great potential in constructing a high-performance anticancer nanodrug delivery system (NDDS) for combining phototherapy and chemotherapy.
APA
Tan F, Lyu J, et al. (2026). The Construction of a Multifunctional Nanoscale Porous Coordination Network-222 Nanodrug for Imaging-Guided Chemotherapy-Photodynamic Therapy.. ACS applied bio materials, 9(4), 2294-2304. https://doi.org/10.1021/acsabm.5c02422
MLA
Tan F, et al.. "The Construction of a Multifunctional Nanoscale Porous Coordination Network-222 Nanodrug for Imaging-Guided Chemotherapy-Photodynamic Therapy.." ACS applied bio materials, vol. 9, no. 4, 2026, pp. 2294-2304.
PMID
41618921
Abstract
Nanoscale metal-organic frameworks have great potential in constructing a high-performance anticancer nanodrug delivery system (NDDS) for combining phototherapy and chemotherapy. However, their practical applications are still challenged by a limited antitumor effect and complex component. In this study, we proposed constructing a multifunctional NDDS simply integrating positron-emitting radionuclide Zr and chemotherapeutic doxorubicin (DOX) into the porous coordination network-222 (PCN-222) featuring intrinsic photoactivity and good guest accommodation ability. It has been demonstrated that the synthesized DOX@Zr-PCN-222 exhibits good stability, favorable nanoscale dimensions, and excellent biocompatibility. More importantly, the prepared DOX@Zr-PCN-222 can provide bioinformation on the constructed nanoformulation from the living cells to the whole body, able to achieve controlled release of cytotoxin as a response to low pH and reductive glutathione (GSH). The excellent tumor binding ability of DOX@Zr-PCN-222 has been confirmed by both fluorescence and nuclear imaging, particularly positron-emission tomography over 7 days. As a result, the prepared NDDS has exhibited remarkable anticancer efficacy to suppress tumor growth and prolong the median survival of a murine breast cancer model, highlighting its great potential for tumor chemo-PDT therapy.
MeSH Terms
Doxorubicin; Animals; Porosity; Mice; Photochemotherapy; Humans; Drug Screening Assays, Antitumor; Biocompatible Materials; Antineoplastic Agents; Particle Size; Nanoparticles; Materials Testing; Mice, Inbred BALB C; Cell Proliferation; Female; Cell Survival; Surface Properties; Antibiotics, Antineoplastic; Cell Line, Tumor
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