Transferrin-Conjugated Manganese Dioxide/Semiconducting Polymer Hybrid Nanoparticles for Targeted Dual-Model Imaging of Orthotopic Glioblastoma AITranslate
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Glioblastoma is one of the important diseases that threaten human health, while the early diagnosis of glioblastoma remains a great challenge. We herein report the development of transferrin (Tf)-conjugated hybrid nanoparticles for targeted magnetic resonance (MR) and near-infrared (NIR) fluorescence dual-model imaging of orthotopic glioblastoma in living mouse models. Tf-stabilized manganese dioxide (MnO2) nanoparticles were conjugated onto the surface of semiconducting polymer nanoparticles (SPNs) to allow the formation of hybrid nanoparticles (Tf@SPNM). Due to the surface modification of Tf that could bind to the Tf receptor, Tf@SPNM would overcome the blood–brain barrier (BBB) and target the glioblastoma cells, which resulted in a more effective delivery of Tf@SPNM into orthotopic glioblastoma sites compared to that of their control nanoparticles. In view of the high r1 relaxation (9.8 mM–1 s–1) and bright NIR fluorescence emission, Tf@SPNM could achieve MR and NIR fluorescence dual-model imaging of orthotopic glioblastoma with obviously improved imaging contrast. Thus, this study provides a multifunctional hybrid nanoplatform for effective diagnosis of orthotopic glioblastoma.
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DOI:https://doi.org/10.1021/acsapm.3c00881
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Glioblastoma is one of the important diseases that threaten human health, while the early diagnosis of glioblastoma remains a great challenge. We herein report the development of transferrin (Tf)-conjugated hybrid nanoparticles for targeted magnetic resonance (MR) and near-infrared (NIR) fluorescence dual-model imaging of orthotopic glioblastoma in living mouse models. Tf-stabilized manganese dioxide (MnO2) nanoparticles were conjugated onto the surface of semiconducting polymer nanoparticles (SPNs) to allow the formation of hybrid nanoparticles (Tf@SPNM). Due to the surface modification of Tf that could bind to the Tf receptor, Tf@SPNM would overcome the blood–brain barrier (BBB) and target the glioblastoma cells, which resulted in a more effective delivery of Tf@SPNM into orthotopic glioblastoma sites compared to that of their control nanoparticles. In view of the high r1 relaxation (9.8 mM–1 s–1) and bright NIR fluorescence emission, Tf@SPNM could achieve MR and NIR fluorescence dual-model imaging of orthotopic glioblastoma with obviously improved imaging contrast. Thus, this study provides a multifunctional hybrid nanoplatform for effective diagnosis of orthotopic glioblastoma.
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| GB/T 7714-2015 | [1] Ningyue Yu, Yue Wang, Jindong Xia, et al. ACS Applied Polymer Materials, 2023(5). DOI:10.1021/acsapm.3c00881. |
| MLA | [1] Ningyue Yu, et al., ACS Applied Polymer Materials, no. 5, 2023, https://doi.org/10.1021/acsapm.3c00881. |
| APA | [1] Ningyue Yu, Yue Wang, Jindong Xia, Viktar Abashkin, Lingzhou Zhao, & Jingchao Li. (2023). ACS Applied Polymer Materials(5). https://doi.org/10.1021/acsapm.3c00881 |
| IEEE | [1] Ningyue Yu, Yue Wang, Jindong Xia, Viktar Abashkin, Lingzhou Zhao, and Jingchao Li, ACS Applied Polymer Materials, no. 5, 2023, doi: 10.1021/acsapm.3c00881. keywords: {molecular imaging;targeting nanoprobes;MR imaging;polymer nanoparticles;orthotopic glioblastoma} |
