| Autor: |
Song‐Yu Wu, Ya‐Xi Ye, Qing Zhang, Qian‐Jin Kang, Zhu‐Min Xu, Shen‐Zhen Ren, Fan Lin, Yong‐Tao Duan, Hao‐Jun Xu, Zi‐Yi Hu, Sui‐Sui Yang, Hai‐Liang Zhu, Mei‐Juan Zou, Zhong‐Chang Wang |
| Rok vydání: |
2022 |
| Předmět: |
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| Zdroj: |
Advanced Science. 10:2203742 |
| ISSN: |
2198-3844 |
| Popis: |
Photodynamic therapy (PDT) under hypoxic conditions and drug resistance in chemotherapy are perplexing problems in anti-tumor treatment. In addition, central nervous system neoplasm-targeted nanoplatforms are urgently required. To address these issues, a new multi-functional protein hybrid nanoplatform is designed, consisting of transferrin (TFR) as the multicategory solid tumor recognizer and hemoglobin for oxygen supply (ODP-TH). This protein hybrid framework encapsulates the photosensitizer protoporphyrin IX (PpIX) and chemotherapeutic agent doxorubicin (Dox), which are attached by a glutathione-responsive disulfide bond. Mechanistically, ODP-TH crosses the blood-brain barrier (BBB) and specifically aggregated in hypoxic tumors via protein homology recognition. Oxygen and encapsulated drugs ultimately promote a therapeutic effect by down-regulating the abundance of multidrug resistance gene 1 (MDR1) and hypoxia-inducible factor-1-α (HIF-1α). The results reveal that ODP-TH achieves oxygen transport and protein homology recognition in the hypoxic tumor occupation. Indeed, compared with traditional photodynamic chemotherapy, ODP-TH achieves a more efficient tumor-inhibiting effect. This study not only overcomes the hypoxia-related inhibition in combination therapy by targeted oxygen transport but also achieves an effective treatment of multiple tumors, such as breast cancer and glioma, providing a new concept for the construction of a promising multi-functional targeted and intensive anti-tumor nanoplatform. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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