Next Materials, Journal Year: 2025, Volume and Issue: 8, P. 100611 - 100611
Published: March 22, 2025
Language: Английский
Next Materials, Journal Year: 2025, Volume and Issue: 8, P. 100611 - 100611
Published: March 22, 2025
Language: Английский
Drug Delivery and Translational Research, Journal Year: 2023, Volume and Issue: 13(5), P. 1500 - 1519
Published: March 29, 2023
Language: Английский
Citations
45International Journal of Biological Macromolecules, Journal Year: 2024, Volume and Issue: 259, P. 129233 - 129233
Published: Jan. 4, 2024
Language: Английский
Citations
19Journal of Materials Chemistry A, Journal Year: 2024, Volume and Issue: 12(17), P. 10316 - 10328
Published: Jan. 1, 2024
A novel modification of zeolitic imidazolate framework-8 with 2-undecylimidazolate was explored to enhance its hydrophobicity and improve compatibility polymer PIM-1 when incorporated as a filler in mixed matrix membranes.
Language: Английский
Citations
18Colloids and Surfaces B Biointerfaces, Journal Year: 2023, Volume and Issue: 232, P. 113612 - 113612
Published: Oct. 26, 2023
Language: Английский
Citations
27Advanced Functional Materials, Journal Year: 2023, Volume and Issue: 34(7)
Published: Nov. 5, 2023
Abstract Cancer immunotherapy has the potential to revolutionize treatment of malignant tumors, but its effectiveness is limited by low immune response rate and immune‐related adverse events. Pyroptosis, as an inflammatory programmed cell death type, triggers strong acute antitumor immunity, converting “cold” tumors “hot”. Particularly, biomaterials loading pyroptosis inducers targeting tumor microenvironment engineer pyroptosis, have achieved great progress in recent years. Herein, design strategy, mechanism pathway, role induce cancer are comprehensively reviewed. The present review focuses on application biomaterials‐induced immunotherapy, including nanogel, polymer prodrug, nanovesicle, mesoporous material. Additionally, synthesis a series stimuli‐responsive nanoplatforms, glutathione‐responsive, pH‐responsive, reactive oxygen species‐responsive, enzyme‐mimicking catalytic performance, described. Meanwhile, it augments multiple processes uptake, antigen presentation, T‐cell activation, expansion. Finally, perspectives pyroptosis‐mediated inflammation break through vascular basement membrane barrier achieving efficient volcanic penetration discussed. Artificial intelligence, multi‐omics analysis, anthropogenic animal models organoids presented, aiming provide guidance assistance for constructing effective controllable pyroptosis‐engineered improving immunotherapy.
Language: Английский
Citations
26Advances in Colloid and Interface Science, Journal Year: 2024, Volume and Issue: 329, P. 103184 - 103184
Published: May 17, 2024
Language: Английский
Citations
12Carbohydrate Polymers, Journal Year: 2022, Volume and Issue: 301, P. 120311 - 120311
Published: Nov. 8, 2022
Language: Английский
Citations
34Journal of Materials Chemistry B, Journal Year: 2023, Volume and Issue: 12(4), P. 872 - 894
Published: Dec. 11, 2023
This review delves into the potential of zeolitic imidazolate framework-8 (ZIF-8) nanoparticles in augmenting efficacy cancer immunotherapy, with a special focus on delivery programmed cell death receptor 1 (PD-1) inhibitors. The multifunctional nature ZIF-8 as drug carriers is emphasized, their ability to encapsulate range therapeutic agents, including PD-1 inhibitors, and facilitate targeted tumor locations. By manipulating pore size surface characteristics nanoparticles, controlled release can be realized. strategic use deliver inhibitors presents precise modality for treatment, reducing off-target impacts enhancing effectiveness. combined strategy addresses existing challenges constraints current immunotherapy techniques, ultimate goal patient outcomes therapy.
Language: Английский
Citations
19Journal of Nanobiotechnology, Journal Year: 2024, Volume and Issue: 22(1)
Published: Jan. 10, 2024
Abstract Radiotherapy (RT) is one of the important treatment modalities for non-small cell lung cancer (NSCLC). However, maximum radiation dose that NSCLC patient can receive varies little. Therefore, exploitation novel RT sensitization approaches a critical need clinical treatment. resistance in linked to tumor microenvironment (TME) hypoxia, cycle arrest and associated genetic alterations. Here, we designed method targeted delivery quercetin (QT) CeO 2 enhance sensitivity. We loaded QT into @ZIF-8-HA nanoparticles prevent its degradation circulatory system successfully delivered tumors. Under protection Zeolitic Imidazolate Framework-8 (ZIF-8), nanocomplexes exhibited excellent catalytic mimetic activity decomposing H O , thus significantly reversing hypoxia TME, while radiosensitizer caused DNA damage directly after RT. In subcutaneous model, overcame enhanced therapeutic efficacy. This multiple strategy combining nanozymes opens promising approach NSCLC.
Language: Английский
Citations
8Talanta, Journal Year: 2024, Volume and Issue: 275, P. 126097 - 126097
Published: April 17, 2024
Language: Английский
Citations
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