Research Square (Research Square), Год журнала: 2024, Номер unknown
Опубликована: Окт. 4, 2024
Язык: Английский
Research Square (Research Square), Год журнала: 2024, Номер unknown
Опубликована: Окт. 4, 2024
Язык: Английский
Journal of Nanobiotechnology, Год журнала: 2025, Номер 23(1)
Опубликована: Фев. 20, 2025
The advent of nanozymes has revolutionized approaches to cancer diagnosis and therapy, introducing innovative strategies that address the limitations conventional treatments. Nanozyme nanostructures with enzyme-mimicking catalytic abilities exhibit exceptional stability, biocompatibility, customizable functions, positioning them as promising tools for theranostics. By emulating natural enzyme reactions, can selectively target eradicate cells, minimizing harm adjacent healthy tissues. Nanozymes also be functionalized specific targeting ligands, allowing precise delivery regulated release therapeutic agents, improving treatment effectiveness reducing adverse effects. However, issues such selectivity, regulatory compliance remain critical challenges clinical application nanozymes. This review provides an overview nanozymes, highlighting their unique properties, various classifications, activities, diverse applications in strategic oncological deployment could profoundly impact future advancements personalized medicine, recent progress prospective directions enzyme-mimetic treatment. summarizes
Язык: Английский
Процитировано
1Advanced Healthcare Materials, Год журнала: 2024, Номер 13(28)
Опубликована: Июль 28, 2024
Conventional phototherapeutic agents are typically used in either photodynamic therapy (PDT) or photothermal (PTT). However, efficacy is often hindered by hypoxia and elevated levels of heat shock proteins the tumor microenvironment (TME). To address these limitations, a formylated, near-infrared (NIR)-absorbing heavy-atom-free Aza-BODIPY dye presented that exhibits both type-I type-II PDT actions with high yield reactive oxygen species (ROS) manifests efficient conversion precise adjustments to conjugate structure electron distribution, leading large amount ROS production even under severe hypoxia. improve biosafety water solubility, an amphiphilic triblock copolymer (Pluronic F-127), yielding BDP-6@F127 nanoparticles (NPs) coated. Furthermore, inspired fact phototherapy triggers release tumor-associated antigens, strategy leverages potential immune activation combining PDT/PTT checkpoint blockade (ICB) amplify systemic response achieve much-desired abscopal effect developed. In conclusion, this study presents promising molecular design integrates multimodal therapeutics for effective approach cancer therapy.
Язык: Английский
Процитировано
4Advanced Science, Год журнала: 2025, Номер unknown
Опубликована: Янв. 9, 2025
Abstract The development of efficient therapeutic strategies to promote ferroptotic cell death offers significant potential for hepatocellular carcinoma (HCC) treatment. Herein, this study presents an HCC‐targeted nanoplatform that integrates bimetallic FeMoO 4 nanoparticles with CO‐releasing molecules, and further camouflaged SP94 peptide‐modified macrophage membrane enhanced ferroptosis‐driven multi‐modal therapy HCC. Leveraging the multi‐enzyme activities multivalent metallic elements, not only decomposes H 2 O generate oxygen alleviate tumor hypoxia but also depletes glutathione inactivate peroxides 4, which amplify sonodynamic under ultrasound (US) irradiation. Meanwhile, catalyzes Fenton reaction produce hydroxyl radicals chemodynamic therapy. Elevated intracellular reactive species trigger cascade release CO, leading lethal lipid peroxidation enhancing ferroptosis‐mediated This demonstrates robust anti‐tumor efficacy US irradiation favorable biosafety in both subcutaneous orthotopic HCC models, representing a promising approach Additionally, findings offer new insights into microenvironment modulation optimize US‐triggered cancer
Язык: Английский
Процитировано
0Microchimica Acta, Год журнала: 2025, Номер 192(4)
Опубликована: Март 13, 2025
Язык: Английский
Процитировано
0Frontiers in Oncology, Год журнала: 2025, Номер 15
Опубликована: Апрель 1, 2025
The rapid development of nanotechnology has significantly advanced the application nanophotocatalysis in medical field, particularly for cancer therapy. Traditional treatments, such as chemotherapy and radiotherapy, often cause severe side effects, including damage to healthy tissues drug resistance. In contrast, nanophotocatalytic therapy offers a promising approach by utilizing nanomaterials that generate reactive oxygen species (ROS) under light activation, allowing precise tumor targeting minimizing collateral surrounding tissues. This review systematically explores latest advancements highly efficient nanophotocatalysts treatment, focusing on their toxicological profiles, underlying mechanisms cell eradication, potential clinical application. Recent research shows nanophotocatalysts, TiO2, In2O3, g-C3N4 composites, along with photocatalysts high conduction band or valence positions, ROS irradiation, which induces oxidative stress leads apoptosis necrosis. These cellular interacting key biological molecules DNA, proteins, lipids, triggering cascade biochemical reactions ultimately result death. Furthermore, strategies S-scheme heterojunctions vacancies (OVs) have been incorporated enhance charge separation efficiency absorption, resulting increased generation, improves photocatalytic performance targeting. Notably, these exhibit low toxicity cells, making them safe effective treatment modality. also discusses challenges associated therapy, limitations penetration need improved biocompatibility. findings suggest technology holds significant precision paving way safer more strategies.
Язык: Английский
Процитировано
0Nature Communications, Год журнала: 2025, Номер 16(1)
Опубликована: Апрель 3, 2025
Malignant pleural effusion (MPE), persistently generated by thorax tumor cells at the advanced stage, remains a major challenge for cancer therapy. Herein, we develop an ultra-sensitive piezoelectric nano-system doping ytterbium in metal-organic framework (O3P@LPYU), which can be triggered physiological intrapleural pressure during breath. Under gently alterative pressure, nanoparticles with notable peroxidase-like activity effectively produce burst of reactive oxygen species and induce immunogenic cell death catalysis carried ozone as well peroxide interstitial fluid. A clear sustained biodistribution is observed tumors upon administration particle. Remarkably, due to abundant substrates oxygen-rich environment cavity, O3P@LPYU particle provides potent reduction MPE volume durable inhibition growth thorax. Our work not only develops bio-responsive nano-system, but also strategy persistent suppression clinics.
Язык: Английский
Процитировано
0Nature Communications, Год журнала: 2025, Номер 16(1)
Опубликована: Апрель 5, 2025
Cancer remains a global health challenge necessitating innovative therapies. We introduce strategy to disrupt cancer cell redox balance using gold nanoparticles (Au NPs) as electron sinks combined with electroactive membranes. Utilizing Shewanella oneidensis MR-1 membrane proteins, we develop liposomes enriched c-type cytochromes. These, coupled Au NPs, facilitate autonomous transfer from cells, disrupting processes and inducing death. Effective across various types, larger NPs show enhanced efficacy, especially under hypoxic conditions. Oxidative stress Au@MIL (MIL: membrane-integrated liposome) treatments, including mitochondrial endoplasmic reticulum lipid oxidation potential changes, triggers apoptosis, bypassing iron-mediated pathways. Surface plasmon band X-ray absorption near-edge structure (XANES) analyses confirm transfer. A SiO2 insulator coating on blocks this transfer, suppressing damage. This approach highlights the of modulated pathways in targeted therapy, offering refined effective treatments.
Язык: Английский
Процитировано
0TrAC Trends in Analytical Chemistry, Год журнала: 2025, Номер 189, С. 118279 - 118279
Опубликована: Апрель 23, 2025
Язык: Английский
Процитировано
0ACS Applied Materials & Interfaces, Год журнала: 2025, Номер unknown
Опубликована: Март 15, 2025
Diabetic wound healing presents a significant medical challenge and requires multistep interventions due to comprehensive environments, such as hyperglycemia, bacterial infection, impaired angiogenesis. However, current are complicated need on-demand sequential release synergy of multicomponents. Herein, H2S-releasing cascade nanozyme (FeS@Au), which is composed ultrasmall gold nanocluster (AuNC) loaded on ferrous sulfide nanoparticle (FeSNP), developed single component regulate glucose level, eliminate promote angiogenesis, achieving for diabetic treatment. The oxidase-like activity AuNC catalyzes into gluconic acid H2O2, not only lowers the local level but also decreases pH increases H2O2 boost peroxidase-like FeSNP generate abundant hydroxyl radical (reactive oxygen species, ROS), inducing ferroptosis-like death in drug-resistant bacteria. Additionally, H2S acidified environment upregulate hypoxia-inducible factor-1 enhance vascularization through upregulating expression vascular endothelial growth factor (VEGF) other angiogenesis-related genes, reducing damage cells caused by excessive ROS produced nanozyme. In full-thickness MRSA-infected rat model, FeS@Au significantly eliminates bacteria, enhances promotes collagen deposition, accelerates healing. This work with H2S-release interventions, providing versatile strategy extensive tissue diabetes.
Язык: Английский
Процитировано
0Journal of Nanobiotechnology, Год журнала: 2024, Номер 22(1)
Опубликована: Авг. 31, 2024
Au@Pt nanozyme, a bimetallic core–shell structure Au and Pt nanoparticle, has attracted significant attention due to its excellent catalytic activity stability. Here, we propose that improves glucose tolerance reduces TG after four weeks administration. The transcriptomic analysis of mouse liver tissues treated with nanozyme showed changes in genes related lipid metabolism signaling pathways, including glycolysis/gluconeogenesis, pyruvate metabolism, PPAR signaling, insulin signaling. Moreover, fecal samples from mice the abundance beneficial gut microbiota such as Dubosiella, Parvibacter, Enterorhabdus, Monoglobus, Lachnospiraceae_UCG-008, Lachnospiraceae_UCG-006, Lachnospiraceae_UCG-001, Christensenellaceae_R-7_group. Combined multi-omics correlation analyses revealed modulation by was strongly correlated hepatic gene expression profiles well microbial profiles. Overall, our integrated demonstrated could modulate regulating key altering composition microbiota, providing new insights into potential applications treatment metabolic disorder.
Язык: Английский
Процитировано
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