Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 7 de 7
Filtrer
1.
Nat Mater ; 2024 Jul 01.
Article de Anglais | MEDLINE | ID: mdl-38951651

RÉSUMÉ

Solution-processed colloidal nanocrystals of lead halide perovskites have been intensively investigated in recent years in the context of optoelectronic devices, during which time their quantum properties have also begun to attract attention. Their unmatched ease of synthetic tunability and unique structural, optical and electronic properties, in conjunction with the confinement of carriers in three dimensions, have motivated studies on observing and controlling coherent light-matter interaction in these materials for quantum information technologies. This Review outlines the recent efforts and achievements in this direction. Particularly notable examples are the observation of coherent single-photon emission, evidence for superfluorescence and the realization of room-temperature coherent spin manipulation for ensemble samples, which have not been achieved for prototypical colloidal CdSe nanocrystals that have been under investigation for decades. This Review aims to highlight these results, point out the challenges ahead towards realistic applications and bring together the efforts of multidisciplinary communities in this nascent field.

2.
Thorac Cancer ; 15(18): 1437-1445, 2024 Jun.
Article de Anglais | MEDLINE | ID: mdl-38757212

RÉSUMÉ

BACKGROUND: The aim of the present study was to evaluate the impact of intratumoral metabolic heterogeneity and quantitative 18F-FDG PET/CT imaging parameters in predicting patient outcomes in thymic epithelial tumors (TETs). METHODS: This retrospective study included 100 patients diagnosed with TETs who underwent pretreatment 18F-FDG PET/CT. The maximum and mean standardized uptake values (SUVmax and SUVmean), metabolic tumor volume (MTV), and total lesion glycolysis (TLG) on PET/CT were measured. Heterogeneity index-1 (HI-1; standard deviation [SD] divided by SUVmean) and heterogeneity index-2 (HI-2; linear regression slopes of the MTV according with different SUV thresholds), were evaluated as heterogeneity indices. Associations between these parameters and patient survival outcomes were analyzed. RESULTS: The univariate analysis showed that Masaoka stage, TNM stage, WHO classification, SUVmax, SUVmean, TLG, and HI-1 were significant prognostic factors for progression-free survival (PFS), while MTV, HI-2, age, gender, presence of myasthenia gravis, and maximum tumor diameter were not. Subsequently, multivariate analyses showed that HI-1 (p < 0.001) and TNM stage (p = 0.002) were independent prognostic factors for PFS. For the overall survival analysis, TNM stage, WHO classification, SUVmax, and HI-1 were significant prognostic factors in the univariate analysis, while TNM stage remained an independent prognostic factor in multivariate analyses (p = 0.024). The Kaplan Meier survival analyses showed worse prognoses for patients with TNM stages III and IV and HI-1 ≥ 0.16 compared to those with stages I and II and HI-1 < 0.16 (log-rank p < 0.001). CONCLUSION: HI-1 and TNM stage were independent prognostic factors for progression-free survival in TETs. HI-1 generated from baseline 18F-FDG PET/CT might be promising to identify patients with poor prognosis.


Sujet(s)
Fluorodésoxyglucose F18 , Tumeurs épithéliales épidermoïdes et glandulaires , Tomographie par émission de positons couplée à la tomodensitométrie , Tumeurs du thymus , Humains , Tomographie par émission de positons couplée à la tomodensitométrie/méthodes , Mâle , Femelle , Tumeurs du thymus/métabolisme , Tumeurs du thymus/imagerie diagnostique , Tumeurs du thymus/anatomopathologie , Tumeurs du thymus/mortalité , Adulte d'âge moyen , Pronostic , Études rétrospectives , Sujet âgé , Adulte , Tumeurs épithéliales épidermoïdes et glandulaires/imagerie diagnostique , Tumeurs épithéliales épidermoïdes et glandulaires/métabolisme , Tumeurs épithéliales épidermoïdes et glandulaires/anatomopathologie , Tumeurs épithéliales épidermoïdes et glandulaires/mortalité , Jeune adulte , Sujet âgé de 80 ans ou plus
3.
ACS Biomater Sci Eng ; 10(2): 1062-1076, 2024 02 12.
Article de Anglais | MEDLINE | ID: mdl-38245905

RÉSUMÉ

Magnesium is a revolutionary biomaterial for orthopedic implants, owing to its eminent mechanical properties and biocompatibility. However, its uncontrolled degradation rate remains a severe challenge for its potential applications. In this study, we developed a self-healing micro arc oxidation (MAO) and dicalcium phosphate dihydrate (DCPD) double-passivated coating on a magnesium membrane (Mg-MAO/DCPD) and investigated its potential for bone-defect healing. The Mg-MAO/DCPD membrane possessed a feasible self-repairing ability and good cytocompatibility. In vitro degradation experiments showed that the Mg contents on the coating surface were 0.3, 3.8, 4.1, 6.1, and 7.9% when the degradation times were 0, 1, 2, 3, and 4 weeks, respectively, exhibiting available corrosion resistance. The slow and sustained release of Mg2+ during the degradation process activated extracellular matrix proteins for bone regeneration, accelerating osteogenic differentiation of human bone marrow mesenchymal stem cells (hBMSCs). The extract solutions of Mg-MAO/DCPD considerably promoted the activation of the Wnt and PI3K/AKT signaling pathways. Furthermore, the evaluation of the rat skull defect model manifested the outstanding bone-healing efficiency of the Mg-MAO/DCPD membrane. Taken together, the Mg-MAO/DCPD membrane demonstrates an optimized degradation rate and excellent bioactivity and is believed to have great application prospects in bone tissue engineering.


Sujet(s)
Phosphates de calcium , Matériaux revêtus, biocompatibles , Magnésium , Rats , Humains , Animaux , Magnésium/pharmacologie , Matériaux revêtus, biocompatibles/pharmacologie , Ostéogenèse , Phosphatidylinositol 3-kinases
4.
Nat Nanotechnol ; 18(2): 124-130, 2023 Feb.
Article de Anglais | MEDLINE | ID: mdl-36536044

RÉSUMÉ

Manipulation of solid-state spin coherence is an important paradigm for quantum information processing. Current systems either operate at very low temperatures or are difficult to scale up. Developing low-cost, scalable materials whose spins can be coherently manipulated at room temperature is thus highly attractive for a sustainable future of quantum information science. Here we report ambient-condition all-optical initialization, manipulation and readout of hole spins in an ensemble of solution-grown CsPbBr3 perovskite quantum dots with a single hole in each dot. The hole spins are initialized by sub-picosecond electron scavenging following circularly polarized femtosecond-pulse excitation. A transverse magnetic field induces spin precession, and a second off-resonance femtosecond-pulse coherently rotates hole spins via strong light-matter interaction. These operations accomplish near-complete quantum-state control, with a coherent rotation angle close to the π radian, of hole spins at room temperature.

5.
Angew Chem Int Ed Engl ; 61(49): e202213065, 2022 12 05.
Article de Anglais | MEDLINE | ID: mdl-36250269

RÉSUMÉ

Colloidal quantum dots (QDs) can photocatalyze diverse organic reactions. However, reported QD-photocatalysts often contain highly-toxic elements Cd or Pb, and have not surpassed prototypical transition-metal complexes in terms of their photoredox power or excited-state energy. Here we report low-toxicity ZnSe/ZnS core/shell QDs as potent visible photocatalysts to drive challenging organic transformations. To overcome the limitation of short excited-state lifetime of the QDs, we functionalize their surfaces with benzophenone ligands which can rapidly extract electrons from photoexcited QDs and sustain long-lived charge-separated states. The benzophenone anions function as potent electron relay to drive dehalogenation of aryl chlorides and additive-free polymerization of acrylates. Alternatively, the QDs are functionalized with biphenyl ligands to store energy in long-lived, energetic triplets, enabling [2+2] homo-cycloaddition of styrene and cycloaddition of carbonyls with alkenes.


Sujet(s)
Boîtes quantiques , Boîtes quantiques/toxicité , Composés du zinc , Sulfures , Benzophénones
6.
Comput Math Methods Med ; 2022: 3058342, 2022.
Article de Anglais | MEDLINE | ID: mdl-36105241

RÉSUMÉ

Matrix metalloproteinase-1 (MMP1) has been reported to play key roles in a variety of cancers by degrading the extracellular matrix. However, its carcinogenic roles have not been shown yet in head and neck squamous cell carcinoma (HNSCC). This study aimed to elucidate its expression pattern and functional roles as well as clinical significance in HNSCC. The Cancer Genome Atlas (TCGA), Gene Expression Omnibus (GEO), and immunohistochemistry (IHC) were utilized to determine the MMP1 expression pattern and the associations between its expression and patients' outcome in HNSCC. Mice tongue squamous cell carcinoma model induced by 4-nitroquinoline 1-oxide (4NQO) and siRNA-mediated cellular assay in vitro were utilized to evaluate the oncogenic role of MMP1. The biological functions and cancer-related pathways involved in MMP1-related genes were found through bioinformatics analysis. Both mRNA and protein abundance of MMP1 were highly increased in HNSCC as compared to its non-tumor counterparts. MMP1 overexpression positively correlated with advanced tumor size, cervical node metastasis, and advanced pathological grade and lower patients' survival. In the 4NQO-induced animal model, MMP1 expression increased along with the progression of the disease. In HNSCC cells, siRNA-mediated knockdown of MMP1 significantly inhibited cell proliferation, migration, and invasion and activated apoptosis and epithelia-mesenchymal transition (EMT). GSEA, GO, and KEGG analyses showed that MMP1 expression was significantly related to cancer-related pathways and cancer-related functions. Together, our results demonstrated MMP1 serves as a novel prognostic biomarker and putative oncogene in HNSCC.


Sujet(s)
Carcinome épidermoïde , Tumeurs de la tête et du cou , Matrix Metalloproteinase 13/métabolisme , Tumeurs de la langue , Animaux , Carcinogenèse/génétique , Carcinome épidermoïde/induit chimiquement , Carcinome épidermoïde/génétique , Carcinome épidermoïde/métabolisme , Régulation de l'expression des gènes tumoraux , Tumeurs de la tête et du cou/génétique , Matrix metalloproteinase 1/génétique , Matrix metalloproteinase 1/métabolisme , Souris , Petit ARN interférent , Carcinome épidermoïde de la tête et du cou/génétique , Tumeurs de la langue/induit chimiquement , Tumeurs de la langue/génétique
7.
Nat Mater ; 21(11): 1282-1289, 2022 Nov.
Article de Anglais | MEDLINE | ID: mdl-36075966

RÉSUMÉ

Anisotropic exchange splitting in semiconductor quantum dots results in bright-exciton fine-structure splitting important for quantum information processing. Direct measurement of fine-structure splitting usually requires single/few quantum dots at liquid-helium temperature because of its sensitivity to quantum dot size and shape, whereas measuring and controlling fine-structure splitting at an ensemble level seem to be impossible unless all the dots are made to be nearly identical. Here we report strong bright-exciton fine-structure splitting up to 1.6 meV in solution-processed CsPbI3 perovskite quantum dots, manifested as quantum beats in ensemble-level transient absorption at liquid-nitrogen to room temperature. The splitting is robust to quantum dot size and shape heterogeneity, and increases with decreasing temperature, pointing towards a mechanism associated with orthorhombic distortion of the perovskite lattice. Effective-mass-approximation calculations reveal an intrinsic 'fine-structure gap' that agrees well with the observed fine-structure splitting. This gap stems from an avoided crossing of bright excitons confined in orthorhombically distorted quantum dots that are bounded by the pseudocubic {100} family of planes.

SÉLECTION CITATIONS
DÉTAIL DE RECHERCHE
...