154 results match your criteria: "Fuzhou University. Fuzhou[Affiliation]"

Treating brain tumors requires a nuanced understanding of the brain, a vital and delicate organ. Location, size, tumor type, and surrounding tissue health are crucial in developing treatment plans. This review comprehensively summarizes various treatment options that are available or could be potentially available for brain tumors, including physical therapies (radiotherapy, ablation therapy, photodynamic therapy, tumor-treating field therapy, and cold atmospheric plasma therapy) and non-physical therapies (surgical resection, chemotherapy, targeted therapy, and immunotherapy).

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Research has shown that the expression level of microRNA-155 (miRNA-155) is positively correlated with clinical stage and depth of invasion in patients with cervical cancer and cervical intraepithelial neoplasia and tends to be highly expressed. Therefore, it is very important to develop sensitive miRNA-155 analysis methods for the early diagnosis, treatment, and prognostic evaluation of cervical cancer. In this study, a near-infrared light-driven fluorescent biosensor based on the metal-enhanced fluorescence effect of polydopamine-coated upconversion nanoparticle (UP/Au) and two toehold-mediated strand displacement (TMSD) steps was constructed for the detection of miRNA-155.

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Near-infrared DNA biosensors based on polysulfonate coatings for the sensitive detection of microRNAs.

Nanoscale Adv

November 2024

Department of Otolaryngology, Fujian Children's Hospital (Fujian Branch of Shanghai Children's Medical Center), College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University Fuzhou 350014 China

MicroRNAs (miRNAs) play crucial roles in the regulation of immune cell differentiation and the immune response during allergic rhinitis (AR). Studies have shown that miRNA-155 is significantly upregulated in AR pathogenesis. Therefore, miRNA-155 can be used as a biomarker for AR diagnosis.

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Zero-dimensional (0D) halide perovskites have garnered significant interest due to their novel properties in optoelectronic and energy applications. However, the mechanisms underlying their phase transformations and fluorescence properties remain poorly understood. In this study, we have synthesized a micron-scale 0D perovskite observable under confocal laser scanning microscopy (CLSM).

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This review is the first to focus on transmembrane transporters derived from aromatic foldamers, with most studies reported over the past decade. These foldamers have made significant strides in mimicking the essential functions of natural ion channel proteins. With their aromatic backbones rigidified by intramolecular hydrogen bonds or differential repulsive forces, this innovative family of molecules stands out for its structural diversity and functional adaptability.

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Hot exciton organic scintillators offer promising prospects due to their efficient generation of bright triplet excitons and ultrafast response time, having potential applications in security detection and medical diagnostics. However, fabricating large-area, highly transparent scintillator screens still remains challenging, impeding the realization of high-resolution X-ray imaging. Herein, we firstly demonstrate a novel highly-transparent hot exciton organic glassy scintillator (>87% transmittance @ 450-800 nm), produced using a low-temperature melt-quenching method with 2',5'-difluoro-4,4,4'',4''-tetraphenyl-[1,1':4',1''-terphenyl]-4,4''-diamine (DTPA2F) powder.

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Snap-through bistability was widely exploited for rapid hopping in micro-electro-mechanical systems and soft robots. However, considerable energy input was required to trigger the transition between discrete buckling states blocked by potential wells. Here a dynamic buckling mechanism of a buckled blister constrained inside an outer ring is explored for eliciting rotary actuation via a localized change of curvature in the blister.

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Materials capable of efficiently converting near-infrared (NIR) light into heat are highly sought after in biotechnology. In this study, two new three-dimensional (3D) porphyrin-based metal-organic frameworks (MOFs) with a -net, CoTCPP-Bi/NiTCPP-Bi, were successfully synthesized. These MOFs feature bismuth carboxylate nodes interconnected by metalloporphyrinic spacers, forming one-dimensional (1D) arrays of closely spaced metalloporphyrins.

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Article Synopsis
  • Some special crystals called thiophosphates are important for electronics but have not been studied much before.*
  • Researchers created three new types of these crystals (α-RbInPS, β-RbInPS, and CsInPS) that show a lot of difference in how light travels through them.*
  • This difference in light behavior, called birefringence, is higher than in regular materials, thanks to how the bonds in the crystals are arranged and the addition of some metals.*
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Poly(3,4-ethylenedioxythiophene) (PEDOT) has emerged as a promising coating for neural electrodes especially through convenient electrodeposition methods. To investigate the influences of solvents and EDOT monomer concentrations on the electrochemical performance and structural characteristics of PEDOT, both aqueous and acetonitrile solutions were employed with varying monomer concentrations during deposition. The prepared PEDOT films were examined for the surface morphology, electrochemical performance, and chemical structures.

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Films of linear conjugated polymer as photoanodes for oxidation reactions.

Chem Sci

August 2024

State Key Laboratory of Photocatalysis on Energy and Environment, College of Chemistry, Fuzhou University 350002 P. R. China

Photoelectrochemical (PEC) devices hold huge potential to convert solar energy into chemical energy. However, the high cost of raw materials and film processing has hindered its practical use. In this study, we attempt to tackle this issue by fabricating straightforward semiconducting polymer films.

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Polyoxometalates (POMs) are a class of anionic metal-oxygen clusters with versatile biological activities. Over the past decade, an increasing number of POMs, especially Sb-rich POMs, have been proven to exert antitumor activity. However, the antitumor effects and mechanisms of POMs in the treatment of non-small cell lung cancer (NSCLC) remain largely unexplored.

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Sialylation-induced stabilization of dynamic glycoprotein conformations unveiled by time-aligned parallel unfolding and glycan release mass spectrometry.

Chem Sci

August 2024

Tianjin Key Laboratory of Biosensing and Molecular Recognition, Research Center for Analytical Science, Frontiers Science Center for New Organic Matter, College of Chemistry, Nankai University Tianjin 300071 China

Sialylation, a critical post-translational modification, regulates glycoprotein structure and function by tuning their molecular heterogeneity. However, characterizing its subtle and dynamic conformational effects at the intact glycoprotein level remains challenging. We introduce a glycoform-resolved unfolding approach based on a high-throughput ion mobility-mass spectrometry (IM-MS) platform.

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P2-type layered materials (Na TMO) have become attractive cathode electrodes owing to their high theoretical energy density and simple preparation. However, they still face severe phase transition and low conductivity. Current research on Na TMO is mostly focused on the modification of bulk materials, and the application performances have been infrequently addressed.

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Article Synopsis
  • Nature typically promotes the formation of closed silver clusters, making the creation of non-closed clusters a challenging task.
  • This research suggests using transition-metal-coordination-cluster substituted polyoxometalates (TMCC-substituted POMs) as effective templates to synthesize non-closed silver clusters, successfully yielding four distinct types of these rare clusters.
  • The strategy relies on the unique bonding interactions of the templates, where specific modules can coordinate with silver ions while others create barriers, preventing the formation of closed clusters.
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mRNA vaccines are regarded as a highly promising avenue for next-generation cancer therapy. Nevertheless, the intricacy of production, inherent instability, and low expression persistence of linear mRNA significantly restrict their extensive utilization. Circular RNAs (circRNAs) offer a novel solution to these limitations due to their efficient protein expression ability, which can be rapidly generated in vitro without the need for extra modifications.

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It remains a challenge to develop a single-component organic photosensitizer that efficiently produces hydroxyl radicals (˙OH) without oxygen involvement, especially while maintaining tumor-targeting capability. Herein, we propose an intelligent molecular design strategy whereby a tumor-targeted phthalocyanine is initially ˙OH-free and can be activated by overexpressed β-nicotinamide adenine dinucleotide sodium salt hydrate (NAD(P)H) in hypoxic tumors to efficiently produce ˙OH under light irradiation. Furthermore, the oligomer models based on the phthalocyanine molecules were constructed by a supramolecular regulation strategy, which were in an intermediate state between monomer and nanoaggregate, to achieve enhanced ˙OH generation.

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Current progress in the regulation of endogenous molecules for enhanced chemodynamic therapy.

Chem Sci

July 2024

New Cornerstone Science Laboratory, MOE Key Laboratory for Analytical Science of Food Safety and Biology, Engineering Technology Research Center on Reagent and Instrument for Rapid Detection of Product Quality and Food Safety in Fujian Province, College of Chemistry, Fuzhou University Fuzhou 350108 China

Article Synopsis
  • - Chemodynamic therapy (CDT) utilizes Fenton chemistry to convert hydrogen peroxide into harmful reactive oxygen species to target and suppress tumor growth, but traditional methods often underperform in effectiveness.
  • - Tumor cells adapt their metabolism, which not only helps them grow but also makes them resistant to various treatments; recent studies show that certain cellular metabolites influence the efficiency of CDT.
  • - The article aims to summarize how these metabolites affect CDT and discusses ongoing challenges, while encouraging future research to manipulate tumor metabolism for improved CDT outcomes in cancer treatment.
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The coupling of the hydrogen evolution reaction (HER) and methanol oxidation reaction (MOR) to produce clean hydrogen energy with value-added chemicals has attracted substantial attention. However, achieving high selectivity for formate production in the MOR and high faradaic efficiency for H evolution remain significant challenges. In light of this, this study constructs an Ru/Ni(OH)/NF catalyst on nickel foam (NF) and evaluates its electrochemical performance in the MOR and HER under alkaline conditions.

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Correction: Halogen-bonded charge-transfer co-crystal scintillators for high-resolution X-ray imaging.

Chem Sci

May 2024

Key Laboratory of Advanced Carbon-Based Functional Materials (Fujian Province University), College of Chemistry, Fuzhou University Fuzhou P. R. China

[This corrects the article DOI: 10.1039/D4SC00735B.].

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It is of great difficulty to create a new antimonite with second-harmonic-generation (SHG) intensity larger than 6 times that of KDP. In this study, a polyfluoroantimonite strategy has been proposed to explore fluoroantimonites with large nonlinear optical (NLO) coefficients. Under the cooperation of chemical (highly asymmetric π-conjugated organic amine) and physical (viscous reaction medium ethylene glycol) methods, two novel polyfluoroantimonites, namely, (3PC)(SbF) and (3AP)(SbF), have been achieved.

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Halogen-bonded charge-transfer co-crystal scintillators for high-resolution X-ray imaging.

Chem Sci

May 2024

Key Laboratory of Advanced Carbon-Based Functional Materials (Fujian Province University), College of Chemistry, Fuzhou University Fuzhou 350116 P. R. China

The development of high-quality organic scintillators encounters challenges primarily associated with the weak X-ray absorption ability resulting from the presence of low atomic number elements. An effective strategy involves the incorporation of halogen-containing molecules into the system through co-crystal engineering. Herein, we synthesized a highly fluorescent dye, 2,5-di(4-pyridyl)thiazolo[5,4-]thiazole (PyTTz), with a fluorescence quantum yield of 12.

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Chiral phosphorus-containing compounds find applications across various fields, including asymmetric catalysis, medicinal chemistry, and materials science. Despite the abundance of reported highly enantioselective methods for synthesizing various chiral phosphorus compounds, the enantioselective synthesis of α-boryl phosphorus compounds still remains an unknown territory. Here, we report a method for the construction of chiral α-boryl phosphates by asymmetric B-H insertion reaction using α-diazo phosphates as carbene precursors, cheap and readily available copper salt as the catalyst and chiral oxazoline as the ligand.

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Regulating electron transfer and orbital interaction within metalloporphyrin-MOFs for highly sensitive NO sensing.

Chem Sci

May 2024

State Key Laboratory of Structural Chemistry, Fujian Provincial Key Laboratory of Materials and Techniques toward Hydrogen Energy, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences Fuzhou Fujian 350002 China

The understanding of electron transfer pathways and orbital interactions between analytes and adsorption sites in gas-sensitive studies, especially at the atomic level, is currently limited. Herein, we have designed eight isoreticular catechol-metalloporphyrin scaffolds, FeTCP-M and InTCP-M (TCP = 5,10,15,20-tetrakis-catechol-porphyrin, M = Fe, Co, Ni and Zn) with adjustable charge transfer schemes in the coordination microenvironment and precise tuning of orbital interactions between analytes and adsorption sites, which can be used as models for exploring the influence of these factors on gas sensing. Our experimental findings indicate that the sensitivity and selectivity can be modulated using the type of metals in the metal-catechol chains (which regulate the electron transfer routes) and the metalloporphyrin rings (which fine-tune the orbital interactions between analytes and adsorption sites).

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