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Developing novel nanoparticle-based bioprobes utilized in clinical settings with imaging resolutions ranging from cell to tissue levels is a major challenge for tumor diagnosis and treatment. Herein, an optimized strategy for designing a FeO-based bioprobe for dual-modal cancer imaging based on surface-enhanced Raman scattering (SERS) and magnetic resonance imaging (MRI) is introduced. Excellent SERS activity of ultrasmall FeO nanoparticles (NPs) was discovered, and a 5 × 10 M limit of detection for crystal violet molecules was successfully obtained. The high-efficiency interfacial photon-induced charge transfer in FeO NPs was promoted by multiple electronic energy levels ascribed to the multiple valence states of Fe, which was observed using ultraviolet-visible diffuse reflectance spectroscopy. Density functional theory calculations were utilized to reveal that the narrow band gap and high electron density of states of ultrasmall FeO NPs significantly boosted the vibronic coupling resonances in the SERS system upon illumination. The subtypes of cancer cells were accurately recognized via high-resolution SERS imaging using the prepared FeO-based bioprobe with high sensitivity and good specificity. Notably, FeO-based bioprobes simultaneously exhibited -weighted MRI contrast enhancement with an active targeting capability for tumors . To the best of our knowledge, this is the first report on the use of pure semiconductor-based SERS-MRI dual-modal nanoprobes in tumor imaging and , which has been previously realized only using semiconductor-metal complex materials. The non-metallic materials with SERS-MRI dual-modal imaging established in this report are a promising cancer diagnostic platform, which not only showed excellent performance in early tumor diagnosis but also possesses great potential for image-guided tumor treatment.
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http://dx.doi.org/10.1016/j.fmre.2022.04.018 | DOI Listing |
Adv Mater
September 2025
Department of Materials Science & Engineering, College of Design and Engineering, National University of Singapore, 9 Engineering Drive 1, Singapore, 117575, Singapore.
To advance the commercial utilization of aqueous electrochemical devices for grid-scale energy storage, it is crucial to address the current limitations related to energy density and cycle stability. Indeed, the lack of high-performance cathodes is still an obstructive issue, not to mention the limited capacities related to the monotonic cation intercalation/deintercalation mechanism. Fortunately, conversion chemistries with redox reactions bring a new dimension, where materials with multiple valence states facilitate multi-electron redox reactions, offering the potential for high-energy-density storage.
View Article and Find Full Text PDFChem Sci
August 2025
School of Materials Science and Engineering, Institutes of Physical Science and Information Technology, Leibniz International Joint Research Center of Materials Sciences of Anhui Province, Anhui University Hefei 230601 China
Aqueous zinc-iodine batteries (ZIBs), exploiting reversible conversion among various iodine species, have drawn significant research interest due to their fast redox kinetics and capability for multi-electron transfer. Although significant progress has been made in ZIBs based on the two-electron I/I redox pathway (2eZIBs), their inherently limited energy density impedes practical deployment. Achieving the additional reversible conversion of high-valence iodine species, particularly the I/I redox chemistry, offers substantial potential for improving energy density up to 630 Wh kg based on the mass of I.
View Article and Find Full Text PDFChem Sci
August 2025
South China Advanced Institute for Soft Matter Science and Technology, School of Emergent Soft Matter, South China University of Technology Guangzhou 510640 China
Cyclic oligomers with multiple redox centers are ideal models for intramolecular electron transfer processes, as they feature well-defined spatial geometries and degenerate energy states. The design and synthesis of such structures with strongly interacting monomers, however, remains a significant challenge. Here, we report a one-pot synthesis of an acetylene-bridged ferrocene macrocycle (9) using alkyne metathesis, with a remarkable 43% isolated yield.
View Article and Find Full Text PDFAdv Mater
September 2025
School of Materials Science and Engineering, Peking University, Beijing, 100871, China.
Ruthenium (Ru)-based dual-site catalysts can efficiently accelerate alkaline hydrogen electrocatalytic kinetics by virtue of the well-balanced competitive adsorptions of multiple reaction intermediates. However, their insufficient mass transfer makes them far away from the applications, largely lying to the challenge of precisely manipulating the interface water structure. Herein, a concept of nitrogen-bridged positively charged dual sites with a robust interfacial hydrogen-bond network is presented for enhancing alkaline hydrogen oxidation and evolution reactions (HOR and HER).
View Article and Find Full Text PDFJ Nanobiotechnology
September 2025
State Key Laboratory of Organic-Inorganic Composites, Beijing Advanced Innovation Center for Soft Matter Science and Engineering, Beijing Key Laboratory of Bioprocess, College of Life Science and Technology, Beijing University of Chemical Technology, Beijing, 100029, China.
Conventional miRNA-based diagnostic methods often treat all biomarkers equally, overlooking the fact that each miRNA contributes differently to disease classification. This differential diagnostic importance is captured by the concept of Cancerous Diagnostic Valence (CDV)-a metric that quantifies both the direction (oncogenic or protective) and magnitude of each miRNA's association with cancer. Here, we introduce a polymerase-based DNA molecular computing system that directly encodes and integrates CDVs to perform weighted molecular classification of non-small cell lung cancer (NSCLC).
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