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Controllable transformation between the bolaamphiphilic molecule assemblies with different morphological nanostructures represents an exciting new direction for materials. However, there are still significant challenges for the quantitative detection and real-time monitoring of a controllable nanoself-assembly process due to insufficient measuring methods. Herein, we propose a new and effective fluorescence technology for realizing quantitative detection of a controllable conversion process of one-dimensional (1D)/two-dimensional (2D) nanoassemblies by introducing AIEgens as the fluorescence signal part. First, an aggregation-induced emission (AIE)-active bolaamphiphilic molecule (TPE-C8-Br) was designed and synthesized by incorporating tetraphenylethene (TPE) as the chromophore into the cationic amphiphile. Subsequently, the 1D nanofibrous morphology of TPE-C8-Br was successfully converted into the 2D rectangular and circular sheet of tosylate (TPE-C8-Ts) and sodium 1-hexanesulfonate (TPE-C8-HS) with the same molecular skeleton by the simple counterion change, respectively. Interestingly, all 2D nanoassemblies exhibited a stronger fluorescence sensitization effect than that of the 1D nanoassembly at the concentration above the critical micelle concentration (CMC) due to the higher degree of aggregation; thus, the rotation of the AIE-active TPE moiety is more restricted in TPE-C8-Ts and TPE-C8-HS. More meaningfully, a rather good linear correlation (FI = 3174.86 + 5282.29MP, = 0.999) and a quadratic correlation (FI = 2113.71 + 5163.56MP - 2966.07MP) were obtained between the molar percentage (MP) of the 2D nanoassembly and the fluorescence intensity (FI). The two proposed methods respond very well with regard to dependability, which can be used for the quantitative calculation of the molar ratio of 1D and 2D components in the controllable nanoself-assembly process. Therefore, this work offers an efficient and practical method for realizing the dynamic monitoring and quantitative detection of mutual conversion between different nanoassemblies.
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http://dx.doi.org/10.1021/acs.langmuir.4c04421 | DOI Listing |
Mol Pharm
September 2025
Department of Nuclear Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Tissue factor (TF) has emerged as a promising target for the diagnosis and treatment of hepatocellular carcinoma (HCC). However, there is limited data available on TF-related PET imaging for longitudinal monitoring of the pathophysiological changes during HCC formation. Herein, we aimed to explore the TF-expression feature and compare a novel TF-targeted PET probe with F-FDG through longitudinal imaging in diethylnitrosamine (DEN)-induced rat HCC.
View Article and Find Full Text PDFJ Phys Chem B
September 2025
Department of Physics, Division of Nano and Biophysics, Chalmers University of Technology, Fysikgränd 3, Göteborg 41296, Sweden.
The detection of biological nanoparticles (NPs), such as viruses and extracellular vesicles (EVs), plays a critical role in medical diagnostics. However, these particles are optically faint, making microscopic detection in complex solutions challenging. Recent advancements have demonstrated that distinguishing between metallic and dielectric signals with twilight off-axis holographic microscopy makes it possible to differentiate between metal and biological NPs and to quantify complexes formed from metal and biological NPs binding together.
View Article and Find Full Text PDFJCI Insight
September 2025
Ragon Institute of Mass General Brigham, Cambridge, United States of America.
Background: The SARS-CoV-2 virus has evolved subvariants since the emergence of the omicron variant in 2021. Whether these changes impact viral shedding and transmissibility is not known.
Methods: POSITIVES is a prospective longitudinal cohort of individuals with mild SARS-CoV-2 infection.
Anal Methods
September 2025
Jilin Province Product Quality Supervision and Inspection Institute, Changchun 130103, China.
A method for determination of ten kinds of sweeteners in soybean products by multi-plug filtration cleanup (-PFC) combined with ultra-high-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) was established. The sample was extracted with acetonitrile (containing 1% formic acid), degreased by using -hexane liquid-liquid extraction and purified by solid phase extraction using an -PFC column (Oasis PRiME HLB). The analytes were separated by using a Waters ACQUITY UPLC® BEH C (2.
View Article and Find Full Text PDFDiscov Nano
September 2025
Department of Rehabilitation Medicine, Rehabilitation Medical Center, Key Laboratory of Rehabilitation Medicine in Sichuan Province, West China Hospital, Sichuan University, Chengdu, 610041, People's Republic of China.
Immunoelectron Microscopy (IEM) is a technique that combines specific immunolabeling with high-resolution electron microscopic imaging to achieve precise spatial localization of biomolecules at the subcellular scale (< 10 nm) by using high-electron-density markers such as colloidal gold and quantum dots. As a core tool for analyzing the distribution of proteins, organelle interactions, and localization of disease pathology markers, it has irreplaceable value, especially in synapse research, pathogen-host interaction mechanism, and tumor microenvironment analysis. According to the differences in labeling sequence and sample processing, the IEM technology system can be divided into two categories: the first is pre-embedding labeling, which optimizes the labeling efficiency through the pre-exposure of antigenic epitopes and is especially suitable for the detection of low-abundance and sensitive antigens; the second is post-embedding labeling, which relies on the low-temperature resin embedding (e.
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