Publications by authors named "Jinxiu Wei"

Extracellular vesicles (EVs) have emerged as promising biomarkers in cancer diagnostics. However, rapid and nondestructive isolation of EVs from plasma remains challenging due to the presence of abundant interferents with smaller sizes (e.g.

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Background: Pancreaticobiliary maljunction (PBM) is a rare congenital abnormality in pancreaticobiliary duct development. PBM is commonly found in children, and it often leads to acute pancreatitis and other diseases as a result of pancreaticobiliary reflux. Roux-en-Y choledochojejunostomy is a common surgical method for the treatment of PBM, but there are several associated complications that may occur after this operation.

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Exosome is a kind of membranous vesicles released from cells and carry a number of important signaling molecules, they play an important role in cellular communication, cell migration, angiogenesis as well as tumor cell growth. Exosome-based cancer diagnosis is usually achieved by detecting exosomal nucleic acids, lipids, and surface proteins, as they reflect tumor type and progression. Here, we proposed a method to rapidly prepare an array of washable magnetic nanoparticles (magnetic beads, MBs) by a magnetic field controlled system, which facilitate the analyzing of exosome phenotypes via super-resolution tricolor fluorescence co-localization (SR-TFC) and pixel counting (CFPP).

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Background: The correlation between serum cotinine and fatty liver index (FLI) needs further investigation for the early identification, prevention, and treatment of metabolic dysfunction-associated steatotic liver disease (MASLD).

Methods: Data from the NHANES database spanning from March 2017 to 2018 was used to perform the population-based study to assess the relationship between serum cotinine and FLI. A variance estimation strategy was applied to address the data volatility.

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Sweat biomarkers have the potential to offer valuable clinical insights into an individual's health and disease condition. Current sensors predominantly utilize enzymes and antibodies as biometric components to measure biomarkers present in sweat quantitatively. However, enzymes and antibodies are susceptible to interference by environmental factors, which may affect the performance of the sensor.

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Article Synopsis
  • Exosomes are promising indicators for early disease detection, particularly cancer, but distinguishing between exosomes from different cell types is challenging due to nonspecific adsorption in detection methods.
  • This study introduces a novel technique (SR-TFC) that effectively mitigates nonspecific adsorption effects using tricolor fluorescence labeling and a pixel counting method (CFPP) developed in MATLAB, enhancing detection reliability at the single-pixel level.
  • As a demonstration, the technique successfully profiles exosomal membrane proteins and identifies different breast cancer subpopulations, suggesting its potential for broader applications in cancer diagnosis and precision medicine.
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Tumor cell-derived extracellular vesicles and their cargo of bioactive substances have gradually been recognized as novel biomarkers for cancer diagnosis. Meanwhile, the PD-L1 (Programmed Death-Ligand 1) protein, as an immune checkpoint molecule, is highly expressed on certain tumor cells and holds significant potential in immune therapy. In comparison to PD-L1 monoclonal antibodies, the inhibitory effect of PD-L1 siRNA (small interfering RNA) is more advantageous.

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Tumor cell exosomes play a very important role in the process of tumor cell proliferation and metastasis. However, due to the nanoscale size and high heterogeneity of exosomes, in-depth understanding of their appearance and biological characteristics is still lacking. Expansion microscopy (ExM) is a method that embeds biological samples in a swellable gel to physically magnify the samples to improve the imaging resolution.

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Ag ions are widely used in various fields of human life due to their unique properties and they threaten the environment and human health. The traditional methods for Ag detection commonly suffer from disadvantages including limited sensitivity, expensive equipment and complicated operating steps. Herein, we developed a highly specific dual-color fluorescence co-localization (DFC) strategy based on the C-Ag-C structure for Ag detection.

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Immunotherapy has become an efficient treatment method of breast cancer. Detection of proteins such as PD-L1 and CTLA-4, which are important immune checkpoint molecules, is attracting more and more attention as they play key roles in immunotherapy. Here, by combining the high resolution of DNA-PAINT (DNA points accumulation for imaging in nanoscale topography) with the qPAINT quantitative analysis method, accurate spatial localization and absolute quantification of PD-L1 and CTLA-4 on the membrane of breast cancer cells could be achieved.

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Programed cell death ligand 1 (PD-L1) is a protein biomarker overexpressed on exosomes derived from tumor cells. It plays an important role in tumor diagnosis, screening, evaluation of therapeutic efficacy, and prognosis. In this study, a facile method is presented to detect PD-L1-overexpressing cancer exosomes with high specificity and sensitivity.

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A bilayer asymmetric photonic crystal slab made of porous SiN/SiO is designed as a biosensor by considering the optical performance of this photonic crystal slab with a square lattice based on rigorous coupled-wave analysis theory and wavelength interrogation methods. The results show that this bilayer asymmetric photonic crystal can be used as a biosensor according to its excellent linearity relationship between the guided resonance peak shift and refractive index of aqueous solution with or without glycerol. The theoretical sensitivity value of the bilayer asymmetric photonic crystal biosensor is achieved as (S>286  nm/RIU) in the wavelength range from 1400 nm to 1600 nm.

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