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Label-free biosensors, including conventional quartz-crystal-microbalance (QCM) biosensors, are seriously affected by nonspecific adsorption of contaminants involved in analyte solution, and it is exceptionally difficult to extract the sensor responses caused only by the targets. In this study, we reveal that this difficulty can be overcome with an ultrahigh-frequency, wireless QCM biosensor. The sensitivity of a QCM biosensor dramatically improves when the quartz resonator is thinned, which also makes the resonance frequency higher, causing high-speed surface movement. Contaminants weakly (nonspecifically) interact with the quartz surface, but they fail to follow the fast surface movement and cannot be detected as the loaded mass. The targets are, however, tightly captured by the receptor proteins immobilized on the surface, and they can move with the surface, contributing to the loaded mass and decreasing the resonant frequency. We have developed a MEMS QCM biosensor in which an AT-cut quartz resonator, 26 μm thick, is packaged without fixing, and we demonstrate this phenomenon by comparing the frequency changes of the fundamental (∼64 MHz) and ninth (∼576 MHz) modes. At ultrahigh-frequency operation with the ninth mode, the sensor response is independent of the amount of impurity proteins, and the binding affinity is unchanged. We then applied this method to the label-free and sandwich-free, direct detection of C-reactive protein (CRP) in serum and confirmed its applicability.
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http://dx.doi.org/10.1021/acs.analchem.9b01414 | DOI Listing |
Adv Healthc Mater
August 2025
Institute of Materials Science, Kiel University, 24143, Kiel, Germany.
Virus sensing and removal are critical for public health, particularly in preventing the spread of infectious diseases and ensuring safe water, air, and clinical environments. Current virus detection tools utilize recognition elements suffering from high cost, low stability, and specificity, and time-consuming production methods. Meanwhile, conventional virus removal techniques are often hindered by inefficiency, complexity, and the potential for harmful byproducts.
View Article and Find Full Text PDFAnal Chem
August 2025
Institute of Industrial Science, The University of Tokyo, Tokyo 153-8505, Japan.
Heparin-induced thrombocytopenia (HIT) is a serious side effect that occurs in patients undergoing heparin therapy. The known risk factor is the presence of antibodies created against platelet factor 4 and heparin complexes (PF4/heparin) in the blood, which activate platelet Fc receptors (FcγRIIA). Although immunoassays have been developed for HIT diagnosis, their specificity remains low (∼50%) due to the binding of nonpathogenic antibodies to the same antigen (PF4/heparin).
View Article and Find Full Text PDFLangmuir
August 2025
Biomedical Engineering Center, Toyo University, 48-1 Oka, Asaka, Saitama 351-8510, Japan.
In label-free biosensors based on graphene, achieving both the specific recognition of target analytes and the suppression of the nonspecific adsorption of interfering substances remains a critical challenge. In this study, a linker molecule possessing a pyrene moiety capable of forming π-π stacking interactions and an active ester group suitable for bioconjugation was employed to construct a selective layer on graphene. Subsequently, a DNA aptamer as the receptor and a phospholipid-mimetic zwitterionic molecule for suppressing nonspecific adsorption were sequentially conjugated to the active ester groups.
View Article and Find Full Text PDFMol Pharm
August 2025
Pre-Pivotal Drug Product Technologies, Process Development, Operations, Amgen, Thousand Oaks, California 91320, United States.
Lipid nanoparticles (LNPs) are an essential delivery platform for nucleic acid payloads that are susceptible to degradation or elimination. Upon administration, a biomolecular corona composed of serum proteins forms around the LNP surface, which is crucial for tissue targeting and biodistribution. One essential protein that drives the distribution of LNPs is apolipoprotein E (ApoE).
View Article and Find Full Text PDFTalanta
January 2026
International Institute for Interdisciplinary and Frontiers, Beihang University, Beijing, 100191, China.
Accurate and synchronized assessment of biochemical parameters, such as biomarker concentration and body fluid viscosity, is crucial for advancing early disease detection and health management. Conventional biomolecular multiparameter detection methods often rely on multiple sensors or analytical techniques, which introduce cross-talk between sensing modalities, data inconsistencies, and complex calibration requirements, ultimately compromising detection precision and adaptability. We propose a streamlined detection approach that leverages a single uncoated Quartz Crystal Microbalance (QCM) sensor to monitor the dynamic magnetized motion of biomolecules under multimodal magnetic field modulation.
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