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Electrorheological Sensor Encapsulating Microsphere Media for Plague Diagnosis with Rapid Visualization
Pai-Chien Chou1,2, Feng-Ping Lin2,3, Hui-Ling Hsu3
1Department of Thoracic Medicine, Taipei Medical University Hospital, Taipei 110, Taiwan, Republic of China.
Abstract:
Plague is a disease infected by an etiological agent, which is transmitted from fleas to a variety of wildlife rodents. Therefore, rapid diagnosis of plague on-site in the field is important. Polystyrene microspheres (SMs) of 2.2 μm diameter were synthesized by emulsion polymerization to adsorb magnetic nanoparticles (FNs), resulting in core-/shell-structured microspheres that generate a significant contrast in relative permittivities between SMs and FNs. Electrorheological displays (EDs) consisting of two indium tin oxide glasses with spacers were constructed to contain core-/shell-structured SM/FN (SM@FN) solutions for observing their transmittance change. The ED encapsulating dispersed SM@FN solution exhibited an opaque state because light was scattered significantly without the application of an alternating electric field (AEF). In the presence of an AEF, the particle chaining behavior results in enhancement of the transmittance of ED. At a specific frequency, the so-called characteristic frequency (Fc), the transmittance reaches a maximum. Fc could be used as an indicator to mark the shell materials. The antibody of Yersinia pestis (ab-Yp) was coated onto the SM@FN as a biosensing medium. The Fc of ab-Yp-modified microspheres shifted from 200 to 750 kHz with antigen coupling of Y. pestis antigen (ag-Yp). In the absence of fluorescence labeling, the large change in ED transmittance could be visualized during the Y. pestis detection. The limit of detection and the limit of quantification were ∼30 and ∼40 ng/μL, respectively, obtained within 30 s according to the highest transmittance of ED under the AEF at 750 kHz. Y. pestis detection was not affected by Escherichia coli and Staphylococcus aureus significantly. Compared with other common immunoassays, including the secondary immunochemical or enzyme-linked steps, this simple electrorheological sensor with high sensitivity and selectivity could be a candidate for on-site plague diagnosis.
Insights
This study developed a novel electrorheological sensor for rapid, on-site plague diagnosis. The sensor detects Yersinia pestis using antibody-modified microspheres, offering high sensitivity and selectivity without fluorescence labeling.
Area of Science:
- Biomaterials Science
- Biosensing Technology
- Electrorheology
Background:
- Plague, caused by Yersinia pestis, requires rapid field diagnosis due to its transmission via fleas to rodents.
- Existing diagnostic methods can be time-consuming and complex, hindering immediate on-site detection.
Purpose of the Study:
- To develop a sensitive and selective biosensor for rapid, on-site detection of Yersinia pestis.
- To utilize electrorheological displays (EDs) for visualizing plague pathogen presence without fluorescence labeling.
Main Methods:
- Synthesis of core-shell structured polystyrene microspheres (SMs) adsorbing magnetic nanoparticles (FNs).
- Construction of electrorheological displays (EDs) containing SM@FN solutions.
- Modification of SM@FN microspheres with antibodies against Yersinia pestis (ab-Yp) for antigen capture.
- Monitoring changes in characteristic frequency (Fc) and transmittance in response to Y. pestis antigen (ag-Yp).
Main Results:
- The electrorheological sensor demonstrated a significant shift in characteristic frequency (Fc) from 200 to 750 kHz upon Y. pestis antigen detection.
- High sensitivity was achieved with a limit of detection around 30 ng/μL within 30 seconds.
- The sensor showed high selectivity, unaffected by common bacteria like Escherichia coli and Staphylococcus aureus.
Conclusions:
- The developed electrorheological sensor offers a simple, sensitive, and selective platform for on-site plague diagnosis.
- This technology bypasses the need for fluorescence labeling, enabling direct visual detection.
- The sensor presents a promising alternative to conventional immunoassays for rapid field identification of Yersinia pestis.
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