4.6 Article

Magnetoelastic Immunosensor via Antibody Immobilization for the Specific Detection of Lysozymes

Journal

ACS SENSORS
Volume 6, Issue 11, Pages 3933-3939

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acssensors.1c00802

Keywords

magnetoelastic immunosensor; lysozyme; resonance frequency shift; surface functionalization; specific detection

Funding

  1. National Natural Science Foundation of China [61501316, 51505324]
  2. Excellent Talents Technology Innovation Program of Shanxi Province of China [201805D211020]
  3. International Cooperation of Science and Technology Projects in Shanxi Province [201903D421063]
  4. Key Research and Development Program in Shanxi Province [201803D221028-5]
  5. Beijing Natural Science Foundation [7202190]

Ask authors/readers for more resources

Lysozymes in urine are important indicators for renal diseases. Current detection methods like ELISA are tedious, while newer methods are time-consuming and complex. A rapid, low-cost, and easy-to-prepare lysozyme detection method is still needed for clinical monitoring.
Lysozymes in human urine have crucial clinical significance as an indicator of renal tubular and glomerular diseases. Most lysozyme detection methods rely on the enzyme-linked immunosorbent assay (ELISA), which is usually a tedious procedure. Meanwhile, aptamer sensors and fluorescence-based techniques for lysozyme detection have emerged in recent studies. However, these methods are time-consuming and highly complex in operation, and some even require exorbitant reagents and instruments, which restricts real-time clinical monitoring as diagnostic approaches. Therefore, a rapid and low-cost lysozyme detection method with facile preparation is still in demand for modern precision medicine. Herein, we propose a magnetoelastic (ME) immunosensor for lysozyme detection by detecting changes in resonance frequency under a magnetostrictive effect. The detection system is composed of a magnetoelastic chip with an immobilized lysozyme antibody, a solenoid coil, and a vector network analyzer. Since the ME sensor is ultrasensitive to mass change, the frequency offset caused by mass change can be utilized to detect the content of lysozyme. The immunosensor is evaluated to possess superior sensitivity of 138 Hz/mu g mL(-1) in terms of the resonance frequency shift (RFS). In addition, our sensor displays an outstanding performance in specificity experiments and shows a relatively lower detection limit (1.26 ng/mL) than other conventional lysozyme detection methods (such as ELISA, chemiluminescence assay, fluorescence, and aptamer biosensors).

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