Skip to main navigation Skip to search Skip to main content

Microstructure and Magnetic Properties of LaSrMnO Nanoparticles and Their Application to Cardiac Immunoassay

  • Woo Seung Ham
  • , Min Kyung Kim
  • , Ji Seok Gim
  • , Ji Sung Lee
  • , Jun Hua Wu
  • , Kyu Back Lee
  • , Young Keun Kim*
  • *Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Though enzyme-linked immunosorbent assay is widely used in laboratory medicine, it has limitations due to interactions between enzymes and secondary antibodies. Here, we propose a new cardiac assay scheme for detecting troponin I antigens based on La(1-x)SrxMnO3 (x=0.10, 0.15, and 0.25) nanoparticles (NPs). These NPs are synthesized via a modified polyol process followed by heat treatment. An increase in x induces changes in crystal structure and increases both Curie temperature and saturation magnetization. The NPs with x=0.15 exhibit a Curie temperature close to the human body temperature. The limit of detection is found to be 0.78 ng/mL. We also confirm that LaSrMnO NPs are reusable after heating the assay plate.

    Original languageEnglish
    Article number7113860
    JournalIEEE Transactions on Magnetics
    Volume51
    Issue number11
    DOIs
    Publication statusPublished - 2015 Nov 1

    Bibliographical note

    Publisher Copyright:
    © 2015 IEEE.

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Keywords

    • Cardiac troponin I (cTnI)
    • Curie temperature
    • LaSrMnO nanoparticles (NPs)
    • immunoassay

    ASJC Scopus subject areas

    • Electronic, Optical and Magnetic Materials
    • Electrical and Electronic Engineering

    Fingerprint

    Dive into the research topics of 'Microstructure and Magnetic Properties of LaSrMnO Nanoparticles and Their Application to Cardiac Immunoassay'. Together they form a unique fingerprint.

    Cite this