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Effects of nanoparticle size and cell type on high sensitivity cell detection using a localized surface plasmon resonance biosensor

  • Fei Liu
  • , Matthew Man Kin Wong
  • , Sung Kay Chiu
  • , Hao Lin
  • , Johnny C. Ho
  • , Stella W. Pang*
  • *Corresponding author for this work
  • City University of Hong Kong
  • Tianjin University

Research output: Contribution to journalArticlepeer-review

Abstract

A localized surface plasmon resonance (LSPR) effect was used to distinguish cell concentration on ordered arrays of Au nanoparticles (NPs) on glass substrates. Human-derived retinal pigment epithelial RPE-1 cells with flatter bodies and higher confluency were compared with breast cancer MCF-7 cells. Nanosphere lithography was used to form Au NPs with average diameters of 500 and 60nm in order to compare cell detection range, resonance peak shift, and cell concentration sensitivity. A larger cell concentration range was detected on the larger 500nm Au NPs compared to 60nm Au NPs (8.56×103-1.09×106 vs. 3.43×104-2.73×105cells/ml). Resonance peak shift could distinguish RPE-1 from MCF-7 cells on both Au NPs. RPE-1 cells consistently displayed larger resonance peak shifts compared to MCF-7 cells until the detection became saturated at higher concentration. For both types of cells, higher concentration sensitivity in the range of ~104-106cells/ml was observed on 500nm compared to 60nm Au NPs. Our results show that cells on Au NPs can be detected in a large range and at low concentration. Optimal cell sensing can be achieved by altering the dimensions of Au NPs according to different cell characteristics and concentrations.

Original languageEnglish
Pages (from-to)141-148
Number of pages8
JournalBiosensors and Bioelectronics
Volume55
DOIs
StatePublished - 15 May 2014
Externally publishedYes

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

  • Au nanoparticles
  • Breast cancer MCF-7 cell
  • Cell concentration detection
  • Human-derived retinal pigment epithelial RPE-1 cell
  • Localized surface plasmon resonance (LSPR)
  • Resonance peak shift

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