Abstract

Quasi three-dimensional (3D) plasmonic nanostructures consisting of Au nanosquares on top of SU-8 nanopillars and Au nanoholes on the bottom were developed and fabricated using nanoimprint lithography with simultaneous thermal and UV exposure. These 3D plasmonic nanostructures were used to detect cell concentration of lung cancer A549 cells, retinal pigment epithelial (RPE) cells, and breast cancer MCF-7 cells. Nanoimprint technology has the advantage of producing high uniformity plasmonic nanostructures for such biosensors. Multiple resonance modes were observed in these quasi 3D plasmonic nanostructures. The hybrid coupling of localized surface plasmon resonances and Fabry–Perot cavity modes in the quasi 3D nanostructures resulted in high sensitivity of 496 nm/refractive index unit. The plasmonic resonance peak wavelength and sensitivity could be tuned by varying the Au thickness. Resonance peak shifts for different cells at the same concentration were distinct due to their different cell area and confluency. The cell concentration detection limit covered a large range of 5 × 102 to 1 × 107 cells ml−1 with these new plasmonic nanostructures. They also provide a large resonance peak shift of 51 nm for as little as 0.08 cells mm−2 of RPE cells for high sensitivity cell detection.

Highlights

  • Measuring cell concentration, especially for cancer cells, is important for disease diagnostics

  • The simulated EM field intensity distributions are shown in figures 3(c)–(e)

  • The EM field intensity distribution for P1 (592 nm) was enhanced between the bottom Au layer and the polymer underneath. This implies that P1 could be attributed to the Bloch wave surface plasmon polaritons (BW-SPPs) involving diffracted light propagating parallel to the bottom of the Au layer–polymer interface

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Summary

Introduction

Especially for cancer cells, is important for disease diagnostics. Localized surface plasmon resonances are collective oscillations of free electrons confined in metallic nanoparticles (NPs) which are excited by an incident light wave, resulting in strong enhancement of local electromagnetic (EM) fields [8,9,10] Their LSPR spectra depend on the size, geometry, distribution, and material of the NPs, as well as the Nanotechnology 27 (2016) 295101 refractive index (RI) of their surrounding medium (i.e. solvent and analyte cells). At the low concentration of 103 cells ml−1, large peak shift of 35 nm was achieved for detecting 1.25 cells mm−2 (based on 60 μl sample volume over 48 mm sample area) of MCF-7 cells using 120 nm diameter (dia.) Au/SiO2/Au nanodisks

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