Abstract

Blue phases (BPs) are mesophases existing between the isotropic and chiral nematic phases of liquid crystals (LCs). In recent years, blue phase LCs (BPLCs) have been extensively studied in the field of LC science and display technology. However, the application of BPLCs in biosensing has not been explored. In this study, a BPLC-based biosensing technology was developed for the detection and quantitation of bovine serum albumin (BSA). The sensing platform was constructed by assembling an empty cell with two glass slides coated with homeotropic alignment layers and with immobilized BSA atop. The LC cells were heated to isotropic phase and then allowed to cool down to and maintained at distinct BP temperatures for spectral measurements and texture observations. At BSA concentrations below 10-6 g/ml, we observed that the Bragg reflection wavelength blue-shifted with increasing concentration of BSA, suggesting that the BP is a potentially sensitive medium in the detection and quantitation of biomolecules. By using the BPLC at 37 °C and the same polymorphic material in the smectic A phase at 20 °C, two linear correlations were established for logarithmic BSA concentrations ranging from 10-9 to 10-6 g/ml and from 10-6 to 10-3 g/ml. Our results demonstrate the potential of BPLCs in biosensing and quantitative analysis of biomolecules.

Highlights

  • Biological detection by liquid crystals (LCs) is an emerging new field in biophotonics that is realized through biomolecules immobilized on solid surfaces or confined in LC–aqueous interfaces, or by utilizing LC-in-water droplets [1]

  • Blue phases (BPs) are mesophases existing between the isotropic and chiral nematic phases of liquid crystals (LCs)

  • A blue phase LCs (BPLCs)-based biosensing technology was developed for the detection and quantitation of bovine serum albumin (BSA)

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Summary

Introduction

Biological detection by liquid crystals (LCs) is an emerging new field in biophotonics that is realized through biomolecules immobilized on solid surfaces or confined in LC–aqueous interfaces, or by utilizing LC-in-water droplets [1]. Traditional LC-based biosensing employs nematic LCs such as 5CB, which is the most extensively applied sensing medium in the detection of biomolecules such as proteins, peptides, and DNA, as well as biomolecular interactions such as the specific binding between antigen and antibody [2,3,4,5]. For biological detection with other phases of LCs, cholesteric LCs (CLCs), produced by incorporating a chiral dopant in nematic LCs, were utilized as droplets in the design of glucose and cholesterol biosensors [11]. A real-time detector based on lyotropic chromonic liquid crystals, a different category of LCs as opposed to nematic ones, was developed to monitor microbial immunocomplexes [13]

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