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Wang, H.;  Xu, T.;  Fu, Y.;  Wang, Z.;  Leeson, M.S.;  Jiang, J.;  Liu, T. Principle of Liquid Crystal Biosensors. Encyclopedia. Available online: https://encyclopedia.pub/entry/26476 (accessed on 19 November 2024).
Wang H,  Xu T,  Fu Y,  Wang Z,  Leeson MS,  Jiang J, et al. Principle of Liquid Crystal Biosensors. Encyclopedia. Available at: https://encyclopedia.pub/entry/26476. Accessed November 19, 2024.
Wang, Haonan, Tianhua Xu, Yaoxin Fu, Ziyihui Wang, Mark S. Leeson, Junfeng Jiang, Tiegen Liu. "Principle of Liquid Crystal Biosensors" Encyclopedia, https://encyclopedia.pub/entry/26476 (accessed November 19, 2024).
Wang, H.,  Xu, T.,  Fu, Y.,  Wang, Z.,  Leeson, M.S.,  Jiang, J., & Liu, T. (2022, August 25). Principle of Liquid Crystal Biosensors. In Encyclopedia. https://encyclopedia.pub/entry/26476
Wang, Haonan, et al. "Principle of Liquid Crystal Biosensors." Encyclopedia. Web. 25 August, 2022.
Principle of Liquid Crystal Biosensors
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This entry is adapted from the peer-reviewed paper 10.3390/bios12080639

Liquid crystals (LCs) are phase transition materials that exist between the liquid and the crystal states, and they can flow as liquids and also have properties such as birefringence of crystals. LCs have been widely used as sensitive elements to construct LC biosensors based on the principle that specific bonding events between biomolecules can affect the orientation of LC molecules.

liquid crystals LC-based biosensors microfluidics

1. Introduction

Liquid crystals (LCs) are phase transition materials that exist between the liquid and the crystal states, and they can flow as liquids and also have properties such as birefringence of crystals [1]. LCs can respond readily to external stimuli such as electromagnetic fields [2][3][4][5][6], pressure [7][8][9], surface effects [10][11][12][13], optical properties [14][15], temperature [16][17][18], and chemical analytes [19][20]. Changes in these factors can be monitored by various characterization techniques. Since LCs have superiorities in sensitivity, reactivity, and fabrications, research works on LCs have been expanded widely to address current technological and scientific challenges [21][22]. Accordingly, LC-based sensing techniques have gradually attracted more and more research attention.
LC molecules can be applied to serve as sensitive materials to respond to environmental changes or the occurrence of binding events. LCs generate macroscopic signals by magnifying and transforming molecular events in their surroundings [23]. The response properties of LCs have been extensively investigated in the context of a variety of sensing applications based on the molecular orientation. These properties form the foundation of LC-based sensing platforms [24][25][26][27][28][29]. A popular biosensing approach employs the optical birefringence properties of LC materials. Signal sensors can detect changes in the phases and the polarization states, since the refractive indices (ordinary and extraordinary refractive indices) vary with the direction of the light beam propagating along LCs. Interactions between biological receptors and ligands change the orientation of LC molecules, and this mechanism allows LCs to respond to biological or chemical materials [30][31][32][33][34]. In addition, LC molecules on the surface can transmit variations in their orientations within a vicinity (maximum 100 μm) to amplify the sensing signal [35]. Considering the optical birefringence properties and the high sensitivity to surface–interface interactions, LC biosensors can avoid the drawbacks of traditional biosensors, such as complex operations and the need for labeling biotargets [36]. Consequently, signals generated by LCs can be used to report subtle molecular events and external stimuli, and a number of materials-based optoelectronic signal transduction systems have been developed for LC-based biosensors [37][38][39].
In response to the rapid advancements of the microfluidic technology, optofluidic systems that combine optics and microfluidic devices have steadily demonstrated their distinct merits and potentials. The microfluidic technique is very important in the biomedical detection since it enables all the functions, including the preparation of biological samples [40], the measurement of concentrations [41][42], the monitoring of biochemical reactions [43][44][45][46], and the detection of products [47], to be implemented on a single biochip. Due to the vital role of the optical technologies in the biomedical detection, the integration of sample analysis, detection, and data transfer significantly enhances the efficiency. Moreover, fluids are excellent carriers of the light and matters, meaning that liquids with varying optical properties can be employed to manipulate the light and convey matters [48]. LCs have both optical anisotropy and liquid shapes, and this makes them perfectly suited for detecting and analyzing extremely small samples in biomedicine and chemistry.

2. Principle of LC-Based Biosensors

The mesophase of LCs is defined by the difference in conditions that create it. LCs can be categorized into two groups: lyotropic liquid crystals (LLCs) and thermotropic liquid crystals (TLCs). LLCs are composed of solvents and amphiphilic compounds. The phase transition of the LLCs depends on both the concentration and the temperature. The amphiphilic feature of one end being hydrophilic and the other end being hydrophobic is required for the lyotropic LCs, and the fabrication is dependent on the interactions between the amphiphilic molecules [49]. In contrast, the TLCs can only develop a liquid crystal phase within a limited temperature range (Figure 1a). Such LCs take on a more turbid appearance at the melting point. They continue to heat up until the clearing point is reached, at which point the LCs become transparent. According to the arrangement of the LC molecules, thermotropic LCs can be divided into three types: nematic liquid crystals (NLCs), cholesteric liquid crystals (CLCs), and smectic liquid crystals (SLCs) (Figure 1b). NLC molecules possess low van der Waals forces, excellent fluidity, and optical birefringence. Due to the high sensitivity to the environmental changes, NLC materials are widely investigated [50]. CLCs, also known as chiral NLC phases, are the chiral variants of orientationally ordered NLC phases. CLC molecules have a director that is periodically rotated along the perpendicular axis; the orientation rotates periodically about a vertical axis, generating a helical superstructure. The CLC possesses exceptional optical properties, including optical rotation, circularly polarized light dichroism, and selective light scattering [51]. An SLC molecule is rod- or strip-shaped. Molecules in SLCs tend to align in layers, and the layers stack on each other. It is noted that all LCs discussed in this research are thermotropic.
Figure 1. Schematic of the properties of LC molecules. (a) The arrangement of thermotropic LC molecules. (b) The variation of thermotropic LC molecules with temperature. (c) Illustration of LC directors in the Cartesian coordinate.

2.1. Optical Anisotropy

LC molecules exhibit the anisotropy in terms of refractive index, dielectric properties, elastic coefficient, etc., due to the structural peculiarities of LCs (between crystals and liquids) [52][53][54][55]. The anisotropy in the refractive index is the most commonly used optical birefringence characteristic. Plane polarized light is decomposed into two linearly polarized rays with different propagation rates, which are called ordinary (no) and extraordinary (ne) rays, respectively [56]. The birefringence property of LC can be described as the difference between the refractive indices of no and ne. This phenomenon will cause a phase change as the light beam outputs from the LC medium. The phase difference is known as the optical retardation δ, and is given by [57]:
δ = 2 π d λ ( n e − n o )
where λ is the wavelength of the light and d is the thickness of the medium. Therefore, LC systems are able to regulate the polarization of light due to the birefringence and convert this into an optical image visible to the naked eye, which can be viewed using a polarized optical microscope (POM).
The birefringence on the surface of LC molecules can cause changes in the optical image, and this means that the monitoring of changes in the optical signal image using a POM allows the indirect detection of the variations in the alignment of LC molecules. Due to the interference of two orthogonal rays, the optical texture of LCs is visible through crossed polarizers. The linearly polarized light beam cannot get through in the case of the homeotropic alignment of the LC molecules, and this will result in dark optical images. The director configuration of LCs restricted inside particular geometries can be identified using the POM, by observing patterns produced by the interaction between the polarized light and LCs [58]. The transmitted light has the following intensity when LCs are sandwiched between crossed polarizers:
I = I 0 sin 2 2 φ sin 2 δ 2
where I0 is the initial intensity of the light and φ is the angle of the LC orientations relative to the polarizer. This formula provides a good explanation of the fact that LC molecules can produce varied optical images when observed under the polarized light [59]. When LCs are positioned between two crossed polarizers, the intensity of the transmitted light I = 0 for the homeotropic alignment of LCs (δ = 0), and a dark optical image is observed. When the LC orientations are disturbed, δ≠0, I≠0, a bright image will be observed.

2.2. Orientations of LCs

Owing to the interaction force between LC molecules and hydrogen bonding, the long axes of LCs tend to align parallel to each other. In addition, the orientation of molecules follows a certain order, and the preferred direction is called the director of phase, which is the average direction that molecules point [60]. The unit vector n→ is used to describe the direction of the preferred orientation, and the spatial orientation of the director is normally specified by the polar angle θ and the azimuth angle φ, as shown in Figure 1c. In general, it can be used to characterize the macroscopic structure and the condition of LCs, as it describes the arrangement direction of LC molecules in space. While LCs are in the dynamic motion, they are oriented along the director for a longer period. Accordingly, an average indicator is required to quantify the degree of LC ordering, i.e., the order parameter S [61], which can be defined as follows:
S = 1 2 ( 3 cos 2 θ − 1 )
where θ is the angle between the long axis of LC molecules and the director. The long axis orientation of molecules in isotropic liquids is disordered, and thus S = 0. At the state of fully parallel LC molecules, we have S = 1. Consequently, the order parameter S, which is utilized to quantify the degree of orientation of molecules with respect to the director, is an important physical property for LCs. However, S is temperature-dependent and will decrease with the increase of the temperature, because LCs will vary from an anisotropic crystalline state to an isotropic liquid state accordingly [11]. The LC director is essential in producing LC biosensors since the spatial orientation significantly affects the characteristics of LCs. As a result of the contact force between LC molecules, an ordered arrangement can be built to realize the function of sensing, and the orientations of LCs will be readjusted by external variables.

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Subjects: Biochemistry & Molecular Biology
Contributors MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register :
Haonan Wang
,
Tianhua Xu
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Yaoxin Fu
,
Ziyihui Wang
,
Mark S. Leeson
,
Junfeng Jiang
,
Tiegen Liu
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