1. Introduction
Biosensor research has attracted considerable attention in the last decades, especially in drug discovery, biomedicine, defense, and security [
1]. A biosensor is a device that uses specific biochemical reactions to produce a measurable signal correlated to the concentration of the target analyte, such as glucose, nucleic acids, proteins, virus, and bacteria. Usually, this analyte is contained in a liquid solution. The biosensor incorporates a biological sensing element that generates a measurable signal from biological interactions. A typical biological interaction can be the binding event between the antibody and the target antigen [
2]. Antibodies are deposited onto the surface of biosensors through a process called functionalization. This process enables the device to react to interactions between the antibodies and the target molecules in the sample, leading to a specific detection response. The biosensor can provide qualitative or quantitative data depending on the correlation mechanism between the response and the amount of bio-analyte detected. The main scope of biosensors is to provide rapid, accurate, and reliable information about the analyte concentration contained in the sensing mean, ideally in real time. From the technological point of view, the essential characteristics of biosensors are stability, sensitivity, selectivity, reproducibility, cost, and size. These parameters compete with each other and are generally chosen after a cost-benefit analysis depending on the specific application.
The scientific field of biosensing is based on several disciplines. Depending on the transduction mechanism, biosensors can be divided into optical, electrochemical, and mechanical. The interaction of the optical field with a biological element is exploited for the operation of optical sensors. They have advantages, such as their high sensitivity and disadvantages, as they suffer from bulky and expensive readout instrumentation [
3]. In contrast, electrochemical sensors take advantage of the enzymatic catalysis of a reaction involving electron exchange. They are generally less sensitive than optical sensors but smaller and more cost-effective [
4]. Mechanical sensors usually offer performance and cost in between the other groups [
5]. Acoustic wave biosensors are a subset of mechanical biosensors that exploit acoustic waves as the transduction mechanism. Acoustic wave biosensors can be divided into two main groups according to the type of acoustic mode: bulk acoustic wave devices (BAW) and surface acoustic wave devices (SAW) [
6]. In the BAW devices, the acoustic wave spreads among the whole volume of the substrate. In SAW devices, the acoustic wave travels on the surface of the substrate, with or without guiding layers. SAW devices can work in the ultra-high-frequency (UHF) range (300 MHz – 3 GHz). Higher frequencies lead to more sensitive devices due to the reduced penetration depth of the acoustic wave into the bulk [
7]. Thus, UHF-SAW devices are very sensitive to substrate surface modifications, such as mass loading, changes in conductivity, and viscosity, [
8] eventually overcoming the sensitivity limitation of mechanical sensors while keeping the low cost.
A possible detection technique that can be used for detecting surface changes in SAW biosensors is the resonant frequency shift technique. This approach involves measuring the variation in the resonance frequency of SAW devices. The interactions on the surfaces lead to a change in the surface density and, thus, to a change in the SAW propagation velocity. This variation can be associated with the concentration of molecules in the sample, thus giving a quantitative analysis. The first attempts to use SAW for biosensing were unsuccessful, as these devices could not function effectively when immersed in fluids. This is because the typical SAW mode, called Rayleigh mode, has a strong displacement component normal to the surface of the substrate. This normal component scatters energy into the fluid and causes pressure waves to be radiated into the liquid. As a result, the SAW is greatly damped and can no longer be exploited for efficient sensing [
9]. To overcome the high attenuation issue, the SAW can be generated as polarized horizontally with respect to the substrate surface. These waves are called shear-horizontal SAW (SH-SAW). SH-SAW devices can be used for measurements also in liquid due to the low coupling of SH-SAW with the solution to be analyzed. [
22] However, they also have disadvantages, such as a low signal-to-noise ratio and limits in the detection performance due to their diffusion into the bulk. [
10] Rayleigh SAW devices, on the other hand, have a higher sensitivity to surface modifications. Recently, SAW technology has been successfully exploited for biosensing even in a liquid environment after a drying step. [
11] Moreover, Rayleigh SAW technology can efficiently perform biosensing and fluid manipulation tasks. [
21] Fluid agitation, mixing, droplet displacement, atomization, and particle displacement within a droplet are all possible with this technology, down to the nanoliter scale. [8, 12-14] Due to the advantages of SAW devices, such as low cost, small size, ease of assembly, and the possibility to work in the UHF range, they have the potential to transform the field of biosensing, where the detection kinetics can be disregarded. [
15]
Several pathologies would benefit from such biosensing technologies. Traumatic brain injuries (TBIs) are one relevant example. Over time, the incidence of traumatic brain injury is increasing significantly. [
16] Early diagnosis is essential to improve the patient's clinical condition. Techniques used for quantification, such as computed tomography (CT), are time-consuming, expensive, and increase the risk of radiation exposure. [
17] Developing a new portable device that can aid the diagnosis of TBIs is an attractive alternative. To this purpose, the glial-fibrillary-acidic-protein (GFAP) has recently become one of the most popular circulating biomarkers for diagnosing TBIs. GFAP levels can reflect the clinical severity and extent of intracranial pathology after TBI. [
18] Therefore, GFAP may be important for diagnosing TBI and other pathologies, intracerebral hemorrhage, or neoplastic diseases, such as glioblastoma multiforme (GBM), are a few examples.
In this work, we characterize UHF-SAW resonator biosensors in terms of acoustic modes generated and biosensing capabilities. We exploit finite element modeling (FEM) techniques to predict the mode behavior for sensing mass adhesion. We then characterize the modes' sensitivity to changes in surface properties, such as temperature and mass changes, and finally test our devices to detect the GFAP biomarker.
4. Conclusions
In this work, we investigated and characterized UHF-SAW resonator biosensors in terms of acoustic modes generated and biosensing capabilities. We used FEM techniques to study the acoustic modes of the resonators and predict their behavior for the detection of bio-analytes. We then characterized the sensitivity of the modes to changes in surface properties, such as temperature and mass changes, and finally tested our devices for GFAP biomarker detection. We observed in such UHF-SAW resonators the presence of two modes, a fast mode and a slow mode, and a strong energy exchange among their components inside the EI. We studied these two modes and showed, using FEM analysis and experimentally with temperature changes and the GFAP biomarker, that the slow mode is generally more sensitive than the fast mode to changes in surface properties, with an average increase of about 1.4 times in sensitivity. This could be due to the fact that inside the EI, the slow mode is more similar to a Rayleigh SAW, while the fast mode is more similar to an SH-SAW. Therefore, since Rayleigh waves are more sensitive, an higher signal to surface change was observed numerically and experimentally. To the best of our knowledge, our work is the first to report the simultaneous presence of these two modes on LN at high frequency and to assess their sensing behavior. Further studies are needed to explain in more detail the sensing mechanisms of these waves in LN or other materials.
Author Contributions
Conceptualization, MA and MC; methodology, AMP and MA; validation, AMP, FL, and DC; investigation, AMP and FL; data curation, AMP, FL, and MA; writing—original draft preparation, AMP and MA; writing—review and editing, FL, DC and MC; supervision, MA; project administration, MA. All authors have read and agreed to the published version of the manuscript.