Detection and Quantification of Multi-Analyte Mixtures Using a Single Sensor and Multi-Stage Data-Weighted RLSE

This work reports the development and experimental verification of a sensor signal processing technique for online identification and quantification of aqueous mixtures of benzene, toluene, ethylbenzene, xylenes (BTEX) and 1, 2, 4-trimethylbenzene (TMB) at ppb concentrations using time-dependent frequency responses from a single polymer-coated shear-horizontal surface acoustic wave sensor. Signal processing based on multi-stage exponentially weighted recursive leastsquares estimation (EW-RLSE) is utilized for estimating the concentrations of the analytes in the mixture that are most likely to have produced a given sensor response. The initial stages of EW-RLSE are used to eliminate analyte(s) that are erroneously identified as present in the mixture; the final stage of EW-RLSE with the corresponding sensor response model representing the analyte(s) present in the mixture is used to obtain a more accurate quantification result of the analyte(s). The success of this method in identifying and quantifying analytes in real-time with high accuracy using the response of just a single sensor device demonstrates an effective, simpler, lower-cost alternative to a sensor array that includes the advantage of not requiring a complex training protocol

Bulk and Surface Acoustic Wave Sensor Arrays for Multi-Analyte Detection: A Review

Bulk acoustic wave (BAW) and surface acoustic wave (SAW) sensor devices have successfully been used in a wide variety of gas sensing, liquid sensing, and biosensing applications. Devices include BAW sensors using thickness shear modes and SAW sensors using Rayleigh waves or horizontally polarized shear waves (HPSWs). Analyte specificity and selectivity of the sensors are determined by the sensor coatings. If a group of analytes is to be detected or if only selective coatings (i.e., coatings responding to more than one analyte) are available, the use of multi-sensor arrays is advantageous, as the evaluation of the resulting signal patterns allows qualitative and quantitative characterization of the sample. Virtual sensor arrays utilize only one sensor but combine itwith enhanced signal evaluation methods or preceding sample separation, which results in similar results as obtained with multi-sensor arrays. Both array types have shown to be promising with regard to system integration and low costs. This review discusses principles and design considerations for acoustic multi-sensor and virtual sensor arrays and outlines the use of these arrays in multi-analyte detection applications, focusing mainly on developments of the past decade

Spiropyran modified PDMS micro-fluidic chip device for photonically controlled sensor array detection of metal ions

Micro‐fluidic chips are particularly attractive in biological and life sciences for analytical purposes because they provide a convenient small platform for rapid analysis and detection [1]. Using micro‐fluidic devices for the determination of ions emerges as a potential solution to some of the challenges not overtaken by conventional techniques e.g. atomic absorption, inductively‐coupled plasma‐optical emission, mass spectrometry and ion‐selective electrodes [2]. For example, these devices can integrate complex sample handling processes, calibration, and detection steps into a compact, portable system. Moreover they require small sample volumes (low μl or nl), consume little power, and are easily constructed for multi‐analyte detection, either through multiple parallel fluidic architectures or by using arrays of detection elements. Organic photochromic compounds like spiropyrans are particularly interesting targets for the development of new approaches to sensing since they offer new routes to multi‐functional materials that take advantage of their photo‐reversible interconversion between two thermodynamically stable states (a spiropyran (SP) form, and a merocyanine (MC) form), which have dramatically different charge, polarity and molecular conformations. Furthermore, they can be easily incorporated into membranes for improved robustness and ease of handling [3], but from our perspective, most interesting of all, they have metal ion‐binding and molecular recognition properties which are only manifested by the MC form. Based on the coordinationinduced photochromism characteristic of the MC form, spiropyrans have been employed as molecular probes for metal ions and organic molecules [4]. In this abstract, we show how through integrating the beneficial characteristics of micro‐fluidic devices and spiropyrans photoswitches, a simple and very innovative chip configured as an on‐line metal ion sensor array can be realised (Figure 1). The micro‐fluidic device consists of five independent 94 μm depth, 150 μm width channels fabricated in polydimethylsiloxane. The spiropyran 1’‐(3‐carboxypropyl)‐3,3’‐dimethyl‐6‐nitrospiro‐1‐benzopyran‐2,2’‐indoline (SP‐COOH) is immobilised by physical adsorption directly on ozone plasma activated PDMS micro‐channel walls. When the colourless, inactive, spiropyran coating absorbs UV light it switches to the highly coloured merocyanine form (MC‐COOH), which also has an active binding site for certain metal ions. Therefore metal ion uptake can be triggered using UV light and subsequently reversed on demand by shining white light on the coloured complex, which regenerates the inactive spiropyran form, and releases the metal ion. When stock solutions of several metal ions (Ca2+, Zn2+, Hg2+, Cu2+, Co2+) are pumped independently through the five channels, different optical responses were observed for each metal (Figure 2), (i.e. complex formation with metal ions is associated with characteristic shifts in the visible spectrum), and the platform can therefore be regarded as a micro‐structured device for online multi‐component monitoring of metal cations

Multi-channel SPR biosensor based on PCF for multi-analyte sensing applications

This paper presents a theoretical investigation of a novel holey fiber (Photonic Crystal Fiber (PCF)) multi-channel biosensor based on surface plasmon resonance (SPR). The large gold coated micro fluidic channels and elliptical air hole design of our proposed biosensor aided by a high refractive index over layer in two channels enables operation in two modes; multi analyte sensing and self-referencing mode. Loss spectra, dispersion and detection capability of our proposed biosensor for the two fundamental modes (HE x 11 and HE y 11 ) have been elucidated using a Finite Element Method (FEM) and Perfectly Matching Layers (PML)

Combined Lab-on-a-Chip and microarray approach for biomolecular interaction sensing using surface plasmon resonance imaging

Surface plasmon resonance imaging (SPR) is a well-established label-free detection technique for real-time biomolecular interaction measurements. An integrated LOC sensing system with fluidic control for sample movement to specific locations on microarray surface in combination with SPR imaging is demonstrated by the measurements of human IgG and anti-IgG interactions from 24 patterned regions.\u

Electroanalytical Sensors and Devices for Multiplexed Detection of Foodborne Pathogen Microorganisms

The detection and identification of pathogen microorganisms still rely on conventional culturing techniques, which are not suitable for on-site monitoring. Therefore, a great research challenge in this field is focused on the need to develop rapid, reliable, specific, and sensitive methods to detect these bacteria at low cost. Moreover, the growing interest in biochip development for large scale screening analysis implies improved miniaturization, reduction of analysis time and cost, and multi-analyte detection, which has nowadays become a crucial challenge. This paper reviews multiplexed foodborne pathogen microorganisms detection methods based on electrochemical sensors incorporating microarrays and other platforms. These devices usually involve antibody-antigen and DNA hybridization specific interactions, although other approaches such as the monitoring of oxygen consumption are also considered

GENETICALLY ENGINEERED AEQUORIN FOR THE DEVELOPMENT OF NOVEL BIOANALYTICAL SYSTEMS

The ability to rationally or randomly modify proteins has expanded their employment in various bioanalytical applications. The bioluminescent protein, aequorin, has been employed as a reporter for decades due to its simplistic, non-hazardous nature and its high sensitivity of detection. More recently aequorin has been subject to spectral tuning. Techniques such as random and site-directed mutagenesis, the incorporation of coelenterazine analogues and the incorporation of non-natural amino acids have expanded the palette of aequorin by altering their emission wavelengths and/or half-lifes. Due to the increased diversity of aequorin, it can be used in multianalyte detection. Although aequorin has been studied extensively and has been used as a reporter in a wide array of applications, it has never been employed as a reporter in systems that involve the splitting of aequorin. Herein we describe the splitting of aequorin in such a way where it becomes the reporter protein in the development of protein-based molecular switches. We have created two distinct protein switches by genetically inserting the glucose-binding protein and the sulfate-binding protein into the aequorin sequence, splitting it in such a manner that it allows for the selective detection of glucose and sulfate, respectively. In a separate investigation, we developed a bioluminescence inhibition binding assay for the detection of hydroxylated polychlorinated biphenyls. These systems have shown that they can be employed in the detection of the respective analyte in biological as well as in environmental samples, which demonstrated a sensitive, fast alternative approach to current methods for on-site screening. Furthermore, we propose the rational design, preparation and use of truncated aequorin fragments in bioanalytical platforms such as multi-analyte detection, protein complementation assays and protein tagging assays based on our discovery that truncated aequorin retains partial bioluminescence emission. One such truncated aequorin demonstrated a large red shift in the emission maximum. It is envisioned that this new red-shifted truncated aequorin will find applications in multi-analyte detection. We anticipate that this work will lead to the discovery of additional functional truncated aequorin fragments that can be employed in novel protein-protein interactions or protein folding systems

A microfluidic device for array patterning by perpendicular electrokinetic focusing

This paper describes a microfluidic chip in which two perpendicular laminar-flow streams can be operated to sequentially address the surface of a flow-chamber with semi-parallel sample streams. The sample streams can be controlled in position and width by the method of electrokinetic focusing. For this purpose, each of the two streams is sandwiched by two parallel sheath flow streams containing just a buffer solution. The streams are being electroosmotically pumped, allowing a simple chip design and a setup with no moving parts. Positioning of the streams was adjusted in real-time by controlling the applied voltages according to an analytical model. The perpendicular focusing gives rise to overlapping regions, which, by combinatorial (bio) chemistry, might be used for fabrication of spot arrays of immobilized proteins and other biomolecules. Since the patterning procedure is done in a closed, liquid filled flow-structure, array spots will never be exposed to air and are prevented from drying. With this device configuration, it was possible to visualize an array of 49 spots on a surface area of 1 mm2. This article describes the principle, fabrication, experimental results, analytical modeling and numerical simulations of the microfluidic chip.\ud \ud \ud \u