This review introduces the basic concepts and terms associated with impedance and techniques of measuring impedance. The focus of this review is on the application of this transduction method for sensing purposes. Examples of its use in combination with enzymes, antibodies, DNA and with cells will be described. Important fields of application include immune and nucleic acid analysis. Special attention is devoted to the various electrode design and amplification schemes developed for sensitivity enhancement. Electrolyte insulator semiconductor (EIS) structures will be treated separately.

The use of electrochemical impedance spectroscopy for biosensing

Publisher Summary The electroactivity of nucleic acids was discovered several years ago. It was shown that at mercury electrodes, adenine and cytosine were reduced in ssDNA while guanine produced an anodic signal due to the oxidation of guanine reduction product. The DNA signals at mercury electrodes are highly sensitive to changes in DNA structure due to DNA denaturation and renaturation, as well as to minor structural changes resulting from DNA premelting and DNA damage. The changes in DNA structure are reflected not only by the DNA faradaic responses but also by non-faradaic signals due to adsorption/desorption of DNA. Several interesting principles have been used in the development of the DNA sensors—such as amplified electrochemical analysis, investigation of charge transport, and tracing of changes in conformation of DNA. The s ensors for DNA hybridization and DNA damage lead the field of the electrochemistry of nucleic acids. The chapter briefly summarizes some properties of the elimination voltammetry with linear scan (EVLS) method. Oscillographic polarography, at controlled alternating current, was used in the electrochemical analysis of nucleic acids.

Electrochemistry of nucleic acids.

Advances in biosensors: Principle, architecture and applications ☆

Effective pathogen detection is an essential prerequisite for the prevention and treatment of infectious diseases. Despite recent advances in biosensors, infectious diseases remain a major cause of illnesses and mortality throughout the world. For instance in developing countries, infectious diseases account for over half of the mortality rate. Pathogen detection platforms provide a fundamental tool in different fields including clinical diagnostics, pathology, drug discovery, clinical research, disease outbreaks, and food safety. Microfluidic lab-on-a-chip (LOC) devices offer many advantages for pathogen detection such as miniaturization, small sample volume, portability, rapid detection time and point-of-care diagnosis. This review paper outlines recent microfluidic based devices and LOC design strategies for pathogen detection with the main focus on the integration of different techniques that led to the development of sample-to-result devices. Several examples of recently developed devices are presented along with respective advantages and limitations of each design. Progresses made in biomarkers, sample preparation, amplification and fluid handling techniques using microfluidic platforms are also covered and strategies for multiplexing and high-throughput analysis, as well as point-of-care diagnosis, are discussed.

Microfluidic designs and techniques using lab-on-a-chip devices for pathogen detection for point-of-care diagnostics

Recent advances in self-assembled monolayers based biomolecular electronic devices.

We investigate the analytical performance of an interdigitated electrode sensor for the label-free detection of DNA, by monitoring the complex impedance of 5 µm wide interdigitated Pt microelectrodes on a glass substrate. We detect the hybridization of unlabeled 38-mer target ssDNA with a complementary probe that is bound on the glass in between the electrodes by a disuccinimidyl terephtalate and aminosilane immobilization procedure. The sensor is mounted in a microfluidic flow cell, in which hybridization is monitored and in situ compared with a reference. After hybridization, the cell is perfused with deionised water and the dependence of the measured conductance due to the immobilized target DNA layer, to target DNA concentrations down to 1 nM is demonstrated. Subsequently, we apply our sensor to the detection of pathogen DNA from Salmonella choleraesuis in dairy food.

Label-free detection of DNA with interdigitated micro-electrodes in a fluidic cell.

Two types of DNA biosensors are presented. Both sensing principles are demonstrated using synthetic oligomer single-stranded DNA (ssDNA) with concentrations in the micromolar range. A first sensor type is based on the detection of fluorescently labeled ssDNA to a complementary probe that is bound to a silicon substrate by a disuccinimidyl terephtalate and aminosilane immobilization procedure. An enhanced fluorescent response is obtained using constructive interference effects in a fused silica layer deposited before immobilization onto the silicon substrate. The selectivity of different DNA probes towards complementary and non-complementary DNA targets is tested. A second type of DNA sensor is based on the impedimetric response of a solution of unlabeled 20-mer ssDNA in de-ionized water. Interdigitated microelectrodes that are 5 μm wide and separated by 5 μm gaps are microfabricated on glass substrates and the complex impedance of the system in the 100 Hz–100 MHz frequency range is investigated. The proportionality between the measured solution resistance and ssDNA concentration is demonstrated.

DNA biosensor using fluorescence microscopy and impedance spectroscopy

A contactless microfluidic dosing system based on actuation by an electrochemical reaction has been designed and tested. The device is composed of two chambers separated by a polydimethylsiloxane (PDMS) plate. One chamber is loaded with the liquid sample to be dosed while the electrochemical reaction occurs in the second chamber. Due to the strict separation between the reaction responsible of the actuation and the sample, the latter is preserved from contamination and/or electrochemical modification. Silicon master microstructures were fabricated using clean-room technologies and subsequently replicated into the PDMS. A full microsystem has been fabricated and tested. Microliter sample solutions can be easily and reproducibly dispensed in a time frame of a few tens of seconds.

Contactless Electrochemical Actuator for Microfluidic Dosing

The scope of this work has been the design of a mechanical actuator in polydimethylsiloxane (PDMS) / glass for precise liquid sampling, based on the electrochemical generation of O2. The device is composed of two chambers separated by a PDMS membrane. In the first chamber, the generated gas bends the membrane, actuating a precise volume of a liquid sample in the second chamber. The linear relationship between the number of transferred charges and the number of gaseous O2 molecules allows a very accurate control of the dispensed volume.

Contactless electrochemical actuator for precise sampling on microchip

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Label-free detection of DNA with interdigitated micro-electrodes in a fluidic cell.

DNA biosensor using fluorescence microscopy and impedance spectroscopy

Contactless Electrochemical Actuator for Microfluidic Dosing

Contactless electrochemical actuator for precise sampling on microchip