Carbon nanotubes (CNTs) promise to advance a number of real-world technologies. Of these applications, they are particularly attractive for uses in chemical sensors for environmental and health monitoring. However, chemical sensors based on CNTs are often lacking in selectivity, and the elucidation of their sensing mechanisms remains challenging. This review is a comprehensive description of the parameters that give rise to the sensing capabilities of CNT-based sensors and the application of CNT-based devices in chemical sensing. This review begins with the discussion of the sensing mechanisms in CNT-based devices, the chemical methods of CNT functionalization, architectures of sensors, performance parameters, and theoretical models used to describe CNT sensors. It then discusses the expansive applications of CNT-based sensors to multiple areas including environmental monitoring, food and agriculture applications, biological sensors, and national security. The discussion of each analyte focuses on the strategies used to impart selectivity and the molecular interactions between the selector and the analyte. Finally, the review concludes with a brief outlook over future developments in the field of chemical sensors and their prospects for commercialization.

Carbon Nanotube Chemical Sensors

Nucleic acid separation is an increasingly important tool for molecular biology. Before modern technologies could be used, nucleic acid separation had been a time- and work-consuming process based on several extraction and centrifugation steps, often limited by small yields and low purities of the separation products, and not suited for automation and up-scaling. During the last few years, specifically functionalised magnetic particles were developed. Together with an appropriate buffer system, they allow for the quick and efficient purification directly after their extraction from crude cell extracts. Centrifugation steps were avoided. In addition, the new approach provided for an easy automation of the entire process and the isolation of nucleic acids from larger sample volumes. This review describes traditional methods and methods based on magnetic particles for nucleic acid purification. The synthesis of a variety of magnetic particles is presented in more detail. Various suppliers of magnetic particles for nucleic acid separation as well as suppliers offering particle-based kits for a variety of different sample materials are listed. Furthermore, commercially available manual magnetic separators and automated systems for magnetic particle handling and liquid handling are mentioned.

Magnetic particles for separation and purification of nucleic acids

The present review (with 205 refs.) addresses the need for microdevices, presents the basic microfluidic equations and describes the relevant numerical and experimental approaches. Various types and designs of passive and active micromixers are presented. In addition, the relevant effective dimensionless or dimensional parameters and the fabrication technology for different micromixer types are introduced. Different general configurations of lamination, obstacle, convergence-divergence and curved-channel are discussed for passive micromixers. The active micromixers are categorized and described as pressure field driven, acoustic field driven, magnetic field driven, electric field driven and thermal field driven.

Active and passive micromixers: A comprehensive review

The unique combination of mechanical, optical and electrical properties offered by carbon nanotubes has fostered research for their use in many kinds of applications, including the biomedical field. However, due to persisting outstanding questions regarding their potential toxicity when considered as free particles, the research is now focusing on their immobilization on substrates for interface tuning or as biosensors, as load in nanocomposite materials where they improve both mechanical and electrical properties or even for direct use as scaffolds for tissue engineering. After a brief introduction to carbon nanotubes in general and their proposed applications in the biomedical field, this review will focus on nanocomposite materials with hydrogel-based matrices and especially their potential future use for diagnostics, tissue engineering or targeted drug delivery. The toxicity issue will also be briefly described in order to justify the safe(r)-by-design approach offered by carbon nanotubes-based hydrogels.

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Overview of Carbon Nanotubes for Biomedical Applications

Electrochemical impedance spectroscopy (EIS) is a powerful technique used for the analysis of interfacial properties related to bio-recognition events occurring at the electrode surface, such as antibody-antigen recognition, substrate-enzyme interaction, or whole cell capturing. Thus, EIS could be exploited in several important biomedical diagnosis and environmental applications. However, the EIS is one of the most complex electrochemical methods, therefore, this review introduced the basic concepts and the theoretical background of the impedimetric technique along with the state of the art of the impedimetric biosensors and the impact of nanomaterials on the EIS performance. The use of nanomaterials such as nanoparticles, nanotubes, nanowires, and nanocomposites provided catalytic activity, enhanced sensing elements immobilization, promoted faster electron transfer, and increased reliability and accuracy of the reported EIS sensors. Thus, the EIS was used for the effective quantitative and qualitative detections of pathogens, DNA, cancer-associated biomarkers, etc. Through this review article, intensive literature review is provided to highlight the impact of nanomaterials on enhancing the analytical features of impedimetric biosensors.

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Electrochemical Impedance Spectroscopy (EIS): Principles, Construction, and Biosensing Applications

Enhancing the performance of paper-based electrochemical impedance spectroscopy nanobiosensors: An experimental approach.

The pandemic of coronavirus disease 2019 (COVID-19) highlights the importance of rapid and sensitive diagnostics of viral infection that enables the efficient tracing of cases and the implementation of public health measures for disease containment. The immediate actions from both academia and industry have led to the development of many COVID-19 diagnostic systems that have secured fast-track regulatory approvals and have been serving our healthcare frontlines since the early stage of the pandemic. On diagnostic technologies, many of these clinically validated systems have significantly benefited from the recent advances in micro- and nanotechnologies in terms of platform design, analytical method, and system integration and miniaturization. The continued development of new diagnostic platforms integrating micro- and nanocomponents will address some of the shortcomings we have witnessed in the existing COVID-19 diagnostic systems. This Perspective reviews the previous and ongoing research efforts on developing integrated micro- and nanosystems for nucleic acid-based virus detection, and highlights promising technologies that could provide better solutions for the diagnosis of COVID-19 and other viral infectious diseases. With the summary and outlook of this rapidly evolving research field, we hope to inspire more research and development activities to better prepare our society for future public health crises.

Fighting COVID-19: Integrated Micro- and Nanosystems for Viral Infection Diagnostics.

The ability to create reproducible and inexpensive nanofluidic chips is essential to the fundamental research and applications of nanofluidics. This paper presents a novel and cost-effective method for fabricating a single nanochannel or multiple nanochannels in PDMS chips with controllable channel size and spacing. Single nanocracks or nanocrack arrays, positioned by artificial defects, are first generated on a polystyrene surface with controllable size and spacing by a solvent-induced method. Two sets of optimal working parameters are developed to replicate the nanocracks onto the polymer layers to form the nanochannel molds. The nanochannel molds are used to make the bi-layer PDMS microchannel–nanochannel chips by simple soft lithography. An alignment system is developed for bonding the nanofluidic chips under an optical microscope. Using this method, high quality PDMS nanofluidic chips with a single nanochannel or multiple nanochannels of sub-100 nm width and height and centimeter length can be obtained with high repeatability.

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Fabrication of polydimethylsiloxane (PDMS) nanofluidic chips with controllable channel size and spacing

The electroosmotic flow (EOF) velocity in single PDMS nanochannels with dimensions as small as 20 nm is investigated systematically by the current slope method in this paper. A novel method for the fabrication of single nanochannels on PDMS surfaces is developed. The effects of channel size, ionic concentration of the electrolyte solution and electric field on the EOF velocity in single nanochannels are investigated. The results show that the EOF velocity in smaller nanochannels with overlapped electric double layers (EDL) is proportional to the applied electric field but is smaller than the EOF velocity in microchannels under the same applied electric field. The EOF velocity in relatively large nanochannels without the overlap of EDLs is independent of the channel size and is the same as that in microchannels under the same applied electric field. Furthermore, in smaller nanochannels with overlapped EDLs, the EOF velocity depends on the ionic concentration and also on the channel size. The experimental results reported in this paper are valuable for the future studies of electrokinetic nanofluidics.

/pdf/electroosmotic-flow-in-single-pdms-nanochannels-20tcg23rgq.pdf

Ran Peng

Papers

Enhancing the performance of paper-based electrochemical impedance spectroscopy nanobiosensors: An experimental approach.

Fighting COVID-19: Integrated Micro- and Nanosystems for Viral Infection Diagnostics.

Fabrication of polydimethylsiloxane (PDMS) nanofluidic chips with controllable channel size and spacing

Electroosmotic flow in single PDMS nanochannels.

Effects of ionic concentration gradient on electroosmotic flow mixing in a microchannel