We propose a novel concept for detecting color transition by the inner product (IP) of RGB unit vectors. A digital microscope-based detector and a Visual Basic program were developed in-house. The concept is applied to indicator-based flow titration. The IP is 1 or < 1 if the vector’s direction is the same or different, respectively. The IP’s change can be used as a criterion for the indicator’s color transition. The present IP-based approach is simple, economical, and versatile because it is applicable to any color transition without selecting an analytical wavelength.

G-quardruplex (G4) DNA forms through the gathering together of G-quartet planes formed with four guanine (G) bases. G4 DNA stabilizes with potassium ions (K⁺) by coordination with the G-quartet center. Fluorometric G4 DNA carrying the fluorescence resonance energy transfer (FRET) chromophore pair at both termini has been applied for the fluorometric sensing or imaging of K⁺ under a homogeneous aqueous medium. This system has realized non-conventional K⁺ selectivity over the sodium ion (Na⁺). The selectivity of the fluorescence G4 was converted to Na⁺ from K⁺ with a modification of its sequence. On the other hand, G4 DNA detection has been achieved in terms of cancer diagnosis because of a strong relationship of G4 DNA and cancer development. Ligands interacting with G4 are expected to have anti-cancer potential. In addition, fluorometric G4 ligands have been developed and tested as tools for the dynamic monitoring of G4 in living cells. Moreover, fluorometric G4 DNA has been utilized to evaluate the G4 ligand performance.

DNA aptamers, which are short, single-stranded DNA sequences that selectively bind to target substances (proteins, cells, small molecules, metal ions), can be acquired by means of the systematic evolution of ligands by exponential enrichment (SELEX) methodology. In the SELEX procedure, one of the keys for the effective acquisition of high-affinity and functional aptamer sequences is the separation stage to isolate target-bound DNA from unbound DNA in a randomized DNA library. In this review, various remarkable advancements in separation techniques for SELEX-based aptamer selection developed in this decade, are described and discussed, including CE-, microfluidic chip-, solid phase-, and FACS-based SELEX along with other methods.

Recently, single cell analysis is becoming more and more important to elucidate cellular heterogeneity. Except for nucleic acid that can be amplified by PCR, the required technical level for single cell analysis is extremely high and the appropriate design of sample preparation and a sensitive analytical system is necessary. Capillary/microchip electrophoresis (CE/MCE) can separate biomolecules in nL-scale solution with high resolution, and it is highly compatible with trace samples like a single cell. Coupled with highly sensitive detectors such as laser-induced fluorescence and nano-electrospray ionization–mass spectrometry, zmol level analytes can be detected. For further enhancing sensitivity, online sample preconcentration techniques can be employed. By integrating these high-sensitive techniques, single cell analysis of metabolites, proteins, and lipids have been achieved. This review paper highlights successful research on CE/MCE-based trace bioanalysis in recent 10 years. Firstly, an overview of basic knowledge on CE/MCE including sensitivity enhancement techniques is provided. Applications to trace bioanalysis are then introduced with discussion on current issues and future prospects.

Carbon materials have been widely used for electrochemical analysis and include carbon nanotubes, graphene, and boron-doped diamond electrodes in addition to conventional carbon electrodes, such as those made of glassy carbon and graphite. Of the carbon-based electrodes, carbon film has advantages because it can be fabricated reproducibly and micro- or nanofabricated into electrodes with a wide range of shapes and sizes. Here, we report two categories of hybrid-type carbon film electrodes for mainly electroanalytical applications. The first category consists of carbon films doped or surface terminated with other atoms such as nitrogen, oxygen and fluorine, which can control surface hydrophilicity and lipophilicity or electrocatalytic performance, and are used to detect various electroactive biochemicals. The second category comprises metal nanoparticles embedded in carbon film electrodes fabricated by co-sputtering, which exhibits high electrocatalytic activity for environmental and biological samples including toxic heavy metal ions and clinical sugar markers, which are difficult to detect at pure carbon-based electrodes.

A nanoporous material has been applied for the development of functional nanobiomaterials by utilizing its uniform pore structure and large adsorption capacity. The structure and stability of biomacromolecules, such as peptide, oligonucleotide, and protein, are primary factors to govern the performance of nanobiomaterials, so that their direct characterization methodologies are in progress. In this review, we focus on recent topics in the structural characterization of protein molecules adsorbed at a nanoporous material with uniform meso-sized pores. The thermal stabilities of the adsorbed proteins are also summarized to discuss whether the structure of the adsorbed protein molecules can be stabilized or not.

Aerosol droplets play a critical role in the development of weather patterns, yet are notoriously difficult to analyze because of their small size, transient nature and potentially complex composition. As a result, there has been a surge in recent years in the development of analysis techniques aimed at the study of aerosol droplets, namely of their surface tension properties, which are thought to play a great role in aerosol/cloud growth and subsequently having an impact on the resulting weather patterns. To capture the state of the field at this key time, we have collected and described some of the most relevant and influential studies, with a focus on those that have had the most impact. This review will present and describe the most used analytical techniques for studying the surface tension of micrometer-sized aqueous droplets, with a focus on historical trends and how the current techniques are posed to revolutionize the field.

Physical forces, such as dielectric, magnetic, electric, optical, and acoustic force, provide useful principles for the manipulation of particles, which are impossible or difficult with other approaches. Microparticles, including polymer particles, liquid droplets, and biological cells, can be trapped at a particular position and are also transported to arbitrary locations in an appropriate external physical field. Since the force can be externally controlled by the field strength, we can evaluate physicochemical properties of particles from the shift of the particle location. Most of the manipulation studies are conducted for particles of sub-micrometer or larger dimensions, because the force exerted on nanomaterials or molecules is so weak that their direct manipulation is generally difficult. However, the behavior, interactions, and reactions of such small substances can be indirectly evaluated by observing microparticles, on which the targets are tethered, in a physical field. We review the recent advancements in the manipulation of particles using a physical force and discuss its potentials, advantages, and limitations from fundamental and practical perspectives.

In this review, we cite references from the period between 2015 and 2020 related to the use of a flow-based system as a tool to obtain a modern analytical system for speeding up data production and improving performance. Based on a great deal of concepts for automatic systems, there are several research groups introduced in the development of flow-based systems to increase sample throughput while retaining the reproducibility and repeatability as well as to propose new platforms of flow-based systems, such as microfluidic chip and paper-based devices. Additionally, to apply a developed system for on-site analysis is one of the key features for development. We believe that this review will be very interested and useful for readers because of its impact on developing novel analytical systems. The content of the review is categorized following their applications including quality control and food safety, clinical diagnostics, environmental monitoring and miscellaneous.

Ion-exclusion chromatography (IEC) is categorized as a type of ion chromatography and is recognized as a simple and convenient water quality monitoring technology for a variety of ionic and nonionic substances. This review, mainly focusing on historical milestone studies by various authors, outlines the archives that concern the separation sciences and practical applications obtained from a variety of IEC modes used for water-quality monitoring as follows: (1) early-developed IEC; (2) IEC using enhanced conductivity detection for weak ionic substance; (3) IEC using nonionic substances eluents such as sugars or polyols; (4) vacancy IEC based on a novel separation concept; (5) applications to the water quality monitoring of inorganic ionic-nutrients; (6) simultaneous IEC and cation-exchange chromatography of anions and cations; and (7) the multicomponent IEC combining different separation modes and detection methods with the expansion of applicable fields, such as for food analysis or material evaluations.

Polyoxometalates (POMs) have been used for spectrophotometric determinations of silicon and phosphorus under acidic conditions, referred to as the molybdenum yellow method and molybdenum blue method, respectively. Many POMs are redox active and exhibit fascinating but complicated voltammetric responses. These compounds can reversibly accommodate and release many electrons without exhibiting structural changes, implying that POMs can function as excellent mediators and can be applied to sensitive determination methods based on catalytic electrochemical reactions. In addition, some rare-earth-metal-incorporated POMs exhibit fluorescence, which enables sensitive determination by the enhancement and quenching of fluorescence intensities. In this review, various analytical applications of POMs are introduced, mainly focusing on papers published after 2000, except for the molybdenum yellow method and molybdenum blue method.

This review summarizes recent progress in solvent extraction of rare earth elements (REEs) using an ionic liquid (IL) as the extraction solvent. These IL extraction systems are advantageous owing to the affinity of ILs for both charged and neutral hydrophobic species, in contrast to conventional organic solvent extraction systems. Herein, REE extraction studies using ILs are detailed and classified based on the type of extraction system, namely extraction using anionic ligands, extraction using neutral ligands, synergistic extraction, extraction without extractants, and a specific system using task-specific ionic liquids (TSILs). In IL extraction systems, the extracted complexes are often different from those in organic solvent systems, and the REE extraction and separation efficiencies are often significantly enhanced. Synergistic IL extraction is an effective approach to improving the extractability and separability of REEs. The development of novel TSILs suitable for IL extraction systems is also effective for REE separation.

In recent years, the utilization of high-technology metals such as rare earth elements (REEs), which exist in extremely low quantities in the Earth, has rapidly increased with the development of new types of industrial materials and pharmaceutical products. This review provides an overview of a new type of potential anthropogenic pollution caused by high-technology metals, with a focus on REEs released into environmental waters from waste treatment plants. In this paper, potential anthropogenic pollution was defined as pollution caused by metals gradually enriched in the environment by human activity, although standard and guideline concentrations of these elements are not regulated by environmental quality standards for water pollution. We review the analytical methods of REEs and the potential anthropogenic pollution of REEs with a focus on Gd, from the viewpoints of a comparison of the degree of Gd anomaly, chemical speciation, ecotoxicology, and bioaccessibility. Moreover, we also highlight the comprehensive analysis based on multielement analysis of high-technology metals as well as REEs for the further screening for potential anthropogenic pollution.

Pyrolysis is considered to be a promising method for polymer characterization (in the field of analytical pyrolysis) and for chemical feedstock recovery from plastic wastes (in the field of applied pyrolysis) because it can decompose any polymeric material into smaller molecules by applying heat alone in an inert atmosphere. Pyrolysis–gas chromatography (Py-GC) involves pyrolyzing polymeric materials in a micropyrolyzer and a subsequent direct GC analysis of pyrolyzates. Py-GC has immense potential for applications in the fields of both analytical and applied pyrolysis, as it allows for rapid and accurate analysis of pyrolyzates. This is beneficial for elucidating microstructure and composition of polymers and for a rapid screening of pyrolysis conditions for designing feedstock recycling processes. In this review, we examined the latest research trends in Py-GC applications for polymer characterization, analysis of plastics in the environment, and chemical feedstock recovery from plastics.

In this review, we summarize the methods of sample introduction into a gas chromatograph. For volatile organic compounds, headspace measurements and purge-trap methods have been used traditionally. Recently, the trapped headspace method has been used in water quality testing. In addition, various solid-state adsorption methods have been developed, including a method in which the adsorbent is placed inside a needle, while new adsorbents and their applications have also been introduced.

The crystalline sponge (CS) method was developed as an X-ray crystallographic molecular structure analysis method that can be performed without the need for crystallization of the analyte. CS has strong molecular-recognition properties and a highly flexible framework. The amount of analyte can be reduced to a sub-milligram level. These features of the crystalline nano-space allow for determining the absolute structure of a trace analyte. In this review, we focus on the discovery of the CS method and its applications to biosynthetic products in combination with NMR spectroscopy. We also describe some examples of the CS method that are used mainly in combination with mass spectrometry (MS). Both approaches demonstrate the potential of microanalysis to determine the molecular structure of an unknown sample. Finally, we mention the use of a crystalline “nano-surface” rather than a crystalline nano-space in MS, which can detect small metabolites as well as post-translation biomolecules.

The kilogram is the unit of mass and was defined in 1889 by the international prototype of the kilogram. The mole is the unit of amount of substance and was defined in 1960 by the number of atoms in 0.012 kg of ¹²C. These definitions were revised in May 2019. The new definitions of the kilogram and the mole are based on the Planck constant h and the Avogadro constant N_A, respectively. The values of h and N_A used in the new definitions were determined by summarizing measurement results of the two physical constants by several national metrology institutes around the world. In this review, the history of the two units and measurement technologies used to derive the new definitions are described. The effect of the revision on the development of new measurement technologies is also introduced.

High-value agricultural products are characterized by the geographical conditions of the production areas such as climatic and soil conditions. These products are protected by the geographical indication (GI) protection system, which has been introduced in more than 100 countries. Because GI products are expensive in the market, products are often mislabeled as GI. Thus, there is an urgent need for the development of analytical methods that enable the tracing of geographical origins of food materials. Stable isotope analysis is used to trace the geographical origin of food materials. In this study, we review the applications for tracing the geographical origin of agricultural products (especially rice, beef, and honey) focusing on an analytical method for analyzing stable isotopes (δD, δ¹³C, δ¹⁵N, δ¹⁸O, and δ³⁴S).

Thermal analysis and calorimetry share a close relationship in the field of thermal research. With regards to the specific heat capacity, researchers have been able to realize absolute measurement techniques by utilizing drop, conduction, and adiabatic methods that are used in calorimetry. Furthermore, it is possible to optimize differential scanning calorimetry, which is a comparative measurement technique for the specific heat capacity used in thermal analysis, by improving the absolute measurement techniques. At the National Metrology Institute of Japan (NMIJ), we developed a new certified reference material (CRM) for comparatively measuring the specific heat capacity, the single-crystalline silicon-NMIJ CRM 5806a, using a new type of cryogenic adiabatic calorimeter equipped with a pulse-tube refrigerator working in the temperature range from 50 to 350 K. This CRM was produced in accordance with the quality specifications of NMIJ, and complies with the ISO/IEC 17025, ISO 17034, and ISO GUIDE 35 standards. This paper reports on the procedure for fabricating this CRM and using it to perform specific heat capacity measurements at low temperatures. The specific heat capacity was measured using a differential scanning calorimeter in the temperature range from 280 to 340 K. NMIJ CRM 5806a was used to calibrate the heat flow. It was found that the uncertainty evaluation became easier because one factor of the uncertainty evaluation could be removed using the CRM. We show that the development of the CRM using the adiabatic calorimeter has led to an improvement in the specific heat capacity measurement results obtained by the differential scanning calorimeter.

Various kinds of polysaccharides found in a wide variety of plants, bacteria, crustaceans and insects form hydrogels via physical aggregation in aqueous media. The major mass of hydrogels is water filled, ca. 95 – 99.5%, in a network structure, although the solid shape of the gel is maintained. In this paper, firstly the wide range of gelation mechanisms are briefly described, and then the thermal analysis of representative gel-forming polysaccharides, such as carrageenan, alginate, galactomannan, and pectin, is introduced. By differential scanning calorimetry (DSC), gel-sol and the sol-gel transition temperature of thermoreversible hydrogels are measured and phase diagram is established. It is suggested that binary systems showing sinusoidal gel-sol-gel transition are capable of being assembled. By thermomechanical analysis (TMA), the dynamic modulus (E′) at around 1 × 10⁴ Pa of thermo-irreversible hydrogels was obtained using a sample holder designed to measure the viscoelastic properties in water. Reliable coordination is shown between the results obtained by DSC and TMA. In this review, the current research and several topics on concerning the thermal properties of polysaccharide physical hydrogels are introduced.