Based on the reversible covalent binding between borates and glycoproteins, we proposed a scheme that can specifically recognize and detect immunoglobulin G (IgG). The application of magnetic materials to enrich SERS probes can provide an enhanced signal and repeatability. The results showed that the prepared sandwich-like complex displayed high sensitivity and excellent selectivity for IgG. The Raman peak intensity showed a good linear relationship in the concentration range of 1 mg/mL – 1 ng/mL. The linear equation was y = 657.93x + 2963.9, R² = 0.996. Parallel testing of this sandwich-like complex proved to have excellent repeatability. This method provided a new possibility for clinical non-immunity and the quantitative detection of IgG.

A simple, sensitive, low-cost, quick and reliable square-wave anodic stripping voltammetric method is described for the determination of the antidiabetic drug Linagliptin (LNG) in pure form, tablets, and spiked human urine and plasma samples. Using a pencil graphite electrode (PGE), cyclic voltammetry (CV) was applied to study the electrochemical behavior of LNG. In a Teorell–Stenhagen buffer (pH 5.5) containing 0.1 M NaClO₄ as a supporting electrolyte, the LNG yields an irreversible well-defined oxidation peak at about 1.2 V vs. Ag/AgCl electrode. The various affecting factors, such as the pH, buffer type, supporting electrolyte, accumulation potential, scan rate and accumulation time, were tested and optimized. Also, square-wave adsorptive anodic stripping voltammetric (SWAdASV) studies show that the peak current various linearly over the LNG concentration range of 0.24 – 5.20 μg mL⁻¹ (R² = 0.9994). The detection and quantification limits were calculated to be 0.10 and 0.33 μg mL⁻¹, respectively. The proposed procedure exhibits a good precision, selectivity, and stability and was applied successfully to determine the LNG in pharmaceutical formulations (tablets) and biological fluids (spiked human urine and plasma samples).

Sodium montmorillonite nanoclay particles were modified by 3-aminopropyltrimetoxysilane using a physical vapor deposition method and applied for the simultaneous removal of Cd, Zn, Pb and Ni heavy metals from wastewater samples. Experiments were performed in both batch and column systems. Several parameters that influence the removal efficiency, such as the pH, contact time, amount of adsorbent, interfering ions, flow rate of sample passage and eluent solvent, were evaluated and optimized. The results showed that the adsorption isotherms obeyed Langmuir isotherms for all heavy metals. Also, interfering ions did not influenced the removal efficiency. Finally, modified nanoclay successfully could remove all heavy metals from real wastewater samples to near completeness.

In this study, core-shell Au@Pt nanoparticles (Au@Pt NPs) with peroxidase catalytic activity were synthesized by the seed-mediated method, and were used to catalyze the reaction of luminol–H₂O₂ to enhance the chemiluminescence (CL) intensity. It was found that thiocyanate (SCN⁻) can effectively inhibit the catalytic activity of Au@Pt NPs. Based on this phenomenon, a method to detect SCN⁻ by using the Au@Pt NPs-catalytic luminol–H₂O₂ CL system was established, which has an ultra-low detection limit and an ultra-wide linear range, as well as the advantages of being simple and having low-cost and convenient operation. The research mechanism indicated that SCN⁻ could be adsorbed on the surface of Au@Pt NPs and occupies the active sites of Pt nanostructures, which led to a decrease in the amount of Pt⁰ and a loss of the excellent catalytic activity of Au@Pt NPs. After optimizing the experimental conditions, this assay for detecting SCN⁻ exhibited a good linear range from 5 to 180 nM, and the low detection limit was 2.9 nM. In addition, this approach has been successfully applied to the detection of SCN⁻ in tap-water samples, which has practical application value and embodies good development prospects.

A near-infrared (NIR) and water-soluble probe was synthesized and studied for the detection of Cys/Hcy in aqueous solution, living cells and mice. The probe was composed of cyanine derivative as the NIR fluorescent reporting unit and pyrimidiny-thioether moiety as the Cys/Hcy responsive unit. Treatment with Cys/Hcy induced the formation of sulfur-substituted products, then intramolecular rearrangement reaction would occur to produce amino-substituted products and resulting in enhanced red fluorescence emissions. It could be applied to sense Cys/Hcy both in solution with the detection limit of 0.17 μM (or 0.32 μM) and in living cells. Cell imaging experiments proved that such a probe exhibited good cell penetration. In addition, the probe could detect Cys/Hcy in live mice with strong turn-on fluorescent response.

Saliva has garnered a lot of interest as a non-invasive, easy to collect, and biochemical rich sample for attenuated total reflection–Fourier transform infrared spectroscopy (ATR-FTIR) based disease diagnosis. Although a large number of studies have explored its potential, the preparation methods used differ greatly. For large scale clinical studies to aid translation into clinics, the collection/processing methodology needs to be standardized. Therefore, in this study, we explored different saliva collection (spitting, method A/cotton soaking, method B) and processing protocols (unprepared, TS; supernatant from the centrifugation, CS; and drying, C) to find which gives the best ATR-FTIR signals. Analysis showed highest proteins, carbohydrates, amino acids, and nucleic acid + proteins/lipids in BTS, BCS, ACS, and BC, respectively. Notably, only BC shows a 1377 cm⁻¹ nucleic acid band that is also uniquely identified in multivariate analysis. We conclude that the collection-processing protocol should be based on a biochemical component that best gives a differential diagnosis.

X-ray fluorescence spectrometry using the “standardless” fundamental parameter method has been studied for the whole elemental analysis of magnesium alloys. Twelve major elements were determined: Mg, Al, Si, Ca, Mn, Fe, Ni, Cu, Zn, Ag, Sn and Pb. The specimens used were over 30 mm in diameter and greater than 10 mm thick to determine Sn Kα which has the largest analyzing depth (9 mm) through the alloy samples. The surfaces of the specimens were polished with fine alumina abrasive paper (#240) to remove the oxide layer and to avoid the influence of any surface roughness variation on the intensities of Mg Kα, Al Kα and Si Kα which have smaller analyzing depths. The total quantitative values of the 12 elements, determined by the FP calculation, were normalized to 100 mass%. The analytical values obtained by this method were comparable to those obtained by the conventional calibration curves method. The relative standard deviations were 6.6% for 0.0014 mass% of Ni, and 0.005% for 93.82 mass% of Mg in AZ91 series Mg alloys. The validation results of the proposed method for 12 elements were successful for the five CRMs tested.

A method for the simultaneous extraction and determination of indoor volatile compounds, including volatile organic compounds (VOCs) and semi-volatile organic compounds (SVOCs), was developed using a multi-bed solid phase extraction (SPE)-type collection device. The collection device was prepared by packing styrene-divinylbenzene polymer particles and activated carbon particles. The collected analytes were completely desorbed by passing 7 mL of acetone, and the solvent was then injected into a gas chromatograph–mass spectrometry without the concentration process. Because the proposed method does not require ultrasonication and a concentration process of eluted solvent, quantitative determination of a relatively volatile compound could be achieved. The total recovery including extraction and elution recoveries for all the investigated analytes were in the range from 91.6 to 109%. The limit of quantification was less than 4.0 ng L⁻¹ for all the investigated analytes, and relative standard deviations of the peak area of the analytes in indoor air were less than 12%. The collection device could be reused for over 50 samplings.

A sensitive sensing method was developed for the determination of alkaline phosphatase (ALP) activity based on gold nanocluster (Au NC)-catalyzed luminol–H₂O₂ chemiluminescent (CL) reaction. The CL signal of luminol–H₂O₂–Au NCs can be quenched by ascorbic acid, which was the product of magnesium ascorbyl phosphate (MAP) hydrolysis reaction catalyzed by ALP. The proposed sensing platform showed convenient, sensitive and selective detection of ALP in the range of 0.0027 – 1.3890 U L⁻¹, with the detection limit of 0.0026 U L⁻¹. The broad detection linear range and ultra-high sensitivity were inherited from the efficient free radical scavenging capability of ascorbic acid on the luminol–H₂O₂–Au NCs CL reaction. The CL sensing platform was applied to the detection of ALP activity in serum samples. We believe that this sensing platform is a universal CL strategy for ALP detection because ascorbic acid is an efficient CL quencher for many CL reactions.

The chemical properties of thin (∼0.6 nm) gold oxide layers prepared by an oxygen-dc glow discharge from gold films at room temperature in various solvents and solutions were studied using a surface plasmon resonance (SPR)-based optical waveguide sensing system and X-ray photoelectron spectroscopy (XPS). New insights into the stability and reactivity of gold oxides under these conditions were obtained. The O 1s XPS spectra show three oxygen species, comprising components I, II, and III in the gold oxides, and components I and II are present in this order from the top surface of the oxide (component III). The gold oxide is stable in various solvents (water, methanol, ethanol, acetone, acetonitrile, diethyl ether, chloroform, hydrocarbons) for 10 – 30 min at room temperature. The gold oxide decomposes in aqueous 10⁻² M solutions of acetaldehyde, hydrochloric acid, and sodium hydroxide during these periods. Gold oxide decomposition in these solutions was monitored by SPR and the decomposition rates were obtained. Decomposition of the gold oxides was confirmed and their surfaces were characterized after decomposition by XPS.

Roselle seeds, a waste biomass of the roselle calyx processing industry, were utilized to recover valuable compounds of oil, vitamin E, and water-soluble saccharides. Firstly, ultrasound-assisted extraction (UAE) and conventional stirring extraction were conducted for saccharide extraction, and the advantage of UAE was confirmed. Secondly, oil, vitamin E, and saccharides extracted from Vietnamese roselle seeds by UAE were analyzed for the first time. Oil of tri-, di-, and mono-glycerides, fatty acids of linoleic-, oleic-, palmitic-, and stearic-acids, vitamin E of γ- and α-tocopherol, and saccharides of sucrose, raffinose, stachyose, etc. were identified, and the amounts of these components were compared with those in other country’s roselle seeds. Thirdly, cascade extraction of oil, vitamin E, and saccharides by UAE was investigated with solvents of hexane, hexane:ethyl acetate binary solvent, and water. The results indicated that the order of using solvents was very important for high and selective extraction: the best order to recover oil (almost 100%), vitamin E (95.7%), and saccharides (86.2%) was hexane, and then water.

Liquid chromatography/electrospray ionization–tandem mass spectrometry (LC/ESI-MS/MS) enables the accurate and precise quantification of various analytes at very low concentrations, but it has room for improvement in analysis throughput. Multiplexing of samples in the same injection could be a promising procedure for enhancing the analysis throughput. This could be achieved by derivatization of the multiple samples with multiple isotopologous reagents. In this study, a sample-multiplexed LC/ESI-MS/MS assay using the 1-[(4-dimethylaminophenyl)carbonyl]piperazine (DAPPZ) isotopologues (²H₀-, ²H₃-, and ²H₆-forms) was developed and validated for the simultaneous determination of primary bile acids in three different plasma samples in a single run. The developed method had satisfactory intra- and inter-assay precisions (≤ 2.3 and ≤ 4.2%, respectively) and accuracy (99.0 – 100.3%), and could reduce the total LC/ESI-MS/MS run time by more than 60% for 42 samples compared to the conventional method. Thus, the derivatization with the DAPPZ isotopologues worked well for enhancing the throughput of the LC/ESI-MS/MS assay of the bile acids.

A sensitive method for the quantification of brominated polycyclic aromatic hydrocarbons (BrPAHs) in environmental samples is yet to be developed. Here, we optimized the analytical conditions for liquid chromatography tandem mass spectrometry with atmospheric pressure photoionization and post-column infusion of dopant (LC-DA-APPI-MS/MS). We then compared the sensitivity of our developed method with that of conventional gas chromatography high-resolution MS (GC-HRMS) by comparing the limits of quantification (LOQs) for a range of BrPAHs. Finally, to evaluate our developed method, 12 BrPAHs in sediments and fish collected from Tokyo Bay, Japan, were analyzed; 9 common PAHs were also targeted. The LOQs of the developed analytical method were 14 – 160 times lower than those of GC-HRMS for the targeted BrPAHs. The developed analytical method is a sensitive approach for determining the concentrations of BrPAHs in sediment and fish samples.

Herein, an electrochemical method is presented for the detection of curcumin in food using a carbon nanotube (CNT)-carboxymethylcellulose (CMC) electrode. The CNT-CMC electrode exhibited ideal characteristics for curcumin detection, namely, a high response current and adequate peak separation toward curcumin oxidation. Cyclic voltammetry revealed two oxidation peaks. In the first scan, only the irreversible peak (Peak I) was observed at a higher potential. In the second scan, the reversible redox peak pairs (Peaks II and II′) appeared at lower potentials, and the potential of Peak I was decreased. Peak I corresponded to oxidation of the hydroxyl groups of the benzene ring to the catechol group via a phenoxy radical, while Peaks II and II′ indicated the redox loop system of the generated catechol group. The current at Peak II was used to quantify the concentration of curcumin in the linear range of 1 – 48 μM and detection limit of 0.084 μM. The concentrations of curcumin determined by the CNT-CMC electrode in real food samples were consistent with those determined by high-performance liquid chromatography.

A flow-injection analytical (FIA) system was developed for the determination of cholesterol concentrations based on enzymatic reactions that occurred in a cholesterol oxidase (CHO_x)-immobilized, fused-silica capillary followed by electrochemical detection. The production of hydrogen peroxide from cholesterol in an enzymatic reaction catalyzed by CHO_x was subsequently oxidized electrochemically at an electrode. Our FlA system demonstrated its cost-effectiveness and utility at an applied potential of 0.6 V (vs. Ag/AgCl), a flow rate of 100 μL/min and, under optimal conditions, the resulting signal demonstrated a linear dynamic range from 50 μM to 1.0 mM with a limit of detection (LOD) of 12.4 μM, limit of quantification (LOQ) of 44.9 μM, and the coefficient of variation of 5.17%. In addition, validation of our proposed system using a reference HDL-cholesterol kit used for clinical diagnosis suggested our FIA system was comparable to commercial kits for the determination of the cholesterol incorporation amount in various aqueous liposomal suspensions. These good analytical features achieved by FIA could make the implementation of this methodology possible for on-line monitoring of cholesterol in various types of samples.

A sparse ZnO nanowire array with aspect ratio of ca. 120 and growth rate of 1 μm/h was synthesized by controlling the density of seeds at the initial stage of nanowire growth. The spatially-separated nanowires were cut off from the growth substrate without breaking, and thus were useful in the construction of a single-nanowire device by photolithography. The device exhibited a linear current–voltage characteristic associated with ohmic contact between ZnO nanowire and electrodes. The device further demonstrated a reliable photoresponse with an I_UV/I_dark of ∼100 to ultraviolet light irradiation.

In this paper, we propose an online dilution system for the rapid quantification of radioactive strontium-90 (⁹⁰Sr) with inductively coupled plasma mass spectrometry coupled solid-phase extraction and O₂ dynamic reaction (cascade ICP-MS). The proposed system automatically provides a higher dilution ratio, which is at most 3.3 ± 0.2-times the ratio obtained by the previous method, without increasing the analysis time (<15 min). A detection limit of 2.7 Bq/kg wet (0.54 pg/kg wet) was achieved. The recovery test results were consistent with two different spiked values.

A simple alternative colorimetric assay of chromium in accessories is proposed. A miniature part of a sample was dissolved by acid digestion. With dithiooxamide (DTO) complexes, metal interferences are retained in polyurethane foam synthesized in the lab, while chromium ions present in the eluate. A 100-μL volume of the eluate was measured for the absorbance using a handy spectrometer. The proposed method was successful for chromium assay and the results obtained agreed with the reference (FAAS) method. The amounts of chromium in accessories were found in the range of 100 to 390 mg g⁻¹.

In order to improve plant factories, an appropriate control system on fertilization is urgently required. An automatic management system to control nutrient concentration was constructed using a programmable logic controller (PLC) and ion selective electrodes (ISEs) of nitrate, phosphate, and potassium ion. The concentration of nutrient components in a culture solution was monitored using these ISEs. When the concentration of the nutrient components diminished to the threshold set as an optimum condition (0.1 – 2.0 mM), an appropriate amount of a concentrated solution of each nutrient component was added to the culture solution using solenoid valves connected with the PLC. The present cultivation system was simply constructed without any computers and pumps. Three kinds of automatic control systems simultaneously worked and did not influence each other.