However, the developed optosensor exhibited better sensitivity, was faster and easier to operate and can be modified for the enrichment and detection of other target analytes in various sample matrices.Interferon gamma (IFNγ) is a cytokine and an immunochemical marker that can be used for revealing of infectious diseases and especially for distinguishing of viral and some types of bacterial infections. Blood tests for IFNγ are typically based on immunoassays like Enzyme-Linked Immunosorbent Assay (ELISA). In this paper, a biosensor working on the principle of quartz crystal microbalance (QCM) was developed as an alternative to the standard analytical methods for IFNγ. The biosensor contained antibodies against IFNγ immobilized on QCM and also on gold nanoparticles. find more A sandwich containing QCM, gold nanoparticles and IFNγ was formed and formation of the sandwich caused decrease of oscillation frequency. The assay exerted limit of detection 5.7 pg/ml for a sample sized 50 μl and one measuring cycle was finished within 90 min. The assay by biosensor fully correlated to standard ELISA. In a conclusion, the biosensor appears to be a fully applicable analytical tool for a simple assay of IFNγ. Overall simplicity and no special requirement on staff and equipment are the major advantages of the here presented assay.In this paper, a supercritical fluid chromatography method using ultra-violet and evaporative light scattering detections (SFC-UV/ELSD) has been developed and validated for the stoichiometry determination of an antiemetic drug with its counter-ion i.e. ondansetron hydrochloride. Seven stationary phases were first screened using a CO2-methanol-diethylamine mobile phase. Best conditions were determined using Derringer's desirability functions regarding chromatographic separation selectivity, resolution, peak shape and runtime. The influence of co-solvent composition on resolution was evaluated. After optimization, best chromatographic results were obtained using 2-ethylpyridine stationary phase and a co-solvent composed of 0.2% diethylamine and 2% water in methanol. While ondansetron was quantified using UV detection (214 nm) and an external calibration curve, the determination of chloride was carried out using ELSD and an internal calibration curve. Then, the method was validated using the accuracy profile approach with a total error included in the ±10%. Finally, the proposed method was applied for the determination of the molar ratio between ondansetron and chloride. A value of 1.001 ± 0.003 demonstrated that the stoichiometry of this drug with its counter-ion was 11.Two probes based on tetrahydroxanthylium unit (probe 1a) and methyltetrahydroxanthylium unit (probe 1b) were designed and synthesized for the detection of hydrazine. Probes 1a-b exhibited turn-on red emission signal and high selectivity toward NH2NH2. The response time of probe 1a to NH2NH2 was more than 60 min, while that of probe 1b was less than 30 min. The detection limits of probes 1a-b were calculated as 210 nM and 110 nM respectively. What's more, the tolerance experiments showed that methyltetrahydroxanthylium unit possessed higher tolerance toward nucleophiles. Moreover, cells imaging experiments demonstrated that probe 1b could detect exogenous NH2NH2 in living HeLa cells.A Multi-Syringe Flow Injection Analysis (MSFIA) fluorometric system based on a 3D printing device hosting a CCD detector has been designed for the determination of quinine in soft drinks. A LED controlled by an electronic circuit was used as a radiation source. The entire system is connected to two USB outputs of a computer. The AutoAnalysis program has been used for data acquisition and treatment. The results are more accurate and precise than those obtained with a manual method using a conventional spectrofluorometer. This developed system is a viable alternative to reduce the consumption of reagents, the impact on the environment and reduce measurement costs.In this work, a portable and reliable optical emission spectrometric (OES) instrument based on solid acid hydride generation (HG) and subsequent in situ dielectric barrier discharge (DBD) preconcentration was first developed for simultaneous and field analysis of ultratrace As and Sb in environmental water. In situ DBD fulfilled both gas phase enrichment (GPE) and excitation; effective enrichment made it possible to use a low-cost charge coupled device (CCD) as detector. To simplify field protocol, solid tablet made from sulfamic acid was first used to replace hydrochloric acid for co-generation of As and Sb hydrides. Moisture interference was eliminated by carrier gas sweeping without any desiccant. After calculating peak volume for emission data handling, detection limits (LODs) were 0.5 μg L-1 for As and 0.2 μg L-1 for Sb, respectively, with 0.995) were 2-200 μg L-1 for As and 1-200 μg L-1 for Sb, respectively. The results agreed with certified values of CRMs and recoveries were 87-97% vs. inductively coupled plasma mass spectrometry. The running costs can be controlled within one dollar per use. This HG-in situ DBD trap-OES scheme, with demonstrated advantages in sensitivity, low-cost, power ( less then 60 W), size (0.6 m × 0.5 m × 0.3 m), weight (15 kg), gas consumption (300 measurements per 4 L tank), and multi-element capability, was implemented in a miniature spectrometer for field analysis.Obtaining the fingerprints of polysaccharides was known to be notoriously difficult by ambient mass spectrometry due to their resistance for desorption and ionization. Ambient mass spectrometry technology has recently been recognized as a quick analysis tool for obtaining fingerprints, which is attributed to its characteristics of no sample pretreatment and easy operation under atmospheric pressure. However, it still remains a challenge for accurate identification of the fingerprints of macromolecular polysaccharides by ambient micro-fabrication glow discharge plasma (MFGDP). In this study, a simplified methylation method was introduced to realize rapid analysis of polysaccharide mixture by MFGDP with the assistance of a temperature-programmed system (TPS). At the optimal temperature of TPS, oligosaccharides, plant polysaccharides and polysaccharide mixtures were all well characterized by TPS-MFGDP. In the proposed method, the characteristic [M + NH4] + adduct ions of oligosaccharides ions of oligosaccharides that are difficult for other ambient mass spectrometric methods were abundantly produced, making it possible to simultaneously identify a mixture of five or more polysaccharides.