Synthesis of Colloidal Silver Using Lignosulfonates

Colloidal silver solutions can be used as catalysts for carrying out various chemical transformations of organic substances and solving the problems of disposal of toxic compounds, as well as antibacterial agents for combating pathogenic microflora, in the manufacture of lubricants and light-absorbing materials, coatings, sensors, conductive pastes, and high-performance electrode materials. The research purpose is to study the synthesis of colloidal silver using a solution of technical lignosulfonates (LST) as a stabilizer. Colloidal silver was synthesized as a result of the reduction-oxidation (redox) reaction of Ag(I) cations with glucose at 100 °C in the presence of lignosulfonates. The reaction was carried out in an alkaline medium, which is provided by the addition of ammonia water. Electronic spectroscopy was used to control the synthesis of colloidal silver. After the reaction, the solution turned dark brown and an intense absorption band with a maximum at 400 nm appeared on the electron spectra. The effects of reagent consumption and synthesis duration were studied. It was found that the optimal reagent consumption in the colloidal silver synthesis is as follows: 2.5–5 g glucose / g Ag, 0.3–1 g LST / g Ag, and 3–5 g NH3 / g Ag. The synthesis duration is 2–5 min. The resulting colloidal silver solution is stable for several months. Partial stratification without precipitation is observed during the solution storage. It is shown experimentally that the stratification is followed by a redistribution of colloidal silver particles. Electron spectroscopy confirmed the absence of colloidal silver particles in the upper layer. The reaction kinetics has been studied in experiments carried out under thermostatically controlled conditions at temperatures from 50 to 100 °C. The kinetic dependence is described by a first-order equation at the initial stage of the reaction, the duration of which depends on the temperature. The duration of the active part of the kinetic curves is 15–90 % of the total reaction time. The logarithm of the rate constant on the active section was proved to depend linearly on the reverse thermodynamic temperature (pair correlation coefficient is 0.9887). The activation energy was 47 kJ/mol. For citation: Plakhin V.A., Khabarov Yu.G., Veshnyakov V.A. Synthesis of Colloidal Silver Using Lignosulfonates. Lesnoy Zhurnal [Russian Forestry Journal], 2021, no. 6, pp. 184–195. DOI: 10.37482/0536-1036-2021-6-184-195

Economical droplet-based microfluidic production of [18F]FET and [18F]Florbetaben suitable for human use

Current equipment and methods for preparation of radiopharmaceuticals for positron emission tomography (PET) are expensive and best suited for large-scale multi-doses batches. Microfluidic radiosynthesizers have been shown to provide an economic approach to synthesize these compounds in smaller quantities, but can also be scaled to clinically-relevant levels. Batch microfluidic approaches, in particular, offer significant reduction in system size and reagent consumption. Here we show a simple and rapid technique to concentrate the radioisotope, prior to synthesis in a droplet-based radiosynthesizer, enabling production of clinically-relevant batches of [18F]FET and [18F]FBB. The synthesis was carried out with an automated synthesizer platform based on a disposable Teflon-silicon surface-tension trap chip. Up to 0.1 mL (4 GBq) of radioactivity was used per synthesis by drying cyclotron-produced aqueous [18F]fluoride in small increments directly inside the reaction site. Precursor solution (10 µL) was added to the dried [18F]fluoride, the reaction chip was heated for 5 min to perform radiofluorination, and then a deprotection step was performed with addition of acid solution and heating. The product was recovered in 80 µL volume and transferred to analytical HPLC for purification. Purified product was formulated via evaporation and resuspension or a micro-SPE formulation system. Quality control testing was performed on 3 sequential batches of each tracer. The method afforded production of up to 0.8 GBq of [18F]FET and [18F]FBB. Each production was completed within an hour. All batches passed quality control testing, confirming suitability for human use. In summary, we present a simple and efficient synthesis of clinically-relevant batches of [18F]FET and [18F]FBB using a microfluidic radiosynthesizer. This work demonstrates that the droplet-based micro-radiosynthesizer has a potential for batch-on-demand synthesis of 18F-labeled radiopharmaceuticals for human use.

Microfluidics-Based Single-Cell Research for Intercellular Interaction

Intercellular interaction between cell–cell and cell–ECM is critical to numerous biology and medical studies, such as stem cell differentiation, immunotherapy and tissue engineering. Traditional methods employed for delving into intercellular interaction are limited by expensive equipment and sophisticated procedures. Microfluidics technique is considered as one of the powerful measures capable of precisely capturing and manipulating cells and achieving low reagent consumption and high throughput with decidedly integrated functional components. Over the past few years, microfluidics-based systems for intercellular interaction study at a single-cell level have become frequently adopted. This review focuses on microfluidic single-cell studies for intercellular interaction in a 2D or 3D environment with a variety of cell manipulating techniques and applications. The challenges to be overcome are highlighted.

A Real-Time Method for Improving Stability of Monolithic Quartz Crystal Microbalance Operating under Harsh Environmental Conditions

Monolithic quartz crystal microbalance (MQCM) has recently emerged as a very promising technology suitable for biosensing applications. These devices consist of an array of miniaturized QCM sensors integrated within the same quartz substrate capable of detecting multiple target analytes simultaneously. Their relevant benefits include high throughput, low cost per sensor unit, low sample/reagent consumption and fast sensing response. Despite the great potential of MQCM, unwanted environmental factors (e.g., temperature, humidity, vibrations, or pressure) and perturbations intrinsic to the sensor setup (e.g., mechanical stress exerted by the measurement cell or electronic noise of the characterization system) can affect sensor stability, masking the signal of interest and degrading the limit of detection (LoD). Here, we present a method based on the discrete wavelet transform (DWT) to improve the stability of the resonance frequency and dissipation signals in real time. The method takes advantage of the similarity among the noise patterns of the resonators integrated in an MQCM device to mitigate disturbing factors that impact on sensor response. Performance of the method is validated by studying the adsorption of proteins (neutravidin and biotinylated albumin) under external controlled factors (temperature and pressure/flow rate) that simulate unwanted disturbances.

A Microfluidic Chip-Based MRS Immunosensor for Biomarker Detection via Enzyme-Mediated Nanoparticle Assembly

Conventional immunoassay methods have their common defects, such as tedious processing steps and inadequate sensitivity, in detecting whole blood. To overcome the above problems, we report a microfluidic chip–based magnetic relaxation switching (MRS) immunosensor via enzyme-mediated nanoparticles to simplify operation and amplify the signal in detecting whole blood samples. In the silver mirror reaction with catalase (CAT) as the catalyst, H2O2 can effectively control the production of Ag NPs. The amount of Ag NPs formed further affects the degree of aggregation of magnetic nanoparticles (MNPS), which gives rise to the changes of transverse relaxation time (T2). Both sample addition and reagent reaction are carried out in the microfluidic chip, thereby saving time and reagent consumption. We also successfully apply the sensor to detect alpha-fetoprotein (AFP) in real samples with a satisfied limit of detection (LOD = 0.56 ng/ml), which is superior to the conventional ELISA.

Green Chemistry: A Simple Manual Apparatus for Potentiometric and Conductometric Micro-Titration of Small Samples for the Educational Laboratory

A simple manual micro-titration method is proposed for the potentiometric and conductometric titration of 200 to 800 µL of liquid samples. The sample to be titrated is dispensed into the titration chamber; the bottom section of a plastic test tube that is glued to the center of a small stirring magnet. After inserting the sensing probe and the tip of the titrant delivery tip into the titration chamber, the chamber-stirring magnet assembly is spun at low speed using a conventional magnetic stirrer. Titrant is delivered (with 0.2 µL resolution) from the submerged tip of a 100-µL capacity micro-pipette by rotating the plunger with the locking ring unlocked. The apparatus has been used for potentiometric titration and conductometric titration of acids and bases usually encountered in educational laboratories. Compared with macro-scale titrations, the obtained accuracy was between +2.2% and -3.9% relative error and the precision ranged between 1.6% and 2.9% relative standard deviation. The proposed procedure cuts the reagent consumption to 1% or less compared with conventional macro-scale titrations.

Application of hydrogen peroxide to intensify in-situ leaching of uranium

The current goal in uranium mining is to ensure the maximum effect at minimized costs. One of the problems when using the in-situ leaching (ISL) technology consists in the incomplete mining of the process blocks due to premature uranium content reduction in the pregnant solutions, leading to increased mining times and excessive reagent consumption. The required complete block mining shall be ensured with the highest possible efficiency. The ISL technology is currently used for the mining of all hydrogenous uranium deposits in the Republic of Kazakhstan, which are often characterized by complex geological and hydrogeological conditions. One of these deposits, Semizbay, rates as complexity type III. The conditions at the deposit require increasing the redox potential of the solution by oxidizing Fe2+ into Fe3+. The article considers the addition of hydrogen peroxide to the leaching solutions to improve the redox potential with due account of the mining and geological features of the Semizbay deposit. The pilot tests have established that this oxidizing agent has a positive effect on the uranium content in the pregnant solution with the concentrations of 0.2–0.3 l/m3, provided that the concentration of sulfuric acid in the leaching solutions is within the range of 13–15 g/l. The studies allowed increasing the concentration of uranium in the pregnant solutions from 74 to 114 g/l (i.e., by over 50 %). The authors are grateful to the staff of the geotechnology department of the Semizbay mine, Semizbay-U LLP, for collecting the data and to the staff of the IVT-Zerde LLP laboratory (branch of the Semizbay mine) for the high-quality laboratory experiments during the pilot tests at the mine.

Direct single-molecule imaging for diagnostic and blood screening assays

Every year, over 100 million units of donated blood undergo mandatory screening for HIV, hepatitis B, hepatitis C, and syphilis worldwide. Often, donated blood is also screened for human T cell leukemia–lymphoma virus, Chagas, dengue, Babesia, cytomegalovirus, malaria, and other infections. Several billion diagnostic tests are performed annually around the world to measure more than 400 biomarkers for cardiac, cancer, infectious, and other diseases. Considering such volumes, every improvement in assay performance and/or throughput has a major impact. Here, we show that medically relevant assay sensitivities and specificities can be fundamentally improved by direct single-molecule imaging using regular epifluorescence microscopes. In current microparticle-based assays, an ensemble of bound signal-generating molecules is measured as a whole. By contrast, we acquire intensity profiles to identify and then count individual fluorescent complexes bound to targets on antibody-coated microparticles. This increases the signal-to-noise ratio and provides better discrimination over nonspecific effects. It brings the detection sensitivity down to the attomolar (10−18 M) for model assay systems and to the low femtomolar (10−16 M) for measuring analyte in human plasma. Transitioning from counting single-molecule peaks to averaging pixel intensities at higher analyte concentrations enables a continuous linear response from 10−18 to 10−5 M. Additionally, our assays are insensitive to microparticle number and volume variations during the binding reaction, eliminating the main source of uncertainties in standard assays. Altogether, these features allow for increased assay sensitivity, wide linear detection ranges, shorter incubation times, simpler assay protocols, and minimal reagent consumption.

Simple-Structured OLEDs Incorporating Undoped Phosphorescent Emitters Within Non-Exciplex Forming Interfaces: Towards Ultraslow Efficiency Roll-Off and Low Driving Voltage for Indoor R/G/B Illumination

To meet the requirement of indoor R/G/B monochrome illumination a simplified OLEDs structure and fabrication process must occur. Herein, a design philosophy of low efficiency roll-off and simple-structure OLEDs incorporating R/G/B phosphorescent ultrathin non-doped emissive layers (EMLs) within non-exciplex forming interfaces a luminescent system by a direct charge trapping mechanism has been reported, which uses bis(2-methyldibenzo[f,h]-quinoxaline)(acetylacetonate)iridium(III) (MDQ)2Ir(acac), bis(3-phenylpyridin-e)iridium(III) (Ir(ppy)3), and bis(3,5-difluoro-2 -(2-pyridyl)phenyl-(2-carboxypyridyl) iridiumII) (Firpic) as R/G/B luminescent dyes, respectively. Although the recombination zone is narrow in the designed OLEDs, the efficiency roll-off of the designed OLEDs are unexpectedly slow, due to stable charge trapping of the emitters and are refrained from concentration quenching in relatively low current density, but the luminance meets the requirement of indoor lighting. With a low threshold voltage of 2.9/2.9/3.5 V, the designed R/G/B phosphorescent OLEDs show an efficiency roll-off as low as 7.6/3.2/4.3% for indoor luminance from 10 cd/m2 to 1,000 cd/m2, respectively. The perspective of R/G/B luminescent dyes on luminous efficiency, chromaticity coordinate drifts, efficiency roll-off, and direct charge trapping has been thoroughly studied. Therefore, our research may help to further develop ideal indoor lighting using a simplified undoped R/G/B OLEDs structure with simultaneous ultraslow efficiency roll-off, low threshold voltage, simplified fabrication process, low reagent consumption, and cost.