scholarly journals Siphon-Induced Droplet Break-Off for Enhanced Mixing on a Centrifugal Platform

Inventions ◽  
2019 ◽  
Vol 5 (1) ◽  
pp. 1 ◽  
Author(s):  
Robert Burger ◽  
David J Kinahan ◽  
Hélène Cayron ◽  
Nuno Reis ◽  
João Fonseca ◽  
...  
Keyword(s):  
Human Plasma ◽  
Spectroscopic Method ◽  
Colorimetric Method ◽  
Phosphate Buffer Solution ◽  
Potassium Thiocyanate ◽  
Single Step ◽  
Buffer Solution ◽  
Batch Mode ◽  
Two Fluids ◽  
Pass Through

We present a powerful and compact batch-mode mixing and dilution technique for centrifugal microfluidic platforms. Siphon structures are designed to discretize continuous flows into a sequence of droplets of volumes as low as 100 nL. Using a passive, self-regulating 4-step mechanism, discrete volumes of two fluids are alternatingly issued into a common intermediate chamber. At its base, a capillary valve acts as a fluidic shift register; a single droplet is held in place while two or more droplets merge and pass through the capillary stop. These merged droplets are advectively mixed as they pass through the capillary valve and into the receiving chamber. Mixing is demonstrated for various combinations of liquids such as aqueous solutions as well as saline solutions and human plasma. The mixing quality is assessed on a quantitative scale by using a colorimetric method based on the mixing of potassium thiocyanate and iron(III) chloride, and in the case of human plasma using a spectroscopic method. For instance, volumes of 5 µL have been mixed in less than 20 s. Single-step dilutions up to 1:5 of plasma in a standard phosphate buffer solution are also demonstrated. This work describes the preliminary development of the mixing method which has since been integrated into a commercially available microfluidic cartridge.

Investigation of the Effects of Various Cyclodextrins on the Stabilisation of Human Serum Albumin by a Spectroscopic Method

2015 ◽  
Vol 68 (12) ◽  
pp. 1894 ◽  
Author(s):  
Mohsen Oftadeh ◽  
Golamreza Rezaei Behbahani ◽  
Ali Akbar Saboury ◽  
Shahnaz Rafiei
Keyword(s):  
Human Serum Albumin ◽  
Serum Albumin ◽  
Human Serum ◽  
Electrostatic Interactions ◽  
Spectroscopic Method ◽  
Phosphate Buffer Solution ◽  
Blue Shift ◽  
Titration Calorimetry ◽  
Tryptophan Residue ◽  
Buffer Solution

The binding parameters between cyclodextrins (CDs) and human serum albumin (HSA) were investigated by isothermal titration calorimetry (ITC), fluorescence quenching, and UV-vis absorption spectroscopy at 300 K in 50 mM phosphate buffer solution. Among the various CDs investigated, β-CD has the greater ability to decrease the aggregation of HSA and the results indicated that the inhibition order is γ-CD < α-CD < β-CD. The obtained heats for HSA+CDs interactions were reported and analysed in terms of the extended solvation model, which was used to reproduce the enthalpies of HSA interactions with CDs over a broad range of complex concentrations. The binding constant and thermodynamic parameters were obtained. These suggested that the binding reaction was driven by both enthalpy and entropy, and electrostatic interactions played a major role in the stabilising of HSA. The parameters and reflected the net effect of β-CD on the HSA stability at low and high cyclodextrin concentrations, respectively. The positive values for indicated that β-CD stabilises the HSA structure at low concentrations. The UV absorption intensity of theses complexes increased and a slight red shift was observed in the absorbance wavelength with increasing the CD concentration. The fluorescence intensity of HSA decreased regularly and a slight blue shift was observed for the emission wavelength with increasing CD concentration. The results indicate that the CD complex could quench the fluorescence of HSA and changes the microenvironment of the tryptophan residue.

Detection of Hepatitis a Virus in Drinking Water by Enzyme -Immunoassay Using Ultracentrifugation for Virus Concentration

1985 ◽  
Vol 17 (10) ◽  
pp. 39-41 ◽  
Author(s):  
A. Schnattinger
Keyword(s):  
Membrane Filtration ◽  
Hepatitis A ◽  
Hepatitis A Virus ◽  
Solid Phase ◽  
Phosphate Buffer Solution ◽  
Enzyme Linked Immunosorbent Assay ◽  
Virus Concentration ◽  
Buffer Solution ◽  
Solution Ph ◽  
Two Stage

Ten litres of tapwater were seeded with 200 µl (8×108 HAV particles) of a commercial (Organon Teknika) suspension of hepatitis A virus. Following WALTER and RÜDIGER (1981), the contaminated tapwater was treated with a two-stage technique for concentration of viruses from solutions with low virus titers. The two-stage technique consists of aluminium hydroxideflocculation (200 mg/l Al2(SO4)3. 18 H2O, pH 5,4-5,6) as first stage, the second stage of a lysis of aluminium hydroxidegel with citric acid/sodium citrate-buffer (pH 4,7; 1 ml/l sample), separation of viruses from the lysate by ultracentrifugation and suspension in 1 ml phosphate buffer solution (pH 7,2). A commercial solid phase enzyme-linked immunosorbent assay (ELISA) was used for the detection of HAV. HAV was detecterl in the 10.000:1 concentrates, but not in the seeded 101 samples. Approximately 4×108 of the inoculated 8×108 HAV particles were found in the 1 ml concentrates. The efficiency of detection is about 50%, the virus concentration 5000-fold. Although the percentage loss of HAV in comparison with concentration by means of membrane filtration is similar, the ultracentrifugation method yields a larger sample/concentrate ratio, so that smaller amounts of HAV can be detected more efficiently because of the smaller end-volume.

Non-enzymatic determination of purine nucleotides using a carbon dot modified glassy carbon electrode

2019 ◽  
Vol 11 (30) ◽  
pp. 3866-3873 ◽  
Author(s):  
R. Karthikeyan ◽  
D. James Nelson ◽  
S. Abraham John
Keyword(s):  
Glassy Carbon ◽  
Low Cost ◽  
Phosphate Buffer Solution ◽  
Purine Nucleotides ◽  
Buffer Solution ◽  
Solution Ph ◽  
Carbon Dot ◽  
Enzymatic Determination ◽  
Sensitive Determination

Selective and sensitive determination of one of the purine nucleotides, inosine (INO) using a low cost carbon dot (CD) modified glassy carbon (GC) electrode in 0.2 M phosphate buffer solution (pH 7.2) was demonstrated in this paper.

scholarly journals Electro-Polymerized Titan Yellow Modified Carbon Paste Electrode for the Analysis of Curcumin

Surfaces ◽  
2021 ◽  
Vol 4 (3) ◽  
pp. 191-204
Author(s):  
Edwin S. D’Souza ◽  
Jamballi G. Manjunatha ◽  
Chenthattil Raril ◽  
Girish Tigari ◽  
Huligerepura J. Arpitha ◽  
...  
Keyword(s):  
Carbon Paste Electrode ◽  
Limit Of Detection ◽  
Phosphate Buffer Solution ◽  
Modified Carbon Paste Electrode ◽  
Carbon Paste ◽  
Buffer Solution ◽  
Solution Ph ◽  
Real Sample Analysis ◽  
Titan Yellow ◽  
Paste Electrode

A modest, efficient, and sensitive chemically modified electrode was fabricated for sensing curcumin (CRC) through an electrochemically polymerized titan yellow (TY) modified carbon paste electrode (PTYMCPE) in phosphate buffer solution (pH 7.0). Cyclic voltammetry (CV) linear sweep voltammetry (LSV) and differential pulse voltammetry (DPV) approaches were used for CRC detection. PTYMCPE interaction with CRC suggests that the electrode exhibits admirable electrochemical response as compared to bare carbon paste electrode (BCPE). Under the optimized circumstances, a linear response of the electrode was observed for CRC in the concentration range 2 × 10−6 M to 10 × 10−6 M with a limit of detection (LOD) of 10.94 × 10−7 M. Moreover, the effort explains that the PTYMCPE electrode has a hopeful approach for the electrochemical resolution of biologically significant compounds. Additionally, the proposed electrode has demonstrated many advantages such as easy preparation, elevated sensitivity, stability, and enhanced catalytic activity, and can be successfully applied in real sample analysis.

Polarographic Determination of Zinc in Compounded Rubber

1950 ◽  
Vol 23 (4) ◽  
pp. 975-980
Author(s):  
F. C. J. Poulton ◽  
L. Tarrant
Keyword(s):  
Zinc Oxide ◽  
Ammonium Acetate ◽  
Potassium Thiocyanate ◽  
Acetate Buffer Solution ◽  
Acid Electrolyte ◽  
Buffer Solution ◽  
Ammonium Acetate Buffer ◽  
Ammonium Acetate Buffer Solution ◽  
Gravimetric Procedure

Abstract Reasons are advanced for the unsatisfactory nature of some of the older methods for the determination of very small amounts of zinc in compounded rubber, particularly in latex mixings. The polarographic technique offers a possible solution, but most of the commoner electrolytes for the electroreduction of this metal are alkaline, and give rise to similar errors as are met in the gravimetric procedure. The development of a suitable acid electrolyte was therefore undertaken, and ways of dealing with likely interferences were examined. The electroltye finally recommended is a potassium thiocyanate-ammonium acetate buffer solution; iron, when present, is reduced to the ferrous condition by potassium iodide. The method was used to determine zinc oxide in a series of mixings of known composition ranging from 0.8 to 40 per cent. In all except the highest proportions of zinc oxide, the figures obtained agree well with the theoretical.

Influence of Red Blood Cell Concentrations on the Measurement of Turbulence Using Hot-Film Anemometer

1983 ◽  
Vol 105 (4) ◽  
pp. 406-410 ◽  
Author(s):  
A. M. Sallam ◽  
N. H. C. Hwang
Keyword(s):  
Phosphate Buffer Solution ◽  
Experimental Information ◽  
Characteristic Change ◽  
Density Functions ◽  
Buffer Solution ◽  
Number Range ◽  
Flow Phenomenon ◽  
Human Red Blood Cells ◽  
Spectral Density Functions ◽  
Hot Film

Measurement of local velocity fluctuations was made with an L-shaped conical hot-film probe in a submerged circular jet. The experiment was carried out in solutions of washed human red blood cells (RBC) in a phosphate buffer solution (PBS), at hematocrit concentrations (Ht percent) of 10, 19, 29, and 38 percent. The viscosity of the testing solutions was kept at 3.2 c.p. by adding proper amount of dextran. The experiment was conducted at Reynolds numbers (NR) 674, 963, 1255 and 1410, based on the jet exit velocity and exit diameter. Statistical analyses were performed on the recorded instantaneous velocity signals to obtain the root-mean-square (rms) values, the probability density functions (PDF) and the power spectral density functions (PSDF) of the signals. Within the range tested, we noticed an incidental rise in rms values at 19 to 29 Ht percent for NR = 963 similar to those reported earlier in the literature. Further analyses using PDF and PSDF, however, showed neither a trend nor any physical significance of this rise. Based on the analyses of both the PDF and the PSDF, we believe that the incidental rise in rms value can be partially attributed to the high spikes registered by the probe in a high RBC concentrations fluid flow. The bombardment of RBC on the probe thermal boundary layer may cause a characteristic change in the probe response to certain flow phenomenon, at least within the Reynolds number range used in this study. Additional theoretical and experimental information is needed to pin point the nature of this response. We thus suggest that the second and higher moments of the HFA signals obtained in a fluctuating flow field involving a liquid with relatively high contaminant concentrations cannot be interpreted as a simple flow phenomenon.

Electrochemical Determination of Uric Acid at CdTe Quantum Dot Modified Glassy Carbon Electrodes

2015 ◽  
Vol 98 (5) ◽  
pp. 1260-1266 ◽  
Author(s):  
Deng Pan ◽  
Shengzhong Rong ◽  
Guangteng Zhang ◽  
Yannan Zhang ◽  
Qiang Zhou ◽  
...  
Keyword(s):  
Uric Acid ◽  
Quantum Dot ◽  
Glassy Carbon ◽  
Semiconductor Nanocrystals ◽  
Phosphate Buffer Solution ◽  
Differential Pulse ◽  
Electrochemical Determination ◽  
Buffer Solution ◽  
Peak Current ◽  
Cdte Quantum Dot

Abstract Cyclic voltammetry and differential pulse voltammetry were used to investigate the electrochemical behavior of uric acid (UA) at a CdTe quantum dot (QD) modified the glassy carbon electrode (GCE). CdTe QDs, as new semiconductor nanocrystals, can greatly improve the peak current of UA. The anodic peak current of UA was linear with its concentration between 1.0 × 10–6 and 4.0 × 10–4 M in 0.1 M pH 5.0 phosphate buffer solution. The LOD for UA at the CdTe electrode (1.0 × 10–7 M) was superior to that of the GCE. In addition, we also determined the effects of scan rate, pH, and interferences of UA for the voltammetric behavior and detection. The results indicated that modified electrode possessed excellent reproducibility and stability. Finally, a new and efficient electrochemical sensor for detecting UA was developed.

Bacterial chemotaxis to fungal propagules in vitro and in soil

1983 ◽  
Vol 29 (9) ◽  
pp. 1104-1109 ◽  
Author(s):  
D. K. Arora ◽  
A. B. Filonow ◽  
J. L. Lockwood
Keyword(s):  
Sandy Loam ◽  
Phosphate Buffer Solution ◽  
Bacterial Chemotaxis ◽  
Macrophomina Phaseolina ◽  
Buffer Solution ◽  
Erwinia Herbicola ◽  
Cochliobolus Victoriae ◽  
Fungal Propagules ◽  
Loam Soil

Erwinia herbicola, Pseudomonas fluorescens, and P. putida were strongly attracted in vitro to substances exuded by conidia of Cochliobolus victoriae and sclerotia of Macrophomina phaseolina, but not to phosphate buffer solution. Numbers of bacteria attracted to propagules of C. victoriae or M. phaseolina in an unsterilized sandy loam soil were significantly (P = 0.05) greater than background populations occurring in soil saturated with buffer. Chemotactic response was greater to C. victoriae than to M. phaseolina both in vitro and in soil. Results suggest that living fungal propagules may act as attractants for motile bacteria in soil.

Surface Morphological Changes Accompanying Dissolution of Bioactive Glass: Effect of Residual Stress

2008 ◽  
Vol 47-50 ◽  
pp. 1302-1306 ◽  
Author(s):  
John A. Nychka ◽  
Ding Li
Keyword(s):  
Residual Stress ◽  
Residual Stresses ◽  
Bioactive Glass ◽  
Morphological Changes ◽  
Phosphate Buffer Solution ◽  
Buffer Solution ◽  
Mechanochemical Effect ◽  
Dissolution Behaviour ◽  
Glass Surfaces

We report our observations concerning the time evolution of surface morphology occurring during the in vitro immersion of bioactive glass surfaces in contact with phosphate buffer solution. We compare regions under intentionally produced residual stresses via micro-indentation to those where no indentation was performed. The sign of the residual stress is shown to be important for predicting dissolution behaviour; compression retards dissolution, whereas tension enhances dissolution. We analyze our results with a simple model for the work of bond dissociation. We report that a highly constrained residual compressive stress state, such as in an indent, leads to a work deficit in comparison to tension, which accounts for the slower dissolution rate of compressed bioactive glass. Such a mechanochemical effect suggests that the presence of residual stresses from the manufacture of biomedical implants and devices could lead to accelerated or delayed dissolution and that careful control of residual stresses should be sought for predictable performance in dissolvable materials.

Controlled Release of Active Substance from Biodegradable Copolymer Matrix

2006 ◽  
Vol 510-511 ◽  
pp. 798-801
Author(s):  
Hyung Suk So ◽  
Hyun Chul Shin ◽  
Beom Suk Kim ◽  
Yeong Seok Yoo
Keyword(s):  
Methylene Blue ◽  
Active Substance ◽  
Phosphate Buffer Solution ◽  
Ultra Violet ◽  
Hydroxyl Groups ◽  
Buffer Solution ◽  
Solution Ph ◽  
Effective Discharge ◽  
Constant Rate ◽  
Long Time

The purpose of this study is to develop a new system to control effective discharge of active substances such as agricultural chemicals. To synthesize a naturally dissolvable polymer; ε-caprolactone and diglycolide were copolymerized with ethylene glycol as an initiator to produce macrodiol. As macrodiol has hydroxyl groups in both ends, they are modified with methacryloyl chloride for photochemical networking. After standard macromonomer produced by this procedure was physically mixed with methylene blue, it was networked with ultra-violet rays to be filmed. This film is naturally dissolvable and hydrolytic. As a result of hydrolytic test with a crosslinked structure of 10 % methylene blue, it decreased by 9 % for seven weeks in 37 °C phosphate buffer solution (pH = 7). Thus, we verified that active substance can be discharged from a crosslinked structure for a long time at a constant rate under room temperature.

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