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Biomedical subjects

Kate Grudpan

Publications and source records attributed to Kate Grudpan.

11 recordsLinked to original sources

Soap bubbles in analytical chemistry. Conductometric determination of sub-parts per million levels of sulfur dioxide with a soap bubble.

Soap bubbles provide a fascinating tool that is little used analytically. With a very low liquid volume to surface area ratio, a soap bubble can potentially provide a very useful interface for preconcentration where mass transfer to an interfacial surface is important. Here we use an automated system to create bubbles of uniform size and film thickness. We utilize purified Triton-X 100, a nonionic surfactant, to make soap bubbles. We use such bubbles as a gas-sampling interface. Incorporating hydrogen peroxide into the bubble provides a system where electrical conductance increases as the bubble is exposed to low concentrations of sulfur dioxide gas. We theoretically derive the conductance of a hollow conducting spherical thin film with spherical cap electrodes. We measure the film thickness by incorporating a dye in the bubble making solution and laser transmission photometry and find that it agrees well with the geometrically computed thickness. With the conductance of the bubble-making soap solution being measured by conventional methods, we show that the measured values of the bubble conductance with known bubble and electrode dimensions closely correspond to the theoretically computed value. Finally, we demonstrate that sub-ppm levels of SO(2) can readily be detected by the conductivity change of a hydrogen peroxide-doped soap bubble, measured in situ, when the gas flows around the bubble.

Journal Article↗

Interaction of trace elements in acid mine drainage solution with humic acid.

The release of metal ions from a coal mining tailing area, Lamphun, Northern Thailand, is studied by leaching tests. Considerable amounts of Mn, Fe, Al, Ni and Co are dissolved in both simulated rain water (pH 4) and 10 mg L(-1) humic acid (HA) solution (Aldrich humic acid, pH 7). Due to the presence of oxidizing pyrite and sulfide minerals, the pH in both leachates decreases down to approximately 3 combined with high sulfate concentrations typical to acid mine drainage (AMD) water composition. Interaction of the acidic leachates upon mixing with ground- and surface water containing natural organic matter is simulated by subsequent dilution (1:100; 1:200; 1:300; 1:500) with a 10 mg L(-1) HA solution (ionic strength: 10(-3) mol L(-1)). Combining asymmetric flow field-flow fractionation (AsFlFFF) with UV/Vis and ICP-MS detection allows for the investigation of metal ion interaction with HA colloid and colloid size evolution. Formation of colloid aggregates is observed by filtration and AsFlFFF depending on the degree of the dilution. While the average HA size is initially found to be 2 nm, metal-HA complexes are always found to be larger. Such observation is attributed to a metal induced HA agglomeration, which is found even at low coverage of HA functional groups with metal ions. Increasing the metal ion to HA ratio, the HA bound metal ions and the HA entities are growing in size from <3 to >450 nm. At high metal ion to HA ratios, precipitation of FeOOH phases and HA agglomeration due to colloid charge neutralization by complete saturation of HA complexing sites are responsible for the fact that most of Fe and Al precipitate and are found in a size fraction >450 nm. In the more diluted solutions, HA is more relevant as a carrier for metal ion mobilization.

Coal Mining↗

Development of sequential injection-lab-at-valve (SI-LAV) micro-extraction instrumentation for the spectrophotometric determination of an anionic surfactant.

The development of instrumentation for sequential injection analysis with a "lab-at-valve" (SIA-LAV) micro-extraction system is presented. The extractive determination of an anionic surfactant using methylene blue was selected as a model. Sample, reagents and organic solvent were sequentially aspirated into an extraction coil connected to the center of a selection valve, where extraction took place by flow reversal. The aqueous and organic phases were separated in a LAV unit attached to one port of the valve. The LAV unit situated a fiber-optic spectrophotometer to monitor the absorbance change of the extract product in the organic phase. The developed SIA-LAV system offers an alternative micro-total analysis system for automated micro-extraction.

Anions↗

Simple sequential injection analysis systems with a dynamic surface tension detector.

Simple sequential injection analysis systems with DSTD (SIA/DSTD) have been developed. One was employed for the study of the effects of the ion contents in solutions to the dynamic surface pressure of ionic surfactants. The results from the studies show the possibility for an alternative simple fast screening, but also a sensitive procedure for water quality determination. Another simple SIA/DSTD system has been demonstrated for the quantification of an anionic surfactant using a single standard calibration.

Calibration↗

Simple spectrophotometric flow injection system with an in-valve minicolumn for enhancement during the determination of chromium(III) using EDTA.

A simple spectrophotometric flow injection (FI) procedure for the determination of Cr(III) using ethylenediaminetetraacetic acid (EDTA) was developed. An FI system with a column packed with Amberlite IR-120(H) was employed for sample pretreatment. This leads to the possibility of a single standard calibration. A linear calibration in a range of 10-27 microg Cr(III) was obtained with a detection limit of 1 microg Cr(III) and RSD of 2% (18 microg Cr(III), n=12). The proposed procedure was applied for determination of Cr(III) in leachate and dietary supplement samples. The results agreed with those obtained by the standard methods.

Chromium↗

Sequential injection titration with spectrophotometric detection for the assay of acidity in fruit juices.

A simple sequential injection analysis (SIA) with spectrophotometric detection for an assay of acidity in fruit juice was investigated. An alkaline reagent (sodium hydroxide), a sample and an indicator (phenolphthalein) were first aspirated and stacked as adjacent zones in a holding coil. With flow reversal through a reaction coil to the detector, zone penetration occurred, leading to a neutralization reaction that caused a decrease in the color intensity of the indicator being monitored for absorbance at 552 nm. The effects of various parameters were studied. Linear calibration graphs for acidities of 0.2 - 1.0 and 0.5 - 2.5% w/v citric acid as a standard, with a relative standard deviation of 1% (acidity of 0.3 - 0.6% w/v as citric acid, n=11) and a sample throughput of 30 samples h(-1), were achieved. The developed method was validated by a standard titrimetric method for assaying the acidity of fruit juice samples.

Beverages↗

Novel approach for mono-segmented flow micro-titration with sequential injection using a lab-on-valve system: a model study for the assay of acidity in fruit juices.

A new concept for micro-titration using a "lab-on-valve"(LOV) system with sequential injection of mono-segmented flow is proposed. The performance of the system was demonstrated by the assay of acidity in fruit juices which is based on acid-base neutralization. A standard/sample solution containing citric acid, indicator, sodium hydroxide, were sandwiched between air segments and were aspirated in microliter volumes through a selection valve into a holding coil. The acid, indicator, and base were mixed by flow reversal. After removing air segments, the solution was pushed to the detector for monitoring of the change in absorbance of the indicator color, which depended on the concentration of the remaining base. With LOV, microliter volumes of the solution can be detected without dispersion of the color zone. A calibration graph (plot of absorbance vs. acidity value) in the range of 0.2-1.2% (w/v) as citric acid was established. Sample throughput of 30 sample h(-1) and good reproducibility (RSD = 1.2%, n= 11 for 0.6% acidity) were achieved. The procedure has been applied to determine acidity in fruit juices.

Beverages↗

Simple bead injection-flow injection system for the determination of copper.

We demonstrate the extended application of a simple bead injection-flow injection system with a modified simple colorimetric detection unit for the determination of low amount of Cu2+ in samples of different matrices (water and supplement tablet samples) with minimal sample pretreatment by employing ammonium pyrrolidinedithiocarbamate (APDC) reagent.

Buffers↗

Flow-injection and sequential-injection determinations of paracetamol in pharmaceutical preparations using nitrosation reaction.

A simple FI and two different SI systems have been investigated for the determination of paracetamol by employing a simple reagent for a nitrosation reaction. It is based on the on-line nitrosation of paracetamol with sodium nitrite in an acidic medium. The formed nitroso derivative species reacts further with sodium hydroxide to convert it to a more stable compound. The yellow product is continuously monitored at 430 nm. The FI system is very simple and cost effective for fast manual operation (60 injections/h; y = 0.268x + 44.314, r2 = 0.9910 for 400 - 1000 mg/l and y = 0.1687x + 145.72, r2 = 0.9970 for 1000 - 2500 mg/l). The two SI systems with different components and configurations are automated and optimized for the conditions for which no extra dilution is to be required for sample handling: one with a syringe pump and two selection valves (60 samples/h; y = 0.1488x - 4.7297, r2 = 0.9946 for 400 - 1000 mg/l and y = 0.0858x + 63.933, r2 = 0.9849 for 1000 - 2500 mg/l); the other is simpler and more cost-effective, with an autoburette and only one selection valve (15 samples/h; y = 0.0072x + 1.1467, r2 = 0.9977 for 200 - 1000 mg/l and y = 0.0028x + 5.4699, r2 = 0.9879 for 1000 - 2500 mg/l). They have all been applied to assay paracetamol in pharmaceutical preparations. The obtained results agree with those by the US Pharmacopeia method.

Journal Article↗

A low-cost light-scattering detector for the flow-injection nephelometric determination of sulfate.

A simple low-cost flow-through light-scattering detector was developed for determining the particle mass concentration in colloidal suspensions. Employing a laser pointer as a light source and a photodiode IC as a light sensor, the detector was shown to have good sensitivity, yet was small and battery operated. The detector was demonstrated to be effective for the flow-injection nephelometric determination of sulfate by precipitation as barium sulfate.

Journal Article↗

Determination of diphenhydramine hydrochloride in some single tertiary alkylamine pharmaceutical preparations by flow injection spectrophotometry.

A simple and rapid spectrophotometric method with flow injection is proposed for determination of diphenhydramine hydrochloride in some single tertiary alkylamine pharmaceutical preparations (capsule and syrup). It is based on ion pair formation with bromocresol green in a pH 3 buffer which a yellow ion pair compound is extracted into chloroform layer. An aqueous layer containing excess bromocresol green is injected into a carrier stream of 0.01 M borax solution and absorbance of the stream is continuously monitored at 610 nm. Diminution of the bromocresol green is related to an amount of diphenhydramine hydrochloride that can be evaluated from a calibration graph established by a plot of diphenhydramine hydrochloride concentration (micro gm l(-1)) and peak height (mV). Optimization will be discussed. The calibration graph is linear over the concentration ranges of 5-21 and 75-188 micro gm l(-1). A throughput of 100 injections h(-1) can be obtained. Application to assay for capsule and syrup samples has been demonstrated. The method is validated by comparing the results with HPLC analyses.

Bromcresol Green↗