Inductively Coupled Plasma Optical Emission Spectrometry Method Research Articles

Evaluation of Trace Elements in Coffee and Mixed Coffee Samples Using ICP-OES Method.

This research examines the concentration of 10 trace elements including arsenic (As), lead (Pb), chromium (Cr), zinc (Zn), iron (Fe), cobalt (Co), cadmium (Cd), nickel (Ni), manganese (Mn), and aluminum (Al) from among 36 different samples of coffee (3 brands and 2 types of simple and instant) and mixed coffee (3 brands and 4 types of simple, creamy, chocolate and sugar free) collected from market of Iran's and analyzed by using ICP-OES (inductively coupled plasma-optical emission spectrometry). The recovery, limit of quantification (LOQ), and limit of detection (LOD) ranged from 93.4 to 103.1%, 0.06 to 7.22, and 0.018 to 2.166 µg/kg, respectively. The findings showed that the highest and lowest average concentrations were 498.72 ± 23.07 μg/kg (Fe) and 3.01 ± 1.30 μg/kg (As) in coffee and mixed coffee samples. Also, in all samples, the maximum concentration of trace elements was related to Fe (1353.61 µg/kg) and the minimum concentration was related to Al, As, Co, Cr, Ni, Pb, and Zn that were not detected (ND). The samples of mixed coffee had highest levels of trace elements compared to coffee samples. In coffee samples, type of instant coffee had highest levels of trace elements compared to simple coffee and mixed coffee samples. The type of creamy mixed coffee had highest levels of trace elements (except Ni and Cr) compared to other type of mixed coffee samples. Finally, trace elements were less than the standard levels of Iran and other countries (in all samples); therefore, it does not threaten Iranian consumers.

Multi-Elemental Composition Data Handled by Chemometrics for the Discrimination of High-Value Italian Pecorino Cheeses.

The multi-elemental composition of three typical Italian Pecorino cheeses, Protected Designation of Origin (PDO) Pecorino Romano (PR), PDO Pecorino Sardo (PS) and Pecorino di Farindola (PF), was determined by Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES). The ICP-OES method here developed allowed the accurate and precise determination of eight major elements (Ba, Ca, Fe, K, Mg, Na, P, and Zn). The ICP-OES data acquired from 17 PR, 20 PS, and 16 PF samples were processed by unsupervised (Principal Component Analysis, PCA) and supervised (Partial Least Square-Discriminant Analysis, PLS-DA) multivariate methods. PCA revealed a relatively high variability of the multi-elemental composition within the samples of a given variety, and a fairly good separation of the Pecorino cheeses according to the geographical origin. Concerning the supervised classification, PLS-DA has allowed obtaining excellent results, both in calibration (in cross-validation) and in validation (on the external test set). In fact, the model led to a cross-validated total accuracy of 93.3% and a predictive accuracy of 91.3%, corresponding to 2 (over 23) misclassified test samples, indicating the adequacy of the model in discriminating Pecorino cheese in accordance with its origin.

Is Mehlich 3 soil extraction a suitable screening method for determination of some risk elements?

Legislation limits for risk elements (As, Be, Cd, Co, Cr, Cu, Ni, Pb, V, Zn) in agricultural soil in the Czech Republic are given for the content of elements extracted by aqua regia. This extraction is time consuming and environmentally unfriendly. The regular soil survey is based on Mehlich 3 universal soil extractant and covers the simultaneous determination of macronutrients, sulphur, and micronutrients by inductively coupled plasma optical emission spectrometry (ICP-OES). Our study focused on the possibility to use Mehlich 3 extractant also for preliminary screening for the determination of the risk elements simultaneously with the other elements by the ICP-OES method. Mehlich 3 was confirmed as a reliable screening method for Cd regarding sensitivity, specificity and precision (> 0.8) when the cut-off value of 0.27 mg/kg in Mehlich 3 extracts was used for the prediction of soils to be above or below the legislation limit, which in turn is based on aqua regia extraction. Very good results were obtained for Be and promising results were received for As, Cu and V. But the available data were not sufficient for the determination of reliable cut-off values for Co, Cr, Ni, Pb and Zn.

The ICP-OES method for determination of zinc in Enchytraeus crypticus and agarose gel from ecotoxicological tests

A simple ICP-OES (inductively coupled plasma optical emission spectrometry) method for determination of zinc in Enchytraeus crypticus and agarose gel samples from ecotoxicological tests is proposed. The E. crypticus individuals are separated, water washed, wet weighed and dissolved in tetramethylammonium hydroxide. The gel is digested in HNO3. The method (limit of detection in mg kg−1: 0.90 for E. crypticus bulk biomass, 14 for one E. crypticus worm and 0.0018 for gel) was employed in the evaluation of ZnO nanoparticles (ZnO-NPs) compared to ZnCl2: bioaccumulation factors were 57–180 for ZnCl2 and 23–65 for ZnO-NPs.

Analytical Method of Silicon Dioxide in Health Functional Food Products using ICP-OES

The analytical method of silicon dioxide (SiO2) in health functional food products was developed employing inductively coupled plasma optical emission spectrometry (ICP-OES) method assisted by acid (hydrofluoric acid and boric acid) digestion in open system without alkali fusion. The limit of detection (LOD) and limit of quantification (LOQ) of this method were found to be 0.07 and 0.20 mg/L, respectively. Linearity (r 2) and linear range were 0.99 and 0.20~20.0 mg/L, respectively. The accuracy and precision of SiO2 (0.4, 1.0, and 2.0%, w/w) in spiked glucosamine exhibited to be the range of 90.22~94.14% and 0.72~1.67%, respectively. The contents of SiO2 in 11 health functional food products were detected in range of 0.02~1.80% (w/w). Every sample showed below content of the permitted use level (2%, w/w) of SiO2. Therefore ICP-OES method with acid can analyze the content of SiO2 in health functional food products easily and rapidly. Consequently, the application of specification analysis of SiO2 in health functional food products could be a significant work.

Comparative Evaluation of Inductively Coupled Plasma-Optical Emission Spectrometry and Colorimetry for Determining Phosphorus in Grain Samples

ABSTRACTThe inductively coupled plasma (ICP)-based method provides the opportunity to determine phosphorus (P) along with other major, secondary, micro and trace elements in plant materials. This study was conducted to compare and evaluate the relative efficacy of the inductively coupled plasma-optical emission spectrometry (ICP-OES) method with that of the colorimetric method using Skalar autoanalyzer, for determining P in 428 grain samples of eight diverse crops. The results on grain P analysis by the two methods, for individual as well as for all crop samples combined, showed that they were highly positively correlated (r varied from 0.84 to 0.98, p < 0.0001 for the eight crops, and R2 for all crop grain samples was 0.9201, p < 0.0001). Moreover, the precision by the ICP method was similar to that determined by the Skalar method. Our results demonstrate that the ICP-OES method can be conveniently used for determining P along with other plant nutrient elements in grain samples of diverse crops.

Determination of Phosphorus in Foods by Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES)

The analytical method for the determination of phosphorus in foods was validated by inductively coupled plasma optical emission spectrometry (ICP-OES) in terms of precision, accuracy, recovery efficiency and linearity. Regression analysis revealed good correlation coefficient, higher than 0.999. Recovery efficiencies of the minerals ranged from 90.36% to 110.63%, and the limit of detection (LOD) and the limit of quantification (LOQ) were 0.0745 mg/ kg and 0.2482 mg/kg, respectively. The value of inter-day and intra-day ranged from 1.43 to 3.23% and from 0.40 to 1.77%. The recovery efficiencies ranged from 97.8 to 110.6%. The method was also compared with Molybdenum blue colorimetric method using certified and statistically significant difference was also not observed in the between two different analytical methods. The ICP-OES method was applied to phosphorus determination in commonly consumed foods. The obtained results suggest that the method verified in the present study may be used as an official analytical method for clear understanding of phosphorus database for national health promotion.

Fabrication of paper-based devices by lacquer spraying method for the determination of nickel (II) ion in waste water

A spraying method with lacquer was developed for the fabrication of paper-based devices. A patterned iron mask was initially placed on a filter paper and held tightly attached by a magnetic plate placed on the opposite side. After that, acrylic lacquer was sprayed on the filter paper to create a hydrophobic area while the hydrophilic area was protected with the iron mask. The optimal conditions for the fabrication of this device were studied including lacquer type and particle retention efficiency of filter paper. Gloss spray lacquer and filter paper No. 4 were chosen as optimal lacquer type and particle retention efficiency of filter paper, respectively. To evaluate its efficiency, the paper-based devices were used to determine nickel using electrochemical detection. Cu-enhancer solution was employed to increase sensitivity of nickel determination with the optimal concentration of 4.5ppm. Under the optimal conditions, linear range was observed in the range of 1–50ppm with a coefficient of determination of 0.9971. The limit of detection (LOD) and the limit of quantitation (LOQ) were found to be 0.5 and 1.97ppm, respectively. Moreover, these paper-based devices coupled with electrochemical detection were applied to determine nickel in waste water of a jewelry factory and compared to those obtained with inductively coupled plasma optical emission spectrometry (ICP-OES). The results indicated that there were no significant variations between this proposed method (4.15±0.043ppm) and the ICP-OES method (4.06±0.013ppm). Therefore, this spraying method was found to be an excellent alternative for the fabrication of paper-based devices due to its ease of use, affordability and simplicity.

Comparison of Binding Parameter Constants between Sevelamer HCl Tablets and Renagel Tablets by a Validated Inductively Coupled Plasma-Optical Emission Spectrometry (ICP-OES) Method

Sevelamer Hydrochloride is a crossolinked polymeric amine; it is the active ingredient in Renagel Tablets. Sevelamer Hydrochloride is indicated for the control of hyperphosphatamiea in patients with end-stage renal disease. The binding parameter constants of Sevelamer Hydrochloride were determined using the Langmuir approximation for the dosage form at pH 4.0 and 7.0 by Inductively Coupled Plasma-Optical Emission Spectrometry. An ICP-OES method has been developed to estimate free phosphate in In-Vitro phosphate binding study of Sevelamer HCl Tablets. The method is selective and capable of detecting phosphate in the presence of placebo matrix. The method has been validated with a lower limit of quantitation of 0.2 mM for Phosphate. A linear response function was established for the range of concentrations 0.2 - 25.0 mM (r > 0.99) for Phosphate. The intra and inter day precision values for Phosphate met the acceptance as per Food and Drug Administrations guidelines. Phosphate was stable in the set of stability studies viz. bench-top and autosampler. The developed method was applied to in-vitro phosphate binding studies of Sevelamer HCl Tablets.

A Validated Inductively Coupled Plasma-Optical Emission Spectrometry (ICP-OES) Method to Estimate Free Calcium and Phosphorus in In Vitro Phosphate Binding Study of Eliphos Tablets

An ICP-OES method has been developed to estimate Calcium and Phosphorous in In vitro phosphate binding study of Eliphos Tablets. The method is selective and is capable of detecting calcium and phosphorous in the presence of other trace elements. The method has been validated using RF power of 1500 watts, plasma flow of 15L/min, Nebuliser flow of 0.8 L/min and plasma view at radial mode for calcium and axial mode for phosphorus. The wavelength was monitored for calcium and phosphorous at 317.933 nm and 213.677 nm respectively. The method has been validated in terms of specificity, precision, linearity, accuracy, limit of quantification and ruggedness. The In vitro binding studies were performed for Eliphos Tablets at eight dif- ferent phosphate concentrations by incubating at 37.0?C and analysis was performed using the validated method to estimate free calcium and phosphorus. The objective of the study is to provide an alternate In vitro method to estimate the binding capacity of calcium acetate tablets to avoid the expensive in-vivo bio clinical studies.

Determination of 28 selected elements in textiles by axially viewed inductively coupled plasma optical emission spectrometry

A simple, robust and reliable analytical procedure for the determination of 28 selected elements, namely Al, As, Ba, Be, Bi, Ca, Cd, Co, Cr, Cu, Fe, K, Hg, Mg, Mn, Mo, Na, Ni, Pb, Sc, Si, Se, Sn, Sm, Sr, Tl, V, and Zn in textile materials by inductively coupled plasma optical emission spectrometry (ICP-OES) after microwave digestion of samples was optimized and validated in this work. The total amount of elements present in textile samples was determined after microwave digestion of materials in 7 mol/L nitric acid within the optimal working program: 5 min at 150 °C (power 250 W), 15 min 180 °C (300 W) and 20 min at the maximum temperature of 200 °C (350 W). For the quality control reasons, which were ascertained by analysis of the certified cotton trace elements reference material IAEA-V9, the ICP-OES method was optimized through several parameters: by comparing Meinhard and Gemcone Low Flow nebulizers efficiency, ranging nebulizer gas flows from 0.6 to 1.0 L/min, ranging sample flows from 0.8 to 1.2 mL/min, testing RF power from 1200 to 1400 W, detecting data acquisition time (read time) from 0 to 527 s, ranging washing (delay) time from 0 to 408 s, as well as by checking the occurring interferences for the optimal line selection. Validation included determination of linearity, selectivity, accuracy, reproducibility, precision and limits of detection calculated for all 28 selected elements of interest. The developed analytical procedure was successfully applied on textile fibers (cotton, flax and hemp) as well as on standard knitted textile sample materials (cotton and wool).

Synthesis and Applications of Poly(Acrylphenylamidrazone-Phenyl-Hydrazide-Acylphenylhydrazine) Chelating Fiber for Preconcentration and Separation of Trae In(III), Zr(IV), Tl(I), V(V), Ga(III) and Ti(IV) from Solution Samples

An ICP-OES method using a new poly (acrylphenylamidrazone-phenylhydrazide-acylphenylhydrazine) chelating fiber to preconcentrate and separate trace In(III), Zr(IV), Tl(I), V(V), Ga(III) and Ti(IV) ions from solution samples has been established. The new chelating fiber was synthesized using polyacrylonitrile fiber as a starting material and the structure of the chelating fiber was determined by FT infrared spectrometry. The acidity, adsorption rate, re-use, capacity and interference on the adsorption of ions on the chelating fiber as well as the conditions of desorption of these ions from the chelating fiber were investigated by means of inductively coupled plasma optical emission spectrometry (ICP-OES). The results show that the relative standard deviations for the determination of 10 ng/ml In, Tl, Ga and 1 ng/ml Zr, V, Ti were lower than 2.5%. The results obtained for these ions in real solution samples by this method were basically in agreement with the given values with average errors of less than 4%.