Chlorine determination in medicinal plants by potentiometry with ion-selective electrode after microwave-induced combustion

A method based on microwave-induced combustion (MIC) was applied for medicinal plants digestion allowing further chlorine determination by potentiometry using ion-selective electrode (ISE). Sample masses ranging from 500 to 1000 mg were evaluated for MIC digestion. Water and 10, 25, 50, and 100 mmol/L NH4OH were investigated as absorbing solutions. The accuracy of the proposed method was evaluated by using certified reference materials (CRMs), by recovery tests (500 µg/g), and also by comparison with the results obtained by inductively coupled plasma optical emission spectrometry (ICP-OES) after microwave-assisted alkaline extraction (MAE). Using water or NH4OH solutions (10 to 100 mmol/L), recoveries close to 100% and relative standard deviation lower than 5% were obtained. Results were in agreement with CRMs values (better than 95%) and also with those values obtained by using the MAE method. The main advantage of the proposed method was the complete combustion of high sample mass (1000 mg) resulting in low quantification limit (12.5 µg/g) and chlorine determination at low concentration by ISE. Another advantage of the proposed method was the high chlorine stability in digests (up to 30 days of storage) even using water as absorbing solution, which is in agreement with green analytical chemistry recommendations. Finally, the proposed MIC method was applied for commercial medicinal plants and the chlorine concentration was in the range of 59.4 ± 1.4 to 2038 ± 70 µg/g. The proposed MIC method was considered suitable for quality control for chlorine determination in medicinal plants

Environmental and human health risks associated with exposure to hazardous elements present in urban dust from Barranquilla, Colombian Caribbean

Urban dust is a mixture of deposited particles from different sources usually linked to potentially toxic elements (PTEs). Despite the industrialization of many South American countries, little is known about the impact of particulate matter in large cities, data necessary to promote environmental policies aiming to protect human health. The main objective of this work was to evaluate the particle size distribution, composition, as well as environmental and human health risks of settled dust particles from Barranquilla, a Colombian Caribbean industrialized area. Trace elements were analyzed by ICP‐MS from thirty‐five different sites, covering all city areas. Dust was mostly composed of 10–70 μm particles. The average concentrations of V, Cr, Mn, Co, Ni, Cu, Zn, As, Se, Mo, Ag, Cd, Sn, Sb, Pb, and Bi were above background. High spatial heterogeneity was observed for Cu, Zn, As, Se, Mo, Ag, Sn, Sb, and Bi. Concentration factors suggest urban dusts are extremely contaminated by Zn and Cu. The ecological risk associated with specific elements decreased in the order Cd > Cu > As > Hg > Pb > Ni > Co ≈ Zn ≈ Cr, and the contamination load index showed that 91% of the samples are polluted by PTEs. Although the carcinogenic risks of Cr, Ni, As, Co, and Cd were low, chronic exposure to several PTEs may be impacting the quality of life. Educational programs, as well as monitoring and greater control on traffic, industry, and construction activities, are needed in order to protect environmental and human healt

Drosophila melanogaster - an embryonic model for studying behavioral and biochemical effects of manganese exposure

Embryonic animals are especially susceptible to metal exposure. Manganese (Mn) is an es-sential element, but in excess it can induce toxicity. In this study we used Drosophila mela-nogaster as an embryonic model to investigate biochemical and behavioral alterations due to Mn exposure. Flies were treated with standard medium supplemented with MnCl2 at 0.1 mM, 0.5 mM or 1 mM from the egg to the adult stage. At 0.5 mM and 1 mM Mn, newly ecloded flies showed significantly enhanced locomotor activity when assessed by negative geotaxis behavior. In addition, a significant increase in Mn levels (p < 0.0001) was observed, while Ca, Fe, Cu, Zn and S levels were significantly decreased. A significant drop in cell viability occurred in flies exposed to 1 mM Mn. There was also an induction of reactive oxygen species at 0.5 mM and 1 mM Mn (p < 0.05). At 1 mM, Mn increased Catalase (p < 0.005), Superoxide Dismutase (p < 0.005) and Hsp83 (p < 0.0001) mRNA expression, without altering Catalase or Superoxide Dismutase activity; the activity of Thioredoxin reductase and Glutatione-S-transferase enzymes was increased. Mn treatment did not alter ERK or JNK1/2 phosphorylation, but at 1 mM caused an inhibition of p38MAPK phosphorylation. Together these data suggest mechanisms of adaptation in the fly response to Mn exposure in embryonic life

Chlorine determination in medicinal plants by potentiometry with ion-selective electrode after microwave-induced combustion

A method based on microwave-induced combustion (MIC) was applied for medicinal plants digestion allowing further chlorine determination by potentiometry using ion-selective electrode (ISE). Sample masses ranging from 500 to 1000 mg were evaluated for MIC digestion. Water and 10, 25, 50, and 100 mmol/L NH4OH were investigated as absorbing solutions. The accuracy of the proposed method was evaluated by using certified reference materials (CRMs), by recovery tests (500 µg/g), and also by comparison with the results obtained by inductively coupled plasma optical emission spectrometry (ICP-OES) after microwave-assisted alkaline extraction (MAE). Using water or NH4OH solutions (10 to 100 mmol/L), recoveries close to 100% and relative standard deviation lower than 5% were obtained. Results were in agreement with CRMs values (better than 95%) and also with those values obtained by using the MAE method. The main advantage of the proposed method was the complete combustion of high sample mass (1000 mg) resulting in low quantification limit (12.5 µg/g) and chlorine determination at low concentration by ISE. Another advantage of the proposed method was the high chlorine stability in digests (up to 30 days of storage) even using water as absorbing solution, which is in agreement with green analytical chemistry recommendations. Finally, the proposed MIC method was applied for commercial medicinal plants and the chlorine concentration was in the range of 59.4 ± 1.4 to 2038 ± 70 µg/g. The proposed MIC method was considered suitable for quality control for chlorine determination in medicinal plants

Development of Green Methods for the Determination of Elemental Impurities in Commercial Pharmaceutical Tablets

In this study, two methods based on the use of diluted acids were developed: microwave-assisted wet digestion (MAWD) and microwave-assisted ultraviolet digestion (MAWD-UV). These methods are evaluated for the digestion of oral pharmaceutical drugs and further determination of elemental impurities from classes 1 (As, Cd, Hg and Pb) and 2A (Co, Ni and V) by inductively coupled plasma optical emission spectrometry (ICP-OES). Commercial drugs for the treatment of type 2 diabetes are used. No prior comminution is performed. For MAWD, the optimized conditions were 2 mol L&minus;1 or 3 mol L&minus;1 HNO3, 1 mL of 50% H2O2 and a 45 min or 55 min irradiation program. For MAWD-UV, the condition using 1 mol L&minus;1 HNO3, 1.6 mL of 50% H2O2 and a 55 min irradiation program enabled the digestion of all samples. In this way, efficient methods are proposed for the digestion of commercial pharmaceutical tablets for further determination of class 1 and 2A elemental impurities (ICH Q3D guidelines)

Development of Green Methods for the Determination of Elemental Impurities in Commercial Pharmaceutical Tablets

In this study, two methods based on the use of diluted acids were developed: microwave-assisted wet digestion (MAWD) and microwave-assisted ultraviolet digestion (MAWD-UV). These methods are evaluated for the digestion of oral pharmaceutical drugs and further determination of elemental impurities from classes 1 (As, Cd, Hg and Pb) and 2A (Co, Ni and V) by inductively coupled plasma optical emission spectrometry (ICP-OES). Commercial drugs for the treatment of type 2 diabetes are used. No prior comminution is performed. For MAWD, the optimized conditions were 2 mol L−1 or 3 mol L−1 HNO3, 1 mL of 50% H2O2 and a 45 min or 55 min irradiation program. For MAWD-UV, the condition using 1 mol L−1 HNO3, 1.6 mL of 50% H2O2 and a 55 min irradiation program enabled the digestion of all samples. In this way, efficient methods are proposed for the digestion of commercial pharmaceutical tablets for further determination of class 1 and 2A elemental impurities (ICH Q3D guidelines)

Combining pyrohydrolysis and ICP-MS for bromine and iodine determination in airborne particulate matter

In this work, a method based on pyrohydrolysis of airborne particulate matter (APM) collected on glass fiber filter and subsequent determination of bromine and iodine by inductively coupled plasma mass spectrometry (ICP-MS) was developed. Samples of APM collected on glass fiber filter were ground using an agate mortar, homogenized and placed on an alumina platform. Samples were mixed with solid V2O5 and introduced into the pyrohydrolysis system. The main operational conditions of pyrohydrolysis (absorbing solution, heating time, sample mass and use of an auxiliary reagent — V2O5) were evaluated. Using selected conditions, samples of APM collected on glass fiber filter (300 mg, including the glass fiber filter) were mixed with 900 mg of V2O5 and heated at 950 °C during 15 min in a quartz tube under water vapor and air flow. The accuracy of the proposed method was evaluated by analyte recovery tests and also by analysis of certified reference material (CRM) with a similar matrix composition (NIST 2709 and NIST 1633b). Results were in agreement better than 104 and 95% for bromine and iodine, respectively, with CRM values. The limits of quantification (LOQs) of bromine (0.05 μg g− 1) and iodine (0.006 μg g− 1) were considered appropriate for APM analysis. The pyrohydrolysis sample preparation method was considered as relatively suitable to be performed in routine analysis and provides a clean solution for analysis by ICP-MS, which is very attractive for bromine and iodine determination in APM samples.Fil: Picoloto, Rochele S.. Universidade Federal se Santa Maria. Campinas; BrasilFil: Cruz, Sandra M.. Universidade Federal se Santa Maria. Campinas; BrasilFil: Melo, Paola A.. Universidade Federal se Santa Maria. Campinas; BrasilFil: Muller, Edson L.. Universidade Federal se Santa Maria. Campinas; BrasilFil: Smichowski, Patricia Nora. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Comisión Nacional de Energía Atómica; ArgentinaFil: Flores, Erico M. M.. Universidade Federal se Santa Maria. Campinas; Brasi

Assessment of inorganic contaminants in golden mussel (Limnoperna fortunei) in Southern Brazil

Elementos traço e majoritários foram determinados em mexilhão dourado (Limnoperna fortunei) coletados no canal São Gonçalo (Rio Grande-RS, Brasil). Digestão assistida por microondas em sistema fechado foi utilizada para decomposição das amostras com subsequente determinação elementar por técnicas espectrométricas. Os resultados mostraram que o tecido de mexilhão contém Ag, Al, As, B, Ba, Ca, Cd, Co, Cr, Cu, Fe, Hg, Li, Mg, Mn, Mo, P, Pb, S, Sn, Sr, Ti, V e Zn, enquanto que na casca foram encontrados os mesmo elementos, exceto Ag e Hg, evidenciando seu potencial como biomarcador. Neste sentido, estes resultados podem ser utilizados para estabelecer um panorama inicial e contribuir para futuros estudos relacionados a contaminantes inorgânicos na área estudada.Major and trace element content was determined in golden mussel (Limnoperna fortunei) collected in the São Gonçalo Channel (Rio Grande City, Brazil). A microwave-assisted digestion procedure in closed vessels was applied to mussel decomposition and subsequent determination of elements by spectrometric techniques. Results showed that the mussel tissue contains Ag, Al, As, B, Ba, Ca, Cd, Co, Cr, Cu, Fe, Hg, Li, Mg, Mn, Mo, P, Pb, S, Sn, Sr, Ti, V and Zn, while the same elements (except Ag and Hg) were quantified in its shell, demonstrating its potential as a biomarker. In this sense, these results can be used to establish an initial view and to contribute to further studies related to element contamination in the area under study