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Antarctic seaweeds are vital components of polar marine ecosystems, playing a crucial role in nutrient cycling and supporting diverse life forms. The sulfur content in these organisms is particularly interesting due to its implication in biogeochemical processes and potential impacts on local and global environmental systems. In this study, we present a comprehensive characterization of seaweed collected in the Antarctic in terms of their total sulfur content and its distribution among different classes of species, including thiols, using various methods and high-sensitivity techniques. The data presented in this paper are unprecedented in the scientific literature. These methods allowed for the determination of total sulfur content and the distribution of sulfur compounds in different fractions, such as water-soluble and proteins, as well as the speciation of sulfur compounds in these fractions, providing valuable insights into the chemical composition of these unique marine organisms. Our results revealed that the total sulfur concentration in Antarctic seaweeds varied widely across different species, ranging from 5.5 to 56 g kg−1 dry weight. Furthermore, our investigation into the sulfur speciation revealed the presence of various sulfur compounds, including sulfate, and some thiols, which were quantified in all ten seaweed species evaluated. The concentration of these individual sulfur species also displayed considerable variability among the studied seaweeds. This study provides the first in-depth examination of total sulfur content and sulfur speciation in brown and red Antarctic seaweeds. [ABSTRACT FROM AUTHOR]

Per and polyfluoroalkylated substances (PFAS) are common additives in ski waxes for their water repellent characteristic. Abrasion of ski wax leaves PFAS on the snow surface, however, little is known about the distribution and concentration of PFAS in snow and soil due to skiing. In this study we analysed different ski waxes, snowmelts and soil from family skiing areas from Alpine locations using targeted high performance liquid chromatography tandem mass spectrometry (HPLC-MS/MS) to understand more about PFAS distribution in the environment. In general, we found a very diverse PFAS pattern in the analysed media. PFAS level was higher in skiing areas compared to the non-skiing ones that were used as control. ∑target PFAS ranged between <1.7 ng L−1 and 143 ng L−1 in snowmelt, <0.62 ng g−1 and 5.35 ng g−1 in soil and <1.89 and 874 ± 240 ng g−1 in ski wax samples. Snowmelt was dominated by short-chained PFAS, while soil and wax contained both short and long-chained PFAS. Extractable organic fluorine (EOF) was several orders of magnitude higher for waxes (0.5–2 mg g−1) than for soils (up to 0.3 μg g−1), while total fluorine (TF) content of the waxes was even higher, up to 31 210 ± 420 μg g−1. We also showed that the ∑ target PFAS accounts for up to 1.5% in EOF content, showing that targeted LC-MS/MS gives a limited measure of the pollution originated from ski waxes and non-targeted analysis and EOF is necessary for a better overview on PFAS distribution. [ABSTRACT FROM AUTHOR]

This document is a summary of an article titled "Elemental Mass Spectrometry for Bioanalysis" published in the journal Analytical & Bioanalytical Chemistry. The article discusses the importance and versatility of mass spectrometry (MS) as an analytical tool for characterizing matter in living and non-living systems. It focuses on elemental mass spectrometry, which involves degrading matter to its basic components, and highlights the use of inductively coupled plasma mass spectrometry (ICP-MS) as a primary source for elemental ions. The article also covers various applications of elemental mass spectrometry in fields such as environmental monitoring, food control, and biological research. The topical collection in the article includes 24 contributions that reflect current research and trends in elemental mass spectrometry for bioanalysis, covering topics such as sample preparation, elemental speciation, protein analysis, and the detection of small objects like cells and nanoparticles. The guest editors express their appreciation for the contributions and hope that the collection serves as a valuable source for readers. The article is authored by Jörg Bettmer, Mario Corte-Rodríguez, and Marcia Foster Mesko, who are experts in the field of analytical chemistry and have published extensively in this area. [Extracted from the article]

Laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) was applied for the determination of Br and I in hair strands of human individuals under treatment with synthetic thyroid hormones. Quantification relied on the use of Br- and I-spiked human hair strands prepared in-house as matrix-matched external calibration standards. The results obtained via LA-ICP-MS agreed with the corresponding Br and I concentrations as determined via pneumatic nebulization-ICP-MS after digestion via microwave-induced combustion. The spatial distributions of Br and I in the spiked hair standards were evaluated by spatially resolved LA-ICP-MS analysis and a homogeneous distribution was established upon scanning longitudinally along the hair strands and across the cross-section. Twenty-five human hair strands from volunteers were analyzed by LA-ICP-MS (7 individuals with hypothyroidism under treatment with synthetic thyroid hormones and 18 individuals considered healthy), and those from subjects under treatment with synthetic thyroid hormones presented a higher I concentration than those from subjects considered healthy. Limits of detection were 0.36 μg g−1 for Br and 0.14 μg g−1 for I, allowing trace level determination in human hair. [ABSTRACT FROM AUTHOR]

In this study, the microwave-induced combustion (MIC) method was evaluated for the sample preparation of the most consumed mushroom species in Brazil (Champignon, Shiitake, and Shimeji) and further halogen determination by ion chromatography (IC). For this, sample mass, combustion aid mass, and absorbing solution (H2O and 50 mmol·L−1, 100 mmol·L−1, or 150 mmol·L−1 NH4OH) were evaluated. Bromine and iodine concentrations, determined by IC, were lower than the limits of detection (LODs, Br: 6 mg·kg−1 and I: 24 mg·kg−1). Inductively coupled plasma mass spectrometry (ICP-MS) was also used for Br and I determination, and the LODs were lower (Br: 0.066 mg·kg−1 and I: 0.014 mg·kg−1) than those obtained by IC. Concentrations of Cl, obtained by IC, ranged from 523 mg·kg−1 to 13053 mg·kg−1 with LOD of 40 mg·kg−1. In turn, Br and I concentrations, obtained by ICP-MS, ranged from 2.49 mg·kg−1 to 5.50 mg·kg−1 and from <0.014 mg·kg−1 to 0.047 mg·kg−1, respectively. Fluorine concentrations, determined by IC, were always lower than LOD (23 mg·kg−1). The trueness of the proposed methods was evaluated by recovery tests using standard solutions and a reference material (RM NIST 8435). When using the standard solution, recoveries ranged from 95% to 103% for halogen determination by IC and from 105% to 109% for Br and I determination by ICP-MS. When using the RM, recoveries of 102% for Cl by IC and of 87% and 86% for Br and I by ICP-MS, respectively, were obtained. [ABSTRACT FROM AUTHOR]

Manganese (Mn) is an essential element that, in excess, seems to be involved in the development of different neurodegenerative conditions. Gamma-oryzanol (Ory) was previously reported to possess antioxidant and neuroprotective properties. Thus, we conducted this study to test the hypothesis that Ory can also protect flies in an Mn intoxication model. Adult wild-type flies were fed over 10 days with Mn (5 mM) and/or Ory (25 μM). Flies treated with Mn had a decrease in locomotor activity and a higher mortality rate compared to those in controls. Mn-treated flies also had a significant increase in acetylcholinesterase (AChE) activity, in Mn accumulation and in oxidative stress markers. Moreover, flies treated with Mn exhibited a significant decrease in dopamine levels and in tyrosine hydroxylase activity, as well as in mitochondrial and cellular viability. Particularly important, Ory protected against mortality and avoided locomotor and biochemical changes associated with Mn exposure. However, Ory did not prevent the accumulation of Mn. The present results support the notion that Ory effectively attenuates detrimental changes associated with Mn exposure in Drosophila melanogaster, reinforcing its neuroprotective action/potential. [ABSTRACT FROM AUTHOR]

Rationale: To increase the consumption of egg powder and its fractions a suitable quality control method is required to obtain more information on its nutritional composition. The proposed method enables the quantification of important elements for the functioning of the human organism, such as halogens and sulfur, in egg powder and its fractions. Methods: Up to 350 mg of egg powder or its fractions (egg white powder and egg yolk powder) were digested by microwave‐induced combustion using 20 bar pressure of oxygen. The analytes were absorbed in 100 mmol L−1 of NH4OH solution. The determination of halogens (chlorine, bromine, fluorine, and iodine) and sulfur was performed in a single analysis using ion chromatography with conductivity detection coupled to mass spectrometry. Results: Using the proposed method, spike recoveries between 99% and 104% for all analytes were obtained, and results agreed with certified values of reference materials (agreements were between 100% and 109%). The relative standard deviations were below 8%. The variation in elemental concentration over a wide range in different fractions (whole egg powder, egg white powder, and egg yolk powder) and different brands was also observed. Conclusions: The proposed method provides reliable information about minerals in whole egg powder and its fractions, contributing to better quality control of these products. Because these food products are widely consumed, these results suggest the safe ingestion levels of these elements. [ABSTRACT FROM AUTHOR]

Rationale: Bromine and iodine have important physiological functions; however, in inadequate concentration, they can also cause several physiological problems. Their mobility assessment in human organisms through biological sampling may help clarify some doubts related to metabolic routes, which are still not well elucidated. In this context, a suitable analytical method for this purpose should be developed. Methods: An analytical method for determining ultratrace levels of bromine and iodine in human nail samples was developed. Inductively coupled plasma mass spectrometry (ICP‐MS) using a conventional nebulization system was immediately chosen as the determination tool because of its powerful sensitivity and selectivity. Sample preparation methods including microwave‐induced combustion (MIC), microwave‐assisted extraction, and microwave‐assisted digestion were evaluated. The compatibility of the final solutions with ICP‐MS analysis was considered while the method was developed. Results: MIC was chosen as the most suitable method for the sample preparation for determining the levels of bromine and iodine in human nail samples using ICP‐MS. Unlike other sample preparation methods, this one fully eliminated interferences related to the carbon content and memory effects. Sample masses up to 100 mg were efficiently digested, and the analytes were quantitatively absorbed using only 50 mmol L−1 NH4OH solution. Recoveries ranged from 93% to 102%, and the relative standard deviation was < 8%. Conclusions: The proposed analytical method presents important characteristics for routine analysis. It allows ultratrace determination even when low sample masses are used because of the low blank values, reduced volume of reagents, and powerful detectability using ICP‐MS. [ABSTRACT FROM AUTHOR]

A suitable and green analytical method using microwave-induced combustion and ion chromatography with conductivity detection (IC-CD) and mass spectrometry detection (IC-MS) was proposed for the halogens and sulfur determination in pet food using a single analysis. Samples (up to 500 mg) were efficiently digested in a closed system under oxygen pressure (20 bar). Ultrapure water and 50 mmol L−1 or 100 mmol L−1 (NH4)2CO3 were evaluated as absorbing solutions. Trueness was evaluated by recovery tests using standard solution and certified reference materials. In both tests, mean recoveries ranging from 91 to 108% for all analytes were obtained using 50 mmol L−1 (NH4)2CO3 as absorbing solution. AOAC International recommended official methods for Cl and F determination in animal feed were also performed. Results for Cl using proposed method were in agreement with those obtained using AOAC official method, while the results for F were not compared between them because the concentration in the samples using AOAC official method was not detected. Precision was evaluated in terms of repeatability and the relative standard deviations (RSDs) using the proposed method were always lower than 8%. The proposed method presents several advantages when compared with AOAC International official methods such as the multielemental determination capability, lower waste generation, lower limits of detection, lower RSDs, and higher sample throughput. Sixteen samples destined to cats or dogs from different manufacturers were analyzed and the results showed a wide variation. These results indicate that an efficient quality control should be performed, and the proposed method is an excellent alternative as a new analytical tool for routine analysis of pet food. [ABSTRACT FROM AUTHOR]

A single analysis of hair for determining halogens (chlorine, bromine, fluorine, and iodine) and sulfur by ion chromatography with suppressed conductivity and mass spectrometry detection (IC-MS) was proposed. Inductively coupled plasma optical emission spectrometry (ICP OES) and inductively coupled plasma mass spectrometry (ICP-MS) were also used to compare the results. For this purpose, 300 mg of human hair were digested by microwave-induced combustion (MIC) using 20 bar of oxygen pressure. The analytes were absorbed in 100 mmol L−1 NH4OH. Trueness of the proposed method was evaluated by analysis of a CRM of human hair; by recovery tests, using standard solution at two levels (50% and 100%), and by comparison of results with those obtained by ICP OES (Cl and S) and ICP-MS (Br and I). Suitable recoveries (ranging from 92 to 105%) were obtained, and the results from CRM analysis did not differ significantly from those described in the certificate. Moreover, results obtained by IC-MS did not present significant differences (p > 0.05) from those obtained by ICP OES and by ICP-MS. Precision was evaluated in terms of repeatability and intermediate precision, and the relative standard deviations were always lower than 8%. The proposed method presented good accuracy and it is a reliable strategy for human hair analysis. Final digests obtained using the MIC method were fully compatible with all proposed determination techniques. Compared to others reported in the literature, the proposed method presents several advantages, especially given that it is possible to determine halogens and sulfur in a single analysis. [ABSTRACT FROM AUTHOR]

In this work, the use of complexing acids (HF and HCl) combined with HNO3 was carefully evaluated for the digestion of several types of lipsticks and further Cd and Pb determination by inductively coupled plasma mass spectrometry (ICP-MS). Creamy, opaque and shimmering lipsticks were digested using HNO3 (6 mL) or a mixture containing HNO3 (6 mL) plus HCl (0.5 or 2 mL) or HNO3 (6 mL) plus HF (2 mL). The results indicate that complexing acids are not required for the subsequent determination of Cd in all types of lipsticks evaluated. On the other hand, complexing acids were essential for ensuring quantitative results for Pb in shimmering lipstick. Thus, by using HNO3 combined with only 0.5 mL of HCl, it was possible to obtain quantitative results for Pb and Cd in lipsticks. Under these conditions, recoveries for Cd and Pb were between 95 and 103%. No statistical difference was observed between the results obtained using the proposed method (HNO3/HCl) and those obtained using HNO3/HF, where a complete dissolution of the lipsticks' inorganic fraction occurred. Moreover, by using HCl, HF was avoided and solutions more compatible with ICP-MS analysis were obtained. The limits of detection for Cd and Pb were 3 and 77 ng g−1, respectively. This method was applied for a variety of lipsticks, and the concentration of Cd and Pb ranged from ＜3 to 31 ng g−1 and 271 to 2250 ng g−1, respectively. [ABSTRACT FROM AUTHOR]

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). [ABSTRACT FROM AUTHOR]

(1) Background: Elevated atmospheric CO2 concentration affects the growth and development of the rice crop. In Southern Brazil, rice is traditionally produced with continuous irrigation, implying a significant amount of water used. Besides, continuous flooding favors the uptake of toxic elements such as arsenic (As) and cadmium (Cd). In this work, one Brazilian rice cultivar (IRGA 424) was tested for the effects of elevated CO2 concentration and different water regimes on rice yield, and As and Cd accumulation in grain. (2) Methods: Rice was grown in two CO2 concentrations (400 and 700 µmol mol−1) and two irrigation regimes (continuous and intermittent). It was evaluated the number of tillers, plant height, aboveground dry weight (ADW), water use efficiency (WUE), rice yield components, and As and Cd concentration in rice grain. (3) Results: Rice plants were taller and had a higher WUE when cultivated at e[CO2]. The ADW and the rice yield component were not affected by CO2 levels nor water regimes. Intermittent flood regimes had a lower average As concentration. The Cd concentration in the samples in both growing seasons and all treatments was below the limit of quantitation (8.76 μg kg−1). (4) Conclusions: Enhanced CO2 concentration did not affect rice yield, increased the WUE, and reduced As concentration in grains. Regarding water management, the intermittent regime enhanced WUE and promoted a reduction in As concentration in grains. [ABSTRACT FROM AUTHOR]