Evaluation of Nickel and Titanium Releasing from Titanium-coated Stainless Steel Crowns Regarding Trimming: An In Vitro Study.

Introduction: Stainless steel crowns (SSCs) are the most durable and effective restorations for primary teeth. Titanium-coated SSCs are newer on the market, and this study was conducted to assess the amount of nickel (Ni) and titanium ions released from titanium-coated SSCs, with and without trim, in artificial saliva. Materials and methods: A total of 60 titanium-coated SSCs were divided into two groups-group I (n = 30, without trim) and group II (n = 30, with trim) and were immersed in 5 mL artificial saliva. The amount of Ni and titanium released in each group was measured by inductively coupled plasma-mass spectrometry on days 1, 7, and 21. Results: The amount of Ni ion released in group I on day 1 was 0.0096 ppm and reduced on day 7 (0.0091 ppm) and day 21 (0.0088 ppm). Whereas the amount of Ni ion released in group II was the same for all 3 days (0.0096 ppm). The amount of titanium ion released in both groups was the same on all 3 days (0.00108 ppm). Conclusion: There was no significant difference seen in the mean Ni and titanium ion release between the two groups on all 3 days. The cumulative release of metals from titanium-coated SSCs in each of the groups was significantly lower than the level required to produce any harmful effects. Any of the groups of commercially available SSCs can be used in pediatric dentistry. How to cite this article: Biradar R, Siaddaiah SB, Bhat PK. Evaluation of Nickel and Titanium Releasing from Titanium-coated Stainless Steel Crowns Regarding Trimming: An In Vitro Study. Int J Clin Pediatr Dent 2024;17(5):524-527.

Adsorption Dynamics of Disodium Octaborate Tetrahydrate on Clay Minerals: Implications for Construction Wood Protection.

The wood preservative disodium octaborate tetrahydrate (DOT) migration is studied in clay. Using boron analysis by inductively coupled plasma optical emission spectroscopy (ICP-OES), DOT spatial and temporal dynamics are surveyed to show how DOT permeates into the wood and the clay using concentration profiles as a function of depth, initial wood moisture, and direction of filling. Atomic force microscopy and chemical imaging using photoinduced force microscopy are used to show the morphology of the wood samples and the distribution of DOT on their surface. ICP-OES results show that the average DOT concentration in the wood samples is originally 0.8 and 1.5 wt% in the bulk and at the surface, respectively. Conditioning of the wood to a moisture content of 19% in a climatic chamber reduces DOT concentration by 8% for the fir and 17% for the spruce. After one week of contact with the clays, the results showed a rapid decrease of 25-40% in DOT concentration in wood. On longer periods (5 months), the spruce shows a tendency to reabsorb the DOT from the clay and the DOT migration stabilizes at 20%. These results contribute to defining the dosage of DOT when the wood is exposed to clay.

Development and validation of a microwave-assisted digestion technique as a rapid sample preparation method for the estimation of selenium in pharmaceutical dosage forms by ICP-OES.

Selenium is a class 2B element according to the International Council for Harmonization Q3D guidelines. Selenium sulfide is an anti-infective agent with antifungal and antibacterial properties used to treat dandruff and seborrheic dermatitis. The literature survey revealed that most of the analytical techniques to estimate selenium were time-consuming and/or required high skill levels. The process involved identifying the isotopes, selecting the measurement approach, and optimizing a typical microwave-aided digesting procedure. Ammonium hydrogen difluoride, water, and concentrated nitric acid were added to the samples. The confirmed microwave digestion program was a two-step program where in the initial step, the samples were ramped at 200°C for 20 min and held for 5 min. Later, samples were cooled and neutralized by boric acid, then ramped for 20 min to a temperature of 180°C and held for 10 min. Selenium was estimated at 196.090 nm by inductively coupled plasma optical emission spectroscopy (ICP-OES). System suitability was run before initiating analysis to ensure that system performance was consistent. Analytical validation parameters, such as the specificity of the method, were demonstrated at 196.090 nm, linearity was proven from 10 ppm to 150 ppm of selenium concentration, the detection limit was 1.28 ppm, and the limit of quantification was 3.89 ppm. Robustness was confirmed for small changes to ICP-OES operating conditions. The precision of the method demonstrated by analyzing the percentage relative standard deviation for six injections was found to be less than 2.0%. Accuracy was confirmed from 10 ppm to 150 ppm, and all the samples were observed to be within the range of 95%-105%. A common microwave-assisted digestion technique was developed and validated as well. The precision, specificity, linearity, accuracy, and robustness of the method for estimating selenium in selenium sulfide drug substances and various pharmaceutical dosage forms were demonstrated. This newly developed microwave-assisted digestion technique has optimum sensitivity and is highly reproducible and time-saving than the existing methods This method can be applied to numerous matrices for a finished dosage of selenium sulfide formulations.

Computer simulation and modeling of glow discharge optical emission coded aperture elemental mapping.

BACKGROUND: Elemental mapping (EM) yields necessary insights into mechanisms of interest in solid samples across multiple disciplines. There are several EM techniques available but long acquisition time is a common limitation. Glow discharge optical emission spectroscopy (GDOES) allows direct quantitative multi-EM at very high throughput (∼10 s s) when coupled to traditional hyperspectral imaging (HSI) techniques. However, GDOES consumes the sample via sputtering, such that traditional HSI sequential scanning requirements lead to loss of information/resolution, which is compounded for multi-EM and limits nanomaterials analysis. Thus, there is a need for faster HSI to enable GDOES multi-EM of nanoscale materials. RESULTS: Here, a new technique is described, Glow discharge Optical emission Coded Aperture elemental Mapping (GOCAM), that takes advantage of compressive coded aperture spectral imaging to enable multi-EM in a single camera exposure. In this first phase of development, computer model simulations were implemented to study the effects of coded aperture parameters on data fidelity, which showed the best fidelity is achieved at smaller mask element sizes and transmittance of 60 %. In addition, SeSCIGPU demonstrated the best fidelity performance compared to several compressed sensing reconstruction algorithms, including TwIST, GAP-TV, SeSCICPU, and ADMM-TV, as evaluated by studying the effects of varying the corresponding hyperparameters. SIGNIFICANCE: This study shows GOCAM's feasibility and provides a starting point for the second phase hardware development currently underway. GOCAM's potential to allow multi-EM from solid surfaces in a fraction of a second will be particularly enabling for nanostructured materials characterization.

Unveiling of a puzzling dual ionic migration in lead- and iodide-deficient halide perovskites (d-HPs) and its impact on solar cell J-V curve hysteresis.

Halide perovskite solar cells are characterized by a hysteresis between current-voltage (J-V) curves recorded on the reverse and on the forward scan directions, and the suppression of this phenomenon has focused great attention. In the present work, it is shown that a special family of 3D perovskites, that are rendered lead -and iodide- deficient (d-HPs) by incorporating large organic cations, are characterized by a large hysteresis. The strategy of passivating defects by K+, which has been successful in reducing the hysteresis of 3D perovskite perovskite solar cells, is inefficient with the d-HPs. By glow discharge optical emission spectroscopy (GD-OES), the existence of the classic iodide migration in these layers is unveiled, which is efficiently blocked by potassium cation insertion. However, it is also shown that it co-exists with the migration of the large organic cations characteristics of d-HPs which are not blocked by the alkali metal ion. The migration of those large cations is intrinsically linked to the special structure of the d-HP. It is suggested that it takes place through channels, present throughout the whole perovskite layer after the substitution of PbI+ units by the large cations, making this phenomenon intrinsic to the original structure of d-HPs.

Validation of a new liquid asymmetric-electrode plasma optical emission spectroscopy (LAEP-OES) method for measurement of total mercury in tuna.

BACKGROUND: Mercury intake is caused by eating seafood, such as tuna and other predatory fish species. To reduce the health risks of mercury intake, it is necessary to continuously measure and monitor mercury concentrations at fish farms and markets. We have developed a compact system that can detect multiple heavy metals by liquid asymmetric-electrode plasma optical emission spectroscopy (LAEP-OES). OBJECTIVE: The validity of the LAEP-OES method for total mercury levels was evaluated using standard solutions, certified substances, and specimens of bluefin tuna and other fish species. METHOD: All specimens were dissolved in 4 M lithium hydroxide solution and then dispensed into a sample reservoir well of the single-use measurement reagent pack. Total mercury levels were automatically measured within 15 min of placement into the dedicated equipment. 102 fish specimens classified into 10 fish species were evaluated using the new method and the results were compared to those obtained from validated analytical methods. RESULTS: Limit of detection (0.02 mg/kg), limit of quantification (0.07 mg/kg), repeatability (4.0%), intermediate precision (9.8%), and trueness (recoveries 107%) of the proposed method were within satisfactory limits for total mercury levels in fish. Additionally, when using various fish species, the method had a strong positive correlation with the results of cold-vapor atomic absorption spectrometry (CV-AAS, the official method) with Spearman rs = 0.984. CONCLUSION: The LAEP-OES method can be used for measuring total mercury levels in bluefin tuna. Total mercury measurement using this new method has the potential to be applied to other fish species. HIGHLIGHTS: Total mercury levels in fish were measured using our unique analysis system. Pacific bluefin tuna, southern bluefin tuna, and Atlantic bluefin tuna distributed in the Japanese market were analyzed for total mercury in their wild and farmed fish varieties.

Imaging the elemental distribution within human malignant melanomas using Laser-Induced Breakdown Spectroscopy.

The diagnosis of malignant melanoma, often an inconspicuous but highly aggressive tumor, is most commonly done by histological examination, while additional diagnostic methods on the level of elements and molecules are constantly being developed. Several studies confirmed differences in the chemical composition of healthy and tumor tissue. Our study presents the potential of the LIBS (Laser-Induced-Breakdown Spectroscopy) technique as a diagnostic tool in malignant melanoma (MM) based on the quantitative changes in elemental composition in cancerous tissue. Our patient group included 17 samples of various types of malignant melanoma and one sample of healthy skin tissue as a control. To achieve a clear perception of results, we have selected two biogenic elements (calcium and magnesium), which showed a dissimilar distribution in cancerous tissue from its healthy surroundings. Moreover, we observed indications of different concentrations of these elements in different subtypes of malignant melanoma, a hypothesis that requires confirmation in a more extensive sample set. The information provided by the LIBS Imaging method could potentially be helpful not only in the diagnostics of tumor tissue but also be beneficial in broadening the knowledge about the tumor itself.

Effect of Femtosecond Ultraviolet and Infrared Laser Wavelength on Plasma Characteristics of Metals, Ceramics and Glass Samples Using Femtosecond Laser-Induced Breakdown Spectroscopy.

In this work, we present studies on the effect of laser wavelengths on the laser-induced plasma characterization using a femtosecond (fs) ytterbium-doped potassium-gadolinium tungstate (Yb:KGW) laser. Plasma plumes of copper, steel, ceramics, and glass samples were induced using a multiple shot of 200 fs laser pulses with 1030 nm and 343 nm wavelengths at fixed laser fluence (10.5J/cm2) and analyzed using the laser-induced breakdown spectroscopy (LIBS) technique. Time-resolved fs-LIBS measurements were performed on the same set of samples and under the same experimental conditions. For the calculation of plasma parameters, the set of spectral lines of Cu(I) (for copper sample), Fe(I) (for steel sample), and Ca(I), K(I) (for glass and ceramics samples) were observed. The plasma electron temperature and density were evaluated from the Boltzmann plots and Stark-broadening profiles of the plasma spectral lines, assuming the local thermodynamic equilibrium condition. Time-resolved plasma temperature and electron density for fs-LIBS using ultraviolet (UV) and infrared (IR) laser wavelengths were analyzed and no significant dependence on fs laser wavelength was observed for any of the samples. However, for all samples the signal-to-noise ratio (SNR) significantly increased using UV laser radiation: copper (∼100%), steel (∼300%), glass (∼400%), and ceramics (∼40%). Therefore, by using a fs UV laser wavelength for laser-induced breakdown spectroscopy experiments, for certain materials the SNR and at the same time the limit of detection can be significantly enhanced.

Carbon-Rich Plasma-Deposited Silicon Oxycarbonitride Films Derived from 4-(Trimethylsilyl)morpholine as a Novel Single-Source Precursor.

4-(trimethylsilyl)morpholine O(CH2CH2)2NSi(CH3)3 (TMSM) was investigated as a single-source precursor for SiCNO films synthesis. Optical emission spectroscopy of plasma generated from TMSM/He, TMSM/H2, and TMSM/NH3 gas mixtures revealed the presence of N2, CH, H, CN, and CO species. The last two are suggested to be responsible for the lowering of carbon concentration in the films in comparison with the precursor. The refractive index ranged from 1.5 to 2.0, and bandgap varied from 2.0 to 4.6 eV, which pointed that some of the films can be used as antireflective coatings in silicon photovoltaic cell technologies and dielectric layers in electronic devices.

Optical Emission Spectroscopy for the Real-Time Identification of Malignant Breast Tissue.

Breast conserving resection with free margins is the gold standard treatment for early breast cancer recommended by guidelines worldwide. Therefore, reliable discrimination between normal and malignant tissue at the resection margins is essential. In this study, normal and abnormal tissue samples from breast cancer patients were characterized ex vivo by optical emission spectroscopy (OES) based on ionized atoms and molecules generated during electrosurgical treatment. The aim of the study was to determine spectroscopic features which are typical for healthy and neoplastic breast tissue allowing for future real-time tissue differentiation and margin assessment during breast cancer surgery. A total of 972 spectra generated by electrosurgical sparking on normal and abnormal tissue were used for support vector classifier (SVC) training. Specific spectroscopic features were selected for the classification of tissues in the included breast cancer patients. The average classification accuracy for all patients was 96.9%. Normal and abnormal breast tissue could be differentiated with a mean sensitivity of 94.8%, a specificity of 99.0%, a positive predictive value (PPV) of 99.1% and a negative predictive value (NPV) of 96.1%. For 66.6% patients all classifications reached 100%. Based on this convincing data, a future clinical application of OES-based tissue differentiation in breast cancer surgery seems to be feasible.

Evidence of direct interaction between cisplatin and the caspase-cleaved prostate apoptosis response-4 tumor suppressor.

Prostate apoptosis response-4 (Par-4) tumor suppressor protein has gained attention as a potential therapeutic target owing to its unique ability to selectively induce apoptosis in cancer cells, sensitize them to chemotherapy and radiotherapy, and mitigate drug resistance. It has recently been reported that Par-4 interacts synergistically with cisplatin, a widely used anticancer drug. However, the mechanistic details underlying this relationship remain elusive. In this investigation, we employed an array of biophysical techniques, including circular dichroism spectroscopy, dynamic light scattering, and UV-vis absorption spectroscopy, to characterize the interaction between the active caspase-cleaved Par-4 (cl-Par-4) fragment and cisplatin. Additionally, elemental analysis was conducted to quantitatively assess the binding of cisplatin to the protein, utilizing inductively coupled plasma-optical emission spectroscopy and atomic absorption spectroscopy. Our findings provide evidence of direct interaction between cl-Par-4 and cisplatin, and reveal a binding stoichiometry of 1:1. This result provides insights that could be useful in enhancing the efficacy of cisplatin-based and tumor suppressor-based cancer therapies.

[Methods, applications, and future perspectives of intraoperative tissue identification]. / Methoden, Anwendungen und Zukunftsperspektiven der intraoperativen Gewebeerkennung.

Over the last century, there has been a steady development of new technologies for intraoperative tissue identification and differentiation. The applications are varied, with the core purpose being to identify target structures while preserving adjacent tissue and thereby follow a general paradigm of minimally invasive medicine. Particularly in oncology, a further asset of these technologies is the identification or classification of neoplastic tissue to support and improve therapy, for example, in breast cancer surgery.Many technologies under consideration make use of the different physical characteristics of treated tissues, such as induced fluorescence, optical coherence, and electrical impedance.Recent developments are focusing on moving from ex vivo to in situ and from asynchronous to real-time assistance of the clinicians, for example, by means of optical emission spectroscopy. Refinements of existing and the creation of new methods will include AI tools to make them more powerful while reducing the inter-operator variability in operative interventions. This talk addresses several aspects of the usage and suitability of these technologies for intraoperative, therapy-supporting application.

A Calibration-Free Optical Emission Spectroscopic Method to Determine the Composition of a Spark Discharge Plasma Used for AuAg Binary Nanoparticle Synthesis.

Spark discharge generators (SDGs) employ controlled gaseous environments to induce spark ablation of non-insulating electrodes, resulting in the formation of various nanostructures in the gas phase. The method offers technological advantages such as continuous particle production, scalable yield, and minimal waste. Additionally, the versatility of the process enables the generation of alloy nanoparticles from various material combinations, including immiscible ones. In order to fully exploit its potential, understanding the atomic mixing process during electrode ablation, particularly in the case of dissimilar electrodes, is crucial. Temporally and spatially resolved optical emission spectroscopy (OES) has been previously demonstrated as an effective characterization tool for spark plasmas in SDGs. However, to gain a deeper insight into the vapor mixing process, it is essential to quantitatively determine the plasma composition in both space and time. This paper introduces a calibration-free OES-based method tailored for spark plasmas utilized in binary nanoparticle generation. The method introduces the so-called multi-element combinatory Boltzmann plots, which use intensity ratios of emission atomic lines from different materials, allowing for the direct estimation of total number concentration ratios. The approach is tested using synthetic spectra and validated with experimental spark spectra obtained near an alloyed gold-silver (AuAg) electrode with a known composition. The study demonstrates the capabilities and robustness of the proposed method, with a focus on the AuAg system due to its significance in plasmonic research and frequent synthesis using spark ablation.

How ICP-OES changed the face of trace element analysis: Review of the global application landscape.

The 50th anniversary of Inductively Coupled Plasma-Optical Emission Spectrometry (ICP-OES) will be observed in 2024. ICP-OES was first commercially available in 1974, and since then, it has become one of the most widely used analytical techniques in the world. ICP-OES is a powerful tool for the determination of trace and ultratrace elemental concentrations in a wide variety of samples specifically for multielement analysis. It is used in a wide range of applications, including environmental monitoring, food analysis, and medical diagnostics. This review aims to explore recent applications of ICP-OES in areas such as food analysis, microplastics, materials, dietary supplements, human tissue, and bodily fluids. The utilization of ICP-OES in these fields has ignited the interest of prospective ICP-OES users and inspired current practitioners, as the 50th anniversary approaches, it is of value of providing an updated review. It is important to note that this work does not seek to encompass a comprehensive review of ICP-OES, given the vast number of published results in this field. Undertaking such a comprehensive task would be a daunting challenge. Consequently, an overview of the ICP-OES instrumental technique is provided, followed by a highlighting of recent significant applications in the aforementioned fields.

Detection of sulfur mustard simulants using the microwave atmospheric pressure plasma optical emission spectroscopy method.

Sulfur mustard (SM) is one kind of highly toxic chemical warfare agent and easy to spread, while existing detection methods cannot fulfill the requirement of rapid response, good portability, and cost competitiveness at the same time. In this work, the microwave atmospheric pressure plasma optical emission spectroscopy (MW-APP-OES) method, taking the advantage of non-thermal equilibrium, high reactivity, and high purity of MW plasma, is developed to detect three kinds of SM simulants, i.e., 2-chloroethyl ethyl sulfide, dipropyl disulfide, and ethanethiol. Characteristic OES from both atom lines (C I and Cl I) and radical bands (CS, CH, and C2) is identified, confirming MW-APP-OES can preserve more information about target agents without full atomization. Gas flow rate and MW power are optimized to achieve the best analytical results. Good linearity is obtained from the calibration curve for the CS band (linear coefficients R 2 > 0.995) over a wide range of concentrations, and a limit of detection down to sub-ppm is achieved with response time on the order of second. With SM simulants as examples, the analytical results in this work indicate that MW-APP-OES is a promising method for real-time and in-site detection of chemical warfare agents.

Application of Micro-Arc Discharges during Anodization of Tantalum for Synthesis of Photocatalytic Active Ta2O5 Coatings.

Ta2O5 coatings were created using micro-arc discharges (MDs) during anodization on a tantalum substrate in a sodium phosphate electrolyte (10 g/L Na3PO4·10H2O). During the process, the size of MDs increases while the number of MDs decreases. The elements and their ionization states present in MDs were identified using optical emission spectroscopy. The hydrogen Balmer line Hß shape analysis revealed the presence of two types of MDs, with estimated electron number densities of around 1.1 × 1021 m-3 and 7.3 × 1021 m-3. The effect of MDs duration on surface morphology, phase and chemical composition, optical absorption, and photoluminescent, properties of Ta2O5 coatings, as well as their applications in photocatalytic degradation of methyl orange, were investigated. The created coatings were crystalline and were primarily composed of Ta2O5 orthorhombic phase. Since Ta2O5 coatings feature strong absorption in the ultraviolet light region below 320 nm, their photocatalytic activity is very high and increases with the time of the MDs process. This was associated with an increase of oxygen vacancy defects in coatings formed during the MDs, which was confirmed by photoluminescent measurements. The photocatalytic activity after 8 h of irradiation was around 69%, 74%, 80%, and 88% for Ta2O5 coatings created after 3 min, 5 min, 10 min, and 15 min, respectively.

Overcoming the matrix effect in the element analysis of steel: Laser ablation-spark discharge-optical emission spectroscopy (LA-SD-OES) and Laser-induced breakdown spectroscopy (LIBS).

The optical emission of plasma on industrial steel samples induced by Laser Ablation-Spark Discharge-Optical Emission Spectroscopy (LA-SD-OES) and by Laser-Induced Breakdown Spectroscopy (LIBS) is investigated and correlated to the volume of ablated steel material. The 36 steel samples investigated have an iron content C(Fe) above 94 wt%. The excitation energy in LIBS (laser pulse of 55 mJ) and in LA-SD-OES (laser pulse of 5 mJ and spark discharge of 50 mJ) is the same. In LA-SD-OES, the optical emission of plasma and the size of ablation craters are very similar for all samples and a linear calibration curve for Mn is measured (R2 = 0.99). In LIBS, however, a pronounced dependence of the plasma emission and of the crater volume on the steel matrix is observed and calibration curves show a strong cross-sensitivity to other elements such as Si (matrix effect). The hardness, grain size, and phase of steel samples are analyzed to correlate the matrix effect in LIBS measurements to a physical property of the specimen. The different behavior for LA-SD-OES and LIBS is probably due to different processes of sampling and plasma excitation. From our results we conclude that LA-SD-OES enables for the element analysis of industrial steel largely independent of composition and structure of samples while in LIBS the matrix effect has to be taken into account.

Generative Adversarial Network-Based Fault Detection in Semiconductor Equipment with Class-Imbalanced Data.

This research proposes an application of generative adversarial networks (GANs) to solve the class imbalance problem in the fault detection and classification study of a plasma etching process. Small changes in the equipment part condition of the plasma equipment may cause an equipment fault, resulting in a process anomaly. Thus, fault detection in the semiconductor process is essential for success in advanced process control. Two datasets that assume faults of the mass flow controller (MFC) in equipment components were acquired using optical emission spectroscopy (OES) in the plasma etching process of a silicon trench: The abnormal process changed by the MFC is assumed to be faults, and the minority class of Case 1 is the normal class, and that of Case 2 is the abnormal class. In each case, additional minority class data were generated using GANs to compensate for the degradation of model training due to class-imbalanced data. Comparisons of five existing fault detection algorithms with the augmented datasets showed improved modeling performances. Generating a dataset for the minority group using GANs is beneficial for class imbalance problems of OES datasets in fault detection for the semiconductor plasma equipment.

Nondestructive characterization of diseased Chinese chive leaves using X-ray intensity ratios with microbeam synchrotron radiation X-ray fluorescence spectrometry.

The Chinese chive (Allium tuberosum) is a core crop grown in Kochi Prefecture, Japan. However, withering symptoms occur during greenhouse growing, which have a negative impact on crop management Chinese chive leaves with physiological disorders (PD) or necrotic streak disease (ND) present with withering as typical blight symptoms. Excess or deficiency of elements may cause such withering in Chinese chive leaves with PD. Therefore, visualizing the elemental distribution in plant bodies may help clarify the cause of this withering. In this study, using synchrotron radiation X-ray fluorescence (SR-XRF) imaging, we examined the elemental distribution conditions in healthy Chinese chive leaves without withering, those that withered due to PD, and those that withered due to ND. Segmentation analysis of inductively coupled plasma-optical emission spectroscopy (ICP-OES) was performed on the SR-XRF imaged Chinese chive leaves and the data from the two analytical methods were compared. SR-XRF imaging provided more detailed data on elemental distribution compared with segmentation analysis using ICP-OES. Based on the SR-XRF imaging results, the X-ray intensity ratios for Ca/K, Fe/Mn, and Zn/Cu were calculated. These findings support that the Ca/K, Fe/Mn, and Zn/Cu X-ray intensity ratios can be used in the early detection of withered leaves and to predict the factors causing withering.

Trace Element Levels in Nails of Residents of Addis Ababa Are Shaped by Social Factors and Geography.

The Akaki catchment in Ethiopia is home to Addis Ababa and about five million people. Its watercourses receive a variety of wastes released by the residents and industries. River water is being used for irrigation, livestock watering, and other domestic purposes. This study tested the hypothesis that the river pollution would be reflected in higher levels of trace elements in the nails of residents living in Akaki-Kality Sub-City in the downstream, as compared to those living in Gullele Sub-City in the upstream of the Akaki catchment. Samples were taken and subsequently analysed for metals using inductively coupled plasma optical emission spectrometry (ICP-OES). The mean concentrations of Fe, Zn, Cu, Mn, Ni, Cr, Pb, and As in nails from Akaki-Kality were 488 ± 49, 106 ± 10, 5.2 ± 0.3, 13 ± 1.5, 11 ± 8, 2.2 ± 0.3, 0.09 ± 0.01, and 0.16 ± 0.01 µg/g, respectively. Likewise, the concentrations of Fe, Zn, Cu, Mn, Ni, Cr, Pb, and As in nails from Gullele were 1035 ± 135, 251 ± 10, 6.6 ± 0.4, 31 ± 3.7, 7.4 ± 1.7, 2.0 ± 0.3, 0.63 ± 0.01, and 0.25 ± 0.01 µg/g, respectively. Co and Cd were not detected. Contrary to the initial hypothesis, higher metal levels were found in nails of residents living in the upstream rather than the downstream area of the catchment. In particular, the concentrations of Fe (p = 0.000), Zn (p = 0.01), and Mn (p = 0.000) were significantly elevated in nails from Gullele and also high in comparison with internationally reported values. Besides, geography and social factors, especially education level, correlated to trace metals in nails. Most of the elements were significantly lower in the nails of individuals with a university degree compared to those who were illiterate or only completed primary school.