TY - JOUR A1 - Reifschneider, O. A1 - Vennemann, A. A1 - Buzanich, Günter A1 - Radtke, Martin A1 - Reinholz, Uwe A1 - Riesemeier, Heinrich A1 - Hogeback, J A1 - Köppen, C. A1 - Großgarten, M. A1 - Sperling, M. A1 - Wiemann, M. A1 - Karst, U. T1 - Revealing Silver Nanoparticle Uptake by Macrophages Using SR-μXRF and LA-ICP-MS JF - Chemical Research in Toxicology N2 - To better study the impact of nanoparticles on both in vitro and in vivo models, tissue distribution and cellular doses need to be described more closely. Here silver nanoparticles were visualized in alveolar macrophages by means of synchrotron radiation micro X-ray fluorescence spectroscopy (SR-μXRF) with high spatial resolution of 3 × 3 μm2. For the spatial allocation of silver signals to cells and tissue structures, additional elemental labeling was carried out by staining with eosin, which binds to protein and can be detected as bromine signal with SR-μXRF. The method was compatible with immunostaining of macrophage antigens. We found that the silver distribution obtained with SR-μXRF was largely congruent with distribution maps from a subsequent laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) of the same tissue sites. The study shows a predominant, though not exclusive uptake of silver into alveolar macrophages in the rat lung, which can be modeled by a similar uptake in cultured alveolar macrophages. Advantages and limitations of the different strategies for measuring nanoparticle uptake at the single cell level are discussed. KW - Synchrotron KW - BAMline KW - XRF KW - Nanoparticle KW - Macrophagen PY - 2020 DO - https://doi.org/10.1021/acs.chemrestox.9b00507 VL - 33 IS - 5 SP - 1250 EP - 1255 PB - American Chemical Society AN - OPUS4-50855 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - De Samber, B. A1 - Scharf, Oliver A1 - Buzanich, Günter A1 - Garrevoet, J. A1 - Tack, P. A1 - Radtke, Martin A1 - Riesemeier, Heinrich A1 - Reinholz, Uwe A1 - Evens, R. A1 - De Schamphelaere, K. A1 - Falkenberg, G. A1 - Janssen, C. A1 - Vincze, L. T1 - Three-dimensional X-ray fluorescence imaging modes for biological specimens using a full-field energy dispersive CCD camera JF - Journal of analytical atomic spectrometry N2 - Besides conventional scanning X-ray fluorescence imaging at synchrotron sources, full-field X-ray fluorescence (FF-XRF) imaging techniques that do not implicitly require spatial scanning of the sample have become available. FF-XRF has become achievable thanks to the development of a new type of energy dispersive CCD-based 2D detector, also referred to as a 'color X-ray camera (CXC)' or 'SLcam'. We report on different imaging schemes for biological samples using FF-XRF imaging: (a) 2D 'zoom' imaging with pinhole optics using the 'camera obscura' principle; (b) 2D 'fixed magnification' imaging using magnifying polycapillary optics; and (c) 3D-FF-XRF imaging using an X-ray sheet beam or computed tomography (CT). The different FF-XRF imaging modes are illustrated using the crustacean Daphnia magna, a model organism for investigating the effects of metals on organism/ecosystem health, and foraminifera, a class of amoeboid protist. Detailed analytical characterization of the set-up is performed through analyzing various reference materials in order to determine limits of detection (LODs) and sensitivities. Experiments were performed using the BAMline at the BESSY synchrotron (Berlin, Germany) and using the P06 Hard X-ray Microprobe at the PETRAIII synchrotron (Hamburg, Germany). KW - CXC KW - BAMline KW - Maia detector KW - Synchrotron PY - 2019 DO - https://doi.org/10.1039/c9ja00198k VL - 34 IS - 10 SP - 2083 EP - 2093 PB - Royal Society of Chemistry CY - Cambridge, United Kingdom AN - OPUS4-49359 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hahn, Michael A1 - Buzanich, Günter A1 - Jähn, Katharina A1 - Reinholz, Uwe A1 - Radtke, Martin T1 - Analysis of cobalt deposition in periprosthetic bone specimens by high-resolution synchroton XRF in undecalcified histological thin sections JF - Materialia N2 - Increasing numbers of implant revisions are a current clinical issue. Interactions of the endoprosthesis biomaterial with the body affect implantation time by wear processes, i.e. corrosion and abrasion. Previously, cobalt-chrome implants were shown to cause high levels of cobalt ions being deposited in the bone matrix. To determine a poten- tial functional role of these ions on bone homeostasis, we have developed a non-destructive dual analysis of highly sensitive elemental analysis by synchrotron XRF directly in undecalcified histological bone thin sections (4 μm). In this study, samples from 28 bone samples from hip endoprosthesis carriers (Surface Replacement Arthroplasty, metal-on-metal bearing) with an implant lifetime of 17–1750 days were used. Results were compared to age- matched control specimens. The histological analysis identified areas of bone cell activity and assigned them for XRF measurements. Co-Cr wear particles were identified in the bone marrow. In addition, Co ions were highly enriched in the mineralized bone matrix. The cobalt deposits were not homogeneously distributed, and areas of high signal intensity were identified. Co was distinctly deposited in the newly formed osteoid layer, but also within deeper layers of the bone matrix, whereby the Co concentration increased with higher degrees of bone matrix mineralization. In the current study, we determined cobalt accumulations in the bone matrix and showed for the first time via synchrotron XRF with a high spatial resolution direct on histological slides, that cobalt deposits in the mineralized bone matrix in a mineral-specific way that is dependent upon the implant lifetime. KW - Implant material KW - Cobalt deposition KW - Bone matrix KW - High-resolution synchrotron XRF KW - Histology PY - 2019 DO - https://doi.org/10.1016/j.mtla.2019.100290 SN - 2589-1529 VL - 6 SP - 100290, 1 EP - 8 PB - Elsevier Inc. CY - Amsterdam, Niederlande AN - OPUS4-47620 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Fretwurst, T. A1 - Buzanich, Günter A1 - Nahles, S. A1 - Woelber, J. P. A1 - Riesemeier, Heinrich A1 - Nelson, K. T1 - Metal elements in tissue with dental peri-implantitis: a pilot study JF - Clinical Oral Implants Research N2 - Objectives: Dental peri-implantitis is characterized by a multifactorial etiology. The role of metal elements as an etiological factor for peri-implantitis is still unclear. The aim of this study was to investigate the incidence of metal elements in bone and mucosal tissues around dental Grade 4 CP titanium implants with signs of peri-implantitis in human patients. Methods: In this prospective pilot study, all patients were enrolled consecutively in two study centers. Bone and soft tissue samples of patients with peri-implantitis with indication for explantation were analyzed for the incidence of different elements (Ca, P, Ti, Fe) by means of synchrotron radiation X-ray fluorescence spectroscopy (SRXRF) and polarized light microscopy (PLM). The existence of macrophages and lymphocytes in the histologic specimens was analyzed. Results: Biopsies of 12 patients (seven bone samples, five mucosal samples) were included and analyzed. In nine of the 12 samples (75%), the SRXRF examination revealed the existence of titanium (Ti) and an associated occurrence with Iron (Fe). Metal particles were detected in peri- implant soft tissue using PLM. In samples with increased titanium concentration, lymphocytes were detected, whereas M1 macrophages were predominantly seen in samples with metal particles. Conclusion: Titanium and Iron elements were found in soft and hard tissue biopsies retrieved from peri-implantitis sites. Further histologic and immunohistochemical studies need to clarify which specific immune reaction metal elements/particles induce in dental peri-implant tissue. KW - Peri-implantitis KW - Metal elements KW - Synchrotron radiation X-ray fluorescence PY - 2016 DO - https://doi.org/10.1111/clr.12718 SN - 0905-7161 VL - 27 IS - 9 SP - 1178 EP - 1186 PB - WILEY-BLACKWELL CY - 111 RIVER ST, HOBOKEN 07030-5774, NJ USA AN - OPUS4-38641 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Radtke, Martin A1 - Buzanich, Günter A1 - de Oliveira Guilherme Buzanich, Ana A1 - Reinholz, Uwe A1 - Riesemeier, Heinrich A1 - Scharf, O. A1 - Scholz, Philipp A1 - Guerra, M.F. T1 - Double Dispersive X-Ray Fluorescence (D2XRF) based on an Energy Dispersive pnCCD detector for the detection of platinum in gold JF - Microchemical Journal N2 - With the aim of improving limits of detection (LOD) of trace elements in a matrix with adjacent fluorescence energies, a simple double dispersive X-ray fluorescence detection system (D2XRF) was constructed to operate at the beamlines BAMline and the mySpot @ BESSY II. This system is based on the combination of a crystal analyzer with an energy resolving single photon counting pnCCD. Without further collimators, the efficient suppression of the background by the pnCCD and the good energy resolution of the crystal results in improved LOD. In first order reflections, an energy resolution of 13 eV for Cu Kα was reached, and an energy range of 1 keV was covered in one shot. This new system was applied to the detection of platinum (Pt) in gold leaves with a LOD of 0.9 mg/kg, which is the lowest attained by totally non-destructive methods nowadays. The presence of Pt in gilded objects from Abydos and Byzantine mosaics provides vital information, as it indicates the alluvial origin of the gold for these examples. KW - Platinum Wavelength dispersive D2XRF KW - Gold Synchrotron XRF PY - 2016 DO - https://doi.org/10.1016/j.microc.2015.10.039 VL - 125 SP - 56 EP - 61 PB - Elsevier Science CY - Amsterdam AN - OPUS4-35777 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Sávoly, Z. A1 - Buzanich, Günter A1 - Pepponi, G. A1 - Streli, C. A1 - Hrács, K. A1 - Nagy, P.I. A1 - Záray, G. T1 - The fate of nano-ZnO and its bulk counterpart in the body of microscopic nematodes: an X-ray spectrometric study JF - Microchemical journal N2 - The distribution and speciation of zinc were studied in the body of female specimens of the soil-inhabiting, plant-feeding nematode, Xiphinema vuittenezi treated with nano-ZnO and its bulk counterpart. Lyophilized nematodes were studied by X-ray absorption near edge structure spectrometry (XANES) in order to characterize the zinc speciation. Furthermore, in the cross-sections prepared by focused ion beam technique, elemental maps were obtained using the electron probe microanalysis (EPMA) technique. XANES spectra were collected from three different regions (head, midbody and tail region) of nematodes in case of two different treatments (50 mg/L bulk and nano-ZnO suspension, 24 h long treatment). The sample spectra were fitted by the spectra of several reference compounds, the main components of the fitted spectra are the following in all cases: bulk/nano-ZnO; Zn–His and Zn3(PO4)2 * xH2O. Consequently, partial biotransformation takes place for both treatments, histidine- and phosphate-rich ligands play dominant role in the binding of zinc. According to the result of the EPMA analysis, it can be established that the distribution of zinc correlates with the calcium and phosphorus distribution for both treatments. Considering the results of the investigations performed by the two microanalytical techniques, it is likely that calcium phosphate granules were formed in order to bind zinc and hereby to take part in zinc detoxification. Apparent difference in the behavior of bulk and nano-sized ZnO in the body of the investigated nematodes was not found. KW - Nematode KW - Elemental distribution KW - X-ray absorption near edge structure (XANES) KW - ZnO nanoparticles KW - Zinc detoxification PY - 2015 DO - https://doi.org/10.1016/j.microc.2014.08.011 SN - 0026-265x VL - 118 SP - 80 EP - 87 PB - Elsevier B.V. CY - Amsterdam [u.a.] AN - OPUS4-31632 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Vasilescu, A. A1 - Constantinescu, B. A1 - Stan, D. A1 - Radtke, Martin A1 - Reinholz, Uwe A1 - Buzanich, Günter A1 - Ceccato, D. T1 - Studies on ancient silver metallurgy using SR XRF and micro-PIXE JF - Radiation physics and chemistry N2 - This work presents a complex evaluation of a series of Geto-Thracian silver adornments found on Romanian territory, part of the 4th century BC Agighiol (Northern Dobruja) hoard and of an ingot from the 1st century BC Geto-Dacian Surcea (Transylvania) hoard, using Synchrotron Radiation X-Ray Fluorescence and micro- Proton Induced X-ray Emission analysis and mapping in order to investigate aspects related to the elemental composition of the metal and the metallurgy implied in their manufacture. One of the samples can be linked to Laurion as the source of metal, and several items contain silver probably originated in Macedonia. The set of silver items was found to be heteregenous as composition and microstructure, and corrosion-related elements could be also identified in the X-Ray maps. KW - Synchrotron radiation XRF KW - Micro-PIXE KW - Archaeological silver PY - 2015 DO - https://doi.org/10.1016/j.radphyschem.2015.07.008 SN - 0969-806X SN - 0020-7055 SN - 0146-5724 VL - 117 SP - 26 EP - 34 PB - Pergamon Press CY - Oxford [u.a.] ; Frankfurt, M. AN - OPUS4-33809 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Curado, Jessica A1 - Radtke, Martin A1 - Buzanich, Günter A1 - Reinholz, Uwe A1 - Riesemeier, Heinrich A1 - Guttler, R.A.S. A1 - Rizzutto, M.A. T1 - μ-SRXRF characterization of Brazilian emeralds JF - Journal of physics / Conference series N2 - The aim of the present study is to characterize emeralds from different mines of Brazil by using Synchrotron Radiation X-ray Fluorescence Microanalysis (µ-SRXRF). The advantage of this technique is that we can analyze a homogeneous, inclusion free area of the stone with the microbeam to distinguish the elemental fingerprint according to the provenance of the emerald. A total of 47 samples belonging to 5 different Brazilian mines were studied in this work and 28 elements were identified. By means of Principal Component Analysis (PCA) it is possible to build different groups according to the provenance of the stones, which allows to assign samples of unknown origin to the according mine. T2 - 22nd International congress on X-ray optics and microanalysis CY - Hamburg, Germany DA - 02.09.2013 KW - µ-SRXRF KW - BAMline KW - Emeralds KW - Geoscience PY - 2014 DO - https://doi.org/10.1088/1742-6596/499/1/012016 SN - 1742-6588 SN - 1742-6596 VL - 499 SP - 012016-1 EP - 012016-5 PB - IOP Publ. CY - Bristol, UK AN - OPUS4-30541 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Rakotondrajoa, Andrianiaina A1 - Buzanich, Günter A1 - Radtke, Martin A1 - Reinholz, Uwe A1 - Riesemeier, Heinrich A1 - Vincze, L. A1 - Raboanary, R. T1 - Improvement of PLS regression-based XRF spectroscopy quantification using multiple step procedure and Monte Carlo simulation JF - X-ray spectrometry N2 - Partial least squares (PLS) regression-based methods have been proven to be a good alternative for quantification in X-ray fluorescence spectroscopy. These methods are fast and easy to use though giving satisfactory results under certain conditions. One of these conditions is the necessity of having a great number of spectra to build the model (training set). The choice of the constituent concentration range in the training set has a big influence on the accuracy of the model. Better accuracy is obtained if the model is built in relatively narrow regions containing (or close to) the real concentration value. In the present work, Monte Carlo (MC) simulated spectra are used to form the training set. The advantage to use MC generated training spectra is the unlimited availability of perfect standards. This paper aims to improve the accuracy of the method by introducing a multiple step procedure in order to build the PLS model using narrow concentration range close to (or containing) the real concentration values in the samples to be measured. This approach consists of an initial guess of the constituents' concentrations and a preliminary PLS model before building the final model. The prediction of ten MC simulated alloy standard samples containing Ti, Mn, Fe, Co, Cu, Zn, Sr, Zr, and Mo using this method allowed to have average relative prediction errors less than 5% for elements with narrow concentration ranges. KW - SR-microXRF KW - Quantification KW - PLS KW - Monte Carlo PY - 2013 DO - https://doi.org/10.1002/xrs.2479 SN - 0049-8246 VL - 42 IS - 4 SP - 183 EP - 188 PB - Wiley CY - Chichester AN - OPUS4-30225 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Ordavo, I. A1 - Ihle, S. A1 - Arkadiev, V. A1 - Scharf, Oliver A1 - Soltau, H. A1 - Bjeoumikhov, A. A1 - Bjeoumikhova, S. A1 - Buzanich, Günter A1 - Gubzhokov, R. A1 - Günther, A. A1 - Hartmann, R. A1 - Holl, P. A1 - Kimmel, N. A1 - Kühbacher, M. A1 - Lang, M. A1 - Langhoff, N. A1 - Liebel, A. A1 - Radtke, Martin A1 - Reinholz, Uwe A1 - Riesemeier, Heinrich A1 - Schaller, G. A1 - Schopper, F. A1 - Strüder, L. A1 - Thamm, C. A1 - Wedell, R. T1 - A new pnCCD-based color X-ray camera for fast spatial and energy-resolved measurements JF - Nuclear instruments and methods in physics research A N2 - We present a new high resolution X-ray imager based on a pnCCD detector and a polycapillary optics. The properties of the pnCCD like high quantum efficiency, high energy resolution and radiation hardness are maintained, while color corrected polycapillary lenses are used to direct the fluorescence photons from every spot on a sample to a corresponding pixel on the detector. The camera is sensitive to photons from 3 to 40 keV with still 30% quantum efficiency at 20 keV. The pnCCD is operated in split frame mode allowing a high frame rate of 400 Hz with an energy resolution of 152 eV for Mn Kα (5.9 keV) at 450 kcps. In single-photon counting mode (SPC), the time, energy and position of every fluorescence photon is recorded for every frame. A dedicated software enables the visualization of the elements distribution in real time without the need of post-processing the data. A description of the key components including detector, X-ray optics and camera is given. First experiments show the capability of the camera to perform fast full-field X-Ray Fluorescence (FF-XRF) for element analysis. The imaging performance with a magnifying optics (3×) has also been successfully tested. KW - X-ray CCD camera KW - pnCCD KW - Fast X-ray imaging KW - XRF KW - Full-field X-ray fluorescence KW - Elemental analysis KW - High quantum efficiency KW - High energy resolution KW - Polycapillary optics PY - 2011 DO - https://doi.org/10.1016/j.nima.2011.05.080 SN - 0168-9002 SN - 0167-5087 VL - 654 SP - 250 EP - 257 PB - North-Holland CY - Amsterdam AN - OPUS4-24370 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -