TY - CONF A1 - Rurack, Knut T1 - Functional polymeric coatings for sensory applications N2 - The growing demand for the detection of relevant chemical compounds as close as possible to their point of origin—whether in industrial processes, for (civilian or military) security, or for environmental monitoring—has increased the importance of functional polymers with molecular recognition capabilities. These materials must meet practical requirements arising from very different real-world scenarios in which simple, robust, and field-deployable approaches are needed and in which bioanalytical binders often suffer significant performance losses. Polymer recognition matrices therefore serve as an essential complement to established laboratory-based analytical technologies. The realization of rapid and reliable onsite detection places specific demands on material design: polymeric recognition layers must be produced with minimal thickness, integrated onto suitable carrier media, and designed for both selectivity and operational robustness. This presentation will introduce our work on molecularly imprinted polymers (MIPs) that have been specifically developed for the detection of relevant contaminants such as pesticides and perfluorinated compounds. Beyond these target analytes, the presentation will show how such polymer layers can support robust, sustainable diagnostic concepts, and it will outline generalizable design principles that enable their extension to a broad spectrum of analytical challenges. T2 - Institutskolloquium des Instituts für Chemie, Humboldt Universität zu Berlin CY - Berlin, Germany DA - 28.01.2026 KW - Functional organic materials KW - Responsive polymers KW - Sensing KW - Molecularly imprinted polymers PY - 2026 AN - OPUS4-65435 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Biyikal, Mustafa T1 - Handgerät für den mobilen Einsatz zur Detektion von Sprengstoffspuren N2 - Mithilfe des EXIST-Forschungstransfers wird ein tragbares und leicht zu bedienendes Handgerät auf der Basis von chemisch-optischen Sensoren entwickelt, welches kleinste Spuren von verschiedensten Sprengstoffen und Markern (z.B. TNT, C4, ANFO, TATP, DMDNB etc.) und reine Salze (z. B. Kaliumnitrat) sicher und ohne größere Querempfindlichkeiten detektieren kann. Das Gerät wurde in den letzten 10 Jahren bei der Bundesanstalt für Materialforschung und -prüfung (BAM) entwickelt und wird von der 2024 ausgegründeten Firma Noxoon GmbH in ein kommerzielles Gerät überführt. Die Vorteile des Handgeräts sind die hohe Selektivität, die hohe Sensitivität, die schnelle Detektion in wenigen Sekunden bis zur Ergebnisanzeige sowie der schnelle und das geringe Gewicht des Gerätes von 900 g. Neben den Vorteilen findet sich auch zahlreiche Alleinstellungsmerkmale in der Benutzung des Gerätes. So können z.B. - reine Salze - Sprengstoffe in Gegenwart von Wasser - Sprengstoffe und Drogen in versiegelten Briefumschlägen detektiert werden. Ein besonderes Alleinstellungsmerkmal ist, dass eine Reinigung des Handgeräts nach Messungen von stark kontaminierten Proben nicht notwendig ist. Für den deutschsprachigen bzw. europäischen Raum existiert noch kein vergleichbares Gerät. Das kommerzielle Gerät soll ab 2025 auf den Markt gebracht werden und wird einen wichtigen Beitrag zur öffentlichen Sicherheit und zum Umweltschutz leisten. T2 - BBK Fachkongress "Forschung für den Bevölkerungsschutz" CY - Bonn, Germany DA - 05.02.2025 KW - Explosivstoffe KW - Detektion KW - Handgerät PY - 2025 AN - OPUS4-65031 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Prakash, Swayam T1 - Development of a Rapid and Sensitive Fluorometric Detection Method for Urobilin Analysis for On-site Water Quality Assessment N2 - The W.H.O. estimated that globally at least 2 billion people use drinking water sources contaminated with faeces and according to UNICEF, most of these faecal contaminants detection methods are expensive, time-consuming (18–24 h time to result), and, with few exceptions, not suited for on-site analysis. Hence, there is an urgent need for the development of rapid analytical methods that allow to unequivocally assess drinking water quality directly on-site. Our approach exploits the weak fluorescence of faecal biomarkers such as urobilin (UB), which is enhanced through complexation with Zn2+ in alcoholic media and is the basis of their detection/estimation, known as Schlesinger’s test.3 However, this method is associated with limitations, as the fluorescence of Zn2+ complexes of UB in water is weak, shows time dependent loss of emission intensity and has strong interference from humic substances that naturally present in surface waters. , To circumvent these issues and achieve the rapid and sensitive on-site detection of FPs, silane-functionalized glass fibre paper test strips were developed following the ‘drop-&-detect’ concept. Drop casting of water samples containing faecal contaminants like UB on specifically functionalized test strips allowed the sensitive detection with a smartphone coupled to a 3D printed optical setup. A series of silanes were used to functionalize glass fibre paper and tune its hydrophobicity, exploiting the influence of matrix tailoring to enhance binding of the Zn2+ salt used as co-reagent to bind UB for optimal fluorometric response. A detection spot was designed by the combination of hydrophilic and hydrophobic silanes with ZnCl2-impregnated test strips. This developed analytical method showed sensitive (nano- and sub-nanomolar concentration) response for UB detection. Furthermore, it can be successfully applied to the analysis of real water samples, allowing for the first time to test for faecal contamination in fresh water directly on-site using a smartphone in only a few minutes, instead of >10 h required for the current standard, i.e., lab-based bacterial tests. T2 - 14th International Conference on Instrumental Methods of Analysis: Modern Trends and Applications CY - Kefalonia, Greece DA - 14.09.2025 KW - Faecal contamination KW - Fluorescence KW - Metal complexes KW - Water analysis KW - Optical and chemical sensing KW - Spectroscopy KW - Onsite analysis KW - Rapid testing PY - 2025 AN - OPUS4-64270 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vinot, Romane T1 - A terpyridine-based fluorescent chemosensor for the selective detection of glyphosate and AMPA in water N2 - Detection of pesticide residues, anthropogenic and persistent environmental contaminants is a public health concern due to their association with various pathologies. Studies have shown a correlation between exposure to these residues in drinking water or food and neurodegenerative disorders, autoimmune conditions, and cancers. In this context, detecting organic molecules such as glyphosate and its primary degradation product: AMPA, presents a significant challenge in sensor development. This is due to factors such as the molecules’ small size, pronounced polarity, and their variable ionic charge. However, fluorescent molecular sensors offer several advantages in terms of versatility, sensitivity, selectivity, response time and low cost. Terpyridine zinc complex derivatives show promise as selective detectors of glyphosate and AMPA due to their inherent specificity towards phosphate moieties4. These complexes are designed to modulate intramolecular charge transfer processes upon interaction with the phosphate moiety of AMPA or glyphosate. A novel series of terpyridine derivatives incorporating complexing moieties for both the phosphate and amine groups of AMPA and carboxylate group of Glyphosate were synthesised to target AMPA and Glyphosate (Figure 1). The absorbance and fluorescence signatures of the probe were investigated upon complexation with the analytes in MeOH/HEPES buffer (10 mM, pH 7.4, 9/1 v/v). The fluorescent sensor displayed high selectivity and sensitivity for glyphosate and AMPA, thanks to two measurements taken a few minutes apart. The detection limit of the sensor for Glyphosate in fluorescence was calculated at 0.14 μM. T2 - Journées Annuelles 2025 de la Subdivision Photochimie, Photophysique et Photosciences (SP2P) CY - Toulouse, France DA - 19.05.2025 KW - Glyphosate KW - AMPA KW - Sensor PY - 2025 AN - OPUS4-63262 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Scharek, Vera T1 - A new elemental analytical approach for microplastic sum parameter analysis in environmental samples – ETV/ICP-MS with CO2 N2 - Plastics are indispensable in our daily lives. Due to their easy processability, durability, and lightweight properties, they are the base material of many consumer and industry products. However, with reported amounts of millions of tons per year, plastic pollution has become a globally emerging problem. In the environment, plastic waste undergoes degradation, leading to the formation of persistent, synthetic particles smaller than 5 mm, known as microplastics (MPs). Toxicological concerns mainly arise from MP uptake by various organisms, including humans. MPs act as transport vectors for hazardous chemicals, e.g., polymer additives, bacteria, and other environmental pollutants. Existing approaches for MP analysis focus on particle size, number, and information on the polymer types. However, there is a lack of analytical tools for a fast and comprehensive assessment of the pollution situation based on the MP mass without limitations to size and polymer types. In this context, a new mass balance approach for the MPs analysis in environmental samples via electrothermal vaporization coupled with inductively coupled plasma-mass spectrometry (ETV/ICP-MS) has been developed as a complementary screening tool to existing methods. With ETV/ICP-MS, the bulk detection of MPs via the 13C isotope as a sum parameter of common polymer types was achievable relatively unaffected by the respective size across the nano-to-micrometer scale. A new mass-based approach through an external gas calibration with carbon dioxide enabled the fast quantification of the MP content in MP-soil mixtures of different portions. By this, the analysis was achievable within a few minutes of analysis time per sample. Furthermore, the potential of polymer heteroatoms and contaminants for the sensitive detection in carbon-rich matrices was investigated. T2 - ANAKON 2025 CY - Leipzig, Germany DA - 10.03.2025 KW - Microplastics KW - Soil KW - Electrothermal Vaporization KW - Inductively coupled plasma-mass spectrometry KW - Sum parameter analysis PY - 2025 AN - OPUS4-62828 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Scharek, Vera T1 - A new elemental analytical approach for microplastic sum parameter analysis in environmental samples – ETV/ICP-MS with CO2 N2 - Plastics are indispensable in our daily lives. Due to their easy processability, durability, and lightweight properties, they are the base material of many consumer and industry products. However, with reported amounts of millions of tons per year, plastic pollution has become a globally emerging problem. In the environment, plastic waste undergoes degradation, leading to the formation of persistent, synthetic particles smaller than 5 mm, known as microplastics (MPs). Toxicological concerns mainly arise from MP uptake by various organisms, including humans. MPs act as transport vectors for hazardous chemicals, e.g., polymer additives, bacteria, and other environmental pollutants. Existing approaches for MP analysis focus on particle size, number, and information on the polymer types. However, there is a lack of analytical tools for a fast and comprehensive assessment of the pollution situation based on the MP mass without limitations to size and polymer types. In this context, a new mass balance approach for the MPs analysis in environmental samples via electrothermal vaporization coupled with inductively coupled plasma-mass spectrometry (ETV/ICP-MS) has been developed as a complementary screening tool to existing methods. With ETV/ICP-MS, the bulk detection of MPs via the 13C isotope as a sum parameter of common polymer types was achievable relatively unaffected by the respective size across the nano-to-micrometer scale. A new mass-based approach through an external gas calibration with carbon dioxide enabled the fast quantification of the MP content in MP-soil mixtures of different portions. By this, the analysis was achievable within a few minutes of analysis time per sample. Furthermore, the potential of polymer heteroatoms and contaminants for the sensitive detection in carbon-rich matrices was investigated. T2 - European Winter Conference on Plasma Spectroscopy CY - Berlin, Germany DA - 02.03.2025 KW - Microplastics KW - Soil KW - Electrothermal Vaporization KW - Inductively coupled plasma-mass spectrometry KW - Sum parameter analysis PY - 2025 AN - OPUS4-62824 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Hernandez Garcia, Maria Amparo T1 - Optical biosensor using free form prototyped elements for targeted explosives immunodetection N2 - Ensuring the safety and security of citizens necessitates a considerable investment of resources and the development of innovative tools by national and international agencies and governments, particularly in the context of explosives detection [1]. The necessity for the detection of improvised explosive devices (IEDs) and homemade explosives (HMEs) at the point of suspicion has increased exponentially due to the simplicity with which the precursors can be obtained, and the reagents synthesised. The restricted availability of immunoanalytical instruments for the detection of homemade explosives (HMEs) offers a valuable opportunity for the development of innovative devices that can rapidly identify and recognise the target analyte with high specificity and sensitivity [2]. In this study, we present the development of an optical biosensor for highly specific and sensitive HME detection. The immunoassay system is situated within a matrix that is permeable to the target analyte and transparent to light, which enables the interrogation via fluorescence. The immunoanalytical system's readout is achieved through the utilisation of supercritical angle fluorescence (SAF), an advanced microscopy technique. To this end, we employed recent, commercially available high-resolution (less than 22 μm) liquid crystal display SLA printers to fabricate a free-form parabolic optical element with a high refractive index (RI greater than 1.5) and transmission values exceeding 90% from commercial photo-resins. The objective is to develop a new generation of sensors that can not only meet the requirements of trace detection but also be used for substance identification. The combination of immunoanalytical recognition with SAF detection offers a modular and versatile solution that is particularly well suited to the measurement of target analytes at trace levels. T2 - ANAKON 2025 CY - Leipzig, Germany DA - 10.03.2025 KW - Biosensor KW - SAF KW - Free-form optics KW - 3D printing KW - Security PY - 2025 AN - OPUS4-62802 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Prakash, Swayam T1 - Fluorescence Spectroscopy as an Analytical Tool for Rapid and Sensitive Faecal Pigments Detection: From Fundamentals to Onsite Applications N2 - W.H.O estimated that globally at least 2 billion people use drinking water sources contaminated with faeces [1] and according to UNICEF, most of these faecal detection methods are expensive, time-consuming (18–24 h time to result),[2] and, with few exceptions, not suited for on-site analysis.[3] Hence, there is an urgent need for the development of analytical methods that allow to unequivocally test for drinking water quality directly on-site. Today, microbial detection methods primarily targeting E. coli, the major faecal indicator bacteria, are still the prevalent methods for detecting faecal contamination of drinking and recreational waters. As an alternative, Schlesinger proposed the detection of urobilin (UB), a metabolic degradation product of haemoglobin occurring in all mammals, as faecal indicator pigment (FIP) through enhancement of its weak fluorescence by complexation with Zn2+ in alcoholic media already 120 years ago.[4] However, the major limitation of this method is the only weak enhancement of the intrinsically very weak UB fluorescence in aqueous media, requiring either the use of organic solvents or very sensitive instrumentation to reach the relevant detection limits, hampering the method’s use outside of a laboratory environment.[3] In the present work, we addressed the shortcomings relying on interfacial and supramolecular chemistry as well as materials functionalization, transforming Schlesinger’s approach into a fluorometric ‘drop and detect’ assay using a smartphone coupled to a 3D-printed optical setup as a simple and portable device. A series of silanes were used to functionalize glass fibre paper and tune its hydrophobicity, exploiting the influence of matrix tailoring to enhance binding of the Zn salt used as co-reagent to UB for optimal fluorescence response. Combination of bis(2-hydroxyethyl)-3-aminopropyltriethoxysilane and N-octyltrimethoxysilane with ZnCl2-impregnated test strips showed the best response for sensitive (nano- and sub-nanomolar concentration) smartphone-based FIP detection. The obtained fluorescence sensing results were validated with a benchtop fluorometer. Furthermore, the developed analytical method was successfully applied to the analysis of real water samples, allowing for the first time to test for faecal water contamination directly on site in a very short time of few minutes. T2 - Anakon 2025 CY - Leipzig, Germany DA - 10.03.2025 KW - Faecal contamination KW - Fluorescence KW - Metal complexes KW - Water analysis KW - Optical and chemical sensing PY - 2025 AN - OPUS4-62795 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bell, Jérémy T1 - Embedded sensor for the detection of TNT in surface and marine waters N2 - In 1945, the Potsdam Conference led to the decision to destroy a significant amount of ammunition from the warring parties of WWII. Dumping was considered the cheapest, quickest, and safest solution to dispose of unused ammunition. However, thin barrels or containers often leak after 50 years, allowing explosives to escape into the marine environment. As the effects of weapons chemicals on ecosystems are well-documented, it is becoming increasingly important to detect, recover and dispose of old ammunition. Physical techniques such as magnetometry and sonar are used to detect ammunition in the sea, but they do not provide chemical information. Detecting leaking organic contaminants like TNT or other explosives in water or soil requires high-end laboratory equipment like HPLC or GC-MS, making remote water testing virtually impossible. As an alternative, a miniaturized method for the selective and sensitive indication of TNT using fluorescence light-up sensing was developed. The visual identification of TNT with a nucleophile that forms a strongly absorbing charge transfer complex (CTC) is a well-known method. This CTC is formed by the attraction of an electron from the donor molecule by the electron-deficient aromatic ring. In this work, a TNT-based CTC was selectively formed by the addition of tetraoctylammonium acetate in N,N-diethylformamide and, as expected, showed strong absorption. Surprisingly, at room temperature, the CTC can be converted into a fluorescent product with an emission band centred at 577 nm. For the detection of TNT in water, a microfluidic chip made of polydimethylsiloxane (PDMS) is used for both the extraction and reaction steps. In addition to miniaturising the experimental steps, the optical system (fluorometer) has been integrated into an autonomous smartphone assembly capable of catalysing the photoreaction and analysing the fluorescence response. Taking advantage of the light-up response, TNT was still easily detectable down to 9.4 ng with the CMOS camera. Further evaluation of this analytical tool consisted of analyses of unfiltered and untreated surface water samples spiked directly with increasing concentrations of TNT to reflect different levels of contamination. LODs of 21 and 40 ng were found for samples from the Teltow Canal in Berlin (DEU) and the Baltic Sea near Greifswald (DEU). Such an analytical tool could be used to monitor water quality in the field, as the release of organic pollutants from munitions into surface and marine waters will become increasingly problematic and concentrations will continue to rise over the coming decades. T2 - ANAKON 2025 CY - Leipzig, Germany DA - 10.03.2025 KW - Explosives KW - Microfluidics KW - Smartphone KW - Sprengstoffe KW - Mikrofluidik KW - Sensor PY - 2025 AN - OPUS4-62767 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gawlitza, Kornelia T1 - Using Dual Fluorescent Molecularly Imprinted Particles Coupled with a Miniaturized Opto-Microfluidic Platform for On-Site Detection of Perfluoroalkyl Carboxylic Acids N2 - Per- and polyfluoroalkyl substances (PFAS) are a group of synthetic organofluorine chemicals widely used in the production of various materials, including firefighting foams, adhesives, and coatings that resist stains and oil. In recent years, PFAS have gained attention as emerging environmental contaminants, with particular emphasis on perfluoroalkyl carboxylic acids (PFCAs), the most common type of PFAS. PFCAs are defined by a fully fluorinated carbon chain and a charged carboxylic acid group. They have been classified as Substances of Very High Concern and included in the REACH Candidate List due to their persistence, resistance to biodegradation, and toxicological impacts. Traditional methods for analyzing PFCAs, like GC-MS, HRMS, and HPLC-based techniques, are time-consuming, non-portable, expensive, and require specialized expertise. On the other hand, fluorescence assays offer a user-friendly, portable, and cost-effective alternative with high sensitivity and quick results, particularly when the binding of the analyte causes a specific increase in the probe’s fluorescence. Combining these probes with a carrier platform and a miniaturized optofluidic device presents a promising approach for PFCA monitoring. In this study, a new guanidine BODIPY fluorescent indicator monomer was synthesized, characterized, and incorporated into a molecularly imprinted polymer (MIP) designed for the specific detection of perfluorooctanoic acid (PFOA). The MIP layer was formed on silica core nanoparticles doped with tris(bipyridine)ruthenium(II) chloride, serving as an optical internal reference for calibration-free assays. In combination with an extraction step prior to sample analysis, this system enables selective and reliable detection of PFCAs in surface water samples, minimizing interference from competing substances, matrix effects, and other factors. When integrated into an opto-microfluidic setup, the assay provided a compact, user-friendly detection system capable of detecting micromolar levels of PFOA in under 15 minutes from surface water samples. T2 - ANAKON2025 CY - Leipzig, Germany DA - 10.03.2025 KW - Perfluorooctanoic Acid (PFOA) KW - On-site detection KW - Fluorescence KW - Microfluidics KW - Molecularly Imprinted Polymers PY - 2025 AN - OPUS4-62712 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Wen, Keqing T1 - In situ analysis of biofilm formation under different flow regimes with the help of a microfluidic platform N2 - Bacteria often live in habitats characterized by fluid flow, which is ubiquitous in a diverse range of environments such as surface waters, wastewater treatment facilities, pipelines, and medical implants. Bacterial adhesion on surfaces may lead to biocorrosion and biodegradation. In comparison to traditional static and macro flow chamber assays for biofilm formation studies, microfluidic chips allow in situ monitoring of biofilm formation and biofilm related gene expression under various flow regimes. We developed a complete microfluidic platform to investigate biofilms under precisely controlled flow conditions. This platform central unit is a single-inlet microfluidic flow cell with a 5 mm wide chamber tested and analyzed by imaging tracking velocimetry (PIV) to achieve ultra-homogenous flow in the central area of the chamber. Additionally, dedicated microstructures were introduced to the chamber’s center to favor and localize bacterial adhesion and biofilm formation pattern. The flows and vortices induced by the structure were analyzed by computational fluid dynamics (CFD) and related to shape and dimension of the biofilm formed by Escherichia coli TG1. The major proteinaceous component of E. coli biofilms are extracellular amyloid fibers (curli) consisting of major (CsgA) and minor (CsgB) subunits. We used the promotor probe plasmid pRU1701 to monitor csgB-promotor activity under different flow regimes in complex and minimal medium. For comparison, csgB promotor activity in a batch liquid culture and curli production on LB and M9 agar plates were assessed. The microfluidic platform represents a powerful and versatile tool for studying biofilm in flow. The setup shows great potential for the yet not too much explored in flow monitoring of biofilm formation and related gene expression under hydrodynamic stresses. T2 - International Biodeterioration and Biodegradation Symposium (IBBS) 19 CY - Berlin, Germany DA - 09.09.2024 KW - Microfluidics KW - Biofilm KW - Escherichia coli KW - Curli PY - 2024 AN - OPUS4-61911 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Hernandez Garcia, Maria Amparo T1 - Fabrication of low-cost free-form optical elements with standard LCD 3D printer for advanced opto-sensing and imaging applications N2 - Nowadays, more and more complex optical elements are used in optical applications, but this can lead to high costs, a time-consuming manufacturing process and limited availability of unconventional elements. Therefore, in this work, we propose LCD 3D printing as alternative cost-effective technique, which is not only user-friendly but also free from design constrains and enables the fabrication of free-form optics. The tested polymeric materials showed promising results for printed optics and optical applications. In addition, 3D printed optical elements were evaluated in terms of their suitability in selected applications with opto-chemical sensors and imaging techniques, with results comparable to those obtained with the corresponding glass optical elements. T2 - 12th European Optical Society Annual Meeting CY - Naples, Italy DA - 09.09.2024 KW - 3D-printing KW - Optics KW - Photopolymerization KW - Rapid prototyping KW - Sensors PY - 2024 AN - OPUS4-61442 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Buchholz, Michelle T1 - Dual Fluorescent Molecularly Imprinted Polymers (MIPs) for Detection of the Prevalent Anti-Inflammatory Drug Diclofenac N2 - Ensuring the purity of air and water is essential for the overall well-being of life on earth and the sustainability of the planet's diverse ecosystems. To achieve the goal of zero pollution, as outlined in the 2020 European Green Deal by the European Commission,[1] significant efforts are in progress. A key aspect of this commitment involves advancing more efficient and economically viable methods for treating wastewater. This includes the systematic monitoring of harmful pollutants such as heavy metals, microplastics, pesticides, and pharmaceuticals. One example is the presence of the anti-inflammatory drug diclofenac in water systems, primarily originating from its use as a gel or lotion for joint pain treatment. Diclofenac contamination in surface waters has been detected at approximately 10 μg L-1 (0.03 μM)[2] which is not solely due to widespread usage but also because of the drug's resistance to microbial degradation. Conventional wastewater treatment plants (WWTPs), which rely on biodegradation, sludge sorption, ozone oxidation, and powdered activated carbon treatment, struggle to efficiently remove diclofenac from wastewater.[3],[4] For instance, to enable WWTPs to efficiently monitor and optimize their processes, it would be advantageous to develop on-site detection and extraction methods for persistent pharmaceutical residues in aqueous samples. In this work, a sol-gel process was used to prepare Nile blue-doped silica nanoparticles (dSiO2-NPs) with a diameter of ca. 30 nm that were further functionalized to enable reversible-addition-fragmentation chain-transfer (RAFT) polymerization. To achieve fluorescence detection, a fluorescent monomer was used as a probe for diclofenac in ethyl acetate, generating stable complexes through hydrogen bond formation. The diclofenac/fluorescent monomer complexes were imprinted into thin molecularly imprinted polymer (MIP) shells on the surface of the dSiO2-NPs. Thus, the MIP binding behaviour could be easily evaluated by fluorescence titrations to monitor the spectral changes upon addition of the analyte. Doping the core substrate with Nile blue generates effective dual fluorescent signal transduction. This approach does not solely depend on a single fluorescence emission band in response to analyte recognition. Instead, it enables the fluorescent core to function as an internal reference, minimizing analyte-independent factors such as background fluorescence, instrumental fluctuation, and operational parameters.[5] Rebinding studies showed that the MIP particles have excellent selectivity towards the imprinted template and good discrimination against the competitor ibuprofen, with a discrimination factor of 2.5. Additionally, the limit of detection was determined to be 0.6 μM. Thus, with further optimization of the MIP, there is potential for the development of a MIP-based biphasic extract-&-detect fluorescence assay for simple, sensitive and specific sensing of diclofenac in aqueous samples down to the required concentrations of 0.03 μM. T2 - MIP2024: The 12th International Conference on Molecular Imprinting CY - Verona, Italy DA - 18.06.2024 KW - Sensor KW - Diclofenac KW - Molecularly Imprinted Polymers KW - Fluorescence KW - Pollutant PY - 2024 AN - OPUS4-60439 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Hernandez Garcia, Maria Amparo T1 - Characterization and testing of commercial photo-resins for the fabrication of free-form optical elements with standard LCD 3D printer for advanced opto-biosensing applications N2 - Optical biosensors often show remarkable performance and can be configured in many ways for sensitive, selective, and rapid measurements. However, the high-quality and advanced optical assemblies required to read out the sensor signals, for example, Total Internal Reflection Fluorescence (TIRF) or Supercritical Angle Fluorescence (SAF) microscopy, which necessitate complex and expensive optical elements. Particularly in optical method development, researchers or developers are often confronted with limitations because conventional manufacturing processes for optical elements can be restrictive in terms of design, material, time, and cost. Modern and high-resolution 3D printing techniques make it possible to overcome these challenges and enable the fabrication of individualized and personalized free-form optical components, which can reduce costs and significantly shorten the prototyping timeline—from months to hours. In this work, we use a modern, high-resolution (< 22 µm) commercial Liquid Crystal Display (LCD)-based 3D printer, for which we spectroscopically and physically characterized commercial photo-resins printable with the LCD technique in the first step (Figure 1). The aim was not only to produce a printed element with a high surface quality that mitigates the inner filter effects caused by attenuation (high optical density (OD) due to reflection and scattering), but also to select a material with a high refractive index (RI>1.5) and high transmission values (>90% transmittance) in the visible to near-infrared spectral range (approx. 450 – 900 nm) that exhibits little or no autofluorescence. Using a selection of suitable resins, lenses and free-form optical elements were manufactured for comparison with standard glass or plastic counterparts. T2 - Europt(r)ode XVI CY - Birmingham, England DA - 24.03.2024 KW - 3D-printing KW - Optics KW - Photopolymerization KW - Sensors KW - Rapid prototyping PY - 2024 AN - OPUS4-59875 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Rurack, Knut T1 - Development of a Lab-on-a-Chip for the Detection of Nerve Agents with a Handheld Device N2 - The development of a Lab-on-a-Chip (LoC) is presented, which can detect reactive phosphorous compounds in the gas phase in combination with an optochemical hand-held sensor. The LoC prototype contains three pairs of sensing materials containing fluorescent indicator dyes in various carrier materials. By measuring the fluorescence response to phosphoryl chloride, a surrogate compound, the detection of chemical warfare agents (CWAs) in gas phase becomes possible within seconds, introducing a novel approach to CWA detection. T2 - IEEE Sensors Conference CY - Vienna, Austria DA - 29.10.2023 KW - Chemical warfare agents KW - Lab-on-a-chip KW - Handheld sensors KW - Toxic industrial chemicals KW - Fluorescence PY - 2023 AN - OPUS4-58815 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Sun, Yijuan A1 - Pérez-Padilla, Víctor A1 - Valderrey, Virginia A1 - Bell, Jérémy A1 - Gawlitza, Kornelia A1 - Rurack, Knut T1 - Fluorescence Detection of Perfluoroalkyl Carboxylic Acids with a Miniaturised Assay N2 - Per- and polyfluoroalkyl substances (PFAS) are a class of man-made organo-fluorine chemicals that have become environmental contaminants of emerging concern, originating from a variety of materials such as adhesive, stain- and oil-resistant coatings, firefighting foams, etc. The high strength of this C-F bond makes PFAS thermodynamically stable and resistant to (bio)degradation, thus retaining them in the environment over time. Perfluoroalkyl carboxylic acids (PFCAs), one category of the most used PFAS, consist of a fully fluorinated carbon backbone and a charged carboxylic acid headgroup, and have been classified as Substances of Very High Concern (SVHC) and added to the REACH Candidate List due to their persistence in the environment, non-biodegradability and toxicological effects.[1-2] Traditional techniques for the analysis of PFCAs include GC-MS, HRMS and HPLC-based approaches, which are laborious, not portable, costly and require trained personnel. In contrast, fluorescence assays can be designed as easy-to-operate, portable and cost-effective methods with high sensitivity and fast response. Integration of fluorescent probes with an adequately miniaturized assay enables a promising alternative for PFCAs analysis. Here, a novel guanidine fluorescent probe has been synthesized and fully characterized for the detection of PFCAs in a biphasic extract-&-detect assay. The fluorescent probe was then incorporated into polymeric matrices supported by a red dye-doped SiO2 nanoparticle to construct a dual-emission sensing platform. Such a system allows precise and selective detection of PFCAs, reducing the interference of competitors, matrix effects and other factors except for the PFCAs. The system was then employed in a droplet-based microfluidic setup which offers a portable and easy to operate detection platform. T2 - IMA 2023 CY - Chania, Greece DA - 18.09.2023 KW - PFAS KW - MIP KW - Fluorescence KW - Microfluidics KW - Fluorezsenz KW - Mikrofluidik PY - 2023 AN - OPUS4-58527 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bell, Jérémy A1 - Climent, Estela A1 - Gotor, Raúl A1 - Tobias, Charlie A1 - Martin-Sanchez, Pedro M. A1 - Rurack, Knut T1 - Dipstick coated with polystyrene-silica core-shell particles for the detection of microbiological fuel contamination N2 - Microbial contamination of fuels by fungi or bacteria poses risks such as corrosion and fuel system fouling, which can lead to critical problems in refineries and distribution systems and has a significant economic impact at every stage of the process. Many factors have been cited as being responsible for microbial growth, like the presence of water in the storage tanks. In fact, only 1 % water in a storage system is sufficient for the growth of microorganisms like bacteria or yeasts, as well as for the development of fungal biomass at the oil/water interface. This work presents a rapid test for the accurate determination of genomic DNA from aqueous fuel extracts. The detection is based on the use of polystyrene-mesoporous silica core-shell particles onto which modified fluorescent molecular beacons are covalently grafted. These beacons contain in the hairpin loop a target sequence highly conserved in all bacteria, corresponding to a fragment of the 16S ribosomal RNA subunit. The designed single-stranded molecular beacon contained fluorescein as an internal indicator and a quencher in its proximity when not hybridized. Upon hybridization in presence of the target sequence, the indicator and the quencher are spatially separated, resulting in fluorescence enhancement. To perform the assay the developed particles were deposited on different glass fibre strips to obtain a portable and sensitive rapid test. The assays showed that the presence of genomic DNA extracts from bacteria down to 50–70 μg L–1 induced a fluorescence response. The optical read-out was adapted for on-site monitoring by fitting a 3D-printed case to a conventional smartphone, taking advantages of the sensitivity of the CMOS detector. Such embedded assembly enabled the detection of genomic DNA in aqueous extracts down to the mg L–1 range and represents an interesting step toward on-site monitoring of fuel contamination. T2 - IMA 2023 CY - Chania, Greece DA - 18.09.2023 KW - Teststreifen KW - Test strip KW - Microbial KW - Mikrobiell KW - Smartphone KW - Particles KW - Partikeln PY - 2023 AN - OPUS4-58526 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Hernandez-Sigüenza, G. T1 - Dye-Displacement-Based Test Implemented in Lateral Flow Strips to Prevent GHB Spiking in Alcoholic Beverages N2 - γ-Hydroxybutyric acid (GHB) is a natural metabolite, which is currently used as a date rape drug. Particularly, GHB is rapidly eliminated and its detection in realistic environments is only possible within 6-12 h after ingestion. Owing to the increasing use of GHB for criminal purposes, a need has arisen to develop simple and in situ efficient assays for its identification in aqueous and alcoholic drinks. Based on the above, we report herein an indicator displacement assay (IDA) for GHB detection that consists of a Cu2+ complex with a tetradentate ligand and the fluorescent dye coumarin 343 (IDA probe 1). Firstly, the tetradentate ligand was synthesized by reductive amination of a 1,2-cyclohexyl diamine with 2-quinoline carboxaldehyde. Subsequently, this ligand was reacted with Cu(CF3SO3)2 to obtain the corresponding copper complex, which generates the final sensing ensemble by coordinating with coumarin 343 (IDA probe 1). The sensing mechanism relies on a displacement of coumarin 343 from the sensing ensemble 1 thus restoring its fluorescence, as a consequence of the higher binding constant between GHB and complex, showing a high sensitivity in MES buffer (50 mM, pH 6.0) (detection limit of 0.03 μM). Likewise, system design and optimization led to a straightforward integration into a lateral-flow assay without further treatment or conditioning of the test strips while guaranteeing fast overall assay times of 1 min (Figure 1). In this way, IDA probe 1 was incorporated into a coated PEG-glass fibre (PEG-GF) membrane to obtain a highly robust and sensitive lateral flow assay for GHB detection in spiked alcoholic drinks with a detection limit of 0.1 μM in less than 1 min coupled to smartphone readout. T2 - XVI International Workshop on Sensors and Molecular Recognition CY - Valencia, Spain DA - 06.07.2023 KW - Schnelltest KW - Vor-Ort-Analytik KW - Drogen KW - Farbstoffe KW - Lateral Flow Assay PY - 2023 AN - OPUS4-57942 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gawlitza, Kornelia T1 - Fluorescent molecularly imprinted polymer particles for direct detection of glyphosate in organic solvents and water N2 - Glyphosate (GPS) is the most widely used pesticide in the world whose use increased dramatically after the introduction of genetically modified crops engineered to resist its herbicidal action during application. In recent years, there have been growing concerns over its toxicity following its classification by the International Agency for Research on Cancer (IARC) as a probable carcinogen as well as reports of its ecotoxicological effects. This resulted in increased efforts to develop quick and sensitive detection methods. In this work, molecular imprinting was combined with direct fluorescence detection of GPS by improving its solubility in organic solvents using tetrabutylammonium (TBA+) and tetrahexylammonium (THA+) as counterions. To achieve fluorescence detection, a fluorescent crosslinker containing urea binding motifs was used as a probe for GPS-TBA and GPS-THA salts in chloroform, generating stable complexes through hydrogen bond formation. The GPS/fluorescent dye complexes were imprinted into 2–3 nm molecularly imprinted polymer (MIP) shells on the surface of sub-micron silica particles. Thus, the MIP binding behavior could be easily evaluated by fluorescence titrations in suspension to monitor the spectral changes upon addition of the GPS analytes. While MIPs prepared with GPS-TBA and GPS-THA both displayed satisfactory imprinting following titration with the corresponding analytes in chloroform, GPS-THA MIPs displayed better selectivity against competing molecules. Moreover, the THA+ counterion was found to be a more powerful phase transfer agent than TBA+, enabling the direct fluorescence detection and quantification of GPS in water in a biphasic assay. A limit of detection of 1.45 µM and a linear range of 5–55 µM, which matches well with WHO guidelines for the acceptable daily intake of GPS in water (5.32 µM), have been obtained. The assay can be further optimized to allow miniaturization into microfluidic devices and shows potential for on-field applications by untrained personnel. T2 - 36th European Colloid & Interface Society Conference CY - Chania, Greece DA - 04.09.2022 KW - Glyphosate KW - Molecular Imprinting KW - Core-Shell Particles KW - Fluorescent Urea Receptors PY - 2022 AN - OPUS4-56311 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Hülagü, Deniz T1 - From 2D and Single Particle to 3D and Batch Analysis as a Routine Quality Check Procedure for the Morphological Characterization of Core-Shell Microparticles N2 - This study presents a practical procedure to give access to more information by tilting the sample holder and hence allowing images of a single particle to be recorded at different orientations under the same view angle. From the analysis of these images, extended information on surface roughness of the particle can be extracted. Thus, instead of obtaining 2D information from a single SEM image, three-dimensional (3D) information is obtained from 2D projections recorded at different particle orientations. T2 - Microscopy & Microanalysis 2022 CY - Online meeting DA - 31.07.2022 KW - Core-shell particles KW - 3D image analysis KW - Roughness KW - SEM tilting KW - Batch analysis PY - 2022 AN - OPUS4-55452 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Rurack, Knut T1 - Approaches to Sensitive and Multiplexed Assays for Robust, Reliable and User-friendly Point-of-Need Analysis N2 - Analytical assays that can be used outside of a dedicated laboratory environment have received unprecedented attention all around the globe during the last one and a half years, in which the world was struggling with and trying to contain the SARS-CoV-2 pandemic. However, besides their current prominence in the field of medical diagnostics, rapid tests and assays have also become increasingly important in other areas ranging from food and feed via security and forensics to environmental management. The advantage is obvious: taking the assay to the sample instead of bringing the sample to the laboratory minimizes the time between first suspicion and first decision taking. Especially today, where mobile communication devices with powerful computing capabilities and onboard cameras are omnipresent, the majority of the global population possesses the basic skills of operating a powerful detector, ready at their fingertips. The stage is thus set for a much broader use of analytical measurements in terms of prognostics and prevention. Today, however, tests for single parameters are still prevailing, whether it is a SARS-CoV-2 biomarker, the glucose level in blood or the concentration of lead in a water sample. Also, for industrial use, many mobile analytical systems still target a single parameter, and several separate runs or tests have to be used even if one wants to screen for only a small number of key parameters. Current challenges in the field thus lie with the development of low-number multiplexing strategies while allowing for robust, reliable, fast, and user-friendly operation and while still reaching the required sensitivities. This lecture will give an overview of various generic approaches developed in BAM’s Chemical and Optical Sensing Division over the years to address these challenges. In particular, it will highlight how the combination of supramolecular (bio)chemistry, luminescence detection, hybrid (nano)materials and device miniaturization can result in powerful (bio)analytical assays that can be used at a point-of-need. Selected examples will introduce key aspects of such systems like tailored signaling mechanisms and recognition elements, materials functionalization and device integration, including hybrid mesoporous nanomaterials, gated indicator release systems, molecularly imprinted polymers, microfluidic devices, test strips and smartphone-based analysis. T2 - Advanced Analytical Technologies Seminar CY - Online meeting DA - 08.12.2021 KW - Rapid tests KW - Multiplexing KW - Trace analysis PY - 2021 AN - OPUS4-54002 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Rurack, Knut T1 - Reaction-based BODIPY dyes as powerful tools in fluorescence sensing applications N2 - The reversible analyte-induced switching between a colourless leuco form of a dye and its coloured all-π-conjugated form is one of the oldest concepts in probe- or indicator-based optical analysis,1 constituting so-called “one-color indicators”.2 In contrast to colour changes in the visible region, for which usually a bond-forming or a non-covalent interaction between a functional group on an indicator and an analyte is responsible, the extraordinarily large shifts of 150–250 nm seen for leuco-to-all-π-conjugated transformation are only possible when the reaction takes place directly at a site that is an intrinsic part of a dye’s π-system; the classic case are triphenylmethane dyes.3 Despite its obvious potential, this approach has not been a very popular area of scientific research for decades, perhaps because it is much more difficult to implement selectivity than by modifying terminal functional groups. However, in recent years, reaction-based fluorescence probes have attracted increasing attention by virtue of their superior sensitivity.4,5 Nowadays, rhodamines and fluoresceins are by far the most prominent groups of reaction-based indicators.5 They are usually switched between a colourless and non-fluorescent and a greenish-yellowish absorbing and yellowish-reddish emitting form. Typically, the coloured and fluorescent form is ionic, while the colourless form is neutral, reactions having mainly be designed to occur at the end groups of the xanthenoid π-system. BODIPY dyes, with their favourable spectroscopic and chemical properties as well as facile wavelength tunability features have only very recently been explored into this direction.6,7 Reaction at the core dipyrrin framework of these dyes led to strong colour and fluorescence modulations with potential applications in materials sciences6 and cell imaging.7 The present contribution will highlight the mechanisms at play and the sensing performance realized so far, and will compare core-reactive approaches to reaction-based signalling that involves π-extension of BODIPYs.8,9 T2 - 11th International Conference on Porphyrins and Phthalocyanines (ICPP-11) CY - Online meeting DA - 26.06.2021 KW - Indicators KW - Fluorescence KW - Sensing KW - BODIPY Dyes PY - 2021 AN - OPUS4-54001 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Climent Terol, Estela T1 - Antibody-gated dye delivery systems for Type-I pyrethroids detection N2 - Type-I pyrethroids are frequently used for disinfection purposes on airplanes from and to tropical areas. The WHO (Word Health Organization) defines “disinfection” as the procedure whereby health measures are taken to control or kill the insect vectors of human diseases including dengue, yellow fever and malaria.1 Due to this, a new effective and rapid method for pyrethroids analysis directly in the plane is needed. To detect type-I pyrethroids, gated materials are constructed for the purpose of finely tuning the movement of a cargo from voids of a mesoporous inorganic support to a solution, in response to a predefined stimulus.2 Antibodies are bound to specific functional groups grafted on the support’s surface with the two-fold aim of closing the mesopores and working as biological receptors for the target compounds.2 A specific opening mechanism, activated selectively in presence of pyrethroids as analytes, is able to control the release of an indicator dye previously loaded inside the inorganic support. As only few molecules of pyrethroids are necessary to open a pore and release a large amount of dyes, the system shows an intrinsic signal amplification quantified as a fluorescence emission intensity.3 Different mesoporous silica supports (from nano- and microparticles to platelets and short fibers) were synthetized, characterized and functionalized following different capping strategies. In this contribution, we will compare the temporal response behaviour of the optimized gated materials to verify if the respective delivery systems are properly closed and how fast they can be opened in presence of the analytes. Our results indicate that the trends of the kinetics observed in solution show a better control of the closing/opening mechanism when the epitope region of the antibody (around 10 nm) properly fits the pore size of the carriers. Because the incorporation of an antibody-gated dye-delivery system with a conventional test-strip-based lateral-flow assay allows for the detection of analytes down to the ppb level in an easy-to-operate manner and an overall assay time of 2–5 min, which is fast for a biochemical test,3 we carried out first model studies for a lateral flow test assay on membranes, using a smartphone setup for read-out. T2 - XV EUROPT(R)ODE 2021 CY - Online meeting DA - 28.11.2021 KW - Antibody-gated materials KW - Lateral flow assay KW - Pyrethroids detection PY - 2021 AN - OPUS4-53862 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Tobias, Charlie T1 - Dip-stick coated with Polystyrene-Silica Core-Shell particles for the detection of microbiological fuel contamination N2 - The microbial contamination of fuels by fungi or bacteria presents risks such as corrosion and fuel system fouling, which can produce critical problems in refineries and distribution systems and has a significant economic impact at every phase of the process. Many factors have been cited as responsible for microbial growth, like the presence of water in the storage tanks. Indeed, only 1 % water in a storage system is enough for the growth of microorganisms like bacteria or yeasts, as well as for the development of fungal biomass at the oil/water interface.1 In this work, a rapid test for the accurate determination of genomic DNA from aqueous fuel extracts is presented. The detection is based on the employment of polystyrene-mesoporous silica core-shell particles, on which modified fluorescent molecular beacons are covalently grafted. Those beacons incorporate in the hairpin loop a target sequence highly conserved in all bacteria, corresponding to a fragment of the 16S ribosomal RNA subunit. The designed single-stranded molecular beacon contained fluorescein as an internal indicator and a quencher in its proximity when not hybridized. Upon hybridization in presence of the target sequence, the indicator and the quencher are spatially separated, resulting in fluorescence enhancement. To perform the assay the designed particles were disposed on different glass fiber strips to try to achieve a portable and sensitive rapid test. Assays showed that presence of genomic DNA extracts from bacteria down to 50–70 μg L-1 induces a fluorescence response. The optical read-out was adapted for on-site monitoring by adapting a 3D-printed case on a conventional smartphone, taking advantages of the CMOS detector sensitivity.2 Such embedded assembly allowed to detect genomic DNA in aqueous extracts down to the mg L-1 range and presents an interesting step toward on-site monitoring of fuel contamination. T2 - Europtrode 2021 CY - Warsaw, Poland DA - 28.11.2021 KW - Bacgteria KW - Fungi KW - Rapid test KW - Fluorescence KW - Smartphone KW - Biofouling PY - 2021 AN - OPUS4-53867 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gornushkin, Igor B. T1 - Optical Detection of Defects during Laser Metal Deposition - Simulations and Experiment N2 - Laser metal deposition is a rapidly evolving method for additive manufacturing that combines high performance and simplified production routine. Quality of production depends on instrumental design and operational parameters that require constant control during the process. In this work, feasibility of using optical spectroscopy as a control method is studied via modeling and experimentally. A simplified thermal model is developed based on the time-dependent diffusion-conduction heat equation and geometrical light collection into detection optics. Intense light emitted by a laser-heated spot moving across a sample surface is collected and processed to yield the temperature and other temperature-related parameters. In a presence of surface defects the temperature field is distorted in a specific manner that depends on a shape and size of the defect. Optical signals produced by such the distorted temperature fields are simulated and verified experimentally using a 3D metal printer and a sample with artificially carved defects. Three quantities are tested as possible metrics for process monitoring: temperature, integral intensity, and correlation coefficient. The shapes of the simulated signals qualitatively agree with the experimental signals; this allows a cautious inference that optical spectroscopy is capable of detecting a defect and, possibly, predicting its character, e.g. inner or protruding. T2 - 28th International Conference on Advanced Laser Technologies CY - Online meeting DA - 06.09.2021 KW - Additive manufacturing KW - Laser metal deposition KW - Optical sensor KW - Optical emission spectroscopy KW - Process control PY - 2021 AN - OPUS4-53246 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gornushkin, Igor B. T1 - Reverse deposition of TI-oxides under nanosecond laser ablation of TI N2 - Processes of laser induced oxidation of metals are typically studied in the framework of heterogeneous chemical reactions occurring on the irradiated surface, which lead to the formation of dense oxide films deposited on it. Such technology has many applications like color-laser marking technology and laser recording on thin metal films for creation of diffractive optical elements . Under the conditions of strong laser ablation, another oxidation mechanism becomes possible: evaporated atoms react with oxygen in a surrounding atmosphere and the products of such reaction are redeposited back onto the substrate. The chemical and phase composition of such deposited layer, its density, morphology and structure depend on the conditions of laser ablation. By varying these conditions, the main properties of such coating can be controlled that is important for some potential application (for example in biomedicine). In our report we present the study of the processes of redeposition of oxides structure under the conditions of multipulse nanosecond laser ablation of titanium (Grade 2) in air atmosphere at normal conditions. Our experiments show that titanium-implants with such deposited oxide layer have increased biocompatibility. Modelling of chemical reaction in laser-induced plasma coupled with experimental methods of plasma optical emission spectroscopy allows us to determine the types of main chemical reactions in laser plasma as well as it influences on the plume dynamics and vapor condensation kinetics. As a result, we propose the general physical picture of reverse deposition of oxides structure under the condition of strong nanosecond laser ablation. The formation of the titanium oxide precipitate is explained not only by collisions in the plasma, but also by the chemical interaction of titanium and oxygen, which leads to the formation of а low pressure area near the substrate and additionally stimulates the reverse deposition of oxides. We expect, similar processes are valid not only for titanium but also for other metals and, possibly, semiconductors. T2 - 28th International Conference on Advanced Laser Technologies CY - Online meeting DA - 06.09.2021 KW - Laser ablation KW - Laser induced plasma deposition KW - Surface coating KW - Emission spectroscopy KW - Titanium dioxide KW - Hydrodynamic model KW - Plasma chemistry PY - 2021 AN - OPUS4-53245 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Hülagü, Deniz T1 - Analysis of the profile roughness of core-shell microparticles by electron microscopy N2 - A particle roughness analysis tool, based on electron microscopy (EM) images. The influence of various parameters on the calculated roughness was also investigated: the setting of the proper threshold, accelerating voltage, etc. The samples were gradually tilted to extend imaging information of more than only one projection. Furthermore, the measurement uncertainty of the profile roughness of particles associated to various orientations was estimated. T2 - Microscopy and Microanalysis 2021 CY - Online Meeting DA - 01.08.2021 KW - MamaLoCA KW - Particle characterization KW - Electron microscopy KW - Roughness KW - Core-shell particles KW - Image processing PY - 2021 AN - OPUS4-53069 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Climent Terol, Estela T1 - Fluorescence-based multiplexed detection on single test strips with antibody-gated mesoporous materials N2 - Rapid testing methods for the use directly at a point-of-need are expected to unfold their true potential especially when offering adequate capabilities for the simultaneous measurement of multiple analytes of interest. However, the implementation of multiplexing features while retaining simplicity, performance and portability is one of the prominent challenges in the field. Keeping in mind these challenges, we decided to combine the use of stimuli-responsive materials for small-molecule sensing relying on chemical signal amplification and their incorporation on paper strips for lateral-flow assays in a straightforward manner. Considering the modularity, high sensitivity and selectivity of antibody-gated indicator delivery systems, a multiplexed assay for three small-molecule explosives TATP, TNT and PETN was developed, allowing to detect the analytes simultaneously with a single test strip at lower ppb concentrations in liquid phase in <5 min, using a fluorescence reader or a smartphone for readout. Because of the versatility of the hybrid material and the modularity of the assay architecture, it is obvious that this generic approach should be easily transferable to food or environmental analysis, point-of-care diagnostics and other areas of application in which the rapid screening for multiple parameters from liquid samples without clean-up in a dedicated laboratory is in demand. T2 - 2021 On-line Symposium on Bioluminiscence, Chemiluminiscence and luminescence spectrometry ISLS-ISBC CY - Online meeting DA - 24.06.2021 KW - Multiplexing KW - Hybrid materials KW - Signal amplification KW - Test Strip analysis KW - Explosives PY - 2021 AN - OPUS4-52889 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Scheuschner, Nils T1 - In-situ Monitoring der Additiven Fertigung von Metallen im LPA Prozess mittels Optischer Emissionsspektrometrie (OES) und Thermografie (TT) N2 - Einer der aussichtsreichsten Ansätze, die Qualität und Sicherheit der gefertigten Teile in der metallbasierten additiven Fertigung (AM) zu erhöhen und die Notwendigkeit aufwändiger und zeitintensiver, zerstörender oder zerstörungsfreier Prüfungen (ZfP) nach der Fertigung zu verringern, liegt in dem Einsatz von in-situ Prozessüberwachungstechniken. Viele wichtige Prozessgrößen bei der additiven Fertigung sind thermischer Natur, wie z.B. die Temperatur des Schmelzbades. Aufgrund der Zugänglichkeit zum Werkstück während des Bauprozesses bieten sich optische Verfahren zur Temperaturbestimmung an. Für die Thermografie und Optische Emissionsspektrometrie im IR-Bereich, welche für die in-situ Anwendung prinzipiell als geeignet angesehen werden können, gibt es allerdings noch wenig konkrete praktische Umsetzungen, da die Möglichkeiten und individuellen Grenzen dieser Methoden, angewendet auf AM, noch nicht ausreichend erforscht sind. Aus diesem Grund verfolgt die BAM mit dem Projekt „Process Monitoring of AM“ (ProMoAM) im Themenfeld Material das Ziel, Verfahren des Prozessmonitorings zur in-situ Bewertung der Qualität additiv gefertigter Metallbauteile weiterzuentwickeln. Im Beitrag wird der Fokus auf eine Versuchsserie gelegt, bei der Aufbau von Probekörpern aus dem austenitischen Edelstahl 316L mittels Laser-Pulver-Auftragschweißen (LPA) durch od. mit Hilfe von IR-Spektrometrie und Thermografie in-situ überwacht wurde. Hierbei stellen u.a. die hohe Bandbreite der zu messenden Temperaturen, die Bestimmung der Emissivität und ihre Änderung bei Phasenübergängen des Metalls große experimentelle Herausforderungen dar, wobei jede Methode individuelle Vor- und Nachteile aufweist, welche verglichen werden. T2 - DGZfP-Jahrestagung 2021 CY - Online meeting DA - 10.05.2021 KW - Additive Manufacturing KW - Thermography KW - Direct Energy Deposition KW - Additive Fertigung KW - Thermografie KW - Laserauftragschweißen PY - 2021 AN - OPUS4-52744 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gawlitza, Kornelia T1 - Long-Term Monitoring of Gaseous Ammonia with a Semi-automated Measuring Device N2 - In the present paper the development of a semi-automated device for long-term monitoring of gaseous ammonia is described. A sensor material was produced that changes its optical properties in the pres-ence of low concentrations of ammonia in air. The implementation into an electronic device enables precise, simple, economic and fast monitoring of low concentrations of harmful gases, like ammonia, and hence can help to improve the climate monitoring in livestock housing, barns or stables. T2 - SMSI 2021 CY - Online meeting DA - 03.05.2021 KW - Spectroscopy KW - Embedded sensor KW - Environment KW - Air quality PY - 2021 AN - OPUS4-52575 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Scheuschner, Nils T1 - In-situ temperature measurements of the LMD process by IR-spectroscopy and Thermography N2 - Temperature measurements of the LMD process by IR-spectroscopy and Thermography are presenet and compared. T2 - 2st Workshop on In-situ Monitoring and Microstructure Development in Additive Manufacturing CY - Online meeting DA - 19.04.2021 KW - Additive Manufacturing KW - Thermography PY - 2021 AN - OPUS4-52565 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gornushkin, Igor B. T1 - Laser induced gas breakdown in reactive mixtures containing halides of boron and silicon: diagnostics and modeling N2 - We run two pilot LIP experiments in reactive gas mixtures. First, LIP is excited in BCl3 or BF3 plus H2 or CH4 to evaluate the efficiency of deposition of solid boron and boron carbide, materials that are largely used for refractory coatings. Second, we investigate a possibility of synthesis of fluorochlorosilanes SiFxCl4-x (x = 1, 2, 3) by LIP induced in SiF4+SiCl4 gas mixtures. Using fluorochlorosilanes with different combinations of F and Cl in the SiFxCly molecule may add flexibility in processes of silicon deposition and etching. The gases used and solid deposits are analyzed by optical emission spectroscopy (OES) and IR and mass spectrometry (MS). We also model the laser induced plasma by performing static equilibrium chemistry calculations to see whether desired reaction products are thermodynamically favorable and dynamic calculations of the expanding plasma plume to see how and where the products form. T2 - International Workshop on Laser Induced breakdown Spectroscopy CY - Online meeting DA - 01.12.2020 KW - Silicon halides KW - Chemical vapor deposition KW - Laser induced dielectric breakdown KW - Hydrogen reduction PY - 2020 AN - OPUS4-51725 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Straße, Anne T1 - In-situ Prozessüberwachung beim Laser-Pulver-Auftragschweißen (LPA) mittels Thermographie, optischer Emissionsspektroskopie (OES) und Schallemission (AE) N2 - In diesem Vortrag wird ein Überblick über die in-situ Messverfahren gegeben, die im Rahmen des Projektes ProMoAM an der LPA- Anlage eingesetzt wurden. Im Speziellen sind das die Thermographie, die optische Emissionsspektroskopie (OES) und die Akustische Emission (AE). T2 - 41. Assistentenseminar der WGF e.V. CY - Online meeting DA - 02.09.2020 KW - Schallemission KW - Laser-Pulver-Auftragschweißen KW - Thermographie KW - Optische Emissionsspektroskopie PY - 2020 AN - OPUS4-51273 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Climent Terol, Estela T1 - Design and synthesis of lateral flow tests containing antibody-gated materials N2 - Methods for the rapid and sensitive detection of target analytes are gaining importance in medical diagnostics and environmental monitoring, in the security, occupational health and safety as well as food sectors. Among all the methods employed for rapid tests, lateral flow assays (LFAs) are the most commonly used. However, some drawbacks are that most of these tests either indicate the analyte only indirectly, and in other cases the sensitivity is not high enough. Keeping in mind these limitations, the use of stimuli-responsive materials for small-molecule sensing relying on chemical signal amplification and utilizing specific interactions between biomolecules such as antibodies and the corresponding analytes are particularly attractive. Such materials can also be incorporated on paper strips for lateral-flow assays in a straightforward manner. These sensing materials comprise mesoporous silica nanoparticles loaded with indicator molecules and containing certain hapten derivative molecules covalently grafted at the surface, which bind to the respective antibody and inhibit the release of a dye as reporter (Scheme 1). In presence of the designated analyte, a displacement of the antibody from the material is observed, allowing the release of dye. Because a large number of indicator molecules can be released when a single analyte molecule binds to an antibody cap, a strong signal amplification is observed. Considering the modularity, high sensitivity and selectivity of these antibody-gated indicator delivery systems, the presentation discusses general aspects of system design as well as analytical performance and highlights the integration into a lateral-flow assay, showing as an example the determination of the explosives TATP, TNT and PETN with a fluorescence readout, in single-substance and multiplexing modes. T2 - International Webinar on Biosensors and Bioelectronics CY - Online meeting DA - 20.07.2020 KW - Multiplexing detection KW - Rapid testing methods KW - Gated hybrid materials KW - Lateral flow tests KW - Explosives detection PY - 2020 UR - https://europeanmeetings.net/conferences/biosensor-bioelectronics AN - OPUS4-51038 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gornushkin, Igor B. A1 - Sennikov, P. T1 - Laser Induced Plasma for Chemical Vapor Deposition: Theory and Experiment N2 - A possibility of deposition from laser-induced plasma (LIP) is investigated in search for an economic and simple method to obtain isotopic compounds from enriched gaseous precursors. A breakdown in mixtures of BCl3 and BCl3 with hydrogen, argon, and methane are studied both theoretically and experimentally. Calculations of expanding plasma of different composition are performed with the use of the fluid dynamic code coupled to the equilibrium chemistry solver. Condensed phases of boron, boron carbide, and graphite are predicted showing maximum concentrations in peripheral zones of the plasma. In experiment LIP is induced in mixtures BCl3, Н2+BCl3, H2+Ar+BCl3, H2+BCl3+CH4, BF3, Н2+BF3, H2+Ar+BF3, and H2+Ar+BF3. The gases are analyzed before, during, and after laser irradiation by optical and mass spectroscopic methods. The composition of reaction products is found to be close to that predicted theoretically. The conversion of precursor gases BCl3 and BF3 into gaseous and condensed products is 100% for BCl3 and 80% for BF3. Solid deposits of up to 30 mg are obtained from all the reaction mixtures. FTIR analysis of BCl3+H2+CH4 deposits points to a presence of condensed boron and boron carbide that are also predicted by the model. Both calculations and preliminary experimental results suggest the chemical vapor deposition by LIP is promising for conversion of gaseous enriched precursors into elemental isotopes and their isotopic compounds. T2 - International Online Meeting on Laser Induced Breakdown Spectroscopy (IIOMLIBS) CY - Online meeting DA - 06.07.2020 KW - Chemical vapor deposition KW - Laser induced plasma PY - 2020 AN - OPUS4-50994 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Kimani, Martha Wamaitha T1 - Design, Synthesis and Characterization of Fluorescent MIP Particles for Labelling of Malignant Cells N2 - Cancer is a leading cause of death worldwide, and its early detection and resultant treatment contributes significantly to patient recovery and survival. Detection is currently based on magnetic resonance imaging and computed tomography, methods that are expensive, while processing of the results is time-consuming1. There is a need for low-cost cancer detection techniques that give conclusive results in the shortest time possible. When equipped with a reporter function, molecularly imprinted polymers (MIPs) targeting tumor markers on cancerous cells may provide a cheaper solution for imaging-based cancer detection. Thin MIP layers immobilized on particle platforms are ideal in this regard, because a fluorescence reporter can be integrated into the particle core and/or MIP shell and such core/shell nanoparticles show faster response times and increased selectivity in comparison to bulk MIPs. Changes in sialylation patterns of cell surface glycans indicate malignancy2. Here, we present the design, synthesis and characterization of MIPs that target sialic acid-terminated glycans (SA MIPs), prepared as a thin layer on a polystyrene core/silica shell nanoparticle platform. The MIP particles contain fluorescent emitters and can be applied in fluorescence imaging of malignant tumors. Dynamic light scattering (DLS) and transmission electron microscopy (TEM) are used for structural characterization. Binding capacity of the MIPs to target glycans and competing sugars is also evaluated and compared to that of the corresponding non-imprinted polymer particles (NIP). T2 - Mini MIP Conference CY - Online meeting DA - 16.06.2020 KW - Cancer KW - MIPs KW - Sialic acid PY - 2020 AN - OPUS4-50901 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Climent Terol, Estela T1 - Antibody-gated indicator releasing mesoporous materials: a potential biosensor platform to be used in the development of rapid tests N2 - The urgent necessity to carry out reliable and relevant analytical measurements directly at a point-of-need is one of the current drivers for the development of miniaturised analytical systems, quick tests and wearables. Despite their simplicity, this type of tests must guarantee analytical relevance and reliability like laboratory-based analysis, e.g., in terms of sensitivity, selectivity, immunity against false positives and false negatives as well as robustness and repeatability. Keeping in mind the high sensitivity offered by gated indicator-releasing micro- and nanoparticles due to their inherent features of signal amplification, we performed several optimisations to develop a potential biosensor platform for use in rapid tests. Conceptually, these gated materials are closely related to drug delivery systems, consisting of high porous materials usually closed with macromolecular “caps” and loaded with indicator molecules that are released in presence of a target analyte. However, the key difference between the two types of functional materials is that many drug delivery systems should deliver their cargo over a longer period, often many hours, whereas the gated materials prepared for sensing should show fast release kinetics, on the order of <5 min. With the aim to optimise and adapt gated materials for sensing purposes, we prepared in this work several antibody-gated materials for small-molecule sensing. The materials consisted of porous silica particles containing indicator molecules in the pores and certain hapten molecules grafted to the particle surface close to the pore openings. The pores were then capped with antibodies binding to these haptens, thus inhibiting the escape of the indicators from inside of the pores. In presence of the corresponding analyte, the antibody is displaced from the surface of the material, allowing the escape of the indicators. This allows the detection of the analyte indirectly through an inherent signal amplification. In this work, the insecticide permethrin, a type-I pyrethroid, was selected as target model, because type-I pyrethroids play an important role in airplane disinfection. A first in-depth study of the various chemical tuning options of such antibody gated systems was performed. Different mesoporous silica supports, different functionalisation routes and different loading sequences were assessed. The materials’ performances were evaluated by studying their temporal response behaviour and detection sensitivity, including the tightness of pore closure (through the amount of blank release in absence of analyte) and the release kinetics. Our results indicate that the better the paratope-accommodating Fab region of the antibody “cap” fits into the host material’s pore openings, the better the closing/opening mechanism can be controlled. Because such materials can be used in various different formats from suspension assays[1] via microfluidic chips[2] to test strip-based lateral flow assays,[3] such materials present a powerful analytical particle platform for the sensitive analytics and diagnostics outside of a laboratory, realising sensitivities down to the µg kg–1 range in less analysis times of less than 5 min as we have recently demonstrated.[4] T2 - Biosensors for Pandemics CY - Online conference DA - 06.05.2020 KW - Hybrid materials KW - Pyrethroids KW - Signal amplification PY - 2020 UR - http://www.confstreaming.com/Biosensors2020/ AN - OPUS4-50744 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gornushkin, Igor B. T1 - Plasma Fundamentals and Diagnostics N2 - This course will provide an introduction to plasma diagnostic techniques. The major focus of the course will be on the discussions of the practical procedures as well as the underlying physical principles for the measurements of plasma fundamental characteristics (e.g., temperatures, thermodynamic properties, and electron number density). Particular emphasis will be placed on inductively coupled plasma–atomic emission spectrometry, but other analytical plasmas will also be used as examples when appropriate. Selected examples on how one can manipulate the operating conditions of the plasma source, based on the results of plasma diagnostic measurements, to improve its performance used for spectrochemical analysis will also be covered. Topics to be covered include thermal equilibrium, line profiles, temperatures, electron densities, excitation processes, microreactions, pump and probe diagnostics, tomography, temporal and spatial resolution. Basis of plasma computer modeling will be presented. T2 - Winter Plasma Conference CY - Tucson, AZ, USA DA - 10.01.2020 KW - Plasma modeling KW - Thermal equilibrium KW - Plasma processes KW - Electron number density KW - Temperatures KW - Emission line profiles KW - Spatial information PY - 2020 AN - OPUS4-50324 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -