TY - JOUR A1 - Sarma, Dominik A1 - Gawlitza, Kornelia A1 - Rurack, Knut T1 - Polystyrene Core−Silica Shell Particles with Defined Nanoarchitectures as a Versatile Platform for Suspension Array Technology N2 - The need for rapid and high-throughput screening in analytical laboratories has led to significant growth in interest in suspension array technologies (SATs), especially with regard to cytometric assays targeting a low to medium number of analytes. Such SAT or bead-based assays rely on spherical objects that constitute the analytical platform. Usually, functionalized polymer or silica (SiO2) microbeads are used which each have distinct advantages and drawbacks. In this paper, we present a straightforward synthetic route to highly monodisperse SiO2-coated polystyrene core−shell (CS) beads for SAT with controllable architectures from smooth to raspberry- and multilayer-like shells by varying the molecular weight of poly(vinylpyrrolidone) (PVP), which was used as the stabilizer of the cores. The combination of both organic polymer core and a structurally controlled inorganic SiO2 shell in one hybrid particle holds great promises for flexible next-generation design of the spherical platform. The particles were characterized by electron microscopy (SEM, T-SEM, and TEM), thermogravimetry, flow cytometry, and nitrogen adsorption/desorption, offering comprehensive information on the composition, size, structure, and surface area. All particles show ideal cytometric detection patterns and facile handling due to the hybrid structure. The beads are endowed with straightforward modification possibilities through the defined SiO2 shells. We successfully implemented the particles in fluorometric SAT model assays, illustrating the benefits of tailored surface area which is readily available for small-molecule anchoring. Very promising assay performance was shown for DNA hybridization assays with quantification limits down to 8 fmol. KW - core-shell particles KW - shell morphology KW - flow cytometry KW - scanning electron microscopy KW - stabilizer PY - 2016 DO - https://doi.org/DOI: 10.1021/acs.langmuir.6b00373 SN - 0743-7463 VL - 32 IS - 15 SP - 3717 EP - 3727 PB - American Chemical Society CY - Washington, DC, USA AN - OPUS4-35833 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gawlitza, Kornelia T1 - Integrating fluorescent molecularly imprinted polymer (MIP) sensor particles with a microfluidic platform for nanomolar small-molecule detection in water N2 - Besides the traditional areas of application such as separation and enrichment which made molecularly imprinted polymers (MIPs) very attractive, they have emerged as a valuable detection tool in the field of environmental analysis due to the low production costs, high stability, format adaptability and the possibility to imprint and thus specifically recognize a wide variety of target analytes. Regarding optical sensing, however, MIPs have only been used in considerably few applications, especially in fluorescence sensors, basically because of the challenge to incorporate a fluorescently responding moiety into a polymer matrix. One way to overcome this limitation is the coating of a thin MIP layer onto the surface of silica nanoparticles using tailor-made fluorescent indicator monomers or cross-linkers for direct transfer of the binding event into an optical signal. Regarding sensors for environmental monitoring, microfluidic devices utilizing optical detection modules are especially appealing because of their versatility in terms of miniaturization and automation. So far, MIPs have only rarely been used in combination with microfluidic sensor devices. Here, we present the hydrogen bond-mediated optical response of fluorescent MIP sensor particles against a typical small-molecule analyte 2,4-D (2,4-dichlorophen¬oxyacetic acid) which is an important herbicide widely used in agriculture and known to cause adverse health effects when ingested by contaminated water. By combining the sensor particles with droplet-based 3D microfluidics, a microfluidic phase-transfer assay was designed which enables the direct analysis of 2,4-D in river and lake water without sample pre-treatment or clean-up. T2 - Bioinspired Materials conference 2017 CY - Manchester, UK DA - 31.08.2017 KW - MIPs KW - Fluorescence KW - Sensor KW - Water-monitoring PY - 2017 AN - OPUS4-41828 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gawlitza, Kornelia T1 - Mesoporous silica materials incorporating BODIPY dyes as a versatile system for the trace detection of hazardous chemical species N2 - There is significant contamination of our water resources and an accelerating accumulation of hazardous species in the aquatic biosphere. Whether for instance mercury as a contaminant constantly released from a multitude of industrial processes or chemical warfare agents (CWAs) such as Tabun (GA), Sarin (GB) or Soman (GD) as highly toxic remnants of World War II, released from dumped containers upon their progressive corrosion, are concerned such hazards can cause serious problems to human health even at low concentration and monitoring them becomes increasingly essential. Conclusively, it is necessary to develop sensors for such hazards that combine high sensitivity, good selectivity, fast responses and can dispense with complex instrumentation. Here, we present SBA-15-type mesoporous silica materials containing boron–dipyrromethene (BODIPY) probes in their pore systems that allow for the sensitive and selective detection of the two target analytes CWAs and Hg2+ in natural waters via a change in the optical properties. In case of Hg2+, the BODIPY dye is directly adsorbed on the (inner and outer) surface of the highly porous material and coordinates the metal ion, leading to an enhancement of fluorescence with a limit of detection (LOD) of 15 ppt. Using the same silica material but incorporating a covalently attached BODIPY dye, the CWAs GA, GD and GB can be detected via fluorescence quenching induced by an intraannular cyclization. The obtained LOD in natural waters is in the pM range and hence below the Maximum Permissible Concentrations for CWAs in drinking water. Aspects of system design as well as application in water and food analysis (fish extracts) will be presented. T2 - Rapid Methods Europe (RME) 2016 CY - Amsterdam, The Netherlands DA - 07.11.2016 KW - Mesoporous silica materials KW - Sensor materials KW - Fluorescence materials PY - 2016 AN - OPUS4-38183 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kyrey, T. A1 - Ganeva, M. A1 - Gawlitza, Kornelia A1 - Witte, J. A1 - von Klitzing, R. A1 - Soltwedel, O. A1 - Di, Z. A1 - Wellert, S. A1 - Holderer, O. T1 - Grazing incidence SANS and reflectometry combined with simulation of adsorbed microgel particles N2 - Adsorbed ethylene glycol based microgel particles on a Silicon surface were studied. Neutron reflectometry (NR) and grazing incidence small-angle neutron scattering (GISANS) were performed to investigate their internal structure. Scattering experiments on soft matter systems such as adsorbed microgels often give only partial Information about the inner structure of the polymer system. In this contribution, we discuss how the detailed inner structure of adsorbed microgel particles can be reconstructed by a combination of the specular Neutron Reflectivity (NR), Grazing Incidence Small Angle Neutron Scattering (GISANS), Atomic Force Microscopy (AFM) and a simulation in the framework of the Distorted Wave Born Approximation. KW - Grazing incidence small-angle neutron scattering KW - Neutron reflectometry KW - BornAgain simulation KW - Adsorbed microgel particles PY - 2018 DO - https://doi.org/10.1016/j.physb.2018.03.049 SN - 0921-4526 VL - 551 SP - 172 EP - 178 PB - Elsevier B.V. AN - OPUS4-47011 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Jiang, Shan A1 - Gawlitza, Kornelia A1 - Rurack, Knut T1 - Dual-Fluorescent Nanoparticle Probes Consisting of a Carbon Nanodot Core and a Molecularly Imprinted Polymer Shell N2 - Dual-fluorescent molecularly imprinted nanoparticles with a red-emissive carbon nanodot-doped silica core and a chlorogenic acid-imprinted fluorescent polymer layer are prepared and their use in ratiometric fluorometric analysis is described. Nanoparticle probes consisting of a shielded and stably emitting core and a shell with embedded binding sites that indicates the presence of an analyte with a change in emission allow for internally referenced measurements potentially accounting for detrimental influences from instrument drifts, light source fluctuations or sensor materials-related inhomogeneities. KW - Molecular imprinting KW - Fluorescence KW - Core-shell particles KW - Chlorogenic acid KW - Ratiometric measurement PY - 2021 DO - https://doi.org/10.1007/978-1-0716-1629-1_17 VL - 2359 SP - 195 EP - 208 PB - Springer CY - Humana, New York, NY AN - OPUS4-53336 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gawlitza, Kornelia A1 - Bartelmeß, Jürgen A1 - Bartholmai, Matthias A1 - Neumann, Patrick P. A1 - Johann, Sergej A1 - Tiebe, Carlo T1 - Fluorescence sensor for the long-term monitoring of gaseous ammonia N2 - Ammonia and its reaction products can cause considerable damage of human health and ecosystems, increasing the necessity for reliable and reversible sensors to monitor traces of gaseous ammonia in ambient air directly on-site or in the field. Although various types of gas sensors are available, fluorescence sensors have gained importance due to advantages such as high sensitivity and facile miniaturization. Here, we present the development of a sensor material for the detection of gaseous ammonia in the lower ppm to ppb range by incorporation of a fluorescent dye, which shows reversible fluorescence modulations as a function of analyte concentration, into a polymer matrix to ensure the accumulation of ammonia. A gas standard generator producing standard gas mixtures, which comply with the metrological traceability in the desired environmentally relevant measurement range, was used to calibrate the optical sensor system. To integrate the sensor material into a mobile device, a prototype of a hand-held instrument was developed, enabling straightforward data acquisition over a long period. T2 - Colloquium of Optical Spectrometry (COSP) 2017 CY - Berlin, Germany DA - 27.11.2017 KW - Ammonia gas sensor KW - Fluorescence KW - Air quality monitoring KW - Standard gas generator KW - Miniaturized sensor device PY - 2017 AN - OPUS4-43143 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Tiebe, Carlo A1 - Banach, Ulrich A1 - Hübert, Thomas A1 - Gawlitza, Kornelia A1 - Bartholmai, Matthias T1 - Development of a gas standard generator N2 - Pollution through emission of toxic gases is an increasing problem for the environment. It affects similarly agricultural, industrial and urban areas. In future, environmental emissions in ambient air must be monitored at even lower concentrations as nowadays. One environmental relevant compound is ammonia and its conversion product ammonium that have strong negative impact on human health and ecosystems. Most ammonia measurements in ambient air are performed in the range below 1000 nmol·mol-1 and thus there is a need for reliable traceable ammonia gas standards and in addition in situ analytical procedures for monitoring (in ambient air to avoid that thresholds are exceeded). Therefore, the use of reference materials is necessary for development accompanying test or for calibration, e. g. of structure-integrated sensors and mobile multi-gas sensors. The developed gas standard generator produces gas mixtures that comply with the metrological traceability for ammonia gas standards in the desired environmentally relevant measurement range. The method is based on the permeation of ammonia through a membrane at constant temperature and pressure. The resulting ammonia penetrant gas flow is then mixed with a carrier gas flow to generate a gas standard flow of known concentration. The dynamic rage is enlarged by using a two dilution steps. Depending on the permeation rate, generable molar fractions are possible in the range nmol·mol-1 to a few µmol·mol-1. We present the design of an ammonia gas standard generator and first results of the characterisation of its individual components supporting the uncertainty assessment according to GUM for stable gas concentrations in this range. The relative uncertainty of the generated ammonia gas standard is smaller than 4 % (k = 2). T2 - Colloquium of Optical Spectrometry (COSP) CY - Berlin, Germany DA - 27.11.2017 KW - Gas standard generator KW - Permeation method KW - Ammonia PY - 2017 AN - OPUS4-43337 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gawlitza, Kornelia A1 - Tiebe, Carlo A1 - Banach, Ulrich A1 - Noske, Reinhard A1 - Bartholmai, Matthias A1 - Rurack, Knut T1 - Novel sensor for long-term monitoring of ammonia in gas phase N2 - Because ammonia and its reaction products can cause considerable damage to human health and ecosystems, there is a need for reliably operating and reversibly interacting sensor materials to monitor traces of gaseous ammonia in ambient air, which at best can be used on-site for in-the-field measurements. Herein, the development of a sensor material for gaseous ammonia in the lower ppm to ppb range using optical fluorescence as transduction mechanism is presented. A fluorescent dye, which shows reversible fluorescence enhancement in the presence of ammonia is incorporated into a polymer matrix, the latter to ensure the accumulation of ammonia. The sensor material is integrated into a prototype of a miniaturized sensor device, facilitating long-term operation. To calibrate the optical sensor system a gas standard generator, producing standard gas mixtures, is used, leading to a sensitivity down to lower ppm concentrations of ammonia. T2 - 13. Dresdner Sensor-Symposium 2017 CY - Dresden, Germany DA - 04.12.2017 KW - Ammonia gas sensor KW - Fluorescence KW - Air quality monitoring KW - Standard gas generator KW - Miniaturized sensor device PY - 2017 DO - https://doi.org/10.5162/13dss2017/P4.02 SP - P4.02, 272 EP - 276 AN - OPUS4-43352 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Sun, Yijuan A1 - Pérez-Padilla, Víctor A1 - Valderrey, Virginia A1 - Bell, Jérémy A1 - Gawlitza, Kornelia A1 - Rurack, Knut T1 - Ratiometric detection of perfluoroalkyl carboxylic acids using dual fluorescent nanoparticles and a miniaturised microfluidic platform N2 - The widespread contamination of soil and water with perfluoroalkyl substances (PFAS) has caused considerable societal and scientific concern. Legislative measures and an increased need for remediation require effective on-site analytical methods for PFAS management. Here we report on the development of a green-fluorescent guanidine-BODIPY indicator monomer incorporated into a molecularly imprinted polymer (MIP) for the selective detection of perfluorooctanoic acid (PFOA). Complexation of PFOA by the indicator, which is mediated by concerted protonation-induced ion pairing-assisted hydrogen bonding, significantly enhances fluorescence in polar organic solvents. The MIP forms as a thin layer on silica nanoparticles doped with tris(bipyridine)ruthenium(II) chloride, which provides an orange emission signal as internal reference, resulting in low measurement uncertainties. Using a liquid-liquid extraction protocol, this assay enables the direct detection of PFOA in environmental water samples and achieves a detection limit of 0.11 µM. Integration into an opto-microfluidic system enables a compact and user-friendly system for detecting PFOA in less than 15 minutes. KW - PFAS KW - Molecular imprinting KW - Microfluidics KW - Fluorescence KW - Onsite assay PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-650270 DO - https://doi.org/10.1038/s41467-025-66872-9 SN - 2041-1723 VL - 16 IS - 1 SP - 1 EP - 16 PB - Springer Science and Business Media LLC AN - OPUS4-65027 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Johann, Sergej A1 - Kohlhoff, Harald A1 - Gawlitza, Kornelia A1 - Bell, Jérémy A1 - Mansurova, Maria A1 - Tiebe, Carlo A1 - Bartholmai, Matthias T1 - Semi-automatic Gas Measurement Device Based on Fluorescent Multi-gas Sensors N2 - This paper describes the development of a semi-automatic gas measurement device presenting potentially a broad range of applications, noteworthy in the agricultural sector. Non-reversible fluorescent molecular sensors were designed and syn-thesized. Upon, integration into a hydrogel matrix with an optimal ratio of co-solvents, the sensors reacting selectively to ammonia were illuminated by excitation light to produce a concentration-correlated fluorescence emission. An automated mechanical-elec-trical device initiates a given gas mixture and thus simulates con-centrations similar to a threshold value. The aim of this project is to develop a sensor or a low-cost method which can monitor low concentrations of harmful gases and aid in their elimination or regulation in livestock housing, barns or stables. T2 - IEEE Sensors 2019 CY - Montreal, Canada DA - 27.10.2019 KW - gas analysis KW - fluorescence KW - embedded sensor KW - spectroscopy KW - environment KW - agricultural economy PY - 2019 SN - 978-1-7281-1634-1 SP - 88 EP - 92 PB - IEEE AN - OPUS4-49506 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - RPRT A1 - Sternbaek, L. A1 - Kimani, Martha Wamaitha A1 - Gawlitza, Kornelia A1 - Janicke, B. A1 - Alm, K. A1 - Gjörloff-Wingren, A. T1 - Digital Holographic Cytometry: Macrophage Uptake of Nanoprobes N2 - Digital holographic cytometry (DHC) is a state-of-the-art quantitative Phase imaging (QPI) method that permits time-lapse imaging of cells without induced cellular toxicity. DHC platforms equipped with semi-automated image segmentation and analysis software packages for assessing cell behavior are commercially available. In this study we investigate the possible uptake of nanoprobes in macrophages in vitro over time. KW - Macrophages KW - MIPs KW - Holographic microscopy KW - Sialic acid PY - 2019 VL - 21 SP - 21 EP - 23 PB - Wiley CY - Imaging and Microscopy AN - OPUS4-47793 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gawlitza, Kornelia T1 - Novel sensor for long-term monitoring of ammonia in gas phase N2 - Pollution through emission of toxic gases is of utmost environmental concern, raising the interest in developing reliable gas sensors. Exemplarily, ammonia and its conversion products can provoke considerable damage on human health and ecosystems. Hence, there is a need for reliable and reversible sensor materials to monitor traces of gaseous ammonia in ambient air, which at best can be used on-site for field measurements. Although various types of sensors such as potentiometric, amperometric, and biological sensors are available for detecting trace amounts of gases, fluorescent sensors have gained importance due to several advantages such as high sensitivity, possible miniaturization, as well as potential multiplexing. Herein, we present the development of a sensor material for gaseous ammonia in the lower ppm or even ppb range using optical fluorescence as transduction mechanism due to its intrinsically high sensitivity and high spatial resolution.[1] Therefore, a fluorescent dye, which shows reversible fluorescence enhancement in the presence of the analyte was incorporated into a polymer matrix, the latter to ensure the accumulation of ammonia. To calibrate the designed optical sensor system a gas standard generator was used, producing standard gas mixtures, which comply with the metrological traceability for ammonia gas standards in the desired environmentally relevant measurement range.[2] Beside the development of a highly sensitive, selective, and reversible sensor, the integration of such systems into mobile sensor devices is addressed. Therefore, a prototype of a miniaturized hand-held instrument was developed enabling a straightforward and long-term read-out of the measurement signal. T2 - 13. Dresdner Sensor Symposium (13. DSS) CY - Dresden, Germany DA - 04.12.2017 KW - Ammonia gas sensor KW - Fluorescence KW - Air quality monitoring KW - Standard gas generator KW - Minitaurized sensor device PY - 2017 AN - OPUS4-43351 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -