TY - CONF A1 - Thünemann, Andreas T1 - Characterization of (bio)macromolecules and polymeric materials with modern scattering methods N2 - The analysis of polymers, biopolymers and polymeric materials is of great interest in biomaterials science. Here small-angle x-ray scattering (SAXS), static light scatterin (SLS) and dynamic light scattering (DLS) are described. Current efforts for digitalization of this methods are explaind with respect to modern data science in biomedical research. T2 - MacroBio Summer School 2018: Biomaterial Science in View of Digitalization CY - Teltow, Germany DA - 24.09.2018 KW - Small-angle x-ray scattering KW - SAXS KW - Static light scattering KW - SLS KW - Dynamic light scattering KW - DLS KW - Biomaterials PY - 2018 AN - OPUS4-46051 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kästner, Claudia A1 - Lampen, A. A1 - Thünemann, Andreas T1 - What happens to the silver ions? – Silver thiocyanate nanoparticle formation in an artificial digestion N2 - An artificial digestion of silver nitrate is reported. It is shown that AgSCN nanoparticles emerge from ionic silver in saliva and remain present during the entire digestion process. The particles were characterized by infrared spectroscopy and small- and wide-angle X-ray scattering (SAXS/WAXS) regarding their composition and size distribution. KW - SAXS KW - WAXS KW - Artificial digestion PY - 2018 DO - https://doi.org/10.1039/c7nr08851e SN - 2040-3364 SN - 2040-3372 VL - 10 IS - 8 SP - 3650 EP - 3653 PB - RSC Publ. CY - Cambridge AN - OPUS4-44277 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bruemmel, Y. A1 - Chan, C. A1 - Renneberg, R. A1 - Thünemann, Andreas A1 - Seydack, M. T1 - On the Influence of Different Surfaces in Nano- and Submicrometer Particle Based Fluorescence Immunoassays KW - Nanoparticles KW - Fluorescence immuno assays PY - 2004 DO - https://doi.org/10.1021/la0486032 SN - 0743-7463 SN - 1520-5827 VL - 20 IS - 21 SP - 9371 EP - 9379 PB - American Chemical Society CY - Washington, DC AN - OPUS4-4573 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Stutz, C. A1 - Bilecka, I. A1 - Thünemann, Andreas A1 - Niederberger, M. A1 - Börner, H.G. T1 - Superparamagnetic core-shell nanoparticles as solid supports for peptide synthesis N2 - Functional superparamagnetic core–shell nanoparticles are synthesized by a microwave assisted route and can be used as colloidal supports for peptide synthesis in 'quasi solution'. KW - Nanotechnology KW - Small-angle X-ray scatering KW - SAXS PY - 2012 DO - https://doi.org/10.1039/c2cc33492e SN - 0022-4936 SN - 0009-241x SN - 1359-7345 SN - 1364-548x VL - 48 IS - 57 SP - 7176 EP - 7178 PB - Royal Society of Chemistry CY - Cambridge AN - OPUS4-26116 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Laschewsky, A. A1 - Mertoglu, M. A1 - Kubowicz, S. A1 - Thünemann, Andreas T1 - Lamellar Structured Nanoparticles Formed by Complexes of a Cationic Block Copolymer and Perfluorodecanoic Acid N2 - A double hydrophilic block copolymer was synthesized by controlled free radical polymerization, namely by the RAFT method, from a poly(ethylene oxide) macromonomer and a cationic acrylate. Stoichiometric complexes with sodium decanoate and with sodium perfluorodecanoate were prepared by self-assembly. Both complexes are soluble in water forming core-shell nanoparticles with hydrodynamic radii of 54 and 22 nm, respectively, and neutral potentials. The complex containing decanoate decomposed upon dilution, while the complex with perfluorodecanoate is stable even against dialysis and in salt solution. Only the nanoparticles containing perfluorodecanoate show a strong contrast in small-angle X-ray scattering (SAXS). It is produced from their cores that have an elliptical shape (short axes = 8.5 nm, long axis = 23.3 nm) and a sharp density transition to the shell. The cores exhibit an internal lamellar structure with a long period of 3.65 nm consisting of fluorocarbon rich lamellae (d1 = 3.00 nm) and lamellae enriched in ionic groups (d2 = 0.65 nm). These fluorinated nanoparticles coexist in physiological buffer with human serum albumin and fibrinogen without inducing aggregation. Moreover, the content of -helix of these serum proteins increased when in solution with the fluorinated nanoparticles. KW - Small-angle X-ray scattering (SAXS) KW - Block-copolymers KW - Polymeric nanoparticles KW - Protein secondary structure PY - 2006 DO - https://doi.org/10.1021/ma061573k SN - 0024-9297 SN - 1520-5835 VL - 39 IS - 26 SP - 9337 EP - 9345 PB - American Chemical Society CY - Washington, DC AN - OPUS4-14392 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Thünemann, Andreas T1 - Small-Angle X-ray Scattering for Nanoparticle Analysis: The Renaissance of an Ancient Method T2 - Workshop of the Max Planck Institute of Colloids and Interfaces on "Trends in Colloid and Interface Science" CY - Potsdam, Germany DA - 2009-06-12 PY - 2009 AN - OPUS4-19376 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Tyagi, R. A1 - Malhotra, S. A1 - Thünemann, Andreas A1 - Sedighi, A. A1 - Weber, M. A1 - Schäfer, A. A1 - Haag, R. T1 - Investigations of host-guest interactions with shape-persistent nonionic dendritic micelles N2 - The interaction of self-assembled dendritic amphiphiles with drugs and dyes in aqueous solutions is of great significance for designing and optimizing shape-persistent delivery systems. Here we present deeper insight for two examples of low molecular weight (LMW) nonionic dendritic amphiphiles as host molecules and a series of selected aromatic guest model molecules (benzene, naphthalene, biphenyl, terphenyl, anthracene, and pyrene). Aromatic guest molecules were incorporated into the self-assemblies of dendritic nanocarriers, and the resultant complexes were studied by a combination of UV, NMR, computational simulation, and small-angle X-ray-scattering (SAXS) techniques in order to determine the loading capacity, localization, and specific interactions in dendritic amphiphiles with guest molecules. Our findings revealed that the localization of guest molecules in the hydrophobic region and the loading capacity of guest molecules are dependent on their size and the arrangement of aromatic rings instead of the loading amount. Furthermore, the shape of self-assembled host molecules was found to be ellipsoidal and highly persistent even after loading the guest molecules. To the best of our knowledge, this is the first systematic host–guest study, particularly with low molecular weight nonionic dendritic amphiphilies and aromatic guest molecules. Thus, this study opens new possibilities and ways to explore the transport behavior of aromatic drugs with such nanocarriers. KW - Nanotechnology PY - 2013 DO - https://doi.org/10.1021/jp401503y SN - 1932-7447 SN - 1089-5639 VL - 117 IS - 23 SP - 12307 EP - 12317 PB - Soc. CY - Washington, DC AN - OPUS4-28710 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Fortes Martin, R. A1 - Thünemann, Andreas A1 - Stockmann, Jörg Manfred A1 - Radnik, Jörg A1 - Koetz, J. T1 - From Nanoparticle Heteroclusters to Filament Networks by Self-Assembly at the Water–Oil Interface of Reverse Microemulsions N2 - Surface self-assembly of spherical nanoparticles of sizes below 10 nm into hierarchical heterostructures is under arising development despite the inherent difficulties of obtaining complex ordering patterns on a larger scale. Due to template-mediated interactions between oil-dispersible superparamagnetic nanoparticles (MNPs) and polyethylenimine-stabilized gold nanoparticles (Au(PEI)NPs) at the water–oil interface of microemulsions, complex nanostructured films can be formed. Characterization of the reverse microemulsion phase by UV–vis absorption revealed the formation of heteroclusters from Winsor type II phases (WPII) using Aerosol-OT (AOT) as the surfactant. SAXS measurements verify the mechanism of initial nanoparticle clustering in defined dimensions. XPS suggested an influence of AOT at the MNP surface. Further, cryo-SEM and TEM visualization demonstrated the elongation of the reverse microemulsions into cylindrical, wormlike structures, which subsequently build up larger nanoparticle superstructure arrangements. Such WPII phases are thus proven to be a new form of soft template, mediating the self-assembly of different nanoparticles in hierarchical network-like filaments over a substrate during solvent evaporation. KW - Small-angle X-ray scattering KW - SAXS KW - Nanoparticle KW - Nano structure PY - 2021 DO - https://doi.org/10.1021/acs.langmuir.1c01348 VL - 37 IS - 29 SP - 8876 EP - 8885 PB - American Chemical Society AN - OPUS4-53034 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Wolf, J. A1 - Stawski, Tomasz A1 - Smales, Glen Jacob A1 - Thünemann, Andreas A1 - Emmerling, Franziska T1 - Towards automation of the polyol process for the synthesis of silver nanoparticles N2 - Metal nanoparticles have a substantial impact across diferent felds of science, such as photochemistry, energy conversion, and medicine. Among the commonly used nanoparticles, silver nanoparticles are of special interest due to their antibacterial properties and applications in sensing and catalysis. However, many of the methods used to synthesize silver nanoparticles often do not result in well-defned products, the main obstacles being high polydispersity or a lack of particle size tunability. We describe an automated approach to on-demand synthesis of adjustable particles with mean radii of 3 and 5 nm using the polyol route. The polyol process is a promising route for silver nanoparticles e.g., to be used as reference materials. We characterised the as-synthesized nanoparticles using small-angle X-ray scattering, dynamic light scattering and further methods, showing that automated synthesis can yield colloids with reproducible and tuneable properties. KW - Sillver KW - Nanoparticles KW - Automated synthesis KW - Chemputer KW - Scattering KW - SAXS PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-546803 DO - https://doi.org/10.1038/s41598-022-09774-w VL - 12 IS - 1 SP - 1 EP - 9 PB - Nature Springer AN - OPUS4-54680 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Klimakow, Maria A1 - Klobes, Peter A1 - Thünemann, Andreas A1 - Rademann, K. A1 - Emmerling, Franziska T1 - Mechanochemical synthesis of metal-organic frameworks: A fast and facile approach toward quantitative yields and high specific surface areas N2 - The strategy of utilizing mechanochemical synthesis to obtain metal–organic frameworks (MOFs) with high surface areas is demonstrated for two model systems. The compounds HKUST-1 (Cu3(BTC)2, BTC = 1,3,5-benzenetricarboxylate) and MOF-14 (Cu3(BTB)2, BTB = 4,4',4''-benzenetribenzoate) were synthesized by ball milling and characterized by powder X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM) and thermal analysis (DTA/DTG/MS). The specific surface area (SSA) of both compounds was characterized by nitrogen adsorption. To verify these results and to understand how the synthetic conditions influence the pore structure and the surface area, additional small-angle X-ray scattering (SAXS) experiments were carried out. Our investigations confirm that this synthesis approach is a promising alternative method for distinct MOFs. This facile method leads to materials with surface areas of 1713 m²/g, which is comparable to the highest given values in the literature for the respective compounds. KW - Metal-organic frameworks KW - Mechanochemistry KW - Green-chemistry synthesis KW - Gas adsorption KW - SAXS KW - Specific surface area PY - 2010 DO - https://doi.org/10.1021/cm1012119 SN - 0897-4756 SN - 1520-5002 VL - 22 IS - 18 SP - 5216 EP - 5221 PB - American Chemical Society CY - Washington, DC AN - OPUS4-21999 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Krause, B. A1 - Meyer, T. A1 - Sieg, H. A1 - Kästner, Claudia A1 - Reichardt, P. A1 - Tentschert, J. A1 - Jungnickel, H. A1 - Estrela-Lopis, I. A1 - Burel, A. A1 - Chevance, S. A1 - Gauffre, F. A1 - Jalili, P. A1 - Meijer, J. A1 - Böhmert, L. A1 - Braeuning, A. A1 - Thünemann, Andreas A1 - Emmerling, Franziska A1 - Fessard, V. A1 - Laux, P. A1 - Lampen, A. A1 - Luch, A. T1 - Characterization of aluminum, aluminum oxide and titanium dioxide nanomaterials using a combination of methods for particle surface and size analysis N2 - The application of appropriate analytical techniques is essential for nanomaterial (NM) characterization. In this study, we compared different analytical techniques for NM analysis. Regarding possible adverse health effects, ionic and particulate NM effects have to be taken into account. As NMs behave quite differently in physiological media, special attention was paid to techniques which are able to determine the biosolubility and complexation behavior of NMs. Representative NMs of similar size were selected: aluminum (Al0) and aluminum oxide (Al2O3), to compare the behavior of metal and metal oxides. In addition, titanium dioxide (TiO2) was investigated. Characterization techniques such as dynamic light scattering (DLS) and nanoparticle tracking analysis (NTA) were evaluated with respect to their suitability for fast characterization of nanoparticle dispersions regarding a particle's hydrodynamic diameter and size distribution. By application of inductively coupled plasma mass spectrometry in the single particle mode (SP-ICP-MS), individual nanoparticles were quantified and characterized regarding their size. SP-ICP-MS measurements were correlated with the information gained using other characterization techniques, i.e. transmission electron microscopy (TEM) and small angle X-ray scattering (SAXS). The particle surface as an important descriptor of NMs was analyzed by X-ray diffraction (XRD). NM impurities and their co-localization with biomolecules were determined by ion beam microscopy (IBM) and confocal Raman microscopy (CRM). We conclude advantages and disadvantages of the different techniques applied and suggest options for their complementation. Thus, this paper may serve as a practical guide to particle characterization techniques. KW - Small-angle X-ray scattering KW - SAXS PY - 2018 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-447057 DO - https://doi.org/10.1039/C8RA00205C SN - 2046-2069 VL - 8 IS - 26 SP - 14377 EP - 14388 PB - The Royal Society of Chemistry AN - OPUS4-44705 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -