@article{62875, author = {{Theile-Rasche, Chantal and Wang, Fuzeng and Prüßner, Tim and Huck, Marten and Steinrück, Hans-Georg and de los Arcos de Pedro, Maria Teresa and Grundmeier, Guido}}, issn = {{0040-6090}}, journal = {{Thin Solid Films}}, publisher = {{Elsevier BV}}, title = {{{Evaluation of anti-adhesive and corrosion protection properties of TiAlSiN-magnetron-sputtered films for applications in polymer processing}}}, doi = {{10.1016/j.tsf.2025.140676}}, volume = {{820}}, year = {{2025}}, } @article{62874, abstract = {{DNA origami adsorption at single-crystalline TiO2 surfaces is investigated at different Mg2+ concentrations. For TiO2(001), DNA origami adsorption is stronger at 5 mM than at 10 mM Mg2+, whereas the opposite is observed for TiO2(110) and TiO2(111).}}, author = {{Xu, Xiaodan and Gołębiowska, Sandra and de los Arcos de Pedro, Maria Teresa and Grundmeier, Guido and Keller, Adrian}}, issn = {{2755-3701}}, journal = {{RSC Applied Interfaces}}, publisher = {{Royal Society of Chemistry (RSC)}}, title = {{{DNA origami adsorption at single-crystalline TiO2 surfaces}}}, doi = {{10.1039/d5lf00109a}}, year = {{2025}}, } @article{60568, author = {{Bocchini, Adriana and Kollmann, S. and Gerstmann, Uwe and Schmidt, Wolf Gero and Grundmeier, Guido}}, issn = {{0039-6028}}, journal = {{Surface Science}}, publisher = {{Elsevier BV}}, title = {{{Phosphonic acid adsorption on α-Bi2O3 surfaces}}}, doi = {{10.1016/j.susc.2025.122776}}, volume = {{760}}, year = {{2025}}, } @article{60913, abstract = {{ABSTRACTSpin‐coated polylactide (PLA) thin films were exposed to nitrogen plasma for varying time intervals. The progressive etching of the PLA film in direct contact with the nitrogen plasma was monitored in situ using polarization modulated infrared reflection absorption spectroscopy (PM‐IRRAS). No appreciative changes in composition were seen with PM‐IRRAS, indicating that the etching did not significantly affect the bulk composition. Atomic force microscopy characterization of the plasma‐etched films showed that the PLA films are homogeneously etched. Subsequent ex situ XPS analysis of the treated surface revealed the presence of C‐N bonds in the surface‐near region that could be associated with amino and/or amide surface species. PLA films were also alternatively exposed to nitrogen ion beams produced by an electron‐cyclotron‐resonance (ECR) plasma source and were investigated in vacuo by XPS. This treatment revealed the partial substitution of surface oxygen species by nitrogen, resulting in a similar surface modification as in the plasma case. The comparison of XPS data and water contact angle studies suggest that the activated surfaces show a reorientation of macromolecular fragments in the surface‐near region depending on the polarity of the phase with which they are in contact. Under ultra‐high vacuum (UHV) conditions, the surface tends to lower its surface energy, while in contact with the aqueous phase, subsurface polar groups orientate outwards, which enables the formation of hydrogen bonds.}}, author = {{Golebiowska, Sandra Alicja and Voigt, Markus and de los Arcos, Teresa and Grundmeier, Guido}}, issn = {{0142-2421}}, journal = {{Surface and Interface Analysis}}, number = {{7}}, pages = {{499--509}}, publisher = {{Wiley}}, title = {{{In Situ PM‐IRRAS and XPS Analysis of Nitrogen Plasma Surface Modification of Polylactide Thin Films}}}, doi = {{10.1002/sia.7406}}, volume = {{57}}, year = {{2025}}, } @article{62936, author = {{Ruhm, Lukas and Neßlinger, Vanessa and Becker, Roman and Meschut, Gerson and Grundmeier, Guido}}, issn = {{0143-7496}}, journal = {{International Journal of Adhesion and Adhesives}}, publisher = {{Elsevier BV}}, title = {{{A contribution to the mechanistic understanding of the improvement of the delamination resistance of adhesives on steel by grit-blasting}}}, doi = {{10.1016/j.ijadhadh.2025.104147}}, volume = {{143}}, year = {{2025}}, } @article{62938, author = {{Müller, Hendrik and Cetin, Ali and Dahlmann, Rainer and de los Arcos, Teresa and Grundmeier, Guido}}, issn = {{0257-8972}}, journal = {{Surface and Coatings Technology}}, publisher = {{Elsevier BV}}, title = {{{Interface chemistry and adhesion of thin bilayer Si-organic PECVD barrier films on post-consumer recycled polypropylene}}}, doi = {{10.1016/j.surfcoat.2025.132392}}, volume = {{512}}, year = {{2025}}, } @article{62939, author = {{Su, Jiangling and Muhle, Marius and Nembot, Nelly and Prüßner, Tim and Xie, Xiaofan and Wittstock, Gunther and Grundmeier, Guido}}, issn = {{0013-4686}}, journal = {{Electrochimica Acta}}, publisher = {{Elsevier BV}}, title = {{{Spontaneous grafting of nitrobenzenediazonium salt on plasma-modified copper substrates}}}, doi = {{10.1016/j.electacta.2025.147810}}, volume = {{546}}, year = {{2025}}, } @article{58853, abstract = {{Abstract While being a promising approach for the treatment of infections caused by drug-resistant, pathogenic bacteria, the clinical implementation of phage therapy still faces several challenges. One of these challenges lies in the high strain-specificity of most bacteriophages, which makes it necessary to screen large phage collections against the target pathogens in order to identify suitable candidates for the formulations of personalized therapeutic phage cocktails. In this work, we evaluate the potential of quartz crystal microbalance with dissipation monitoring (QCM-D) to identify and detect phage infection and subsequent lysis of bacteria immobilized on the surfaces of the QCM-D sensors. Using lytic Escherichia coli phage T7 as a model, we show that phage infection of E. coli cells results in various unique alterations in the behaviors of the frequency (Δf) and dissipation (ΔD) signals, which are not observed during exposure of the E. coli strain to non-infectious Bacillus subtilis phage phi29 at similar concentration. To aid future phage screening campaigns, we furthermore identify a single measurement parameter, i.e., the spread between the different overtones of ΔD, that can be used to detect phage-induced lysis. For T7 infection of E. coli, this is achieved within 4 h after inoculation, including immobilization and growth of the bacteria on the sensor surface, as well as the completed phage propagation cycle. Given the commercial availability of highly automated multichannel systems and the fact that this approach does not require any sensor modifications, QCM-D has the potential to become a valuable tool for screening medium-sized phage collections against target pathogens. Graphical Abstract }}, author = {{Pothineni, Bhanu K. and Probst, René and Kiefer, Dorothee and Dobretzberger, Verena and Barišić, Ivan and Grundmeier, Guido and Keller, Adrian}}, issn = {{1618-2642}}, journal = {{Analytical and Bioanalytical Chemistry}}, publisher = {{Springer Science and Business Media LLC}}, title = {{{Monitoring phage infection and lysis of surface-immobilized bacteria by QCM-D}}}, doi = {{10.1007/s00216-025-05803-5}}, year = {{2025}}, } @article{60507, abstract = {{DNA origami nanostructures are powerful molecular tools for the controlled arrangement of functional molecules and thus have important applications in biomedicine, sensing, and materials science. The fabrication of DNA origami...}}, author = {{Tomm, Emilia and Grundmeier, Guido and Keller, Adrian}}, issn = {{2040-3364}}, journal = {{Nanoscale}}, publisher = {{Royal Society of Chemistry (RSC)}}, title = {{{Cost-efficient folding of functionalized DNA origami nanostructures via staple recycling}}}, doi = {{10.1039/d5nr01435b}}, year = {{2025}}, } @article{60606, abstract = {{Streptavidin binding to DNA origami-supported high-density biotin arrays is investigated for selected experimental parameters. While bidentate binding and steric hindrance can be minimized, molecular crowding limits the binding yields in 2D arrays.}}, author = {{Rabbe, Lukas and Tomm, Emilia and Grundmeier, Guido and Keller, Adrian}}, issn = {{2046-2069}}, journal = {{RSC Advances}}, number = {{30}}, pages = {{24536--24543}}, publisher = {{Royal Society of Chemistry (RSC)}}, title = {{{Toward high-density streptavidin arrays on DNA origami nanostructures}}}, doi = {{10.1039/d5ra03393d}}, volume = {{15}}, year = {{2025}}, } @article{60709, abstract = {{Self-assembled DNA origami lattices have promising applications in the fabrication of functional surfaces for sensing and plasmonics via molecular lithography. While surface-assisted DNA origami lattice assembly at mica surfaces is...}}, author = {{Omoboye, Adekunle and Pothineni, Bhanu and Grundmeier, Guido and She, Zhe and Keller, Adrian}}, issn = {{2755-3701}}, journal = {{RSC Applied Interfaces}}, publisher = {{Royal Society of Chemistry (RSC)}}, title = {{{Surface potential-dependent assembly of DNA origami lattices at SiO2 surfaces}}}, doi = {{10.1039/d5lf00169b}}, year = {{2025}}, } @article{60973, abstract = {{The specific binding of DNA origami nanostructures (DONs) to bacteria is an important prerequisite for their application in pathogen targeting and antimicrobial drug delivery. So far, targeting bacteria with DONs has been achieved exclusively via aptamers, which suffer from drawbacks such as sensitivity toward environmental conditions and reduced binding after immobilization or conjugation. Here, an alternative approach is presented based on the modification of DONs with the cell wall‐binding glycopeptide antibiotic vancomycin. Using strain‐promoted azide‐alkyne cycloaddition, azide‐modified vancomycin is conjugated to selected staple strands and subsequently incorporated into 2D DON triangles. The resulting constructs show specific binding to the Gram‐positive species Bacillus subtilis (B. subtilis) and Staphylococcus capitis (S. capitis), and remarkably, to Gram‐negative Escherichia coli (E. coli), but no antimicrobial activity at vancomycin concentrations up to at least 2.91 μM. For B. subtilis and E. coli, DONs with vancomycin modifications on both sides exhibit better binding than DONs modified on only one side. However, both variants bind equally well to S. capitis. These results demonstrate the great potential of small molecule drug compounds for the robust, broad‐spectrum targeting of bacteria with DONs. Targeting a ubiquitous cell wall component of most pathogenic bacteria, vancomycin‐modified DONs have many potential applications in the prevention and treatment of nosocomial infections.}}, author = {{Coşkuner Leineweber, Özge and Pothineni, Bhanu K. and Schumann, Nils and Hofmann, Ulrike and Möser, Christin and Smith, David M. and Grundmeier, Guido and Zhang, Yixin and Keller, Adrian}}, issn = {{2688-4062}}, journal = {{Small Structures}}, publisher = {{Wiley}}, title = {{{Vancomycin‐Modified DNA Origami Nanostructures for Targeting Bacterial Pathogens}}}, doi = {{10.1002/sstr.202500246}}, year = {{2025}}, } @article{51121, abstract = {{DNA origami nanostructures are a powerful tool in biomedicine and can be used to combat drug‐resistant bacterial infections. However, the effect of unmodified DNA origami nanostructures on bacteria is yet to be elucidated. With the aim to obtain a better understanding of this phenomenon, the effect of three DNA origami shapes, i.e., DNA origami triangles, six‐helix bundles (6HBs), and 24‐helix bundles (24HBs), on the growth of Gram‐negative Escherichia coli and Gram‐positive Bacillus subtilis is investigated. These results reveal that while triangles and 24HBs can be used as a source of nutrients by E. coli and thereby promote population growth, their effect is much smaller than that of genomic single‐ and double‐stranded DNA. However, no effect on E. coli population growth is observed for the 6HBs. On the other hand, B. subtilis does not show any significant changes in population growth when cultured with the different DNA origami shapes or genomic DNA. The detailed effect of DNA origami nanostructures on bacterial growth thus depends on the competence signals and uptake mechanism of each bacterial species, as well as the DNA origami shape. This should be considered in the development of antimicrobial DNA origami nanostructures.}}, author = {{Garcia-Diosa, Jaime Andres and Grundmeier, Guido and Keller, Adrian}}, issn = {{1439-4227}}, journal = {{ChemBioChem}}, keywords = {{Organic Chemistry, Molecular Biology, Molecular Medicine, Biochemistry}}, publisher = {{Wiley}}, title = {{{Effect of DNA Origami Nanostructures on Bacterial Growth}}}, doi = {{10.1002/cbic.202400091}}, year = {{2024}}, } @article{53621, abstract = {{The coupling of structural transitions to heat capacity changes leads to destabilization of macromolecules at both, elevated and lowered temperatures. DNA origami not only exhibit this property but also provide...}}, author = {{Dornbusch, Daniel and Hanke, Marcel and Tomm, Emilia and Kielar, Charlotte and Grundmeier, Guido and Keller, Adrian and Fahmy, Karim}}, issn = {{1359-7345}}, journal = {{Chemical Communications}}, keywords = {{Materials Chemistry, Metals and Alloys, Surfaces, Coatings and Films, General Chemistry, Ceramics and Composites, Electronic, Optical and Magnetic Materials, Catalysis}}, publisher = {{Royal Society of Chemistry (RSC)}}, title = {{{Cold denaturation of DNA origami nanostructures}}}, doi = {{10.1039/d3cc05985e}}, year = {{2024}}, } @article{54644, abstract = {{DNA origami nanostructures (DONs) are able to scavenge reactive oxygen species (ROS) and their scavenging efficiency toward ROS radicals was shown to be comparable to that of genomic DNA. Herein, we demonstrate that DONs are highly efficient singlet oxygen quenchers outperforming double‐stranded (ds) DNA by several orders of magnitude. To this end, a ROS mixture rich in singlet oxygen is generated by light irradiation of the photosensitizer methylene blue and its cytotoxic effect on Escherichia coli cells is quantified in the presence and absence of DONs. DONs are found to be vastly superior to dsDNA in protecting the bacteria from ROS‐induced damage and even surpass established ROS scavengers. At a concentration of 15 nM, DONs are about 50 000 times more efficient ROS scavengers than dsDNA at an equivalent concentration. This is attributed to the dominant role of singlet oxygen, which has a long diffusion length and reacts specifically with guanine. The dense packing of the available guanines into the small volume of the DON increases the overall quenching probability compared to a linear dsDNA with the same number of base pairs. DONs thus have great potential to alleviate oxidative stress caused by singlet oxygen in diverse therapeutic settings.}}, author = {{Garcia-Diosa, Jaime Andres and Grundmeier, Guido and Keller, Adrian}}, issn = {{0947-6539}}, journal = {{Chemistry – A European Journal}}, publisher = {{Wiley}}, title = {{{Highly Efficient Quenching of Singlet Oxygen by DNA Origami Nanostructures}}}, doi = {{10.1002/chem.202402057}}, year = {{2024}}, } @article{55310, abstract = {{DNA origami nanostructures are promising carries for drug delivery applications. However, their limited stability under relevant conditions often presents a challenge. Herein, the structural stability of DNA origami nanostructures is investigated in a setting compatible with their application in photodynamic therapy (PDT). To this end, DNA origami triangles and six‐helix bundles (6HBs) are loaded with the clinically tested photosensitizer methylene blue, which upon irradiation with red light generates reactive oxygen species (ROS) that attack the DNA origami nanostructures. ROS‐induced structural damage is observed to depend on the ionic composition of the surrounding medium and becomes more severe at low ionic strength. Mg2+ ions can efficiently protect the DNA origami nanostructures from ROS‐induced damage and may even heal some of the damage obtained under Mg2+‐free conditions when added after irradiation. Finally, the employed DNA origami 6HBs are more resistant toward ROS‐induced structural damage than the triangles, which is attributed to their markedly different mechanical properties. These results thus provide some fundamental insights into the stabilizing role of DNA origami superstructure that may guide the selection or design of DNA origami nanocarriers with optimized stability for their application in PDT.}}, author = {{Rabbe, Lukas and Garcia‐Diosa, Jaime Andres and Grundmeier, Guido and Keller, Adrian}}, issn = {{2688-4062}}, journal = {{Small Structures}}, publisher = {{Wiley}}, title = {{{Ion‐Dependent Stability of DNA Origami Nanostructures in the Presence of Photo‐Generated Reactive Oxygen Species}}}, doi = {{10.1002/sstr.202400094}}, year = {{2024}}, } @article{62236, abstract = {{AbstractDue to its excellent biocompatibility, pure iron is a very promising implant material, but often features corrosion rates that are too low. Using additive manufacturing and modified powders the microstructure and, thus, the material properties, e.g., the corrosion properties, can be tailored for specific applications. Within the scope of this study, pure iron powder was modified with different amounts of CeO2 or Fe2O3 nanoparticles and subsequently processed by Electron Beam Powder Bed Fusion (PBF-EB/M). The corrosion-fatigue behavior of CeO2 and Fe2O3 modified iron was investigated using rotation bending tests under the influence of simulated body fluid (m-SBF). While the modification using Fe2O3 showed reduced fatigue and corrosion-fatigue strengths, it could be demonstrated that the modification with CeO2 is characterized by improved fatigue properties. The superior fatigue properties in air are attributed to the positive impact of dispersion strengthening. Additionally, an increased degradation rate compared to pure iron could be observed, eventually promoting an earlier failure of the specimens in the corrosion fatigue tests.}}, author = {{Wackenrohr, Steffen and Torrent, Christof Johannes Jaime and Herbst, Sebastian and Nürnberger, Florian and Krooss, Philipp and Frenck, Johanna-Maria and Ebbert, Christoph and Voigt, Markus and Grundmeier, Guido and Niendorf, Thomas and Maier, Hans Jürgen}}, issn = {{2397-2106}}, journal = {{npj Materials Degradation}}, number = {{1}}, publisher = {{Springer Science and Business Media LLC}}, title = {{{Corrosion fatigue behavior of nanoparticle modified iron processed by electron powder bed fusion}}}, doi = {{10.1038/s41529-024-00470-w}}, volume = {{8}}, year = {{2024}}, } @article{62828, author = {{Ruhm, Lukas and Löseke, Jannik and Vieth, Pascal and Prüßner, Tim and Grundmeier, Guido}}, issn = {{0169-4332}}, journal = {{Applied Surface Science}}, publisher = {{Elsevier BV}}, title = {{{Adhesion promotion and corrosion resistance of mixed phosphonic acid monolayers on AA 2024}}}, doi = {{10.1016/j.apsusc.2024.160655}}, volume = {{670}}, year = {{2024}}, } @article{62873, abstract = {{AbstractVapor phase infiltration (VPI) has emerged as a promising tool for fabrication of novel hybrid materials. In the field of polymeric gas separation membranes, a beneficial impact on stability and membrane performance is known for several polymers with differing functional groups. This study for the first time investigates VPI of trimethylaluminum (TMA) into poly(1‐trimethylsilyl‐1‐propyne) (PTMSP), featuring a carbon–carbon double bond as functional group. Saturation of the precursor inside the polymer is already attained after 60 s infiltration time leading to significant densification of the material. Depth profiling proves accumulation of aluminum in the polymer itself, but a significantly increased accumulation is visible in the gradient layer between polymer and SiO2 substrate. A reaction pathway is proposed and supplemented by density‐functional theory (DFT) calculations. Infrared spectra derived from both experiments and simulation support the presented reaction pathway. In terms of permeance, a favorable impact on selectivity is observed for infiltration times up to 1 s. Longer infiltration times yield greatly reduced permeance values close or even below the detection limit of the measurement device. The present results of this study set a strong basis for the application of VPI on polymers for gas‐barrier and membrane applications in the future.}}, author = {{Jenderny, Jonathan and Boysen, Nils and Rubner, Jens and Zysk, Frederik and Preischel, Florian and de los Arcos de Pedro, Maria Teresa and Damerla, Varun Raj and Kostka, Aleksander and Franke, Jonas and Dahlmann, Rainer and Kühne, Thomas D. and Wessling, Matthias and Awakowicz, Peter and Devi, Anjana}}, issn = {{2196-7350}}, journal = {{Advanced Materials Interfaces}}, number = {{28}}, publisher = {{Wiley}}, title = {{{Tuning the Permeation Properties of Poly(1‐trimethylsilyl‐1‐propyne) by Vapor Phase Infiltration Using Trimethylaluminum}}}, doi = {{10.1002/admi.202400171}}, volume = {{11}}, year = {{2024}}, } @article{62942, abstract = {{AbstractNanostructured bilayer thin films with superhydrophobic and superhydrophilic surfaces were prepared using Ti6Al4V alloy substrates which allowed for the comparative analysis of polyvinyl acetate (PVAc) particle adsorption as a function of the interface structure. The PVAc particles were obtained from emulsion polymerization of vinyl acetate. A superhydrophilic TiO2 nanofiber-based 3D network was created on the Ti6Al4V alloy substrate by application of a hydrothermal method. Subsequent UV-grafting of ultra-thin polydimethylsiloxane (PDMS) layers resulted in a superhydrophobic surface. The modification steps were followed via Diffuse Reflectance Infrared Fourier Transform Spectroscopy, X-ray Photoelectron Spectroscopy, Field Emission-Scanning Electron Microscopy, contact angle and Electrochemical Impedance Spectroscopy. A mechanism for the adsorption of PVAc at the two electrolyte/substrate interfaces could be revealed.}}, author = {{Neßlinger, Vanessa and Atlanov, Jan and Grundmeier, Guido}}, issn = {{3004-9261}}, journal = {{Discover Applied Sciences}}, number = {{6}}, publisher = {{Springer Science and Business Media LLC}}, title = {{{Interactions of polyvinyl acetate dispersions with nanostructured superhydrophilic and superhydrophobic Ti6Al4V alloy surfaces}}}, doi = {{10.1007/s42452-024-05916-z}}, volume = {{6}}, year = {{2024}}, }