TY - JOUR A1 - Kasper, J. A1 - Herrmanns, M.I. A1 - Bantz, C. A1 - Utech, S. A1 - Koshkina, Olga A1 - Maskos, Michael A1 - Brochhausen, C. A1 - Pohl, C. A1 - Fuchs, S. A1 - Unger, R. E. A1 - Kirkpatrick, C.J. T1 - Flotillin-involved uptake of silica nanoparticles and responses of an alveolar-capillary barrier in vitro N2 - Drug and gene delivery via nanoparticles across biological barriers such as the alveolar-capillary barrier of the lung constitutes an interesting and increasingly relevant field in nanomedicine. Nevertheless, potential hazardous effects of nanoparticles (NPs) as well as their cellular and systemic fate should be thoroughly examined. Hence, this study was designed to evaluate the effects of amorphous silica NPs (Sicastar) and (poly)organosiloxane NPs (AmOrSil) on the viability and the inflammatory response as well as on the cellular uptake mechanisms and fate in cells of the alveolar barrier. For this purpose, the alveolar epithelial cell line (NCI H441) and microvascular endothelial cell line (ISO-HAS-1) were used in an experimental set up resembling the alveolar-capillary barrier of the lung. In terms of IL-8 and sICAM Sicastar resulted in harmful effects at higher concentrations (60 µg/ml) in conventional monocultures but not in the coculture, whereas AmOrSil showed no significant effects. Immunofluorescence counterstaining of endosomal structures in NP-incubated cells showed no evidence for a clathrin- or caveolae-mediated uptake mechanism. However, NPs were enclosed in flotillin-1 and -2 marked vesicles in both cell types. Flotillins appear to play a role in cellular uptake or trafficking mechanisms of NPs and are discussed as indicators for clathrin- or caveolae-independent uptake mechanisms. In addition, we examined the transport of NPs across this in vitro model of the alveolar-capillary barrier forming a tight barrier with a transepithelial electrical resistance of 560 ± 8 Ω cm². H441 in coculture with endothelial cells took up much less NPs compared to monocultures. Moreover, coculturing prevented the transport of NP from the epithelial compartment to the endothelial layer on the bottom of the filter insert. This supports the relevance of coculture models, which favour a differentiated and polarised epithelial layer as in vitro test systems for nanoparticle uptake. KW - Silica nanoparticles KW - Alveolar-capillary barrier KW - NP uptake KW - NP-transport KW - Endocytosis KW - Flotillin-1/-2-dependent uptake/trafficking PY - 2013 DO - https://doi.org/10.1016/j.ejpb.2012.10.011 SN - 0939-6411 SN - 1873-3441 VL - 84 IS - 2 SP - 275 EP - 287 PB - Elsevier B.V. CY - Amsterdam AN - OPUS4-28841 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CHAP A1 - Maskos, Michael A1 - Stauber, R.H. ED - Ducheyne, P. ED - Healy, K.E. ED - Hutmacher, D.W. ED - Grainger, D.W. ED - Kirkpatrick, C.J. T1 - Characterization of nanoparticles in biological environments N2 - Deliberate and accidental exposure of the ecosystem including humans to nanoparticles becomes inevitable as nanomaterials are increasingly used. In biological fluids, biomolecules associate with nanoparticles, leading to the formation of a dynamic biomolecule “corona” that critically defines the biological identity of the particle. As the bio-physical properties of such a decorated particle often differ significantly from those of the formulated particle a detailed characterization of nanoparticles in biological environments becomes increasingly important though, nevertheless also technically challenging. Here, we introduce experimental methods currently employed for nanoparticle characterization, present examples underlining the complexity of the nano-bio interface, and discuss the need for further technical and conceptual developments. A deep and mechanistic bio-physical understanding of the nano-bio interface is a challenge but also fundamental prerequisite for future applications in nanobiology, nanomedicine and nano(eco)toxicology. KW - Amorphous silica nanoparticles KW - Dynamic light scattering DLS KW - Interparticle interactions KW - Field-flow fractionation FFF KW - Cryogenic transmission electron microscopy cryo-TEM PY - 2011 SN - 978-0-08-055302-3 VL - 3 IS - Chapter 3.319. SP - 329 EP - 339 PB - Elsevier AN - OPUS4-27283 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Eslahian, Kyriakos-Alexandros A1 - Maskos, Michael T1 - Hofmeister effect in thermal field-flow fractionation of colloidal aqueous dispersions N2 - In this study, the retention of colloidal polystyrene beads in aqueous dispersion in thermal field-flow fractionation (ThFFF) is investigated as function of various types and concentrations of electrolytes in the carrier liquid. A specific ion effect is observed and can be interpreted in terms of Hofmeister series. Addition of salt composed of chaotropic anions to the carrier liquid increases particle retention with increasing ionic strength up to several mM. This effect is less pronounced the more kosmotropic the anions are, up to a decrease of retention by increasing concentration of sulphate and citrate. It is demonstrated that the effect of varying cations is minor as compared to the one of anions with this model system. KW - Thermal field-flow fractionation KW - Hofmeister series KW - Specific ion effects KW - Thermophoresis KW - Soret coefficient PY - 2012 DO - https://doi.org/10.1016/j.colsurfa.2012.02.003 SN - 0927-7757 SN - 1873-4359 VL - 413 SP - 65 EP - 70 PB - Elsevier CY - Amsterdam AN - OPUS4-27432 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Thiermann, Raphael A1 - Mueller, W. A1 - Montesinos-Castellanos, A. A1 - Metzke, D. A1 - Löb, P. A1 - Hessel, V. A1 - Maskos, Michael T1 - Size controlled polymersomes by continous self-assembly in micromixers N2 - The formation of vesicles based on the self-assembly of amphiphilic poly(butadiene)-b-poly(ethylene oxide) (PB130-b-PEO66) block copolymer in water has been studied using THF as co-solvent. To obtain a highly controlled mixing process for the polymer/THF- and the water-phase, we employed micro mixers with different mixing geometries. The high impact of this preparation method on the self-assembling process was verified by TEM and DLS characterization of the obtained structures. Spherical micelles, vesicles and worm-like micelles were found depending on the parameters of mixing. By additional parameter adjustment in the vesicle regime, the size of the assembled vesicles was controlled between 45 and 100 nm. This demonstrates the continuous preparation of narrowly distributed vesicle structures with controlled sizes. KW - Vesicles KW - Polymersomes KW - Micromixers PY - 2012 DO - https://doi.org/10.1016/j.polymer.2012.03.058 SN - 0032-3861 SN - 1873-2291 VL - 53 IS - 11 SP - 2205 EP - 2210 PB - Springer CY - Berlin AN - OPUS4-25884 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Koshkina, Olga A1 - Bantz, C. A1 - Würth, Christian A1 - Lang, Thomas A1 - Resch-Genger, Ute A1 - Maskos, Michael T1 - Fluorophore-labeled siloxane-based nanoparticles for biomedical applications N2 - We present the synthesis and characterization of multifunctional fluorophore-labeled poly(organosiloxane) nanoparticles with core-shell architecture, where the fluorescent dye is incorporated into the core. Grafting of heterobifunctional poly(ethylene oxide) (PEO) onto the particle surface leads to water-soluble biocompatible nanoparticles. Two different strategies have been used for the synthesis: The encapsulation of dye-labeled monomers during the polycondensation with additional PEO coating and subsequent dye labeling by covalent attachment of the fluorescent dye rhodamine B to the (chloromethylphenyl)siloxane groups in the core after polymerization and grafting of PEO onto the surface. Comparison of the fluorescence quantum yields of the nanoparticles before and after PEO coating show a decrease in quantum yield after PEO coating. KW - Biocompatibility KW - Core-shell KW - Fluorescence KW - Fluorescence quantum yield KW - Nanoparticles KW - PEO PY - 2011 DO - https://doi.org/10.1002/masy.201100041 SN - 1022-1360 SN - 0258-0322 SN - 1521-3900 VL - 309/310 IS - 1 SP - 141 EP - 146 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-25143 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Noskov, Sergey A1 - Scherer, Christian A1 - Maskos, Michael A1 - Thünemann, Andreas T1 - Determination of Hamaker constants of polymeric nanoparticles in organic solvents by asymmetrical flow field-flow fractionation N2 - Interaction forces between all objects are either of repulsive or attractive nature. Concerning attractive interactions, the determination of dispersion forces are of special interest since they appear in all colloidal systems and have a crucial influence on the properties and processes in these systems. One possibility to link theory and experiment is the description of the London–Van der Waals forces in terms of the Hamaker constant, which leads to the challenging problem of calculating the van der Waals interaction energies between colloidal particles. Hence, the determination of a Hamaker constant for a given material is needed when interfacial phenomena such as adhesion are discussed in terms of the total potential energy between particles and substrates. In this work, the asymmetrical flow field-flow fractionation (AF-FFF) in combination with a Newton algorithm based iteration process was used for the determination of Hamaker constants of different nanoparticles in toluene. KW - Hamaker constant KW - Asymmetrical flow field flow fractionation KW - Lifshitz KW - Van der Waals KW - London KW - Thermodynamic KW - Interaction PY - 2013 DO - https://doi.org/10.1016/j.chroma.2012.12.001 SN - 0021-9673 VL - 1274 SP - 151 EP - 158 PB - Elsevier B.V. CY - Amsterdam AN - OPUS4-27625 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Scherer, Christian A1 - Utech, S. A1 - Scholz, S. A1 - Noskov, S. A1 - Kindervater, P. A1 - Graf, R. A1 - Thünemann, Andreas A1 - Maskos, Michael T1 - Synthesis, characterization and fine-tuning of bimodal poly(organosiloxane) nanoparticles N2 - The acid catalyzed sol–gel type synthesis of polyorganosiloxane core-shell nanoparticles with removable PDMS core in aqueous dispersion leads to the inherent formation of a bimodal size distribution with smaller spheres having approximately 26 nm radii and larger nanoparticles with 60 nm in radius. The origin of the self-organized bimodality is investigated and finally attributed to a combination of stabilization of the growing particles due to i) a miniemulsion-type stabilization by the ultrahydrophobe PDMS and ii) by surface co-stabilization by the employed surfactant. The significant influence of temperature, pH, stirrer speed and amount of the surfactant on the particle sizes allows for the design and fine-tuning of different nanoparticles sizes and distributions. KW - Nanoparticles KW - Polyorganosiloxane KW - Field-flow fractionation (FFF) PY - 2010 DO - https://doi.org/10.1016/j.polymer.2010.09.065 SN - 0032-3861 SN - 1873-2291 VL - 51 IS - 23 SP - 5432 EP - 5439 PB - Springer CY - Berlin AN - OPUS4-22476 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CHAP A1 - Thünemann, Andreas A1 - Eckelt, J. A1 - Maskos, Michael A1 - Wolf, B. A. ED - Matyjaszewski, K. ED - Möller, M. T1 - Fractionation N2 - The enormous diversity of polymers with respect to molecular weight, molecular architecture, and – in the case of copolymers – also the content and arrangement of dissimilar monomers requires well-targeted methods for the separation of the different species that are contained in a given sample. This chapter presents the most abundant fractionation procedures, which are either based on thermodynamic driving forces (like in the case of liquid–liquid phase separation) or on kinetic effects (as with field-flow fractionation). KW - Field-flow fractionation KW - Polymer science KW - Asymmetrical flow field-flow fractionation (AF-FFF) KW - Baker-Williams fractionation KW - Chemical composition distribution (CCD) KW - Circular asymmetrical flow field-flow eluation (CAFFFE) KW - Continuous polymer fractionation (CPF) KW - Crystallization analysis fractionation (CRYSTAF) KW - Crystallization–dissolution fractionation (CDF) KW - Liquid-liquid phase separation KW - Temperature rising elution fractionation (TREF) KW - Phase distribution chromatography (PDC) PY - 2012 SN - 978-0-444-53349-4 DO - https://doi.org/10.1016/B978-0-444-53349-4.00022-4 VL - 2 IS - Chapter 2.04 SP - 65 EP - 91 PB - Elsevier CY - Amsterdam AN - OPUS4-26265 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kasper, J. A1 - Hermanns, M. A1 - Bantz, C. A1 - Maskos, Michael A1 - Stauber, R. A1 - Pohl, C. A1 - Unger, R. E. A1 - Kirkpatrick, J.C. T1 - Inflammatory and cytotoxic responses of an alveolar-capillary coculture model to silica nanoparticles: comparison with conventional monocultures N2 - To date silica nanoparticles (SNPs) play an important role in modern technology and nanomedicine. SNPs are present in various materials (tyres, electrical and thermal insulation material, photovoltaic facilities). They are also used in products that are directly exposed to humans such as cosmetics or toothpaste. For that reason it is of great concern to evaluate the possible hazards of these engineered particles for human health. Attention should primarily be focussed on SNP effects on biological barriers. Accidentally released SNP could, for example, encounter the alveolar-capillary barrier by inhalation. In this study we examined the inflammatory and cytotoxic responses of monodisperse amorphous silica nanoparticles (aSNPs) of 30 nm in size on an in vitro coculture model mimicking the alveolar-capillary barrier and compared these to conventional monocultures. Methods Thus, the epithelial cell line, H441, and the endothelial cell line, ISO-HAS-1, were used in monoculture and in coculture on opposite sides of a filter membrane. Cytotoxicity was evaluated by the MTS assay, detection of membrane integrity (LDH release), and TER (Transepithelial Electrical Resistance) measurement. Additionally, parameters of inflammation (sICAM-1, IL-6 and IL-8 release) and apoptosis markers were investigated. Results Regarding toxic effects (viability, membrane integrity, TER) the coculture model was less sensitive to apical aSNP exposure than the conventional monocultures of the appropriate cells. On the other hand, the in vitro coculture model responded with the release of inflammatory markers in a much more sensitive fashion than the conventional monoculture. At concentrations that were 10-100fold less than the toxic concentrations the apically exposed coculture showed a release of IL-6 and IL-8 to the basolateral side. This may mimic the early inflammatory events that take place in the pulmonary alveoli after aSNP inhalation. Furthermore, a number of apoptosis markers belonging to the intrinsic pathway were upregulated in the coculture following aSNP treatment. Analysis of the individual markers indicated that the cells suffered from DNA damage, hypoxia and ER-stress. Conclusion We present evidence that our in vitro coculture model of the alveolar-capillary barrier is clearly advantageous compared to conventional monocultures in evaluating the extent of damage caused by hazardous material encountering the principle biological barrier in the lower respiratory tract. KW - Silica nanoparticles KW - Alveolar-capillary coculture model KW - Cytotoxicity PY - 2011 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-254217 DO - https://doi.org/10.1186/1743-8977-8-6 SN - 1743-8977 VL - 8 IS - 6 SP - 1 EP - 16(?) PB - BioMed Central CY - London AN - OPUS4-25421 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Pretsch, Thorsten A1 - Ecker, Melanie A1 - Schildhauer, Markus A1 - Maskos, Michael T1 - Switchable information carriers based on shape memory polymer N2 - Herein we demonstrate the realization of a new technological concept, which enables the use of shape memory polymers (SMPs) as switchable information carriers. At first, we applied a surface-specific dyeing process based on 'guest-diffusion' on two sophisticated polymeric host materials, including a thermoplastic poly(ester urethane) SMP and a thermoset epoxy-based SMP. Upon drying, self-assembly of the dye molecules inside the polymer surfaces occurred, resulting in homogeneous color penetration depths of about 100 µm. Subsequently, the colored surfaces were patterned with quick response (QR) codes. For this purpose, laser ablation was used. The resulting cavity depth was exceeding the color penetration depth. This assured sufficient surface contrast and rendered the QR codes machine-readable. In a progressive approach, two thermo-mechanical functionalization protocols were designed in accordance with the thermal properties of the polymers. As a result of programming, the tag prototypes were converted into stable, temporary shapes with non-decodable QR code information. When thermally triggering the shape memory effect on the functionalized tags, we verified the mostly complete recovery of the polymer surface and the associated restoration into the almost original shape. As such, the QR code could again precisely be read out. We anticipate that tagging products with these information carriers is helpful for the purpose of secure one-time identification. KW - Shape memory polymer KW - Epoxy-based polymer KW - Poly(ester urethane) KW - Thermo-responsive polymer KW - Laser ablation KW - Laser marking KW - QR code KW - Functionalized tags KW - Tag technology KW - Smart tagging KW - Switchable information carrier KW - Authentification KW - Identification KW - Surface-specific dyeing KW - Guest diffusion PY - 2012 DO - https://doi.org/10.1039/c2jm16204k SN - 0959-9428 SN - 1364-5501 VL - 22 IS - 16 SP - 7757 EP - 7766 PB - Royal Society of Chemistry CY - Cambridge AN - OPUS4-25737 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -