TY - CONF A1 - Bertin, Annabelle T1 - Bioinspired hybrid organic-inorganic copolymers N2 - The demand for high-performance materials has strongly increased over the last decade. One way to improve their performance is to introduce material gradients as found in Nature (for example squid beaks, spider fangs, mussel byssal threads). One path towards the achievement of such material gradients is the synthesis of hybrid (gradient) copolymers, for instance based on silane and organic monomers. Since not all gradient copolymers can be synthesized by utilising the reactivity ratios of the monomers, forced gradients have to be used. However, in order to obtain gradient copolymers at high conversions, living or pseudo-living copolymerizations have to be performed and so far only few hybrid (organic / inorganic) gradient copolymers have been reported. In this contribution we will present the synthesis of a novel organic / inorganic hybrid copolymer via controlled radical polymerization. T2 - 5th International Conference on Multifunctional, Hybrid and Nanomaterials CY - Lisbon, Portugal DA - 06.03.2017 KW - Hybrid organic-inorganic copolymers KW - RAFT polymerization KW - ATRP polymerization PY - 2017 AN - OPUS4-39464 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle T1 - Temperature Sensitive Aggregation Behavior of Poly(Acrylamide-co-Acrylonitrile) in Water N2 - Thermoresponsive polymers have shown great potential in applications such as bioseparation, drug delivery and diagnostic. Only few thermoresponsive polymers that present an upper critical solution temperature (UCST), i.e. phase separate from solution upon cooling, in a relevant temperature range have been reported so far. Herein, a robust UCST-type copolymer of acrylamide (AAm) and acrylonitrile (AN) (poly(AAm-co-AN)) was prepared by reversible addition fragmentation chain transfer (RAFT) polymerization and its thermo-induced aggregation behavior in aqueous media was studied. We propose a model for the temperature-induced aggregation behaviour of UCST-type poly(AAm-co-AN) copolymer in aqueous solution on the basis of turbidity measurements, SLS, DLS, SANS and cryo-TEM. T2 - German Physical Society - Spring Meeting 2017 CY - Dresden, Germany DA - 19.03.2017 KW - Thermoresponsive polymers KW - UCST-type copolymer PY - 2017 AN - OPUS4-39465 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle T1 - Functional polymer based on 2,6-diaminopyridine with tunable UCST behaviour in water/alcohol mixture N2 - Thermoresponsive polymers are of great importance in numerous applications such as bioseparation, drug delivery, diagnostic and microfluidic applications. Only few thermoresponsive polymers that present an upper critical solution temperature (UCST), i.e. phase separate from solution upon cooling, in a relevant temperature range and green solvents such as water or ethanol have been reported. Indeed, polymers with UCST behavior below 60°C in alcohol or water/alcohol mixtures are extremely promising for the preparation of smart materials for sensing. In this work two novel functional polymers of based on a 2,6-diaminopyridine motif were synthesized by free radical polymerization. Their UCST-type transition temperature is tunable by varying either their concentration in solution or the type of solvent. Insights into this phenomenon will be given based on turbidimetry and temperature dependent dynamic light scattering T2 - German Physical Society - Spring Meeting 2017 CY - Dresden, Germany DA - 19.03.2017 KW - Thermoresponsive polymers KW - USCT-type polymers KW - Polymers based on 2,6-diaminopyridine PY - 2017 AN - OPUS4-39466 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle T1 - Phase transition and aggregation behavior of thermoresponsive copolymer poly(acrylamide-co-acrylonitrile) N2 - Thermoresponsive polymers have shown great potential in applications such as bioseparation, drug delivery and diagnostic. Only few thermoresponsive polymers that present an upper critical solution temperature (UCST), i.e. phase separate from solution upon cooling, in a relevant temperature range have been reported so far. Moreover, the most studied UCST type polymers namely polybetaines are difficult to use under physiological conditions, which significantly restricts their potential applications. Therefore, UCST polymers with sharp and robust phase transition in physiological conditions (in the presence of salts, etc.) are highly needed in order to extend the range of applications of this class of polymers. A robust UCST-type copolymer of acrylamide (AAm) and acrylonitrile (AN) (poly(AAm-co-AN)) was prepared by reversible addition fragmentation chain transfer (RAFT) polymerization and its thermo-induced aggregation behavior in aqueous media was studied by turbidimetry, dynamic and static light scattering. At temperature below the UCST, the poly(AAm-co-AN) copolymer chains were aggregated together. The aggregate size was found to be larger with increasing AN contents and became smaller upon dilution of the copolymer solutions. While above the UCST, the poly(AAm-co-AN) copolymer chains were expanded and weekly associated in solution. The association between the copolymer chains formed smaller aggregates with increasing the AN contents or the concentration of the solutions. A model is proposed to explain such association-aggregation behavior of the poly(AAm-co-AN) copolymer depending on the AN contents and concentration of the solutions. T2 - Biennial meeting GDCh-Division of Macromolecular Chemistry CY - Halle, Germany DA - 11.09.2016 KW - Thermoresponsive polymers PY - 2016 AN - OPUS4-37365 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle T1 - Phase transition and aggregation behavior of thermoresponsive copolymer Poly(acrylamide-co-acrylonitrile) N2 - The results of a study on the phase transition and aggregation behavior of the thermoresponsive copolymer Poly(acrylamide-co-acrylonitrile) are presented. T2 - Warwick Polymer Conference 2016 CY - Warwick, England DA - 11.07.2016 KW - Thermoresponsive polymers PY - 2016 AN - OPUS4-37366 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle T1 - Controlled self-assembly of dendritic amphiphiles in micromixers N2 - The controlled synthesis of supramolecular aggregates formed by the self-assembly of dendritic amphiphiles is a challenging task. Conventional batch-based techniques such as the solvent injection method or the film hydration method typically go along with a lack of control over mixing and thus over size, morphology and size distribution. The micromixer technology is a promising method for the controlled preparation of supramolecular assemblies as it allows control of mixing at microscale level. In addition, such microfluidic systems benefit from a high mixing efficiency, a low mixing time as well as from a reproducible and continuous synthesis. Herein, we report on the microfluidic-controlled self-assembly of several dendritic amphiphiles and the impact of the mixing parameters on the self-assembly process. T2 - 251st American Chemical Society National Meeting CY - San Diego, USA DA - 13.03.2016 KW - Dendritic amphiphiles KW - Self-assembly KW - Micromixer PY - 2016 AN - OPUS4-37371 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle T1 - Dendron-based macromolecules and supramolecular architectures for medical diagnosis and therapy T2 - Invited talk by Prof. Rolf Mülhaupt at Albert-Ludwigs-Universität Freibung CY - Freiburg, Germany DA - 2015-09-30 PY - 2015 AN - OPUS4-34534 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle T1 - Dendron-based macromolecules and supramolecular architectures for medical diagnosis and therapy T2 - Invited talk at "Habilitanden-Workshop der Fachgruppe Makromolekulare Chemie der GDCh 2015" CY - Leverkusen, Germany DA - 2015-09-28 PY - 2015 AN - OPUS4-34535 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle T1 - Dendron-based macromolecules and supramolecular architectures for medical diagnosis and therapy T2 - Invited lecture at Leibnitz-Institut für Polymerforschung Dresden CY - Dresden DA - 2015-06-09 PY - 2015 AN - OPUS4-34031 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle T1 - Functional Thermoresponsive Polymers based on 2,6-Diaminopyridine with Tunable UCST Behavior N2 - Thermoresponsive polymers are of great importance in numerous applications such as bioseparation, drug delivery, diagnostic and microfluidic applications. Only few thermoresponsive polymers that present an upper critical solution temperature (UCST), i.e. phase separate from solution upon cooling, in a relevant temperature range and green solvents such as water or ethanol have been reported. In this work two novel functional polymers of based on a 2,6-diaminopyridine motif, namely poly(N-(6-aminopyridin-2-yl)acrylamide) (PNAPAAm) and poly(N-(6-acetamidopyridin-2-yl)acrylamide) (PNAcAPAAm), were synthesized by free radical polymerization. The obtained polymers displayed UCST-type reversible thermoresponsive behaviour in water/alcohol mixtures. Insights into this phenomenon will be given based on visual observations, temperature-dependent turbidimetry and dynamic light scattering as well as 1H-NMR measurements. The UCST phase transition behaviour of the polymers was tunable by varying either the concentration of the polymer solution, the nature of the alcohol or the composition of the solvent mixture. The cloud point temperature of PNAcAPAAm was found to decrease with increasing alcohol content (MeOH, EtOH and iPrOH) in water/alcohol mixtures. Past a critical amount of EtOH or iPrOH in water the cloud point temperature of PNAcAPAAm increased by further addition of EtOH or iPrOH. These polymers with UCST behavior below 60°C in water/alcohol mixtures show great promises for the preparation of smart materials for sensing. T2 - European Polymer Congress Lyon 2017 CY - Lyon, France DA - 02.07.2017 KW - Cosolvency KW - UCST polymer KW - 2,6-diaminopyridine PY - 2017 AN - OPUS4-40965 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle T1 - Controlled Self-Assembly of Janus Dendrimers via Microfluidics N2 - Unilamellar vesicles self-assembled in water from natural and synthetic phospholipids (liposomes), amphiphilic block copolymers (polymersomes), and more recently amphiphilic Janus dendrimers (dendrimersomes) as hollow soft structures in the nano size regime have attracted increasing interest as they can mimic primitive and contemporary biological membranes, and can be configured into biomimetic nanocapsules with application in nanomedicine such as gene, proteins and drug carriers or theranostics. Compared to other amphiphilic structures, the molecular structure of Janus dendrimers can be precisely controlled: by using the vast range of tools from organic chemistry their size, architecture, density, generation as well as the number of endgroups of the individual dendrons can be modified as desired. Unfortunately, the controlled production of the supramolecular aggregates made thereof is still a challenging task. Conventional batch-based techniques such as the solvent injection method or the film hydration method typically go along with a lack of control over mixing and thus over size, morphology and size distribution. The micromixer technology is a promising method for the controlled preparation of supramolecular assemblies as it allows control of mixing at microscale level. In addition, such microfluidic systems benefit from a high mixing efficiency, a low mixing time as well as from a reproducible and continuous synthesis. Herein, we report on the microfluidic-controlled self-assembly of Janus dendrimers as dendrimersomes and the impact of the mixing parameters on the self-assembly process. T2 - 10th International Dendrimer Symposium CY - Weihai, China DA - 05.08.2017 KW - Micromixers KW - Janus dendrimers KW - Vesicles KW - Self-assembly PY - 2017 AN - OPUS4-41464 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Taabache, Soraya A1 - Bertin, Annabelle T1 - Vesicles from amphiphilic dumbbells and Janus dendrimers: bioinspired self-assembled structures for biomedical applications N2 - The current review focuses on vesicles obtained from the self-assembly of two types of dendritic macromolecules, namely amphiphilic Janus dendrimers (forming dendrimersomes) and amphiphilic dumbbells. In the first part, we will present some synthetic strategies and the various building blocks that can be used to obtain dendritic-based macromolecules, thereby showing their structural versatility. We put our focus on amphiphilic Janus dendrimers and amphiphilic dumbbells that form vesicles in water but we also encompass vesicles formed thereof in organic solvents. The second part of this review deals with the production methods of these vesicles at the nanoscale but also at the microscale. Furthermore, the influence of various parameters (intrinsic to the amphiphilic JD and extrinsic—from the environment) on the type of vesicle formed will be discussed. In the third part, we will review the numerous biomedical applications of these vesicles of nano- or micron-size. KW - Janus dendrimers KW - Amphiphilic dumbbells KW - Self-assembled structures KW - Dendrimersomes KW - Artificial cells PY - 2017 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-418245 DO - https://doi.org/10.3390/polym9070280 SN - 2073-4360 VL - 9 IS - 7 SP - Article 280, 1 EP - 36 AN - OPUS4-41824 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hentrich, D. A1 - Taabache, Soraya A1 - Brezesinski, G. A1 - Lange, Nele A1 - Unger, Wolfgang A1 - Kübel, C. A1 - Bertin, Annabelle A1 - Taubert, A. T1 - A dendritic amphiphile for efficient control of biomimetic calcium phosphate mineralization N2 - The phase behavior of a dendritic amphiphile containing a Newkome-type dendron as the hydrophilic moiety and a cholesterol unit as the hydrophobic segment is investigated at the air–liquid interface. The amphiphile forms stable monomolecular films at the air–liquid interface on different subphases. Furthermore, the mineralization of calcium Phosphate beneath the monolayer at different calcium and phosphate concentrations versus mineralization time shows that at low calcium and Phosphate concentrations needles form, whereas flakes and spheres dominate at higher concentrations. Energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, and electron diffraction confirm the formation of calcium phosphate. High-resolution transmission electron microscopy and electron diffraction confirm the predominant formation of octacalcium phosphate and hydroxyapatite. The data also indicate that the final products form via a complex multistep reaction, including an association step, where nano-needles aggregate into larger flake-like objects. KW - Dendritic amphiphile KW - Calcium phosphate KW - Biomineralization PY - 2017 DO - https://doi.org/10.1002/mabi.201600524 SN - 1616-5187 SN - 1616-5195 VL - 17 IS - 8 SP - Article 1600524, 1 EP - 14 AN - OPUS4-41825 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle T1 - Upper critical solution temperature (UCST)- type thermoresponsive polymers from acrylamide-based monomers N2 - UCST-type thermoresponsive polymers that phase separate from solution upon cooling present a tremendous potential not only in aqueous media where they can be used in drug delivery, diagnostic and microfluidic applications, but also in water/alcohol mixtures, where they can be used for instance in sensing systems for alcohol-soluble drugs. However, only a few thermoresponsive polymers have been reported that present an UCST in a relevant temperature range and “green” solvents such as water or ethanol. In this context, acrylamide-based monomers can be very useful building blocks for designing novel UCST-type polymers because of their hydrophilic nature (with the right side chain) and propensity to form hydrogen bonds. We want to present our latest results on the copolymer poly(acrylamide-co-acrylonitrile) (P(AAm-co-AN)) that present a UCST in water as well as on two homopolymers based on an acrylamide derivative of 2,6-diaminopyridine, namely poly(N-(6-aminopyridin-2-yl)acrylamide) (PNAPAAm) and poly(N-(6-acetamidopyridin-2-yl)acrylamide) (PNAcAPAAm) that show UCST-type thermoresponsiveness in water/alcohol mixtures. Our focus for P(AAm-co-AN)) is its aggregation behaviour above and below its phase transition temperature as the size of thermoresponsive polymeric systems is of prime importance for biomedical applications (as size dependent processes take place in the body) and is linked to the optical properties of a material that matter in materials science. In the case of PNAPAAm and PNAcAPAAm, we focused on the co-solvency/co-non solvency effect on the phase transition temperature in water/alcohol mixture. Indeed, polymers with UCST behavior below 60°C in water/alcohol mixtures are extremely promising for the preparation of “smart” materials for sensing. T2 - 31st Conference of the European Colloid and Interface Society (ECIS 2017) CY - Madrid, Spain DA - 03.09.2017 KW - Thermoresponsive polymers KW - UCST polymers KW - Acrylamide based polymers PY - 2017 AN - OPUS4-41902 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle T1 - Controlled self-assembly of Janus dendrimers via microfluidics N2 - Vesicles self-assembled in water from natural and synthetic phospholipids (liposomes), amphiphilic block copolymers (polymersomes), and more recently amphiphilic Janus dendrimers (dendrimersomes) as hollow soft structures in the nano size regime have attracted increasing interest as they can mimic primitive and contemporary biological membranes, and can be configured into biomimetic nanocapsules with application in nanomedicine such as gene, proteins and drug carriers or theranostics. Compared to other amphiphilic structures, the molecular structure of Janus dendrimers can be precisely controlled: by using the vast range of tools from organic chemistry their size, architecture, density, generation as well as the number of end groups of the individual dendrons can be modified as desired. Unfortunately, the controlled production of the supramolecular aggregates made thereof is still a challenging task. Conventional batch-based techniques such as the solvent injection method or the film hydration method typically go along with a lack of control over mixing and thus over size, morphology and size distribution. The micromixer technology is a promising method for the controlled preparation of supramolecular assemblies as it allows control of mixing at microscale level. In addition, such microfluidic systems benefit from a high mixing efficiency, a low mixing time as well as from a reproducible and continuous synthesis. Herein, we report on the microfluidic-controlled self-assembly of Janus dendrimers as dendrimersomes and the impact of the mixing parameters on the self-assembly process. T2 - 6th Annual workshop on biomaterials and their interactions with biological and model membranes 2017 CY - Altafulla, Spain DA - 07.09.2017 KW - Janus dendrimers KW - Dendrimersomes KW - Microfluidic PY - 2017 AN - OPUS4-41903 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle T1 - Efficient one-pot synthesis of polymer-coated USPIOs for image-guided nanoparticle-mediated cancer gene therapy T2 - 9th International Conference on the Scientific and Clinical Applications of Magnetic Carriers CY - Minneapolis, MN, USA DA - 2012-05-22 PY - 2012 AN - OPUS4-25916 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bleul, Regina A1 - Bachran, D. A1 - Thiermann, Raphael A1 - Bertin, Annabelle A1 - Fuchs, H. A1 - Maskos, Michael T1 - Probing polymersome-protein and -cell interactions: influence of different end-groups and environments N2 - Developing polymersomes for drug delivery purposes requires a deeper understanding of their behavior in physiological environment. We performed the self-assembly and in-situ loading of polybutadiene-block-polyethyleneoxide (PB-b-PEO) polymersomes in a continuous process using micromixers. Varying the length and end-groups of the starting block copolymer allows us to control the polymer membrane thickness and surface functionalities (hydroxyl or carboxylic acid), required to realize a further coupling with specific cell targeting ligands. To get a deeper understanding of these polymersomes in physiological environment, we studied the cellular response (HeLa cells) in presence of various polymersomes, and showed by cytotoxicity tests the relative biocompatibility of the systems. Flow cytometry experiments at 4?°C in PBS buffer showed a different behavior of hydroxyl-functionalized vesicles compared to carboxylic acid-functionalized vesicles. On the contrary cell binding in DMEM medium supplemented with 10% FCS was almost completely blocked with both kinds of polymersomes. Protein adsorption measurements by dynamic light scattering confirmed that protein binding occurs in all cases, which apparently influences the particle-cell interaction. This study contributes towards a deeper understanding of polymersomes in biological environment and further investigations will help us to design highly effective polymersomes for in vitro as well as in vivo applications. KW - Drug delivery KW - End-group functionality KW - Particle-cell interaction KW - Physiologic environment KW - Polymersomes KW - Protein adsorption PY - 2011 DO - https://doi.org/10.1002/masy.201100042 SN - 1022-1360 SN - 0258-0322 SN - 1521-3900 VL - 309/310 IS - 1 SP - 134 EP - 140 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-25246 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle T1 - Effect of multivalent biocompatible (macro)molecules on the one-pot synthesis of nanoparticles for biomedical applications T2 - 2nd International Symposium on "Multivalency in Chemistry and Biochemistry" CY - Berlin, Germany DA - 2012-10-18 PY - 2012 AN - OPUS4-26787 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bertin, Annabelle T1 - Emergence of polymer stereocomplexes for biomedical applications N2 - Polylactide (PLA) and poly(methyl methacrylate) (PMMA) constitute, already for several decades, the gold standards for various biomedical applications due to their biocompatibility/inertness. Moreover, they have an additional property: they can form stereocomplexes (SCs) that have a more compact crystalline structure than the individual components. As a result, polymer SCs display improved thermal and mechanical properties, as well as delayed drug release and biodegradation rate in the case of drug delivery systems and biomaterials based on PLA, which is of prime importance in the biomedical field. In this article, the potential of SCs for biomedical applications in the areas of drug delivery, tissue engineering, and nanostructured surfaces is highlighted. KW - Biomedical applications of polymers KW - Polylactide KW - Poly(methyl methacrylate) KW - Self-assembly KW - Stereocomplexation PY - 2012 DO - https://doi.org/10.1002/macp.201200143 SN - 1022-1352 SN - 1521-3935 VL - 213 IS - 22 SP - 2329 EP - 2352 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-27212 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle T1 - Effect of multivalent biocompatible (macro)molecules on the one-pot synthesis of nanoparticles for biomedical applications T2 - NanoGEM-Abschlusskonferenz CY - Berlin, Germany DA - 2013-06-12 PY - 2013 AN - OPUS4-28699 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Koshkina, Olga A1 - Westmeier, D. A1 - Lang, Thomas A1 - Bantz, C. A1 - Hahlbrock, A. A1 - Würth, Christian A1 - Resch-Genger, Ute A1 - Braun, Ulrike A1 - Thiermann, Raphael A1 - Weise, C. A1 - Eravci, M. A1 - Mohr, B. A1 - Schlaad, H. A1 - Stauber, R. H. A1 - Docter, D. A1 - Bertin, Annabelle A1 - Maskos, M. T1 - Tuning the surface of nanoparticles: Impact of poly(2-ethyl-2-oxazoline) on protein adsorption in serum and cellular uptake N2 - Due to the adsorption of biomolecules, the control of the biodistribution of nanoparticles is still one of the major challenges of nanomedicine. Poly(2-ethyl-2-oxazoline) (PEtOx) for surface modification of nanoparticles is applied and both protein adsorption and cellular uptake of PEtOxylated nanoparticles versus nanoparticles coated with poly(ethylene glycol) (PEG) and non-coated positively and negatively charged nanoparticles are compared. Therefore, fluorescent poly(organosiloxane) nanoparticles of 15 nm radius are synthesized, which are used as a scaffold for surface modification in a grafting onto approach. With multi-angle dynamic light scattering, asymmetrical flow field-flow fractionation, gel electrophoresis, and liquid chromatography-mass spectrometry, it is demonstrated that protein adsorption on PEtOxylated nanoparticles is extremely low, similar as on PEGylated nanoparticles. Moreover, quantitative microscopy reveals that PEtOxylation significantly reduces the non-specific cellular uptake, particularly by macrophage-like cells. Collectively, studies demonstrate that PEtOx is a very effective alternative to PEG for stealth modification of the surface of nanoparticles. KW - Poloxazolines KW - Protein corona KW - Cellular uptake PY - 2016 DO - https://doi.org/10.1002/mabi.201600074 SN - 1616-5187 SN - 1616-5195 VL - 16 IS - 9 SP - 1287 EP - 1300 AN - OPUS4-37369 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle T1 - Thermoresponsive fluorescent hybrid core-shell-shell nanoparticles T2 - 14th Biennal International Bayreuth Polymer Symposium CY - Bayreuth, Germany DA - 2015-09-20 PY - 2015 AN - OPUS4-34457 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle T1 - Endowing nanoparticles with orthogonal functionalities via core / shell / shell architecture N2 - Dual orthogonal functionality in a single material is highly desirable in many fields such as bio-imaging, sensing, coating or diagnostic and therapy. However, combining two different functionalities in a precise and controlled way is still a challenging task. Here we present how simply dual functional hybrid nanoparticles consisting of a silica core with a fluorescent and a thermoresponsive polymeric layers can be prepared. As a first step of this work, silica core particles were coated by a fluorescent layer using surface-initiated reversible addition-fragmentation chain transfer polymerization. Afterwards, the fluorescent silica nanoparticles were completely enclosed in a switchable protective coating made of thermoresponsive poly(N-isopropylacrylamide). The thermoresponsive poly(N-isopropylacrylamide) changes its properties with varying the surroundings temperature and this behavior is reversible and controllable. To the best of our knowledge these types of hybrid dual functional core-shell-shell nanoparticles have not yet been prepared, despite the prospect of many potential applications. T2 - World Congress on Living Polymerizations and Polymers - LPP16 CY - Budapest, Hungary DA - 29.05.2016 KW - Fluorescent and thermoresponsive nanoparticles KW - Core KW - Shell KW - Shell nanoparticles PY - 2016 AN - OPUS4-37367 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle T1 - Endowing nanoparticles with orthogonal functionalities via core / shell / shell architecture N2 - Dual orthogonal functionality in a single material is highly desirable in many fields such as bio-imaging, sensing, coating or diagnostic and therapy. However, combining two different functionalities in a precise and controlled way is still a challenging task. Here we present how simply dual functional hybrid nanoparticles consisting of a silica core with a fluorescent and a thermoresponsive polymeric layers can be prepared. As a first step of this work, silica core particles were coated by a fluorescent layer using surface-initiated reversible addition-fragmentation chain transfer polymerization. Afterwards, the fluorescent silica nanoparticles were completely enclosed in a switchable protective coating made of thermoresponsive poly(N-isopropylacrylamide). The thermoresponsive poly(N-isopropylacrylamide) changes its properties with varying the surroundings temperature and this behavior is reversible and controllable. To the best of our knowledge these types of hybrid dual functional core-shell-shell nanoparticles have not yet been prepared, despite the prospect of many potential applications. T2 - 251st American Chemical Society National Meeting CY - San Diego, USA DA - 13.03.2016 KW - Fluorescent and thermoresponsive nanoparticles KW - Core / shell / shell / nanoparticles PY - 2016 AN - OPUS4-37370 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle T1 - The role of coating materials and zeta potential in iron oxide nanoparticle uptake in human intestinal cells T2 - NANOTOX 2014, 7th International Nanotoxicology Congress CY - Antalya, Turkey DA - 2014-04-23 PY - 2014 AN - OPUS4-30664 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Czarnecki, Sebastian A1 - Bertin, Annabelle T1 - Hybrid silicon-based organic/inorganic block copolymers with sol-gel active moieties: Synthetic advances, self-assembly and applications in biomedicine and material science N2 - Abstract: Hybrid silicon-based organic/inorganic (multi)block copolymers are promising polymeric precursors to create robust nano-objects and nanomaterials due to their sol–gel active moieties via self-assembly in solution or in bulk. Such nano-objects and nanomaterials have great potential in bio-medicine as nanocarriers or scaffolds for bone regeneration as well as in materials science as Pickering emulsifiers, pho- tonic crystals or coatings/films with antibiofouling, antibac- terial or water- and oil-repellent properties. Thus, this Review outlines recent synthetic efforts in the preparation of these hybrid inorganic/organic block copolymers, gives an overview of their self-assembled structures and finally presents recent examples of their use in the biomedical field and material science. KW - Organic/inorganic block copolymer KW - Robust nano objects KW - Self-assembly KW - Synthesis KW - Biomedical application KW - Material science PY - 2018 DO - https://doi.org/10.1002/chem.201705286 SN - 1521-3765 SN - 0947-6539 VL - 24 IS - 14 SP - 3354 EP - 3373 PB - WILEY-VCH Verlag GmbH & Co. KGaA CY - Weinheim AN - OPUS4-43953 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Roszak, I. A1 - Oswald, L. A1 - Ouahabi, A. A. A1 - Bertin, Annabelle A1 - Laurent, E. A1 - Felix, O. A1 - Carvin-Sergent, I. A1 - Charles, L. A1 - Lutz, J.-F. T1 - Synthesis and sequencing of informational poly(amino phosphodiester)s N2 - Sequence-defined poly(amino phosphodiester)s containing main-chain tertiary amines were synthesized by automated solid-phase phosphoramidite chemistry. These polymers were prepared using four monomers with different substituents. The formed polymers were characterized by HPLC and mass spectrometry. These methods evidenced preparation of molecularly-defined polymers. Furthermore, the presence of tertiary amines in the polymer backbones facilitates sequencing by tandem mass spectrometry. KW - Poly(amino phosphodiester) KW - Synthesis KW - HPLC KW - Mass spectrometry PY - 2021 DO - https://doi.org/10.1039/d1py01052b SN - 1759-9954 VL - 12 IS - 37 SP - 5279 EP - 5282 PB - Royal Society of Chemistry AN - OPUS4-53732 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Asadujjaman, Asad A1 - Ahmadi, Vahid A1 - Franc, Antoine Michel Claude A1 - Bertin, Annabelle T1 - 2,6-Diaminopyridine and Acrylamide-Based Copolymers with Upper Critical Solution Temperature-type Behavior in Aqueous Solution N2 - A novel cop olyme r based on supramolecular motif2,6-diaminopyridin e and water-soluble acrylamide, poly[N-(6-ace tamidopyridin-2-yl) acrylamide-co-acrylamide], was synthe-size d via rev ersible addi tion–fragmentation chain transfer (RAFT)polymerization with various monomer compositions. The thermo-respon sive behavior of the copolymers was studied by turbidime-try and dynamic light scattering (DLS). The obtained copolymersshowed an upper critical solution temperature (UCST)-typ e phasetransition behavior in water and electrolyte solution. The phasetransition temperature was found to increase with decreasingam ount of acrylamide in the copolymer and increasing concentra-tion of the solution. Furth ermore, the phase transition temperatureva ried in aqueous solutions of electrolytes according to the naturean d concentration of the electrolyte in accordance with theHoffmeister series. A dramatic solvent isotope effect on thetransition temperature was o bserved in this study, as the transitiontemperature was almost 10–12C higher in D2OthaninH2Oatthesame concentration and acrylamide co mposition. The size of theaggregates below the transition temperature was larger in D2Ocompared to that in H2O that can be explained by deuterium iso-tope effect. The thermoresponsive behavior of the copolymers wasalso investigated in different cell medium and found to be exhibitedUCST-type phase transition behavior in different cell medium.Such behavior of the copo lyme rs can be useful in many a pplica-tions including biomedical, microfluidics, optical materials, and indrug delivery. KW - 2,6-diaminopyridine KW - Acrylamide KW - Stimuli-responsive polymers KW - Thermo-responsive polymers KW - UCST polymers PY - 2019 DO - https://doi.org/10.1002/pola.29474 SN - 0887-624X VL - 57 IS - 19 SP - 2064 EP - 2073 PB - Wiley AN - OPUS4-49297 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Asadujjaman, Asad A1 - Kent, B. A1 - Bertin, Annabelle T1 - Phase transition and aggregation behaviour of an UCST-type copolymer poly(acrylamide-coacrylonitrile) in water: effect of acrylonitrile content, concentration in solution, copolymer chain length and presence of electrolyte N2 - An UCST-type copolymer of acrylamide (AAm) and acrylonitrile (AN) (poly(AAm-co-AN)) was prepared by reversible addition fragmentation chain transfer (RAFT) polymerization and its temperature-induced phase transition and aggregation behaviour studied by turbidimetry, static and dynamic light scattering, small angle neutron scattering (SANS) and cryo-transmission electron microscopy (cryo-TEM) measurements. The phase transition temperature was found to increase with increasing AN content in the copolymer, concentration of the solutions and copolymer chain length. A significant effect was observed onto the phase transition temperature by addition of different electrolytes into the copolymer solution. The copolymer chains were aggregated below the phase transition temperature and disaggregated above it. The size of the aggregates increases with increasing AN contents and concentration of the copolymer solutions below the phase transition temperature. The copolymer chains were expanded and weekly associated in solution above the phase transition temperature. A model is proposed to explain such association–aggregation behaviour of poly(AAm-co-AN) copolymers depending on AN contents and concentration of the copolymer solutions as a function of temperature. KW - Thermoresponsive polymers KW - UCST-type copolymer PY - 2017 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-394636 DO - https://doi.org/10.1039/c6sm02262f SN - 1744-683X SN - 1744-6848 VL - 13 IS - 3 SP - 658 EP - 669 PB - RSC AN - OPUS4-39463 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle T1 - Colloidal clusters of superparamagnetic iron oxide nanoparticles stabilized with bioactive catechols for magnetic particle imaging T2 - European Summit for Clinical Nanomedicine 2013, Clinical Nanomedicine & Targeted Medicine: From Antibodies to Nanodrugs, Diagnostic Systems and Targeted Delivery (CLINAM 2013) CY - Basel, Switzerland DA - 2013-06-24 PY - 2013 AN - OPUS4-28743 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Koshkina, Olga A1 - Lang, Thomas A1 - Thiermann, R. A1 - Docter, D. A1 - Stauber, R.H. A1 - Secker, C. A1 - Schlaad, H. A1 - Weidner, Steffen A1 - Mohr, B. A1 - Maskos, M. A1 - Bertin, Annabelle T1 - Temperature-triggered protein adsorption on polymer-coated nanoparticles in serum N2 - The protein corona, which forms on the nanoparticle's surface in most biological media, determines the nanoparticle’s physicochemical characteristics. The formation of the protein corona has a significant impact on the biodistribution and clearance of nanoparticles in vivo. Therefore, the ability to influence the formation of the protein corona is essential to most biomedical applications, including drug delivery and imaging. In this study, we investigate the protein adsorption on nanoparticles with a hydrodynamic radius of 30 nm and a coating of thermoresponsive poly(2-isopropyl-2-oxazoline) in serum. Using multiangle dynamic light scattering (DLS) we demonstrate that heating of the nanoparticles above their phase separation temperature induces the formation of agglomerates, with a hydrodynamic radius of 1 µm. In serum, noticeably stronger agglomeration occurs at lower temperatures compared to serum-free conditions. Cryogenic transmission electron microscopy (cryo-TEM) revealed a high packing density of agglomerates when serum was not present. In contrast, in the presence of serum, agglomerated nanoparticles were loosely packed, indicating that proteins are intercalated between them. Moreover, an increase in protein content is observed upon heating, confirming that protein adsorption is induced by the alteration of the surface during phase separation. After cooling and switching the surface back, most of the agglomerates were dissolved and the main fraction returned to the original size of approximately 30 nm as shown by asymmetrical flow-field flow fractionation (AF-FFF) and DLS. Furthermore, the amounts of adsorbed proteins are similar before and after heating the nanoparticles to above their phase-separation temperature. Overall, our results demonstrate that the thermoresponsivity of the polymer coating enables turning the corona formation on nanoparticles on and off in situ. As the local heating of body areas can be easily done in vivo, the thermoresponsive coating could potentially be used to induce the agglomeration of nanoparticles and proteins and the accumulation of nanoparticles in a targeted body region. PY - 2015 DO - https://doi.org/10.1021/acs.langmuir.5b00537 SN - 0743-7463 SN - 1520-5827 VL - 31 IS - 32 SP - 8873 EP - 8881 PB - American Chemical Society CY - Washington, DC AN - OPUS4-34163 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -