@article{LangeBrauneLuetzowetal.2012, author = {Lange, Maik and Braune, Steffen and Luetzow, Karola and Richau, Klaus and Scharnagl, Nico and Weinhart, Marie and Neffe, Axel T. and Jung, Friedrich and Haag, Rainer and Lendlein, Andreas}, title = {Surface functionalization of poly(ether imide) membranes with linear, methylated oligoglycerols for reducing thrombogenicity}, series = {Macromolecular rapid communications}, volume = {33}, journal = {Macromolecular rapid communications}, number = {17}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {1022-1336}, doi = {10.1002/marc.201200426}, pages = {1487 -- 1492}, year = {2012}, abstract = {Materials for biomedical applications are often chosen for their bulk properties. Other requirements such as a hemocompatible surface shall be fulfilled by suitable chemical functionalization. Here we show, that linear, side-chain methylated oligoglycerols (OGMe) are more stable to oxidation than oligo(ethylene glycol) (OEG). Poly(ether imide) (PEI) membranes functionalized with OGMes perform at least as good as, and partially better than, OEG functionalized PEI membranes in view of protein resistance as well as thrombocyte adhesion and activation. Therefore, OGMes are highly potent surface functionalizing molecules for improving the hemocompatibility of polymers.}, language = {en} } @article{vonRuestenLangeLuetzowNeffeetal.2012, author = {von R{\"u}sten-Lange, Maik and Luetzow, Karola and Neffe, Axel T. and Lendlein, Andreas}, title = {Characterization of oligo(ethylene glycol) and oligoglycerol functionalized poly(ether imide) by angle-dependent X-ray photoelectron spectroscopy}, series = {Journal of applied biomaterials \& functional materials}, volume = {10}, journal = {Journal of applied biomaterials \& functional materials}, number = {3}, publisher = {Wichtig}, address = {Milano}, issn = {2280-8000}, doi = {10.5301/JABFM.2012.10345}, pages = {215 -- 222}, year = {2012}, abstract = {Purpose: Previous investigations have shown that poly(ether imide) (PEI) membranes can be functionalized with aminated macromolecules. In this study we explored whether the characterization of PEI functionalized with oligo(ethylene glycol) (OEG) or linear, side chain methylated oligoglycerols (OGMe), by angle-dependent X-ray induced photoelectron spectroscopy (XPS) can be used to prove the functionalization, give insight into the reaction mechanism and reveal the spatial distribution of the grafts. Methods: PEI membranes were functionalized under alkaline conditions using an aqueous solution with 2 wt\% of alpha-amino-methoxy oligo(ethylene glycol) (M-n = 1,320 g.mol(-1)) or linear, side chain methylated monoamine oligoglycerols (M-n = 1,120, 1,800 or 2,270 g.mol(-1)), respectively. The functionalized membranes were investigated using XPS measurements at different detector angles to enable comparison between the signals related to the bulk and surface volume and were compared with untreated and alkaline-treated PEI membranes. Results: While at a perpendicular detector angle the bulk signals of the PEI were prominent, at larger surface volume-related detector angles, the signals for OGMe and OEG were determinable. Conclusion: The surface functionalization of PEI with OEG and OGMe could be verified by the angle-dependent XPS. The observations proved the functionalization at the PEI surface, as the polyethers were detected at angles providing signals of the surface volume. Furthermore, the chemical functions determined verified a covalent binding via the nucleophilic addition of the amine functionalized OGMe and OEG to the PEI imide function.}, language = {en} } @misc{ReicheKratzHofmannetal.2011, author = {Reiche, J{\"u}rgen and Kratz, Karl and Hofmann, Dieter and Lendlein, Andreas}, title = {Current status of Langmuir monolayer degradation of polymeric biomaterials}, series = {The international journal of artificial organs}, volume = {34}, journal = {The international journal of artificial organs}, number = {2}, publisher = {Wichtig}, address = {Milano}, issn = {0391-3988}, doi = {10.5301/IJAO.2011.6401}, pages = {123 -- 128}, year = {2011}, abstract = {Langmuir monolayer degradation (LMD) experiments with polymers possessing outstanding biomedical application potential yield information regarding the kinetics of their hydrolytic or enzymatic chain scission under well-defined and adjustable degradation conditions. A brief review is given of LMD investigations, including the author's own work on 2-dimensional (2D) polymer systems, providing chain scission data, which are not disturbed by simultaneously occurring transport phenomena, such as water penetration into the sample or transport of scission fragments out of the sample. A knowledge-based approach for the description and simulation of polymer hydrolytic and enzymatic degradation based on a combination of fast LMD experiments and computer simulation of the water penetration is briefly introduced. Finally, the advantages and disadvantages of this approach are discussed.}, language = {en} } @article{ZaupaNeffePierceetal.2011, author = {Zaupa, Alessandro and Neffe, Axel T. and Pierce, Benjamin F. and N{\"o}chel, Ulrich and Lendlein, Andreas}, title = {Influence of tyrosine-derived moieties and drying conditions on the formation of helices in gelatin}, series = {Biomacromolecules : an interdisciplinary journal focused at the interface of polymer science and the biological sciences}, volume = {12}, journal = {Biomacromolecules : an interdisciplinary journal focused at the interface of polymer science and the biological sciences}, number = {1}, publisher = {American Chemical Society}, address = {Washington}, issn = {1525-7797}, doi = {10.1021/bm101029k}, pages = {75 -- 81}, year = {2011}, abstract = {The single and triple helical organization of protein chains strongly influences the mechanical properties of gelatin-based materials. A chemical method for obtaining different degrees of helical organization in gelatin is covalent functionalization, while a physical method for achieving the same goal is the variation of the drying conditions of gelatin solutions. Here we explored how the introduction of desaminotyrosine (DAT) and desaminotyrosyl tyrosine (DATT) linked to lysine residues of gelatin influenced the kinetics and thermodynamic equilibrium of the helicalization process of single and triple helices following different drying conditions. Drying at a temperature above. the helix-to-coil transition temperature of gelatin (T > T-c, called nu(short)) generally resulted in gelatins with relatively lower triple helical content (X-c,X-t = 1-2\%) than lower temperature drying (T < T-c, called nu(long)) (X-c,X-t = 8-10\%), where the DAT(T) functional groups generally disrupted helix formation. While different helical contents affected the thermal transition temperatures only slightly, the mechanical properties were strongly affected for swollen hydrogels (E = 4-13 kPa for samples treated by nu(long) and E = 120-700 kPa for samples treated by nu(short)). This study shows that side group functionalization and different drying conditions are viable options to control the helicalization and macroscopic properties of gelatin-based materials.}, language = {en} } @article{PilusoHieblGorbetal.2011, author = {Piluso, Susanna and Hiebl, Bernhard and Gorb, Stanislav N. and Kovalev, Alexander and Lendlein, Andreas and Neffe, Axel T.}, title = {Hyaluronic acid-based hydrogels crosslinked by copper-catalyzed azide-alkyne cycloaddition with tailorable mechanical properties}, series = {The international journal of artificial organs}, volume = {34}, journal = {The international journal of artificial organs}, number = {2}, publisher = {Wichtig}, address = {Milano}, issn = {0391-3988}, doi = {10.5301/IJAO.2011.6394}, pages = {192 -- 197}, year = {2011}, abstract = {Biopolymers of the extracellular matrix are attractive starting materials for providing degradable and biocompatible biomaterials. In this study, hyaluronic acid-based hydrogels with tunable mechanical properties were prepared by the use of copper-catalyzed azide-alkyne cycloaddition (known as "click chemistry"). Alkyne-functionalized hyaluronic acid was crosslinked with linkers having two terminal azide functionalities, varying crosslinker density as well as the lengths and rigidity of the linker molecules. By variation of the crosslinker density and crosslinker type, hydrogels with elastic moduli in the range of 0.5-4 kPa were prepared. The washed materials contained a maximum of 6.8 mg copper per kg dry weight and the eluate of the gel crosslinked with diazidostilbene did not show toxic effects on L929 cells. The hyaluronic acid-based hydrogels have potential as biomaterials for cell culture or soft tissue regeneration applications.}, language = {en} } @article{NeffeLoebusZaupaetal.2011, author = {Neffe, Axel T. and Loebus, Axel and Zaupa, Alessandro and St{\"o}tzel, Christian and M{\"u}ller, Frank A. and Lendlein, Andreas}, title = {Gelatin functionalization with tyrosine derived moieties to increase the interaction with hydroxyapatite fillers}, series = {Acta biomaterialia}, volume = {7}, journal = {Acta biomaterialia}, number = {4}, publisher = {Elsevier}, address = {Oxford}, issn = {1742-7061}, doi = {10.1016/j.actbio.2010.11.025}, pages = {1693 -- 1701}, year = {2011}, abstract = {Combining gelatins functionalized with the tyrosine-derived groups desaminotyrosine or desaminotyrosyl tyrosine with hydroxyapatite (HAp) led to the formation of composite materials with much lower swelling ratios than those of the pure matrices. Shifts of the infra-red (IR) bands related to the free carboxyl groups could be observed in the presence of HAp, which suggested a direct interaction of matrix and filler that formed additional physical cross-links in the material. In tensile tests and rheological measurements the composites equilibrated in water had increased Young's moduli (from 200 kPa up to 2 MPa) and tensile strengths (from 57 kPa up to 1.1 MPa) compared with the matrix polymers without affecting the elongation at break. Furthermore, an increased thermal stability of the networks from 40 to 85 degrees C could be demonstrated. The differences in the behaviour of the functionalized gelatins compared with pure gelatin as a matrix suggested an additional stabilizing bond between the incorporated aromatic groups and the HAp as supported by the IR results. The composites can potentially be applied as bone fillers.}, language = {en} } @inproceedings{NeffeZaupaLendlein2011, author = {Neffe, Axel T. and Zaupa, Alessandro and Lendlein, Andreas}, title = {Physical crosslinking of gelatin a supramolecular approach tobiomaterial}, series = {The international journal of artificial organs}, volume = {34}, booktitle = {The international journal of artificial organs}, number = {8}, publisher = {Wichtig}, address = {Milano}, issn = {0391-3988}, pages = {656 -- 656}, year = {2011}, language = {en} } @article{ZaupaNeffePierceetal.2011, author = {Zaupa, Alessandro and Neffe, Axel T. and Pierce, Benjamin F. and Lendlein, Andreas and Hofmann, Dieter}, title = {A molecular dynamic analysis of gelatin as an amorphous material Prediction of mechanical properties of gelatin systems}, series = {The international journal of artificial organs}, volume = {34}, journal = {The international journal of artificial organs}, number = {2}, publisher = {Wichtig}, address = {Milano}, issn = {0391-3988}, doi = {10.5301/IJAO.2010.6083}, pages = {139 -- 151}, year = {2011}, abstract = {Biomaterials are used in regenerative medicine for induced autoregeneration and tissue engineering. This is often challenging, however, due to difficulties in tailoring and controlling the respective material properties. Since functionalization is expected to offer better control, in this study gelatin chains were modified with physically interacting groups based on tyrosine with the aim of causing the formation of physical crosslinks. This method permits application-specific properties like swelling and better tailoring of mechanical properties. The design of the crosslink strategy was supported by molecular dynamic (MD) simulations of amorphous bulk models for gelatin and functionalized gelatins at different water contents (0.8 and 25 wt.-\%). The results permitted predictions to be formulated about the expected crosslink density and its influence on equilibrium swelling behavior and on elastic material properties. The models of pure gelatin were used to validate the strategy by comparison between simulated and experimental data such as density, backbone conformation angle distribution, and X-ray scattering spectra. A key result of the simulations was the prediction that increasing the number of aromatic functions attached to the gelatin chain leads to an increase in the number of physical netpoints observed in the simulated bulk packing models. By comparison with the Flory-Rehner model, this suggested reduced equilibrium swelling of the functionalized materials in water, a prediction that was subsequently confirmed by our experimental work. The reduction and control of the equilibrium degree of swelling in water is a key criterion for the applicability of functionalized gelatins when used, for example, as matrices for induced autoregeneration of tissues.}, language = {en} } @article{TronciNeffePierceetal.2010, author = {Tronci, Giuseppe and Neffe, Axel T. and Pierce, Benjamin Franklin and Lendlein, Andreas}, title = {An entropy-elastic gelatin-based hydrogel system}, issn = {0959-9428}, doi = {10.1039/C0jm00883d}, year = {2010}, abstract = {Gelatin is a non-immunogenic and degradable biopolymer, which is widely applied in the biomedical field e. g. for drug capsules or as absorbable hemostats. However, gelatin materials present limited and hardly reproducible mechanical properties especially in aqueous systems, particularly caused by the uncontrollable partial renaturation of collagen-like triple helices. Therefore, mechanically demanding applications for gelatin-based materials, such as vascular patches, i.e. hydrogel films that seal large incisions in vessel walls, and for induced autoregeneration, are basically excluded if this challenge is not addressed. Through the synthesis of a defined chemical network of gelatin with hexamethylene diisocyanate (HDI) in DMSO, the self-organization of gelatin chains could be hindered and amorphous gelatin films were successfully prepared having Young's moduli of 60-530 kPa. Transferring the crosslinking reaction with HDI and, alternatively, ethyl lysine diisocyanate (LDI), to water as reaction medium allowed the tailoring of swelling behaviour and mechanical properties by variation of crosslinker content while suppressing the formation of helices. The hydrogels had Young's moduli of 70-740 kPa, compressive moduli of 16-48 kPa, and degrees of swelling of 300-800 vol\%. Test reactions investigated by ESI mass spectrometry allowed the identification and quantification of reaction products of the crosslinking reaction. The HDI crosslinked networks were stabilized by direct covalent crosslinks (ca. 10 mol\%), supported by grafting (50 mol\%) and blending of hydrophobic oligomeric chains. For the LDI- based networks, less crosslinked (3 mol\%) and grafted species (5 mol\%) and much higher amounts of oligomers were observed. The adjustable hydrogel system enables the application of gelatin-based materials in physiological environments.}, language = {en} } @article{HeilmannGrothSchossigetal.2007, author = {Heilmann, Katja and Groth, Thomas and Schossig, Michael and Lendlein, Andreas and Micheel, Burkhard}, title = {Modulation of hybridoma cell growth and antibody production by coating cell culture material with extracellular matrix proteins}, issn = {1369-703X}, doi = {10.1016/j.bej.2007.01.035}, year = {2007}, abstract = {The influence of coating polystyrene tissue culture plates with different proteins on murine hybridoma cell growth and antibody production was investigated. Fibronectin, collagen I, bovine serum albumin and laminin were used to coat NUNC and COSTAR cell culture plates. Cell number and antibody concentration in culture fluids were quantified as indicators for cell viability, proliferation and productivity. Adhesive behaviour, morphology, expression of surface receptors of hybridoma cells and the presence of tyrosine-phosphorylated proteins in cell lysates were characterized by cell adhesion experiments, microscopy, flow cytometry and Western Blot analysis. It was shown that coatings with fibronectin (0.2 ;g/ml) lead to a substantial improvement of cell growth by 50-70\% and an increase of monoclonal antibody production by 100-120\%. Collagen I coatings showed an improvement in cell growth by 30-70\% and by 60\% for the production of monoclonal antibodies. Coatings with BSA and laminin had minor effects on these parameters. It was found that the hybridoma cell lines used in this study did not express the ;2-chain of the ;2;1-integrin, which is responsible for binding to collagen and laminin. However, the presence of ;1- integrin on the cell surface was shown, which should enable hybridoma cells to bind fibronectin. We propose, therefore, that fibronectin adsorption to cell culture materials may be a promising approach to enhance the production of monoclonal antibodies by cultivated hybridoma cells.}, language = {en} } @article{HeilmannGrothBehrsingetal.2005, author = {Heilmann, Katja and Groth, Thomas and Behrsing, Olaf and Wagner, Albrecht and Schossig-Tiedemann, Michael and Lendlein, Andreas and Micheel, Burkhard}, title = {The influence of the chemical composition of cell culture material on the growth and antibody production of hybridoma cells}, year = {2005}, abstract = {The multiplication and antibody production of murine hybridoma cells cultured on five different polymer membranes were tested and compared with conventional tissue culture polystyrene (TCPS). Membranes were prepared from polyacrylonitrile (PAN) and acrylonitrile copolymerized with N-vinylpyrrolidone (NVP20, NVP30), Na-methallylsulfonate (NaMAS) and N-(3-amino-propyl-methacrylamide-hydrochloride) (APMA). Cell number and antibody concentration were quantified as criteria for viability and productivity. Adhesion of hybridoma cells was characterized by vital and scanning electron microscopy. The results suggest that a strong adhesion of cells, observed on APMA and TCPS, increased cell growth but reduced monoclonal antibody production. In contrast membranes with lowered adhesivity such as NVP20 provided favourable conditions for monoclonal antibody production. In addition it was shown that this membrane also possessed a minor fouling as indicated by the low decrease of water flux across the membrane after protein adsorption. It was concluded that NVP20 could be a suitable material for the development of hollow fibre membranes for bioreactors.}, language = {en} } @article{RickertLendleinKelchetal.2005, author = {Rickert, D and Lendlein, Andreas and Kelch, S and Franke, R. P. and Moses, M. A.}, title = {Cell proliferation and cellular activity of primary cell cultures of the oral cavity after cell seeding on the surface of a degradable, thermoplastic block copolymer}, year = {2005}, abstract = {Using standard cell biological and biochemical methods we were able to test the ability of a degradable, thermoplastic block copolymer to support the adhesion, proliferation, and the cellular activity of primary cell cultures of the oral cavity in vitro. The delicate balance between a group of endogenous enzymes, Matrix Metalloproteinases (MMPs), and their inhibitors (Tissue Inhibitor of MMPs, TIMPs) have a decisive function in the remodeling of the extracellular matrix during processes like wound healing or the integration of biomaterials in surrounding tissues after implantation. Recently developed, biodegradable thermoplastic elastomers with shape-memory properties may be the key to develop new therapeutical options in head and neck surgery. Primary cell cultures of the oral cavity of Sprague-Dawley rats were seeded on the surface of a thermoplastic block copolymer and on a polystyrene surface as control. Conditioned media of the primary cells were analyzed for MMPs and TIMPs after different periods of cell growth. The MMP and TIMP expression was analysed by zymography and a radiometric enzyme assay. No statistically significant differences in the appearance and the kinetic of MMP-1, MMP-2, MMP-9 and TIMPs were detected between cells grown on the polymer surface compared to the control. An appropriate understanding of the molecular processes that regulate cellular growth and integration of a biomaterial in surrounding tissue is the requirement for an optimal adaptation of biodegradable, polymeric biomaterials to the physiological, anatomical, and surgical conditions in vivo to develop new therapeutic options in otolaryngology and head and neck surgery}, language = {en} } @article{FengKelchRickertetal.2004, author = {Feng, Y. and Kelch, S. and Rickert, D. and Fuhrmann, R. and Franke, R. P. and Lendlein, Andreas}, title = {Biokompatible abbaubare Formged{\"a}chtnispolymersysteme als intelligente Implantatmaterialien}, year = {2004}, language = {de} } @article{KelchLendleinSchulte2004, author = {Kelch, S. and Lendlein, Andreas and Schulte, J.}, title = {Kunststoffe mit Formged{\"a}chtnis : die erstaunlichen F{\"a}higkeiten intelligenter Materialien}, issn = {0344-5690}, year = {2004}, language = {de} } @misc{LendleinKelchSchulteetal.2004, author = {Lendlein, Andreas and Kelch, S. and Schulte, J. and Kratz, K.}, title = {Shape-memory polymers}, year = {2004}, language = {en} } @article{GrothLendlein2004, author = {Groth, Thomas and Lendlein, Andreas}, title = {In-vivo-Reparatur von Blutgef{\"a}ßen durch alternierende Adsorption von Polyelektrolyten}, year = {2004}, language = {de} } @article{SantosoSchroeterWagneretal.2004, author = {Santoso, F. and Schroeter, M. and Wagner, Albrecht and Lendlein, Andreas and Sckomaecker, R.}, title = {Simultane Funktionalisierung und Poren{\"o}ffnung von Polyetherimid-Membranen zur Entwicklung neuer Tr{\"a}germaterialien f{\"u}r die Apharese}, year = {2004}, language = {de} } @article{GrothLendlein2004, author = {Groth, Thomas and Lendlein, Andreas}, title = {Layer-by-layer deposition of polyelectrolytes : a versatile tool for the in vivo repair of blood vessels and the preparation of biocompatible implant coatings}, year = {2004}, language = {en} } @article{RickertLendleinKelchetal.2004, author = {Rickert, D. and Lendlein, Andreas and Kelch, S. and Moses, M. A. and Franke, R. P.}, title = {Biokompatibilit{\"a}tstestung von bioabbaubaren Shape Memory Polymeren in vivo}, year = {2004}, language = {de} } @article{BinzenLendleinKelchetal.2004, author = {Binzen, Eva and Lendlein, Andreas and Kelch, S. and Rickert, D. and Franke, R. P.}, title = {Biomaterial-microvasculature interaction on polymers after implantation in mice}, year = {2004}, language = {en} } @article{RickertLendleinSchmidtetal.2003, author = {Rickert, D. and Lendlein, Andreas and Schmidt, A. M. and Kelch, S. and Roehlke, W. and Fuhrmann, R. and Franke, R. P.}, title = {In vitro cytotoxicity testing of AB-polymer networks based on oligo(epsilon-caprolactone) segments after different sterilization techniques}, year = {2003}, language = {en} } @article{RickertMosesLendleinetal.2003, author = {Rickert, D. and Moses, M. A. and Lendlein, Andreas and Kelch, S. and Franke, R. P.}, title = {The importance of angiogenesis in the interaction between polymeric biomaterials and surrounding tissue}, year = {2003}, language = {en} } @article{KelchLendleinMuellenetal.2003, author = {Kelch, S. and Lendlein, Andreas and M{\"u}llen, A. and Ridder, U.}, title = {Textile Polymer Scaffolds for Tissue Engineering}, year = {2003}, language = {en} } @article{KelchLendleinMuellenetal.2003, author = {Kelch, S. and Lendlein, Andreas and M{\"u}llen, A. and Ridder, U.}, title = {Textile Polymerger{\"u}ste f{\"u}r das Tissue Engineering}, year = {2003}, language = {de} }