@article{BommGuenterStumpe2012,
  author    = {Bomm, Jana and G{\"u}nter, Christina and Stumpe, Joachim},
  title     = {Synthesis and optical characterization of thermosensitive, luminescent gold nanodots},
  series = {The journal of physical chemistry : C, Nanomaterials and interfaces},
  volume    = {116},
  journal   = {The journal of physical chemistry : C, Nanomaterials and interfaces},
  number    = {1},
  publisher = {American Chemical Society},
  address   = {Washington},
  issn      = {1932-7447},
  doi       = {10.1021/jp206260r},
  pages     = {81 -- 85},
  year      = {2012},
  abstract  = {A facile one-pot synthesis for preparing thermosensitive, luminescent gold nanodots with diameters of 1-2 nm is presented. The influence of the alkyl chain length of the surface ligands (alkyl thiols) on the optical properties of the gold nanodots was investigated. The synthesized gold nanodots show strong thermosensitive photoluminescence. A photoluminescence quantum yield of 16.6\% was observed at room temperature, which could be improved to a value of 28.6\% when cooling the gold nanodot solutions to -7 degrees C. The synthesized thermosensitive, luminescent gold nanodots are interesting candidates for optoelectronic devices, medical imaging, sensing, or security labels.},
  language  = {en}
}
@article{BastianRobelSchmidtetal.2021,
  author    = {Bastian, Philipp U. and Robel, Nathalie and Schmidt, Peter and Schrumpf, Tim and G{\"u}nter, Christina and Roddatis, Vladimir and Kumke, Michael U.},
  title     = {Resonance energy transfer to track the motion of lanthanide ions},
  series = {Biosensors : open access journal},
  volume    = {11},
  journal   = {Biosensors : open access journal},
  number    = {12},
  publisher = {MDPI},
  address   = {Basel},
  issn      = {2079-6374},
  doi       = {10.3390/bios11120515},
  pages     = {23},
  year      = {2021},
  abstract  = {The imagination of clearly separated core-shell structures is already outdated by the fact, that the nanoparticle core-shell structures remain in terms of efficiency behind their respective bulk material due to intermixing between core and shell dopant ions. In order to optimize the photoluminescence of core-shell UCNP the intermixing should be as small as possible and therefore, key parameters of this process need to be identified. In the present work the Ln(III) ion migration in the host lattices NaYF4 and NaGdF4 was monitored. These investigations have been performed by laser spectroscopy with help of lanthanide resonance energy transfer (LRET) between Eu(III) as donor and Pr(III) or Nd(III) as acceptor. The LRET is evaluated based on the Forster theory. The findings corroborate the literature and point out the migration of ions in the host lattices. Based on the introduced LRET model, the acceptor concentration in the surrounding of one donor depends clearly on the design of the applied core-shell-shell nanoparticles. In general, thinner intermediate insulating shells lead to higher acceptor concentration, stronger quenching of the Eu(III) donor and subsequently stronger sensitization of the Pr(III) or the Nd(III) acceptors. The choice of the host lattice as well as of the synthesis temperature are parameters to be considered for the intermixing process.},
  language  = {en}
}
@article{HamedMisbahSantosQuintanillaetal.2017,
  author    = {Hamed Misbah, Mohamed and Santos, Mercedes and Quintanilla, Luis and G{\"u}nter, Christina and Alonso, Matilde and Taubert, Andreas and Carlos Rodriguez-Cabello, Jose},
  title     = {Recombinant DNA technology and click chemistry: a powerful combination for generating a hybrid elastin-like-statherin hydrogel to control calcium phosphate mineralization},
  series = {Beilstein journal of nanotechnology},
  volume    = {8},
  journal   = {Beilstein journal of nanotechnology},
  publisher = {Beilstein-Institut zur F{\"o}rderung der Chemischen Wissenschaften},
  address   = {Frankfurt, Main},
  issn      = {2190-4286},
  doi       = {10.3762/bjnano.8.80},
  pages     = {772 -- 783},
  year      = {2017},
  abstract  = {Understanding the mechanisms responsible for generating different phases and morphologies of calcium phosphate by elastin-like recombinamers is supreme for bioengineering of advanced multifunctional materials. The generation of such multifunctional hybrid materials depends on the properties of their counterparts and the way in which they are assembled. The success of this assembly depends on the different approaches used, such as recombinant DNA technology and click chemistry. In the present work, an elastin-like recombinamer bearing lysine amino acids distributed along the recombinamer chain has been cross-linked via Huisgen [2 + 3] cycloaddition. The recombinamer contains the SN(A)15 peptide domains inspired by salivary statherin, a peptide epitope known to specifically bind to and nucleate calcium phosphate. The benefit of using click chemistry is that the hybrid elastin-like-statherin recombinamers cross-link without losing their fibrillar structure. Mineralization of the resulting hybrid elastin-like-statherin recombinamer hydrogels with calcium phosphate is described. Thus, two different hydroxyapatite morphologies (cauliflower- and plate-like) have been formed. Overall, this study shows that crosslinking elastin-like recombinamers leads to interesting matrix materials for the generation of calcium phosphate composites with potential applications as biomaterials.},
  language  = {en}
}
@article{ChemamHadjzobirDaifetal.2018,
  author    = {Chemam, Asma and Hadjzobir, Soraya and Daif, Menana and Altenberger, Uwe and G{\"u}nter, Christina},
  title     = {Provenance analyses of the heavy-mineral beach sands of the Annaba coast, northeast Algeria, and their consequences for the evaluation of fossil placer deposit},
  series = {Journal of earth system science},
  volume    = {127},
  journal   = {Journal of earth system science},
  number    = {8},
  publisher = {Indian Academy of Science},
  address   = {Bangalore},
  issn      = {0253-4126},
  doi       = {10.1007/s12040-018-1019-z},
  pages     = {25},
  year      = {2018},
  abstract  = {The paper presents the first study of heavy-mineral sand beaches from the Mediterranean coast of Annaba/Algeria. The studied beaches run along the basement outcrops of the Edough massif, which are mainly composed by micaschists, tourmaline-rich quartzo-feldspathic veins, gneisses, skarns and marbles. Sand samples were taken from three localities (Ain Achir, Plage-Militaire and El Nasr). The heavy-mineral fraction comprises between 74 and 91 vol\%. The garnets of the beaches are almandine rich and tourmalines vary with respect to their location from schorl to dravite. Tourmaline at Ain Achir and the Plage-Militaire is schorlits, while at El Nasr beach dravite is ubiquitous. The World Shale Average normalised REE of the sands and the basement outcrops reveal: (i) Ain Achir beach: REE pattern of sand and the coastal rocks from the studied beaches reflects a multiple sources; (ii) Plage-Militaire: the sand and the coastal outcrops show similar LREE and a strong enrichment in HREE, suggesting the presence HREE-rich phases found as inclusions in staurolite; (iii) El Nasr: two types of sand patterns are found: one with flat REE pattern similar to the proximal rocks and other one enriched in HREE suggesting a mixed source.},
  language  = {en}
}
@article{LoebbickeChananaSchlaadetal.2011,
  author    = {L{\"o}bbicke, Ruben and Chanana, Munish and Schlaad, Helmut and Pilz-Allen, Christine and G{\"u}nter, Christina and M{\"o}hwald, Helmuth and Taubert, Andreas},
  title     = {Polymer Brush Controlled Bioinspired Calcium Phosphate Mineralization and Bone Cell Growth},
  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    = {10},
  publisher = {American Chemical Society},
  address   = {Washington},
  issn      = {1525-7797},
  doi       = {10.1021/bm200991b},
  pages     = {3753 -- 3760},
  year      = {2011},
  abstract  = {Polymer brushes on thiol-modified gold surfaces were synthesized by using terminal thiol groups for the surface initiated free radical polymerization of methacrylic acid and dimethylaminotheyl methacrylate, respectively. Atomic force microscopy shows that the resulting poly(methacrylic acid (PMAA) and poly(dimethylaminothyl methacrylate) (PDM- AEMA) brushes are homogeneous. Contact angle measurements show that the brushes are pH responsive and can reversibly be protonated and deprotonated. Mineralization of the brushes with calcium phosphate at different pH yields homogeneously mineralized surfaces, and preosteoblastic cells proliferate-on be number of living cells on the mineralized hybrid surface is ca. 3 times (P corresponding nonmineralized brushes.},
  language  = {en}
}
@article{MaiBoyeYuanetal.2015,
  author    = {Mai, Tobias and Boye, Susanne and Yuan, Jiayin and V{\"o}lkel, Antje and Gr{\"a}wert, Marlies and G{\"u}nter, Christina and Lederer, Albena and Taubert, Andreas},
  title     = {Poly(ethylene oxide)-based block copolymers with very high molecular weights for biomimetic calcium phosphate mineralization},
  series = {RSC Advances : an international journal to further the chemical sciences},
  journal   = {RSC Advances : an international journal to further the chemical sciences},
  number    = {5},
  publisher = {RSC Publishing},
  address   = {London},
  issn      = {2046-2069},
  doi       = {10.1039/c5ra20035k},
  pages     = {103494 -- 103505},
  year      = {2015},
  abstract  = {The present article is among the first reports on the effects of poly(ampholyte)s and poly(betaine)s on the biomimetic formation of calcium phosphate. We have synthesized a series of di- and triblock copolymers based on a non-ionic poly(ethylene oxide) block and several charged methacrylate monomers, 2-(trimethylammonium)ethyl methacrylate chloride, 2-((3-cyanopropyl)-dimethylammonium)ethyl methacrylate chloride, 3-sulfopropyl methacrylate potassium salt, and [2-(methacryloyloxy)ethyl]dimethyl-(3-sulfopropyl)ammonium hydroxide. The resulting copolymers are either positively charged, ampholytic, or betaine block copolymers. All the polymers have very high molecular weights of over 106 g mol-1. All polymers are water-soluble and show a strong effect on the precipitation and dissolution of calcium phosphate. The strongest effects are observed with triblock copolymers based on a large poly(ethylene oxide) middle block (nominal Mn = 100 000 g mol-1). Surprisingly, the data show that there is a need for positive charges in the polymers to exert tight control over mineralization and dissolution, but that the exact position of the charge in the polymer is of minor importance for both calcium phosphate precipitation and dissolution.},
  language  = {en}
}
@misc{MaiBoyeYuanetal.2015,
  author    = {Mai, Tobias and Boye, Susanne and Yuan, Jiayin and V{\"o}lkel, Antje and Gr{\"a}wert, Marlies and G{\"u}nter, Christina and Lederer, Albena and Taubert, Andreas},
  title     = {Poly(ethylene oxide)-based block copolymers with very high molecular weights for biomimetic calcium phosphate mineralization},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-85299},
  year      = {2015},
  abstract  = {The present article is among the first reports on the effects of poly(ampholyte)s and poly(betaine)s on the biomimetic formation of calcium phosphate. We have synthesized a series of di- and triblock copolymers based on a non-ionic poly(ethylene oxide) block and several charged methacrylate monomers, 2-(trimethylammonium)ethyl methacrylate chloride, 2-((3-cyanopropyl)-dimethylammonium)ethyl methacrylate chloride, 3-sulfopropyl methacrylate potassium salt, and [2-(methacryloyloxy)ethyl]dimethyl-(3-sulfopropyl)ammonium hydroxide. The resulting copolymers are either positively charged, ampholytic, or betaine block copolymers. All the polymers have very high molecular weights of over 106 g mol-1. All polymers are water-soluble and show a strong effect on the precipitation and dissolution of calcium phosphate. The strongest effects are observed with triblock copolymers based on a large poly(ethylene oxide) middle block (nominal Mn = 100 000 g mol-1). Surprisingly, the data show that there is a need for positive charges in the polymers to exert tight control over mineralization and dissolution, but that the exact position of the charge in the polymer is of minor importance for both calcium phosphate precipitation and dissolution.},
  language  = {en}
}
@article{MaiBoyeYuanetal.2015,
  author    = {Mai, Tobias and Boye, Susanne and Yuan, Jiayin and Voelkel, Antje and Graewert, Marlies and G{\"u}nter, Christina and Lederer, Albena and Taubert, Andreas},
  title     = {Poly(ethylene oxide)-based block copolymers with very high molecular weights for biomimetic calcium phosphate mineralization},
  series = {RSC Advances},
  volume    = {5},
  journal   = {RSC Advances},
  number    = {125},
  publisher = {Royal Society of Chemistry},
  address   = {Cambridge},
  issn      = {2046-2069},
  doi       = {10.1039/c5ra20035k},
  pages     = {103494 -- 103505},
  year      = {2015},
  abstract  = {The present article is among the first reports on the effects of poly(ampholyte)s and poly(betaine) s on the biomimetic formation of calcium phosphate. We have synthesized a series of di- and triblock copolymers based on a non-ionic poly(ethylene oxide) block and several charged methacrylate monomers, 2-(trimethylammonium) ethyl methacrylate chloride, 2-((3-cyanopropyl)-dimethylammonium)ethyl methacrylate chloride, 3-sulfopropyl methacrylate potassium salt, and [2-(methacryloyloxy)ethyl]dimethyl-(3-sulfopropyl) ammonium hydroxide. The resulting copolymers are either positively charged, ampholytic, or betaine block copolymers. All the polymers have very high molecular weights of over 10(6) g mol(-1). All polymers are water-soluble and show a strong effect on the precipitation and dissolution of calcium phosphate. The strongest effects are observed with triblock copolymers based on a large poly(ethylene oxide) middle block (nominal M-n = 100 000 g mol(-1)). Surprisingly, the data show that there is a need for positive charges in the polymers to exert tight control over mineralization and dissolution, but that the exact position of the charge in the polymer is of minor importance for both calcium phosphate precipitation and dissolution.},
  language  = {en}
}
@article{MaiRakhmatullinaBleeketal.2014,
  author    = {Mai, Tobias and Rakhmatullina, Ekaterina and Bleek, Katrin and Boye, Susanne and Yuan, Jiayin and Voelkel, Antje and Graewert, Marlies and Cheaib, Zeinab and Eick, Sigrun and G{\"u}nter, Christina and Lederer, Albena and Lussi, Adrian and Taubert, Andreas},
  title     = {Poly(ethylene oxide)-b-poly(3-sulfopropyl methacrylate) block copolymers for calcium phosphate mineralization and biofilm inhibition},
  series = {Biomacromolecules : an interdisciplinary journal focused at the interface of polymer science and the biological sciences},
  volume    = {15},
  journal   = {Biomacromolecules : an interdisciplinary journal focused at the interface of polymer science and the biological sciences},
  number    = {11},
  publisher = {American Chemical Society},
  address   = {Washington},
  issn      = {1525-7797},
  doi       = {10.1021/bm500888q},
  pages     = {3901 -- 3914},
  year      = {2014},
  abstract  = {Poly(ethylene oxide) (PEO) has long been used as an additive in toothpaste, partly because it reduces biofilm formation on teeth. It does not, however, reduce the formation of dental calculus or support the remineralization of dental enamel or dentine. The present article describes the synthesis of new block copolymers on the basis of PEO and poly(3-sulfopropyl methacrylate) blocks using atom transfer radical polymerization. The polymers have very large molecular weights (over 10(6) g/mol) and are highly water-soluble. They delay the precipitation of calcium phosphate from aqueous solution but, upon precipitation, lead to relatively monodisperse hydroxyapatite (HAP) spheres. Moreover, the polymers inhibit the bacterial colonization of human enamel by Streptococcus gordonii, a pioneer bacterium in oral biofilm formation, in vitro. The formation of well-defined HAP spheres suggests that a polymer-induced liquid precursor phase could be involved in the precipitation process. Moreover, the inhibition of bacterial adhesion suggests that the polymers could be utilized in caries prevention.},
  language  = {en}
}
@article{UnuabonahKolawoleAgunbiadeetal.2017,
  author    = {Unuabonah, Emmanuel I. and Kolawole, Matthew O. and Agunbiade, Foluso O. and Omorogie, Martins O. and Koko, Daniel T. and Ugwuja, Chidinma G. and Ugege, Leonard E. and Oyejide, Nicholas E. and G{\"u}nter, Christina and Taubert, Andreas},
  title     = {Novel metal-doped bacteriostatic hybrid clay composites for point-of-use disinfection of water},
  series = {Journal of Environmental Chemical Engineering},
  volume    = {5},
  journal   = {Journal of Environmental Chemical Engineering},
  publisher = {Elsevier},
  address   = {Oxford},
  issn      = {2213-3437},
  doi       = {10.1016/j.jece.2017.04.017},
  pages     = {2128 -- 2141},
  year      = {2017},
  abstract  = {This study reports the facile microwave-assisted thermal preparation of novel metal-doped hybrid clay composite adsorbents consisting of Kaolinite clay, Carica papaya seeds and/or plantain peels (Musa paradisiaca) and ZnCl2. Fourier Transformed IR spectroscopy, X-ray diffraction, Scanning Electron Microscopy and Brunauer-Emmett-Teller (BET) analysis are employed to characterize these composite adsorbents. The physicochemical analysis of these composites suggests that they act as bacteriostatic rather than bacteriacidal agents. This bacterostactic action is induced by the ZnO phase in the composites whose amount correlates with the efficacy of the composite. The composite prepared with papaya seeds (PS-HYCA) provides the best disinfection efficacy (when compared with composite prepared with Musa paradisiaca peels-PP-HYCA) against gram-negative enteric bacteria with a breakthrough time of 400 and 700 min for the removal of 1.5 x10(6) cfu/mL S. typhi and V. cholerae from water respectively. At 10(3) cfu/mL of each bacterium in solution, 2 g of both composite adsorbents kept the levels the bacteria in effluent solutions at zero for up to 24 h. Steam regeneration of 2 g of bacteria-loaded Carica papaya prepared composite adsorbent shows a loss of ca. 31\% of its capacity even after the 3rd regeneration cycle of 25 h of service time. The composite adsorbent prepared with Carica papaya seeds will be useful for developing simple point-of-use water treatment systems for water disinfection application. This composite adsorbent is comparatively of good performance and shows relatively long hydraulic contact times and is expected to minimize energy intensive traditional treatment processes.},
  language  = {en}
}