TY  - JOUR
A1  - Hentrich, Doreen
A1  - Junginger, Mathias
A1  - Bruns, Michael
A1  - Boerner, Hans G.
A1  - Brandt, Jessica
A1  - Brezesinski, Gerald
A1  - Taubert, Andreas
T1  - Interface-controlled calcium phosphate mineralization: effect of oligo(aspartic acid)-rich interfaces
JF  - CrystEngComm
N2  - The phase behavior of an amphiphilic block copolymer based on a poly(aspartic acid) hydrophilic block and a poly(n-butyl acrylate) hydrophobic block was investigated at the air-water and air-buffer interface. The polymer forms stable monomolecular films on both subphases. At low pH, the isotherms exhibit a plateau. Compression-expansion experiments and infrared reflection absorption spectroscopy suggest that the plateau is likely due to the formation of polymer bi- or multilayers. At high pH the films remain intact upon compression and no multilayer formation is observed. Furthermore, the mineralization of calcium phosphate beneath the monolayer was studied at different pH. The pH of the subphase and thus the polymer charge strongly affects the phase behavior of the film and the mineral formation. After 4 h of mineralization at low pH, atomic force microscopy shows smooth mineral films with a low roughness. With increasing pH the mineral films become inhomogeneous and the roughness increases. Transmission electron microscopy confirms this: at low pH a few small but uniform particles form whereas particles grown at higher pH are larger and highly agglomerated. Energy-dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy confirm the formation of calcium phosphate. The levels of mineralization are higher in samples grown at high pH.
Y1  - 2015
U6  - https://doi.org/10.1039/c4ce02274b
SN  - 1466-8033
VL  - 17
IS  - 36
SP  - 6901
EP  - 6913
PB  - Royal Society of Chemistry
CY  - Cambridge
ER  - 
TY  - JOUR
A1  - Hentrich, Doreen
A1  - Junginger, Mathias
A1  - Bruns, Michael
A1  - Börner, Hans Gerhard
A1  - Brandt, Jessica
A1  - Brezesinski, Gerald
A1  - Taubert, Andreas
T1  - Interface-controlled calcium phosphate mineralization
BT  - effect of oligo(aspartic acid)-rich interfaces
JF  - CrystEngComm
N2  - The phase behavior of an amphiphilic block copolymer based on a poly(aspartic acid) hydrophilic block and a poly(n-butyl acrylate) hydrophobic block was investigated at the air–water and air–buffer interface. The polymer forms stable monomolecular films on both subphases. At low pH, the isotherms exhibit a plateau. Compression–expansion experiments and infrared reflection absorption spectroscopy suggest that the plateau is likely due to the formation of polymer bi- or multilayers. At high pH the films remain intact upon compression and no multilayer formation is observed. Furthermore, the mineralization of calcium phosphate beneath the monolayer was studied at different pH. The pH of the subphase and thus the polymer charge strongly affects the phase behavior of the film and the mineral formation. After 4 h of mineralization at low pH, atomic force microscopy shows smooth mineral films with a low roughness. With increasing pH the mineral films become inhomogeneous and the roughness increases. Transmission electron microscopy confirms this: at low pH a few small but uniform particles form whereas particles grown at higher pH are larger and highly agglomerated. Energy-dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy confirm the formation of calcium phosphate. The levels of mineralization are higher in samples grown at high pH.
Y1  - 2015
U6  - https://doi.org/10.1039/C4CE02274B
SN  - 1466-8033
IS  - 17
SP  - 6901
EP  - 6913
PB  - Royal Society of Chemistry
CY  - London
ER  - 
TY  - GEN
A1  - Hentrich, Doreen
A1  - Junginger, Mathias
A1  - Bruns, Michael
A1  - Börner, Hans Gerhard
A1  - Brandt, Jessica
A1  - Brezesinski, Gerald
A1  - Taubert, Andreas
T1  - Interface-controlled calcium phosphate mineralization
BT  - effect of oligo(aspartic acid)-rich interfaces
N2  - The phase behavior of an amphiphilic block copolymer based on a poly(aspartic acid) hydrophilic block and a poly(n-butyl acrylate) hydrophobic block was investigated at the air–water and air–buffer interface. The polymer forms stable monomolecular films on both subphases. At low pH, the isotherms exhibit a plateau. Compression–expansion experiments and infrared reflection absorption spectroscopy suggest that the plateau is likely due to the formation of polymer bi- or multilayers. At high pH the films remain intact upon compression and no multilayer formation is observed. Furthermore, the mineralization of calcium phosphate beneath the monolayer was studied at different pH. The pH of the subphase and thus the polymer charge strongly affects the phase behavior of the film and the mineral formation. After 4 h of mineralization at low pH, atomic force microscopy shows smooth mineral films with a low roughness. With increasing pH the mineral films become inhomogeneous and the roughness increases. Transmission electron microscopy confirms this: at low pH a few small but uniform particles form whereas particles grown at higher pH are larger and highly agglomerated. Energy-dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy confirm the formation of calcium phosphate. The levels of mineralization are higher in samples grown at high pH.
T3  - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 213 
Y1  - 2015
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-89540
SP  - 6901
EP  - 6913
ER  -