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Crystallization of calcium oxalate monohydrate at dipalmitoylphosphatidylcholine monolayers in the presence of chondroitin sulfate A

Year: 2004

Journal: -, 20111221

Authors: Jian-Ming Ouyang, Sui-Ping Deng, Jiu-Ping Zhong, Bernd Tieke, Shu-Hong Yu

Organizations: aInstitut für Physikalische Chemie, Universität zu Köln, Luxemburgerstr, 116, D-50939 Köln, Germany bInstitute of Biomineralization and Lithiasis Research, Jinan University, Guangzhou 510632, PR China cDepartment of Materials Science and Engineering & Structure Research Laboratory of CAS, University of Science and Techonology of China, Hefei 230026, PR China

The growth and aggregation of calcium oxalate monohydrate (COM) crystals beneath dipalmitoylphosphatidylcholine (DPPC) monolayers in the presence of chondroitin sulfate A (C4S) was systematically examined under different surface pressure. The results indicated that the addition of C4S can inhibit the crystal growth and prevent the aggregation of COM crystals. Under a DPPC monolayer, well-defined three-dimensional hexagonal prisms and threedimensional rhombus prisms with sharply angled tips were obtained. The DPPC monolayer at a surface pressure of 10mN/m can match the Ca2+ distance of the (101) face of COM better than at 20 mN/m. The addition of C4S could cooperatively modulate the interaction strength between the monolayer (or itself) with the specific morphology determining faces such as (101) and (0 2 0), and thus results in remarkable stabilization of the (101) faces. The dramatic changes in morphological details were due to the strong electrostatic interactions between the Ca2+-rich (101) crystal faces of COM and the polyanionic polysaccharide C4S together with the negatively charged sites of the zwitterionic DPPC monolayers. The increase of the concentration of C4S can further enhance the stabilization of the (101) face.