No abstract

Poly(amidoamine) (PAMAM) dendrimers, known as artificial proteins, have unique and well-defined molecular size and structure. It has previously been used to mimic protein-crystal interaction during biomineralization. In this study, generation 4.5 (4.5G) PAMAM with carboxylic acid (PAMAM-COOH) was synthesized and utilized to remineralize the surface of etched enamel in vitro. Using confocal laser scanning microscopy, Fourier transform infrared spectroscopy, X-ray diffraction analysis and scanning electron microscopy we observed that 4.5G PAMAM-COOH can be absorbed on the etched enamel surface and that it can induce the formation of hydroxyapatite crystals with the same orientation as that of the enamel prisms on longitudinal and transversal enamel surfaces. The self-assembly behavior of PAMAM in the mineralization solution was also investigated and the result showed that 4.5G PAMAM can assemble to microribbon structure similar to the behavior of amelogenins. Therefore, we concluded that 4.5G PAMAM-COOH assemblies can act as the organic template on enamel surface and in mineralization solution to control the nucleation site and morphology of new-grown crystals to form the biomimetic structure of human enamel, which may open a new way for repairing damaged enamel.

The application of biomass-based composites in the field of adsorption has attracted extensive attention. Herein, soybean dreg/hydrocalumite composites were prepared by in situ self-assembly from soybean dregs and applied to the adsorption of Congo Red (CR). The composites were characterized by scanning electron microscopy, X-ray diffraction, Fourier infrared spectroscopy, and N2 physical adsorption–desorption. The results showed that the adsorption property of soybean dregs/hydrocalumite for CR was better than that of soybean dregs or hydrocalumite. Effects of preparation and adsorption conditions on the adsorption of CR by soybean dregs/hydrocalumite were also investigated. The removal rate of soybean dregs/hydrocalumite (30%BD-LDH) prepared under the optimized conditions reached 97.4% with a 486.8 mg·g–1 adsorption capacity. Also, the adsorption capacity of 30%BD-LDH was about 2.4 times and 3.0 times that of hydrocalumite and soybean dregs, respectively. In addition, the adsorption process of CR by 30%BD-LDH was more in line with the pseudo-second-order kinetic and Langmuir isothermal models.

No abstract

The purpose of this study is to detect the effect of gallic acid (GA) on hydroxyapatie crystal growth and find the mechanism of the regulation. We evaluated the morphology of HAP crystals grown under various amounts of GA (0, 0.05, 1, and 4 gL −1 ). Subsequently, the chemical composition, crystal size and the morphology were investigated via the energy-dispersive X-ray spectrometer, attenuated total fourier transform infrared spectroscopy, thermogravimetric analysis, X-ray diffraction analysis, transmission electron microscope and scanning electron microscopy. In all groups, the Ca/P ratio was closed to 1.67. In the absence of GA, crystals did not arrange, while in the presence of GA, crystals tended to form spherules. The size of the crystals decreased with the concentration of GA increased. These results indicated the role of GA on the growth and morphology of hydroxyapatite crystals, which might be the key mechanism for gallic acid regulating the mineralization.