Papers by Author: Ji Dong Li

Abstract: In this paper, isoniazid (INH)-loaded poly (ε-caprolactone) microspheres with a special microporous surface and relatively high drug loading were fabricated by an oil-in-oil (O/O) solvent evaporation method. Meanwhile the microspheres were produced by an oil-in-water (O/W) method for comparison. The technological parameters such as the concentration of surfactant, the volume of continuous phase and the quantity of the drug were investigated systematically. The microspheres morphology, their size distribution and the viscosity of both the dispersed and continuous phase were characterized. The results indicate that the O/O solvent evaporation method is a feasible approach to encapsulate micromolecular and hydrophilic drugs in PCL. This opens the door for INH-loaded microspheres able to release drugs and thereby improve the therapy of tuberculosis of bones and joints in the future.

Abstract: Using nano-hydroxyapatite/polyamide66 composite (n-HA/PA66) and a special foamer as start materials, a porous species for bone defect repair was successfully developed by thermal-pressing method. The resulting material presented: (1) high compressive strength which reached 13~46MPa; (2) excellent porous structure, the average diameter of pores in the matrix was in range of 280μm to 500μm and porosity of 36% to 57%. The porous architecture could be adjusted by the combination of processing parameters such as the weight of start mixture used per mold and the ratio of composite to foamer as well as n-HA content in the composite. No apparent change in composition and structure of n-HA/PA66 composite was found by XRD and IR determination before and after formation of porous species. According to Sherrer equation, the value of D(002) of n-HA crystals in porous material and start powder were about 70nm, indicating no occurrence of change in size of n-HA during the thermal-pressing procedure. Additionally, no foamer residual was detected in porous species.

Abstract: A new method was studied for improving stainless steel antibacterial capability. The Na2FeO4 coating was prepared on steel surface throughout NaOH treatment, then steel samples were immersed into the solution coantaining Ag+, Zn2+ and TiO2. The antibacterial-ions were fixated firmly on the stainless steel with chemical bond. Scanning electronic microscopy(SEM), X-ray(XRD) and atomic absoption spectroscopy(AAS) were employed to analyze the materials, and the results showed that the antibacterial membrane included silver citrate and silver peroxide. Quinn test was also carried out, in which Staphylococus and E.coli. the results showed that the steel has a bacteriostasis rate of 99.48% to Staphylococus, and 99.09% to E.coli.

Abstract: Nano-hydroxyapatite (n-HA) slurry was synthesized at normal pressure, and (Cu2+, Zn2+)-bearing nano-hydroxyapatite (Cu-Zn-HA) was prepared by ion exchange reaction in water medium. The properties of n-HA and Cu-Zn-HA were characterized by AAS, TEM, XRD and FTIR. The results of XRD analysis indicate that Cu2+ and Zn2+ can occupy Ca2+ sites and enter the crystal lattice of hydroxyapatite. Through the antibacterial experiments, it was found that Cu-Zn-HA had better antibacterial ability on Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus). After heat treatment at 400°C for an hour, the materials still had good antibacterial effect. The accelerated aging method was employed to test antibacterial durability of the material and the results indicated that the durability was good. The results of the security assessment, including skin stimulation test of rabbit, acute toxicity test by stomach filling and the micronucleus test in bone marrow polychromatic erythrocytes of mice, showed that the security of the material was excellent.

Abstract: In this paper, using sodium phosphate and calcium nitrate as reagents, nano-hydroxyapatite (n-HA) was synthesised under 8 conditions. The morphology and crystallinity of these prepared HA were investigated by Transmission Electron Microscope (TEM) and X-ray diffraction pattern (XRD). The Ca/P molar ratio of n-HA was tested by chemical method. In order to find a better way to obtain purer nano-hydroxyapatite, the phases transition and purification of these 8 samples before and after sintering at 1000°C were compared. The results indicated that all these samples showed similar, poorly crystallized apatite structures before sintering. The adding order between calcium and phosphate would affect the crystallinity, structure and Ca/P molar ratio of hydoxyapatite significantly. XRD analysis showed that adding sodium phosphate into calcium nitrate could gain more HA phase after sintering at 1000°C. The pH of reaction system had obvious effects on the structure of hydroxyapatite. Besides the pH of reactants also affected the structure of hydoxyapatite.

Abstract: The compatibility efficiency on different compatibilizer for nano-hydroxyapatite (n-HA) reinforced polyamide 66 (PA66) and high density polyethylene (HDPE) blends at a composition of 40/42/18 as functionalized biomaterial was investigated by mechanical properties testing and scanning electron microscopy (SEM). The results showed that mechanical properties of compatibilized blends were much improved by the compatibilizers of maleic anhydride grafted polyethylene (PE-g-MAH) and ethylene/methacrylic acid ionomer-sodium ion (ION) compared with the uncompatibilized blends. Blends had peak mechanical values of different compatibilizer. Both PE-g and ION formed adhesion during melt mixing and stabilized the morphology and significantly reduced the size of dispersed PE phase. PE-g gave the blends with PE spheres ranging from 1 to 4µm and ION with well-dispersed spheres with an average diameter of 1µm. The more enlarged interphase of the blends containing ION reduced the lower interfacial energy to increase the miscibiliy of the blends. Consequently, ION had better contribution to rigidity properties than PE-g for n-HA/PA/PE blends.

Abstract: In this paper a series of silver ions-substituted hydroxyapatites (HA) were prepared. The antibacterial activities of these materials on textiles against bacteria have been investigated. Titania (TiO2) was selectively added into the materials to decrease the silver-ions concentration to get the same active antimicrobial effects. The microstructure, the shape and size, concentration of silver, and the groups of the composite materials were characterized using transmission electron microscopy (TEM), infrared spectroscopy (IR), Atomic absorption spectroscopy (AAS), and X-ray diffraction (XRD). The results showed that there was a dose dependent-effect of silver-ions concentration from the disk diffusion test. The higher the silver-ions concentration, the better the antibacterial activity of the composite materials was. Keeping silver-ions concentration constant, the antibacterial activity of the materials for adding Titania was better than that of without Titania. Moreover, the addition of Titania would inhibit the discolouration of the composite materials. The antibacterial activities of the composite materials differentiate to some extent with the bacterial strains.