Synthesis and characterization of biocomposite materials of hydroxyapatite (HA) and yttrium oxide (Y2O3) were investigated. HA nanoparticles powder was obtained from mussel shells via a wet chemical precipitation routine. HA powder was doped with 1 and 2 wt% of Y2O3 . For microstructural examination, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), and scanning electron microscopy (SEM) coupled with energy dispersive X-rays (EDX) were used. In addition, the dielectric and electrical properties and antimicrobial activities were investigated. XRD patterns reveal the crystallization of the oxyapatite. The peak intensities of pristine HA are inferior compared to the yttrium containing HA composites, thus suggesting that the addition of yttrium promotes the crystallization of HA due to the variance in their ionic radii. FT-IR shows a variation in the phosphate wavenumber, indicating the integration of yttrium into the HA matrix. SEM reveals nanorod- or worm-like crystals arose in clusters. With increasing Y2O3, from 1 to 2 wt%, the DC conductivity reduces from 16 to 9.3 nS/cm, which confirms that high amounts of Y3+ substitute Ca2+ in the HA matrix. In the high-frequency range, the AC conductivity linearly increases with increasing frequency following the universal power law. Further, antimicrobial activity results showed that the addition of yttrium in HA improves the antimicrobial effects against pathogenic bacteria and fungi. Additional research is needed to investigate the doping concentration of yttrium ions, and an anticipated property could be comprehended for several forthcoming biomedical applications
Two levels Plackett-Burman experimental design was employed to screen the main factors that significantly affect the synthesis of bioactive silver nanoparticles. Scenedesmus obliquus ethanol extract, Scenedesmus obliquus dried algal powder and Spirulina platensis aqueous extract were the most favorable reducing and capping agents. Also the high pH value (10), rpm (150), high concentration of AgNO3 (4 mM) and dark conditions had the highest significant influence on biosynthesis of active nanoparticles. Characterizations of the formed AgNPs were approved by UV–Visible Spectroscopy, Transmission Electron Microscopy and Fourier Transform Infrared spectroscopy. The nanoparticles were varied in sizes and shape that ranged between 2.83 and 27.17nm, depending on the organism used and the method of biosynthesis. Valuable inhibitory effects were showed by all bio-synthesized nanoparticles against four tested Gram- positive and Gram- negative bacteria, except that formed by Spirulina platensis powder. Moreover, the nanoparticles exhibited wide range of antifungal activities. AgNPs prepared from ethanol extract of Spirulina platensis was the most active against HepG2 and MCF-7 cell lines, with IC50values 62.1 and 56.2 ug/mL, respectively. The obtained results, indicated the advantages of AgNPs from microalgae and possible industrial applications as a source of antifungal, antibacterial, and antitumor formulation.
Antimicrobial and antifungal materials we prepared from Zn-containing wollastonite set by wet precipitation method.Wollastonite, hardystonite, willemite and very little quartz were developed after sintering at 1100°C/2h, however, the Raman spectroscopy approved the later phases by their characteristic Raman shift bands. The microstructure exhibited accumulated rounded to irregular clusters containing nano-size particles (< 500nm) developed in all sintered samples. Zeta potential; exposed negative values for all powdered samples from − 2.64 to -17.6 mV (i.e., for Zn-free to highest Zn-containing samples). It can be easily noticed that the lowest ZnO-content exhibits a varied range of antibacterial activities in contrast to Gram-negative (E. coli) and Gram-positive (S. aureus & B. subtilis). Correspondingly, the CZS5 exhibits good inhibitory effect against the lamentous pathogenic fungus (A. niger).
Antimicrobial and antifungal materials we prepared from Zn-containing wollastonite set by wet precipitation method. Wollastonite, hardystonite, willemite and very little quartz were developed after sintering at 1100°C/2h, however, the Raman spectroscopy approved the later phases by their characteristic Raman shift bands. The microstructure exhibited accumulated rounded to irregular clusters containing nano-size particles (< 500nm) developed in all sintered samples. Zeta potential; exposed negative values for all powdered samples from − 2.64 to -17.6 mV (i.e., for Zn-free to highest Zn-containing samples). It can be easily noticed that the lowest ZnO-content exhibits a varied range of antibacterial activities in contrast to Gram-negative (E. coli) and Gram-positive (S. aureus & B. subtilis). Correspondingly, the CZS5 exhibits good inhibitory effect against the filamentous pathogenic fungus (A. niger).
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