Combination of Selective Etching and Impregnation toward Hollow Mesoporous Bioactive Glass Nanoparticles

In this study, binary SiO2-CaO hollow mesoporous bioactive glass nanoparticles (HMBGNs) are prepared by combing selective etching and impregnation strategies. Spherical silica particles (SiO2 NPs) are used as hard cores to assemble cetyltrimethylammonium bromide (CTAB)/silica shells, which are later removed by selective etching to generate a hollow structure. After the removal of CTAB by calcination, the mesoporous shell of particles is formed. Calcium (Ca) is incorporated into the particles using impregnation by soaking the etched SiO2 NPs in calcium nitrate aqueous solution. The amount of incorporated Ca is tailorable by controlling the ratio of SiO2 NPs:calcium nitrate in the soaking solution. The produced HMBGNs are bioactive, as indicated by the rapid formation of hydroxyapatite on their surfaces after immersion in simulated body fluid. In a direct culture with MC3T3-E1 cells, HMBGNs were shown to exhibit concentration-dependent cytotoxicity and can stimulate osteogenic differentiation of MC3T3-E1 cells at concentrations of 1, 0.5, and 0.25 mg/mL. Our results indicate that the combination of selective etching and impregnation is a feasible approach to produce hierarchical HMBGNs. The produced hollow particles have potential in drug delivery and bone tissue regeneration applications, and should be further investigated in detailed in vitro and in vivo studies.European Union’s Horizon 2020 research and innovation program 685872-MOZAR

Cerium and gallium containing mesoporous bioactive glass nanoparticles for bone regeneration: Bioactivity, biocompatibility and antibacterial activity

In recent years, mesoporous bioactive glass nanoparticles (MBGNPs) have generated great attention in biomedical applications. In this study, cerium and gallium doped MBGNPs were prepared by microemulsion assisted sol-gel method in the binary SiO2-CaO system. MBGNPs with spheroidal and pineal shaped morphology were obtained. Nitrogen sorption analysis elucidated the mesoporous structure of synthesized nanoparticles with high specific surface area. X-ray diffraction analysis confirmed the amorphous nature of the nanoparticles. The chemical compositions of all samples were determined by inductively coupled plasma-optical emission spectrometry (ICP-OES), which revealed that the contents of cerium and gallium could be tailored by adjusting the concentrations of the precursors used for the synthesis. All MBGNPs exhibited in vitro bioactivity when immersed in simulated body fluid, except the particles doped with higher amounts than 1 mol% of cerium. MBGNPs showed antibacterial activity against S. aureus and E. coli without exhibiting cytotoxicity towards MG-63 osteoblast-like cells. Mentioned features of the obtained Ce and Ga-doped MBGNPs make them useful for multifunctional applications such as drug delivery carriers or bioactive fillers for bone tissue engineering applications. © 2021 The AuthorsEuropean Union's Horizon 2020 research and innovation program [739566]; project "Centre of Polymer System plus" - Ministry of Education, Youth and Sports of the Czech Republic-Program NPU I [LO1504]; Ministry of Education, Youth and Sports of the Czech Republic -DKRVO [RP/CPS/2020/006]; [VEGA 1/0098/19]; [SAS-MOST JRP 2018/02]RP/CPS/2020/006; Ministerstvo Školství, Mládeže a Tělovýchovy, MŠMT: LO1504; Vedecká Grantová Agentúra MŠVVaŠ SR a SAV, VEGA: 1/0098/19, SAS-MOST JRP 2018/02; Horizon 2020: 73956

Polymeric Hydrogel Systems as Emerging Biomaterial Platforms to Enable Hemostasis and Wound Healing

Broad interest in developing new hemostatic technologies arises from unmet needs in mitigating uncontrolled hemorrhage in emergency, surgical, and battlefield settings. Although a variety of hemostats, sealants, and adhesives are available, development of ideal hemostatic compositions that offer a range of remarkable properties including capability to effectively and immediately manage bleeding, excellent mechanical properties, biocompatibility, biodegradability, antibacterial effect, and strong tissue adhesion properties, under wet and dynamic conditions, still remains a challenge. Benefiting from tunable mechanical properties, high porosity, biocompatibility, injectability and ease of handling, polymeric hydrogels with outstanding hemostatic properties have been receiving increasing attention over the past several years. In this review, after shedding light on hemostasis and wound healing processes, the most recent progresses in hydrogel systems engineered from natural and synthetic polymers for hemostatic applications are discussed based on a comprehensive literature review. Most studies described used in vivo models with accessible and compressible wounds to assess the hemostatic performance of hydrogels. The challenges that need to be tackled to accelerate the translation of these novel hemostatic hydrogel systems to clinical practice are emphasized and future directions for research in the field are presented

Combination of Selective Etching and Impregnation toward Hollow Mesoporous Bioactive Glass Nanoparticles

In this study, binary SiO2-CaO hollow mesoporous bioactive glass nanoparticles (HMBGNs) are prepared by combing selective etching and impregnation strategies. Spherical silica particles (SiO2 NPs) are used as hard cores to assemble cetyltrimethylammonium bromide (CTAB)/silica shells, which are later removed by selective etching to generate a hollow structure. After the removal of CTAB by calcination, the mesoporous shell of particles is formed. Calcium (Ca) is incorporated into the particles using impregnation by soaking the etched SiO2 NPs in calcium nitrate aqueous solution. The amount of incorporated Ca is tailorable by controlling the ratio of SiO2 NPs:calcium nitrate in the soaking solution. The produced HMBGNs are bioactive, as indicated by the rapid formation of hydroxyapatite on their surfaces after immersion in simulated body fluid. In a direct culture with MC3T3-E1 cells, HMBGNs were shown to exhibit concentration-dependent cytotoxicity and can stimulate osteogenic differentiation of MC3T3-E1 cells at concentrations of 1, 0.5, and 0.25 mg/mL. Our results indicate that the combination of selective etching and impregnation is a feasible approach to produce hierarchical HMBGNs. The produced hollow particles have potential in drug delivery and bone tissue regeneration applications, and should be further investigated in detailed in vitro and in vivo studies

Crystallization kinetics of binary Yb2O3-Al2O3 glass

The ytterbium aluminum garnet composition YbAG (62.5 mol.% Al2O3, 37.5 mol.% Yb2O3) was prepared in the form of glass microspheres by flame synthesis. Precursor powder for flame synthesis with high homogeneity was prepared by modified sol-gel Pechini method. XRD pattern of prepared glass microspheres indicated predominantly amorphous nature of the sample. Detailed study of morphology of the microspheres by scanning electron microscopy revealed the presence of a small fraction of partially or fully crystallized microspheres. The high-temperature X-ray powder diffraction analysis (HT XRD) was carried out in the temperature interval 750-1450 degrees C: The temperature dependence of phase composition was determined. Crystallization of Yb3Al5O12-ytterbium aluminum garnet phase-was observed in the temperature range 900-1200 degrees C. The DSC analysis with heating rates 2, 4, 6, 8, 10 degrees C min(-1)in temperature interval 25-1200 degrees C was performed in N(2)atmosphere to study thermal behavior and crystallization kinetics of prepared glass microspheres. The two exothermic effects at 918 and 939 degrees C were observed, which were attributed to Yb(3)Al(5)O(12)crystallization. The crystallization kinetics of prepared sample was examined with the use of JMAK model, and the kinetic triplet-frequency factorA = (1.8 +/- 2.2) 10(+28)min(-1)(for the first peak),A = (1.2 +/- 1.6) 10(+55)min(-1)(for the second peak), apparent activation energyE(app) = (6.4 +/- 0.1) 10(+02) kJ mol(-1)(for the first peak),E-app = (1.3 +/- 0.1) 10(+03)kJ mol(-1)(for the second peak) and the Avrami coefficientm = 3 (for the first peak) andm = 2 (for the second peak)-was determined using RSS,Radj2, AIC andW(AIC)criteria