scholarly journals Highly Efficient and Stable Removal of Arsenic by Live Cell Fabricated Magnetic Nanoparticles

2019 ◽  
Vol 20 (14) ◽  
pp. 3566
Author(s):  
Hyo Kyeong Kim ◽  
Sun-Wook Jeong ◽  
Jung Eun Yang ◽  
Yong Jun Choi
Keyword(s):  
Photoelectron Spectroscopy ◽  
Iron Nanoparticles ◽  
Deinococcus Radiodurans ◽  
Specific Treatment ◽  
Arsenic Species ◽  
Live Cell ◽  
Toxic Substances ◽  
X Ray ◽  
Removal Capacity

As concerns about public health and environmental problems regarding contamination by toxic substances increase worldwide, the development of a highly effective and specific treatment method is imperative. Although physicochemical arsenic treatment methods have been developed, microbial in vivo remediation processes using live cell fabricated nanoparticles have not yet been reported. Herein, we report the development of magnetic iron nanoparticles immobilized an extremophilic microorganism, Deinococcus radiodurans R1, capable of removing toxic arsenic species. First, in vivo synthesis of magnetic iron nanoparticles was successfully achieved with the D. radiodurans R1 strain and characterized by scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDX), dynamic light scattering (DLS), zeta-potential, Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) analysis. Second, the maximum removal capacity of the magnetic iron nanoparticle-immobilized D. radiodurans R1 strain (DR-FeNPs) for arsenic [As(V)] was evaluated under the optimized conditions. Finally, the removal capacity of DR-FeNPs in the presence of various competitive anions was also investigated to simulate the practical application. More than 98% of As(V) was efficiently removed by DR-FeNPs within 1 h, and the removal efficiency was stably maintained for up to 32 h (98.97%). Furthermore, the possibility of recovery of DR-FeNPs after use was also suggested using magnets as a proof-of-concept.

scholarly journals Surface-Modified Poly(l-lactide-co-glycolide) Scaffolds for the Treatment of Osteochondral Critical Size Defects—In Vivo Studies on Rabbits

2020 ◽  
Vol 21 (20) ◽  
pp. 7541
Author(s):  
Małgorzata Krok-Borkowicz ◽  
Katarzyna Reczyńska ◽  
Łucja Rumian ◽  
Elżbieta Menaszek ◽  
Maciej Orzelski ◽  
...  
Keyword(s):  
Bone Tissue ◽  
Tissue Regeneration ◽  
Photoelectron Spectroscopy ◽  
Sessile Drop ◽  
Bone Tissue Regeneration ◽  
In Vivo Studies ◽  
In Vivo Model ◽  
Type I ◽  
X Ray

Poly(l-lactide-co-glycolide) (PLGA) porous scaffolds were modified with collagen type I (PLGA/coll) or hydroxyapatite (PLGA/HAp) and implanted in rabbits osteochondral defects to check their biocompatibility and bone tissue regeneration potential. The scaffolds were fabricated using solvent casting/particulate leaching method. Their total porosity was 85% and the pore size was in the range of 250–320 µm. The physico-chemical properties of the scaffolds were evaluated using scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), X-ray diffractometry (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR), sessile drop, and compression tests. Three types of the scaffolds (unmodified PLGA, PLGA/coll, and PLGA/HAp) were implanted into the defects created in New Zealand rabbit femoral trochlears; empty defect acted as control. Samples were extracted after 1, 4, 12, and 26 weeks from the implantation, evaluated using micro-computed tomography (µCT), and stained by Masson–Goldner and hematoxylin-eosin. The results showed that the proposed method is suitable for fabrication of highly porous PLGA scaffolds. Effective deposition of both coll and HAp was confirmed on all surfaces of the pores through the entire scaffold volume. In the in vivo model, PLGA and PLGA/HAp scaffolds enhanced tissue ingrowth as shown by histological and morphometric analyses. Bone formation was the highest for PLGA/HAp scaffolds as evidenced by µCT. Neo-tissue formation in the defect site was well correlated with degradation kinetics of the scaffold material. Interestingly, around PLGA/coll extensive inflammation and inhibited tissue healing were detected, presumably due to immunological response of the host towards collagen of bovine origin. To summarize, PLGA scaffolds modified with HAp are the most promising materials for bone tissue regeneration.

scholarly journals Removal Efficiency and Mechanism of Cr(VI) from Aqueous Solution by Maize Straw Biochars Derived at Different Pyrolysis Temperatures

Water ◽  
2019 ◽  
Vol 11 (4) ◽  
pp. 781 ◽  
Author(s):  
Wang ◽  
Zhang ◽  
Lv
Keyword(s):  
Aqueous Solution ◽  
Removal Efficiency ◽  
Photoelectron Spectroscopy ◽  
Low Cost ◽  
X Ray ◽  
Removal Capacity ◽  
Maize Straw ◽  
Efficient Adsorbent ◽  
Positively Charged ◽  
Maximum Removal

The removal efficiency and mechanism of Cr(VI) removal from aqueous solution on semi-decomposed maize straw biochars pyrolyzed at 300 to 600 °C were investigated. The removal of Cr(VI) by the biochars decreased with pyrolysis temperature increasing from 300 to 600 °C, and the maximum removal capacity of Cr(VI) for maize straw biochar pyrolyzed at 300 °C was 91 mg/g at pH 2.0. The percentage removal of Cr(VI) rapidly decreased with pH increasing from 2.0 to 8.0, with the maximum (>99.9%) at pH 2.0. The variation of Cr(VI) and Cr(III) concentrations in the solution after reaction showed that Cr(VI) concentration decreased while Cr(III) increased and the equilibrium was reached after 48 h, while the redox potential after reaction decreased due to Cr(VI) reduction. X-ray photoelectron spectroscopy (XPS) semi-quantitative analysis showed that Cr(III) accounted for 75.7% of the total Cr bound to maize straw biochar, which indicated reductive adsorption was responsible for Cr(VI) removal by the biochars. Cr(VI) was firstly adsorbed onto the positively charged biochar surface and reduced to Cr(III) by electrons provided by oxygen-containing functional groups (e.g., C=O), and subsequently part of the converted Cr(III) remained on the biochar surface and the rest released into solution. Fourier transform infrared (FTIR) data indicated the participation of C=O, Si–O, –CH2 and –CH3 groups in Cr(VI) removal by the biochars. This study showed that maize straw biochar pyrolyzed at 300 °C for 2 h was one low-cost and efficient adsorbent for Cr(VI) removal from aqueous solution.

scholarly journals The Surface Characterisation of Fused Filament Fabricated (FFF) 3D Printed PEEK/Hydroxyapatite Composites

Polymers ◽  
2021 ◽  
Vol 13 (18) ◽  
pp. 3117
Author(s):  
Krzysztof Rodzeń ◽  
Mary Josephine McIvor ◽  
Preetam K. Sharma ◽  
Jonathan G. Acheson ◽  
Alistair McIlhagger ◽  
...  
Keyword(s):  
3D Printing ◽  
Photoelectron Spectroscopy ◽  
High Performance ◽  
Secondary Ion Mass Spectrometry ◽  
Fused Filament Fabrication ◽  
Surface Characterisation ◽  
X Ray ◽  
3D Printed

Polyetheretherketone (PEEK) is a high-performance thermoplastic polymer which has found increasing application in orthopaedics and has shown a lot of promise for ‘made-to-measure’ implants via additive manufacturing approaches. However, PEEK is bioinert and needs to undergo surface modification to make it at least osteoconductive to ensure a more rapid, improved, and stable fixation that will last longer in vivo. One approach to solving this issue is to modify PEEK with bioactive agents such as hydroxyapatite (HA). The work reported in this study demonstrates the direct 3D printing of PEEK/HA composites of up to 30 weight percent (wt%) HA using a Fused Filament Fabrication (FFF) approach. The surface characteristics and in vitro properties of the composite materials were investigated. X-ray diffraction revealed the samples to be semi-crystalline in nature, with X-ray Photoelectron Spectroscopy and Time-of-Flight Secondary Ion Mass Spectrometry revealing HA materials were available in the uppermost surface of all the 3D printed samples. In vitro testing of the samples at 7 days demonstrated that the PEEK/HA composite surfaces supported the adherence and growth of viable U-2 OS osteoblast like cells. These results demonstrate that FFF can deliver bioactive HA on the surface of PEEK bio-composites in a one-step 3D printing process.

scholarly journals A new insight into the restriction of Cr(VI) removal performance of activated carbon under neutral pH condition

2021 ◽  
Author(s):  
Yi Fang ◽  
Ke Yang ◽  
Yipeng Zhang ◽  
Changsheng Peng ◽  
Aurora Robledo-Cabrera ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Removal Efficiency ◽  
Photoelectron Spectroscopy ◽  
Toxic Heavy Metal ◽  
X Ray ◽  
Neutral Ph ◽  
Removal Capacity ◽  
Ph Conditions ◽  
Neutral Conditions ◽  
The Impact

Abstract Activated carbon has been widely used to remove hazardous Cr(VI), however, the impact of Cr2O3 precipitate on gradually declined removal ability as pH increased has received little attention. Herein, to investigate the effect of Cr2O3, SEM-EDX (scanning electron microscope-energy dispersive X-ray analysis) coupling elements mapping of chromium loaded powder activated carbon (PAC) revealed that a chromium layer was formed on the PAC exterior after being treated with Cr(VI) at pH 7. XPS (X-ray photoelectron spectroscopy) study confirmed that 69.93% and 39.91% Cr2O3 precipitated on the PAC surface at pH 7 and pH 3, respectively, corresponding to 17.77 mg/g and 20 mg/g removal capacity. Exhausted PAC had a removal efficiency of 92.43% after Cr2O3 being washed by H2SO4 solution, which was much higher than the removal efficiency of 51.27 % after NaOH washing. This further verified the intrinsically developed Cr2O3 precipitate on PAC under neutral conditions limited the durability of PAC as an adsorbent. Consecutive elution assessments confirmed that adsorption and reduction ability both declined as pH increased. Raman spectroscopy and C 1s spectra of materials demonstrated two distinct Cr(VI) removal mechanisms under pH 3 and pH 7. In conclusion, the exhausted AC after Cr(VI) adsorption can be rejuvenated after the surface coated Cr2O3 being washed by the acid solution which can expand the longevity of AC and recover Cr(III). HIGHLIGHT In this work, we scrutinized the mechanism of poor removal capacity of commercial activated carbon on toxic heavy metal Cr(VI) under neutral pH conditions. Differing from the most accepted view that electrostatic repulsion is the main consideration, our study suggested that the relatively more Cr2O3 precipitate on the surface of activated carbon under higher pH led to the low Cr(VI) sequestration capability.

scholarly journals A Simple Low-Cost Method to Prepare Lignocellulose-Based Composites for Efficient Removal of Cd(II) from Wastewater

Polymers ◽  
2019 ◽  
Vol 11 (4) ◽  
pp. 711 ◽  
Author(s):  
Yingying Wen ◽  
Yong Ji ◽  
Shifeng Zhang ◽  
Jie Zhang ◽  
Gaotang Cai
Keyword(s):  
Photoelectron Spectroscopy ◽  
Low Cost ◽  
Agricultural Waste ◽  
Value Added ◽  
Particle Structure ◽  
X Ray ◽  
Removal Capacity ◽  
Secondary Reactions ◽  
Green Separation ◽  
Surface Modified

The fabrication of functional lignocellulose-based materials has drawn considerable attention because it acts as a green separation/absorption material owing to its multi-porous mesostructure. In this study, a surface functionalized lignocellulose-based adsorbent for the highly efficient capture of Cd(II) ions was prepared through facile in situ co-deposition of wood waste-derived saw powder (SP) in the presence of tannic acid (TA) and aminopropyltriethoxysilane (APTES) mixed aqueous solution. The SP was first modified using TA-APTES coating to synthesize the functional SP substrate (SP-(TA-APTES)). The SP-(TA-APTES) hybrids served as reactive platforms, which enabled further decoration with amino-rich polyethylenimine (PEI) due to the outstanding secondary reactions of the TA-APTES layer. The surface morphology of the resulting SP-(TA-APTES)-PEI (SP-TAPI) composites were investigated using Fourier-transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), thermogravimetric analysis (TGA), and scanning electron microscopy (SEM). Significantly, the combined advantages of the lignocellulosic skeleton, the layer-particle structure, and the hybrid coating contributed to the enhanced adsorption capacity of Cd(II) (up to 22.66 mg/g at pH = 5.0). This removal capacity was higher than that of most reported agricultural waste-based or lignocellulose-based materials. The Cd(II) adsorption mechanism of the surface-modified SP-TAPI composites was studied in detail. These results provide new insights into the high value-added utilization of agricultural waste for water purification applications.

scholarly journals Optimized Synthesis of FeS Nanoparticles with a High Cr(VI) Removal Capability

2016 ◽  
Vol 2016 ◽  
pp. 1-9 ◽  
Author(s):  
Yuanyuan Liu ◽  
Wenyan Xiao ◽  
Jiajia Wang ◽  
Zakaria A. Mirza ◽  
Tao Wang
Keyword(s):  
Photoelectron Spectroscopy ◽  
Chemical Precipitation ◽  
High Reactivity ◽  
Precipitation Method ◽  
Hydrodynamic Diameter ◽  
X Ray ◽  
Removal Capacity ◽  
Promising Tool ◽  
Horizontal Oscillation ◽  
Average Size

FeS nanoparticles were synthesized using chemical precipitation method involving sulfide and ferrous solutions. Effects of important synthesis parameters including stabilizer, time taken for titration, horizontal oscillation speed, and initial salt concentration on the size of synthesized FeS nanoparticles were investigated by Orthogonal Array design. Increasing the CMC dosage significantly made the hydrodynamic diameter decrease between 0.05 wt.% and 0.15 wt.% while Na2S titration, oscillation rate, and Na2S concentration did not show significant influence on the hydrodynamic diameter of FeS nanoparticles. The synthesized FeS nanoparticles were characterized by using XRD (X-ray diffraction), TEM (transmission electron microscopy), and XPS (X-ray photoelectron spectroscopy). The as-synthesized FeS nanoparticles had an average size of 25 ± 10 nm and had a better long-term stability after storage for 150 days compared to bare FeS particles. Because of the optimized process parameters, the synthesized FeS nanoparticles had a higher Cr(VI) removal capacity of 683 mg per gram of FeS in comparison to the previously reported cases, and up to 92.48% Cr(VI) was removed from aqueous solutions. The small size, special surface property, and high reactivity make the synthesized FeS nanoparticles a promising tool for the remediation of Cr(VI) contaminated soil and groundwater.

Characterization of Carbon-Encapsulated Nickel and Iron Nanoparticles by Means of X-ray Absorption and Photoelectron Spectroscopy

2010 ◽  
Vol 114 (51) ◽  
pp. 22413-22416 ◽  
Author(s):  
V. R. Galakhov ◽  
A. S. Shkvarin ◽  
A. S. Semenova ◽  
M. A. Uimin ◽  
A. A. Mysik ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Iron Nanoparticles ◽  
X Ray ◽  
X Ray Absorption

scholarly journals Surface Modified β-Tricalcium phosphate enhanced stem cell osteogenic differentiation in vitro and bone regeneration in vivo

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Cheuk Sing Choy ◽  
Wei Fang Lee ◽  
Pei Ying Lin ◽  
Yi-Fan Wu ◽  
Haw-Ming Huang ◽  
...  
Keyword(s):  
Bone Regeneration ◽  
Tricalcium Phosphate ◽  
Photoelectron Spectroscopy ◽  
Osteoblastic Differentiation ◽  
Water Soluble ◽  
Glow Discharge Plasma ◽  
Micro Computed Tomography ◽  
X Ray ◽  
Micro Particles

AbstractA major number of studies have demonstrated Beta-tricalcium phosphate (β-TCP) biocompatibility, bioactivity, and osteoconductivity characteristics in bone regeneration. The aim of this research was to enhance β-TCP's biocompatibility, and evaluate its physicochemical properties by argon glow discharge plasma (GDP) plasma surface treatment without modifying its surface. Treated β-TCP was analyzed by scanning electron microscopy (SEM), energy-dispersive spectrometry, X-ray photoelectron spectroscopy (XPS), X-ray diffraction analysis, and Fourier transform infrared spectroscopy characterization. To evaluate treated β-TCP biocompatibility and osteoblastic differentiation, water-soluble tetrazolium salts-1 (WST-1), immunofluorescence, alkaline phosphatase (ALP) assay, and quantitative real-time polymerase chain reaction (QPCR) were done using human mesenchymal stem cells (hMSCs). The results indicated a slight enhancement of the β-TCP by GDP sputtering, which resulted in a higher Ca/P ratio (2.05) than the control. Furthermore, when compared with control β-TCP, we observed an improvement of WST-1 on all days (p < 0.05) as well as of ALP activity (day 7, p < 0.05), with up-regulation of ALP, osteocalcin, and Osteoprotegerin osteogenic genes in cells cultured with the treated β-TCP. XPS and SEM results indicated that treated β-TCP’s surface was not modified. In vivo, micro-computed tomography and histomorphometric analysis indicated that the β-TCP test managed to regenerate more new bone than the untreated β-TCP and control defects at 8 weeks (p < 0.05). Argon GDP treatment is a viable method for removing macro and micro particles of < 7 μm in size from β-TCP bigger particles surfaces and therefore improving its biocompatibility with slight surface roughness modification, enhancing hMSCs proliferation, osteoblastic differentiation, and stimulating more new bone formation.

scholarly journals Impact of Crystal Habit on the Dissolution Rate and In Vivo Pharmacokinetics of Sorafenib Tosylate

Molecules ◽  
2021 ◽  
Vol 26 (11) ◽  
pp. 3469
Author(s):  
Chi Uyen Phan ◽  
Jie Shen ◽  
Kaxi Yu ◽  
Jianming Mao ◽  
Guping Tang
Keyword(s):  
Dissolution Rate ◽  
Photoelectron Spectroscopy ◽  
Class Ii ◽  
Crystal Habit ◽  
Factors Affecting ◽  
X Ray ◽  
Bcs Class Ii ◽  
Rate Limiting Step ◽  
In Vivo Pharmacokinetics

The dissolution rate is the rate-limiting step for Biopharmaceutics Classification System (BCS) class II drugs to enhance their in vivo pharmacokinetic behaviors. There are some factors affecting the dissolution rate, such as polymorphism, particle size, and crystal habit. In this study, to improve the dissolution rate and enhance the in vivo pharmacokinetics of sorafenib tosylate (Sor-Tos), a BCS class II drug, two crystal habits of Sor-Tos were prepared. A plate-shaped crystal habit (ST-A) and a needle-shaped crystal habit (ST-B) were harvested by recrystallization from acetone (ACN) and n-butanol (BuOH), respectively. The surface chemistry of the two crystal habits was determined by powder X-ray diffraction (PXRD) data, molecular modeling, and face indexation analysis, and confirmed by X-ray photoelectron spectroscopy (XPS) data. The results showed that ST-B had a larger hydrophilic surface than ST-A, and subsequently a higher dissolution rate and a substantial enhancement of the in vivo pharmacokinetic performance of ST-B.

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