Advances and Perspectives in Dental Pulp Stem Cell Based Neuroregeneration Therapies

Human dental pulp stem cells (hDPSCs) are some of the most promising stem cell types for regenerative therapies given their ability to grow in the absence of serum and their realistic possibility to be used in autologous grafts. In this review, we describe the particular advantages of hDPSCs for neuroregenerative cell therapies. We thoroughly discuss the knowledge about their embryonic origin and characteristics of their postnatal niche, as well as the current status of cell culture protocols to maximize their multilineage differentiation potential, highlighting some common issues when assessing neuronal differentiation fates of hDPSCs. We also review the recent progress on neuroprotective and immunomodulatory capacity of hDPSCs and their secreted extracellular vesicles, as well as their combination with scaffold materials to improve their functional integration on the injured central nervous system (CNS) and peripheral nervous system (PNS). Finally, we offer some perspectives on the current and possible future applications of hDPSCs in neuroregenerative cell therapies.     

Isolation and identification of high pressure‐resistant bacteria naturally contaminating strawberry pulp

The inactivation of bacteria naturally present in strawberry pulp was investigated after high hydrostatic pressure (HHP) treatment at pressure levels up to 600 MPa at 25 °C for 5 ~ 25 min. Five strains of pressure‐resistant bacteria designated as A, B, C, D and E were isolated and identified. The five strains were gram‐positive, spore‐forming, rods or rod in chains. Growth of the strains was observed at 30 ~ 45 °C, and strain B also grew well at 55 °C. They could produce acid from glucose and were catalase‐positive. Analysis of 16S rRNA gene sequences showed that the five strains belonged to the genus Bacillus. Strain A and D exhibited the greatest 16S rRNA gene sequence similarity of 99% with B. licheniformis and B. firmus, respectively. By combination of phenotypic characteristics and 16S rRNA gene sequences, strain C was B. mycoides and E was B. pumilus. On the basis of physiological and biochemical characteristics, gyrB gene sequences analysis and whole‐cell fatty acids analysis, strain B was B. amyloliquefaciens. Further studies showed that strain B (B. amyloliquefaciens) exhibited the highest pressure resistance, and it was reduced by 4.62‐log after treatment at 600 MPa for 25 min at 25 °C as the most effective observed inactivation.     

Assessment of selected properties of LDPE composites reinforced with sugar beet pulp

This study measured the effect of sugar beet pulp (SBP) and maleated polyethylene (MAPE) concentrations on the properties of low density polyethylene (LDPE) composites. SBP concentration has significantly increased density, thickness swelling (TSW), water absorption (WA), flexural strength (FS), tensile modulus (TM) and flexural modulus (FM) of composites while reducing tensile strength (TS), elongation at break (EatB) and impact strength (IS). Presence of MAPE has improved TSW, WA, TS, FS, TM and FM. However, EatB and IS were slightly worsened by MAPE use. Composites showed two main decomposition peaks; one coming from SBP (360–368 °C) and the second one from LDPE degradation (484–490 °C). SEM images showed improved dispersion of SBP. The composites has provided less than 2% weight loss and classified as ‘very durable material’ against white-rot and brown-rot fungi attack. Through this study, potential utilization of SBP in LDPE matrix was demonstrated.     

Modified nanoporous carbon as a novel sorbent before solvent-based de-emulsification dispersive liquid–liquid microextraction for ultra-trace detection of cadmium by flame atomic absorption spectrophotometry

Combination of different extraction methods is an interesting work in the field of sample pretreatment. In the current study, for the first time, solid phase extraction combined with solvent-based de-emulsification dispersive liquid–liquid microextraction (SPE-SD-DLLME) was developed for preconcentration and trace detection of cadmium in water samples using flame atomic absorption spectrophotometry (FAAS). The adsorbed cadmium ions on prepared SPE (75 mL of aqueous solution) were eluted by optimized elution solvent and introduced to the second microextraction step. The effective variables of SPE including the pH of sample, flow rates, type, concentration and volume of the eluent and the effect of potentially interfering ions of the separation of cadmium were evaluated and optimized. Also, several factors that influence the SD-DLLME step such as pH, neocuproine concentration (the cadmium binding ligand), type of dispersed/de-emulsifier solvent, volume of disperser/de-emulsifier solvent and type and volume of extraction solvents were investigated. SPE-SD-DLLME provides a preconcentration factor of 165 for cadmium ions. Calibration plot was linear in the range of 0.1–50 μg L⁻¹ with correlation of determination (r²) of 0.988. The precision and limit of detection of proposed method were 5.1% (RSD%, n = 8) and 0.03 μg L⁻¹, respectively.     

Utility of solid phase spectrophotometry for the modified determination of trace amounts of cadmium in food samples

A modified selective, highly sensitive and accurate procedure for the determination of trace amounts of cadmium which reacts with 1-(2-benzothiazolylazo)-2-hydroxy-3-naphthoic acid (BTAHNA) to give a deep violet complex with high molar absorptivity (7.05 × 10⁶ L mol⁻¹ cm⁻¹, 3.92 × 10⁷ L mol⁻¹ cm⁻¹, 1.78 × 10⁸ L mol⁻¹ cm⁻¹, and 4.10 × 10⁸ L mol⁻¹ cm⁻¹), fixed on a Dowex 1-X8 type anion-exchange resin for 10 mL, 100 mL, 500 mL, and 1000 mL, respectively. Calibration is linear over the range 0.2-3.5 μg L⁻¹ with RSD of ?1.14% (n = 10). The detection and quantification limits were calculated. Increasing the sample volume can enhance the sensitivity. The method has been successfully applied for the determination of Cd(II) in food samples, water samples and some salts samples without interfering effect of various cations and anions.     

β-Cyclodextrin Based Molecularly Imprinted Solid Phase Extraction for Class Selective Extraction of Priority Phenols in Water Samples

Molecular imprinted polymer (MIP MAA-β-CD) with 2,4-dichlorophenol (2,4-DCP) and methacrylic acid functionalized β-cyclodextrin (MAA-β-CD) as the template molecule and the functional monomer, respectively, was prepared and used in molecular imprinted-solid phase extraction (MISPE) for the extraction of phenols (2,4-dichlorophenol, 2-chlorophenol, 4-chloro-3-methylphenol, 4-chlorophenol, 2,4,6-trichlorophenol, and 2-nitrophenol) from water samples. The MISPE method was optimized prior to the determination using gas chromatography coupled with a flame ionization detector (GC-FID). Under the optimized conditions, the MIP MAA-β-CD sorbent showed good linearity (0.01-12 mgL^?1), low limits of detection (0.14-0.75 µgL^?1), and good repeatability (RSD 2.3-3.6%, n = 3). Good recoveries were obtained in the range of 97-115% for tap water and between 88-103% for river water. The developed MIP MAA-β-CD SPE was then compared with other adsorbents. The unique properties of β-CD and presence of imprinted cavities explains the higher extraction recoveries obtained for phenols when using MIP MAA-β-CD SPE.     

Highly sensitive toxin microarray assay for aflatoxin B1 detection in cereals

We report a rapid, highly sensitive microarray method for quantitative aflatoxin B₁ (AFB₁) detection in cereal samples. Following optimisation using an indirect competitive immunoassay, optimised amounts of AFB₁-bovine serum albumin (AFB₁-BSA)-conjugate were contact-printed onto 16 isolated sub-arrays on multi-pad nitrocellulose coated slides subsequently used in competitive binding assays.The toxin microarray working range for AFB₁ was established in the range of 15 pg g⁻¹ to 3.04 ng g⁻¹, with a detection limit of 1 pg g⁻¹. To determine assay sensitivity in contaminated food models, wheat flour and barley grains samples were spiked with AFB₁ standard dilutions. Following extraction, the working ranges of 0.11–4.15 and 0.18–4.31 ng g⁻¹ were determined, with detection limits of 30 and 90 pg g⁻¹, respectively. The sensitivity of the developed assay is below the European commission limit set for AFB₁ detection and the assay procedure was completed in 3 h time. Good recoveries (98% ± 11%) obtained demonstrate the suitability of the proposed method for rapid and sensitive quantification of AFB₁ in contaminated cereal samples.     

Application Of Superconducting High Gradient Magnetic Separation Technology On Silica Extraction From Iron Ore Beneficiation Tailings

Comprehensive utilization of tailings resources not only solves environmental problems but also creates huge economic benefits. In this paper, fine weakly magnetic particles were extracted from iron ore beneficiation tailings and silica (SiO₂) was separated and purified using a superconducting high gradient magnetic separator. Based on plenty of contrast experiments, SiO₂ content of the magnetic concentrate could be increased from 68.67% to 92.57% with the selected optimal parameter combination, i.e., a magnetic flux density of 3.2 T, a pulp concentration of 40 g/L and a slurry flow velocity of 500 mL/min. The concentrate can be utilized as low-grade normal SiO₂ sands for industrial use, or act as the raw materials for preparing high-purity SiO₂ product.