[en] An alizarin-modified electrode for the voltammetric determination of aluminium(III) is reported. The single-use modified electrode is simply prepared by dip-coating a high-density graphite electrode in an N,N-dimethylformamide solution of alizarin. Optimum experimental conditions for aluminium(III) determination include a solution pH of 8.4±0.2, an accumulation time of 1 min and use of the differential-pulse mode for measurement of the oxidation peak of the aluminium(III)-alizarin complex. The detection limit is 1.5x10^-7 M, the response is linear up to 1.0x10^-5 M and the relative standard deviation for replicate preparations of the electrode [at 7.5x10^-6 M Al(III)] is 3.8%. The determination of aluminium in soil samples is reported. (author). 14 refs.; 5 figs.; 2 tabs

[en] Advanced oxidation processes (AOPs) based on persulfate activated by zero valent iron (ZVI) were used to remove azo dyes in water. Activated persulfate generate to strong free radicals SO₄ (E⁰ = 2.6V) and HO (E⁰ = 2.8 V). The UV light was used to improve the efficiency of this activated persulfate. This study focused on determining a kinetic model, reaction rate constants and concentrations of SO₄ and HO in processes of persulfate activated by ZVI with or without UV light to degrade alizarin yellow R (AY). By using both experimental resultsand data analysis using the developed pseudo-first-order kinetic model, the reaction rate constants for the reaction of AY at pH 4.5 were determined to be 6.98×10^-4 s^-1 and 1.38×10^-3 s^-1 in condition without UV light and with UV light, respectively. The concentrations of SO₄, HO at 30 minutes of the process were 9.41×10^-4 mM, 4.12×10^-7 mM without UV and 8.58×10^-4 mM, 8.10×10^-7 mM with UV, respectively. (author)

[en] An accurate and precise determination of thorium is proposed. Precision of about 0,1% is required for the determination of macroquantities of thorium processed. After an extensive literature search concerning this subject, spectrophotometric titration has been chosen, using disodium ethylenediaminetetraacetate (EDTA) solution and alizarin S as indicator. In order to obtain such a precision, an amount of 0,025 M EDTA solution precisely measured has been added and the titration was completed with less than 5 ml of 0,0025 M EDTA solution. It is usual to locate the end-point graphically, by plotting added titrant versus absorbance. The non-linear minimum square fit, using the Fletcher e Powell's minimization process and a computer program. (author)

[en] To dye poly(lactic acid) (PLA) fiber with natural dyes has gained importance in recent years due to the production of the fully eco-friendly textile products. In this study, pure and modified PLA fibers with two different POSS nanoparticles, namely N-phenyl aminopropyl POSS (AP-POSS) and octa (aminophenyl) polyhedral oligomeric silsesquioxane (OAPPOSS), are dyed with three different natural dyes including alizarin, lawsone and indigo. The effects of the dyeing conditions including dyeing temperature and time, POSS nanoparticle concentration, natural dye types and concentrations are investigated on the dyeability properties of the PLA fiber samples. The wash and light fastness of the fiber samples are also investigated. According to the dyeability results, it is concluded that POSS nanoparticles are effective for increasing the dyeability of the PLA fiber with all natural dyes used in this study. As the added amount of the POSS nanoparticle increases, the dyeability of the PLA fiber increases. When the performances of the POSS nanoparticles are compared, it is seen that OAP-POSS is more effective than the AP-POSS nanoparticle.

[en] 3-aminomethylalizarn-N-N diacetic acid chromogenic dye (AMADA) was used for the first time in uranium and thorium spectrophotometric estimation with accurate and sensitive result, their complexes having a maximum absorbance at 575 nm for U and at 510 nm for Th. This system allows uranium and thorium content to be calculated with a detection limit (LOD) of 0.16 µg L^-1 and 0.14 µg L^-1, respectively. The first-derivative spectra and EDTA were investigated to eliminate interference and provide selective estimation of uranium and thorium in presence of each other. This new spectrophotometric method was applied for the determination of U(VI) and Th(IV) in the standard reference materials (granite and Syenite) and some cataclastic rock samples with accurate results. (author)

[en] Ossification of the ligamentum flavum (OLF) is a debilitating disease resulting from the development of ectopic bone formation, which leads to the compression of the spinal cord. Nicotinamide phosphoribosyltransferase (NAMPT) was found to be upregulated and microRNA-182 (miR-182) was downregulated in OLF tissue. We investigated the effects of NAMPT and miR-182 expression in OLF cells and the influence on proteins associated with osteogenic differentiation. MiR-182 overexpression inhibited NAMPT, RUNX2, OCN and OPN mRNA and protein expression in OLF cells. Alkaline phosphatase (ALP) assay and Alizarin red staining confirmed reduced levels of osteogenic differentiation and mineralized nodule formation. Knockdown of NAMPT and the NAMPT inhibitor FK866 also inhibits RUNX2, OCN and OPN mRNA expression and protein levels, whereas overexpression of NAMPT promotes the expression of RUNX2, OCN and OPN and the generation of bone nodules. Dual-luciferase reporter assays revealed that miR-182 directly targets NAMPT and downregulates its expression. Transfection of OLF cells with miR-182 downregulated NAMPT and suppressed the regulation of RUNX2, OCN, and OPN by NAMPT overexpression. Overall, these data demonstrate that miR-182 suppresses OLF by downregulating NAMPT.

[en] Stem cells derived from oral tissue represent a highly attractive alternative source for clinical bone regeneration because they can be collected by non-invasive or minimally invasive procedures. Herein, we describe the human dental stem cells (DSCs) deriving from buccal fat pads (BFP), dental pulp (DP) of impacted teeth, and periodontal ligaments (PDL) to obtain BFPSCs, DPSCs, and PDLSCs, respectively. Cells were purified with selected medium and expanded through passages in stem cell culture medium. Purified cells were characterized for stemness by their growth rate, immunostaining, and multilineage differentiation ability. They showed plastic adherence, expression of stemness-specific markers, and multilineage differentiation potential. Immunocytochemistry analysis confirmed that DPSCs had more osteogenic potential than BFSCs and PDLSCs. Calcium-rich deposits, evaluated by von Kossa and Alizarin red staining, showed greater mineralization when DPSCs were cultured on collagen type I matrix than without collagen. Furthermore, DPSC-seeded collagen type I matrix maintained consistent osteogenesis and boosted mineral formation by 1–2 weeks over that in DPSCs cultured without collagen. Radiographic analysis of DPSC-seeded collagen type I matrix transplanted into rat cranial defects showed significant bone regeneration after 8 weeks. These results suggested that the redundant oral tissue can be used as a source of adult multipotent stem cells for clinical bone regeneration.

Graphical abstract

Triple overlay images with biomarkers (red), nuclei (blue) and bright field morphology of DPSCs. The specifically osteo-differentiation shown by osteocalcin (left) expression and lack of sox9 (right) expressed in the images below which were cultured with collagen matrix, contrast with no collagen matrix group above.

[en] Vascular calcification is extremely common and associated with major adverse cardiovascular events. Fibroblast growth factor (FGF) 21 has been identified as a potent metabolic regulator and a protector of the cardiovascular system. In this study, we aimed to investigate the effect of FGF21 on calcification of vascular smooth muscle cell (VSMC) and its mechanism. FGF21 inhibited beta-glycerophosphate (BGP) induced mineralization in VSMCs as determined by calcium concentration and Alizarin Red S. FGF21 suppressed BGP-induced BMP2/Smad signaling pathway components as well as osteoblast differentiation markers. FGF21 and Noggin could synergistically inhibit BGP-induced BMP2/Smad pathway expressions and calcification. Taken together, FGF21 inhibits vascular calcification in vitro by modulating BMP2/Smad signaling pathway.

[en] Highlights: • Performance of a strategy of constructing a novel tissue-engineered bone (TEB). • Simvastatin could release in a sustained manner after incorporated in the TEB. • This novel TEB could promote the bone formation capability of hASCs more effectively. To repair bone defects, we evaluate the in-vitro and in-vivo osteogenic activities of a novel tissue-engineered bone (TEB) by elaborately combining biomimetic calcium phosphate (BioCaP) granules with internally-incorporated simvastatin (SIM) and human adipose-derived stem cells (hASCs). First, we constructed BioCaP with SIM internally incorporated (SIM-BioCaP). Then we characterized the morphology and chemical composition of SIM-BioCaP. The release kinetics of SIM was monitored in vitro spectroscopically. Thereafter, we explored the in-vitro cellular responses of hASCs to SIM-BioCaP by performing scanning electron microscopy observation, proliferation assay, alkaline phosphatase (ALP) activity assay, alizarin red staining and real-time PCR. Finally, we investigated the in-vivo osteogenic activities of the novel TEB in a subcutaneous bone induction model in nude mice. We found that SIM was successfully incorporated internally in BioCaP and showed a slow release manner without significantly affecting the attachment and proliferation of hASCs. The released SIM from BioCaP could significantly enhance the proliferation, ALP activities, mineralized nodules formation and osteogenic genes of hASCs. The in-vivo tests showed this TEB could induce new bone formation while the other groups could not. Taken together, the present data show that this novel TEB represented a very promising construct to treat critical-volume bone defects.

[en] It was demonstrated that the mechanism of the inner filter effect (IFE) can emerge well in the resonance Rayleigh scattering (RRS) technique and be utilized as a new analytical method in the design of innovative IFE-based sensors. To prove this process, silver nanocubes (Ag NCs) with tunable extinction spectra were selected as RRS probes, and three analytes, doxorubicin (DOX), sunitinib (SUN), and Alizarin Red S (ARS), were considered as the typical absorbers. In addition, in the presence of SUN as a typical analyte, the quenching of the RRS signal of Ag NCs, with λ_max of 419 nm, was linear in the range 0.01 to 2.5 µM of SUN. The limit of detection (LOD) was 0.0025 µM. The introduced method was then used to develop a dual-signal assay for the ratiometric determination of Al³⁺ ions. The suggested dual-signal assay was based on the color changes of ARS caused by Al³⁺ and the IFE between ARS and Ag NCs. The obtained results showed that the two characteristics of response sensitivity and linear dynamic range are very satisfactory for sensing Al³⁺ ions. The findings of this study demonstrate that the newly developed IFE mechanism can be employed as an attractive and highly efficient analytical technique for measuring different analytes. Graphical