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Non-availability of an ideal alternative for autografts in treating critical-size bone defects is a major challenge in orthopedics. Phytocompounds have been proven to enhance osteogenesis via various osteogenic signaling pathways, but its decreased bioavailability and increased renal clearance limit its application. In this study, we designed a biocomposite scaffold comprising gelatin (Gel) and nanohydroxyapatite (nHAp) incorporated with diosmin (DM) and we investigated its bone forming potential in vitro and in vivo . Physiochemical characterization of the scaffold showed that DM had no effect on altering the material characteristics of the scaffold. The addition of DM enhanced the osteoblast differentiation potential of the scaffold in mouse mesenchymal stem cells at both cellular and molecular levels, possibly via the integrin-mediated activation of FAK and ERK signaling components. Using the rat tibial bone defective model, we identified the effect of DM in Gel/nHAp scaffold on enhancing bone formation in vivo . Based on our results, we suggest that Gel/nHAp/DM can be a potential therapeutic agent in scaffold-mediated bone regeneration.

Most of the precursors and/or degradation products related to the Chemical Weapons Convention (CWC) are polar. Identification of these molecules in environmental samples provides clues regarding the alleged usage and/or synthesis of the parent toxic chemicals. Such polar compounds need to be derivatized in order to analyze them by gas chromatography–mass spectrometry (GC–MS). In this study, we developed a new derivatizing reagent, para -tolyl isocyanate (PTI), for derivatization of polar CWC-related compounds. The PTI reagent selectively derivatizes the –OH and/or−SH functional groups with high efficiency, but does not react with carboxylic acid (−COOH) or phosphonic acid (−(O)P(OH) 2 ) groups. The PTI derivatives of dialkyl aminoethanols, dialkyl aminoethanol- N -oxides, and 3-quinuclidinol were successfully eluted through GC, and their electron ionization (EI) mass spectra were distinct and provided the structure information by which the isomeric compounds can be easily distinguished. We also calculated the GC-retention index values that can be used for further confirmation of the target compounds. All the studied PTI derivatives can be analyzed by EI-MS with direct insertion probe and/or by direct electrospray ionization mass spectrometry (ESI-MS) together with the MS–MS data; both sets of data provide full structure information. The PTI reagent was found to be better in some respects than the conventional bistrimethylsilyl trifluoroacetamide (BSTFA), a trimethyl silylating reagent. The PTI reagent is commercially available, and the PTI derivatives are highly stable for months and are not sensitive to moisture. The applicability of the PTI derivatization for trace-level determination of the target CWC-related polar compounds in environmental matrices and in human plasma samples is also evaluated. Fig. a ᅟ

The kinetic method, which is known to be simple, fast and precise, is used for the measurement of proton affinity values of fifteen selected matrix-assisted laser desorption/ionization matrices under electrospray ionization conditions. The stabilization of [M − H] −/[M + Matrix − H] − ions for β-cyclodextrin in negative ion mode has been rationalized based on the proton affinity values of the matrices.

Thirteen orange-pigmented bacteria associated with cyanobacterial mat samples collected from four different lakes in McMurdo, Antarctica, were isolated. Twelve of the isolates, which were coccoid in shape, were very similar and possessed all the characteristics of the genus Planococcus and represented a new species, which was assigned the name Planococcus antarcticus sp. nov. (CMS 26or(T)). Apart from the phenotypic differences, P. antarcticus differed from all reported species of Planococcus by more than 2.5% at the 16S rRNA gene sequence level. In addition, at the DNA-DNA hybridization level, it exhibited very little similarity either with P. mcmeekinii (30%-35%), P. okeanokoites (26%-29%), or CMS 53or(T) (15%-25%), the three species with which it is closely related at the rRNA gene sequence level (2.5%-2.9%). P. antarcticus also showed only 2.5% difference in its 16S rRNA gene sequence compared with the P. alkanoclasticus sequence. But it was distinctly different from P. alkanoclasticus, which exists only as rods, is mesophilic and phosphatase positive, can hydrolyze starch, cannot utilize succinate, glutamate, or glucose, and cannot acidify glucose. Most important, P. antarcticus and P. alkanoclasticus varied distinctly in their fatty acid composition in that C(15:0), C(15:1), C(16:0), iso-C(16:1), and C(17:0) were present only in P. antarcticus but absent in P. alkanoclasticus. CMS 53or(T), the thirteenth isolate, was also identified as a new species of Planococcus and was assigned the name Planococcus psychrophilus sp. nov. This species was distinctly different from all the reported species, including the new species P. antarcticus, with respect to a number of phenotypic characteristics. At the 16S rRNA gene sequence level, it was closely related to P. okeanokoites (98.1%) and P. mcmeekinii (98%), but with respect to the DNA-DNA hybridization, the similarity was only 35%-36%. The type strain of P. antarcticus is CMS 26or(T) (MTCC 3854; DSM 14505), and that of P. psychrophilus is CMS 530r(T) (MTCC 3812; DSM 14507).

Kattedan is an industrial area near Hyderabad, Andhra Pradesh, India, contaminated with high concentrations of metals attributed to industrial sources (battery manufacturing, metal plating, textile and pharmaceuticals production and others). Twelve different locations in the Kattedan industrial area were assessed for concentrations of metals (Zn, Cr, Cu, Ni, Co, Pb, Hg, Cd, and As) in soils, waters, and vegetation. Application of sequential extraction technique for the soils revealed relatively high percentages of Zn, Cu, and Cr associated with mobile fractions, and correspondingly high concentrations of Zn, Cr, Cu, and Pb in forage grass samples and a high degree of bioavailability to humans. Human exposure assessment revealed high concentrations of Pb, Zn, and Cr in blood and urine samples from the residents of the study area showing a direct pathway and a potential for toxicological hazard due to heavy metal pollution.

Beta haemolytic streptococci belonging to Lancefield group A, B, C and G cause a wide spectrum of clinical diseases. Hence there is a need for rapid and accurate typing of these strains. The present study was undertaken to evaluate the use of intact cell matrix assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) for rapid discrimination between strains of beta haemolytic streptococci. Colonies of beta haemolytic streptococci were emulsified with chemical matrix on the sample slide, dried and analyzed by MALDI-TOF-MS. The reproducibility of results for all groups of beta haemolytic streptococci was good and spectra obtained for Lancefield group A, C and G streptococci showed discrimination between the groups on visual comparison. A finer difference in spectrum was observed among group A streptococci isolated from different locations at different periods of time. MALDI-TOF-MS may be a potential tool in discriminating between strains of beta haemolytic streptococci, and also in the characterisation of untypable strains of group A streptococci.

A series of O,O-dialkyl N,N-dialkyl phosphoramidates ( 1– 25) were analyzed under GC-EIMS conditions. Clear-cut differences are found in the fragmentation of O,O-dialkyl N,N-dimethyl phosphoramidates (Series 1) and O,O-dimethyl N,N-dialkyl phosphoramidates (Series 2). The phosphoramidates comprising of mixed/crossed alkyl groups on nitrogen and oxygen (Series 3) showed mixed fragmentation pattern corresponding to both Series 1 and 2 depending on the nature of alkyl groups. All the possible isomers among the studied compounds showed distinguishable EI mass spectra. Although the major ions in the EI mass spectra for the isomers containing O-n-propyl or O-isopropyl and N,N-diethyl or N-isopropyl N-methyl are similar, the isomers could be distinguished by characteristic ions of low abundance at low mass region. The differences are prominent in the metastable ion spectra of characteristic ions.

During INDOEX IFP-99, the samples of aerosols were collected onboard ORV Sagar Kanya over Indian Ocean along the cruise track, for chemical characterization and identification of dominating sources of aerosols. The concentrations of nss-SO4, nss-Ca, nss-Mg, NO3, K, NH4 and SO2 were observed to be significantly higher before ITCZ in northern hemisphere than across ITCZ in southern hemisphere. In this study, variation of concentrations of nss-SO4, nss-Ca and nss-K with respect to change in latitude, wind direction, wind speed and relative humidity have been highlighted. North of ITCZ, nss-SO4 varied from 2.20 to 18.31 μg/m3 and south of ITCZ from 0.50 to 2.79 μg/m3 while nss-Ca varied from 0.02 to 0.72 μg/m3 north of ITCZ and from 0.01 to 0.14 μg/m3 south of ITCZ. nss-K ranged 0.09–1.43 μg/m3 and 0.07–0.60 μg/m3 before ITCZ and across ITCZ respectively. nss-Ca and nss-SO4 were contributed mainly by NNW and ENE winds while nss-K was observed to be contributed mainly by SSW and ENE winds. Wind speed greater than 4.5 m/s negatively influenced the concentration of nss-Ca concentrations. Correlation coefficients of nss-SO4 with SO2 (r = 0.7) and RH (r = 0.5) suggested a significant contribution of nss-SO4 by aqueous phase oxidation of SO2. Using PCA, four major sources namely sea salt, biogenic combustion, secondary SO4 and crustal contribution were identified over Indian Ocean during INDOEX period.