Research progress in analytical methods of carbon nanomaterials

 With the mass production and application of carbon nano materials, the detection and characterization methods of carbon nano materials in different media are particularly important. This paper reviews the commonly used characterization and detection technologies of carbon nanomaterials. Firstly, the separation and enrichment technology of carbon nanomaterials, including extraction separation, is introduced. The sample pretreatment technology of fractional separation and the combination of various separation methods, and then the electron microscope is reviewed. Spectrum. Thermal analysis. Electrochemical analysis. Isotope labeling, imaging and other characterization techniques, as well as fluorescence spectroscopy. Laser induced breakdown spectroscopy. Mass spectrometry. Scanning Raman microscope and quantitative analysis methods combined with various technologies, and some new carbon nano materials and some special characterization and detection methods are introduced. Finally, the future development trend and Prospect of carbon nano materials are prospected

Overexpression of serine racemase in retina and overproduction of D-serine in eyes of streptozotocin-induced diabetic retinopathy

<p>Abstract</p> <p>Background</p> <p>Recent data indicate that inflammatory mechanisms contribute to diabetic retinopathy (DR). We have determined that serine racemase (SR) expression is increased by inflammatory stimuli including liposaccharide (LPS), amyloid β-peptide (A-beta), and secreted amyloid precursor protein (sAPP); expression is decreased by the anti-inflammatory drug, dexamethasone. We tested possibility that SR and its product, D-serine, were altered in a rat model of DR.</p> <p>Methods</p> <p>Intraperitoneal injection of streptozotocin (STZ; 70 mg/kg body weight) to Sprague-Dawley rats produced type-I diabetic mellitus (fasting blood sugar higher than 300 mg/dL). At 3 and 5 months after STZ or saline injection, retinas from some rats were subjected to cryosectioning for immunofluorescent analysis of SR and TUNEL assay of apoptosis. Retinal homogenates were used to detect SR levels and Jun N-terminal kinase (JNK) activation by immunoblotting. Aqueous humor and retina were also collected to assay for neurotransmitters, including glutamate and D-serine, by reverse-phase HPLC.</p> <p>Results</p> <p>Compared to saline-injected rats, STZ-injected (diabetic) rats showed elevation of SR protein levels in retinal homogenates, attributed to the inner nuclear layer (INL) by immunofluorescence. Aqueous humor fluid from STZ-injected rats contained significantly higher levels of glutamate and D-serine compared to controls; by contrast, D-serine levels in retinas did not differ. Levels of activated JNK were elevated in diabetic retinas compared to controls.</p> <p>Conclusions</p> <p>Increased expression of SR in retina and higher levels of glutamate and D-serine in aqueous humor of STZ-treated rats may result from activation of the JNK pathway in diabetic sequelae. Our data suggest that the inflammatory conditions that prevail during DR result in elevation of D-serine, a neurotransmitter contributing to glutamate toxicity, potentially exacerbating the death of retinal ganglion cells in this condition.</p

Comparison of two pretreatment methods for mercury stable isotope analysis in Antarctic moss

Mercury (Hg) stable isotope analysis can provide new insight for understanding the biogeochemistry and sources of Hg in the polar regions. To completely extract the low contents of Hg in polar samples and to avoid isotopic fractionation during the sample preparation stage, an effective and reliable pretreatment method is needed. In this work, two different pretreatment methods were compared for measuring Hg stable isotopes in Antarctic moss samples. One method was acid digestion (HNO3︰ H2O2=5︰3, v/v) and the second was a combustion-trapping treatment with a trapping solution (HNO3:HCl=2:1, v/v). There were no significant differences in the analytical results obtained with the two methods. The overall mean values and uncertainties of total Hg (THg) and the isotopic compositions of Hg in the referenced materials were all in good agreement with the certified and reported values, indicating that both methods were accurate and applicable. Acid digestion is highly efficient, while the combustion-trapping method can be used to treat samples with low Hg content. The proposed methods were successfully used to determine the Hg isotopic compositions in moss samples collected from the Antarctic

The Proteasome Is a Molecular Target of Environmental Toxic Organotins

BACKGROUND: Because of the vital importance of the proteasome pathway, chemicals affecting proteasome activity could disrupt essential cellular processes. Although the toxicity of organotins to both invertebrates and vertebrates is well known, the essential cellular target of organotins has not been well identified. We hypothesize that the proteasome is a molecular target of environmental toxic organotins. OBJECTIVES: Our goal was to test the above hypothesis by investigating whether organotins could inhibit the activity of purified and cellular proteasomes and, if so, the involved molecular mechanisms and downstream, events. RESULTS: We found that some toxic organotins [e.g., triphenyltin (TPT)] can potently and preferentially inhibit the chymotrypsin-like activity of purified 20S proteasomes and human breast cancer cellular 26S proteasomes. Direct binding of tin atoms to cellular proteasomes is responsible for the observed irreversible inhibition. Inhibition of cellular proteasomes by TPT in several human cell lines results in the accumulation of ubiquitinated proteins and natural proteasome target proteins, accompanied by induction of cell death. CONCLUSIONS: The proteasome is one of the molecular targets of environmental toxic organotins in human cells, and proteasome inhibition by organotins contributes to their cellular toxicity