ONLINE FLOW-INJECTION COBALT-AMMONIUM PYRROLIDIN-1-YLDITHIOFORMATE COPRECIPITATION FOR PRECONCENTRATION OF TRACE AMOUNTS OF METALS IN WATERS WITH SIMULTANEOUS DETERMINATION BY INDUCTIVELY-COUPLED PLASMA-ATOMIC EMISSION-SPECTROMETRY

The technique of on-line flow injection (FI) cobalt-ammonium pyrrolidin-1-yldithioformate (Co-APDC) coprecipitation for the preconcentration of trace amounts of the heavy metals Cd, Cu, Fe, Ni, Pb and Zn in rain water samples with simultaneous determination by inductively coupled plasma atomic emission spectrometry (KP-AES) has been developed. A precipitate collector system, consisting of a poly(tetrafluoroethylene) (PTFE) membrane on a polypropylene support filtering device combined with a 1.5 m reaction coil, was selected. An inorganic solution of concentrated nitric acid and hydrogen peroxide was applied as the dissolution reagent. The technique is characterized by high retention efficiency (which ranged from 77 to 99% for the six elements of interest), good enrichment factors (ranging from 10 to 50 for 100 s preconcentration depending on the elements studied) and satisfactory accuracy and precision (recoveries from two standard additions to a rain sample ranged from 92 to 104%, with relative standard deviations ranging from 1.9 to 5%). The sample throughput is 20 per hour

Suppression of gas species signals in direct current glow discharge time-of-flight mass spectrometry

The possibility of suppressing gas species in direct current glow discharge mass spectrometry (dc-GDMS) with a linear time-of-flight mass analyzer was investigated. With this tic-GD ion source, a 'clean' mass spectrum rich in analyte could be obtained when the dc-GD was operated under a discharge current of 15-30 mA and a gas pressure of 300-500 Pa, in contrast to the strong signals of gas species in convention dc-GDMS, which operates at lower currents and pressures (typically 1-5 mA and 100 Pa). Such an experimental result is believed to be due to increased sputtering at higher pressures and currents, and the different ionization mechanisms of analyte and gas species. For a possible GD design to eliminate the background gas ions, a new discharge configuration was developed by attaching a TM,,, microwave resonator to the GD ion source. The mass spectrum of the cathode sample showed a low gas species background when the microwave-induced plasma (MIP) discharge was 'off' under different dc-GD parameters. The mass spectra of analyte and gas species obtained with 'MIP + dc-GD' and 'MIP only' modes are also compared and discussed. It was found that the analyte signals decrease and the gas species signals increase in the presence of the MIP, and that the analyte signals nearly disappear in the 'MIP only' mode. Preliminary results suggest that, for specific discharge conditions and with a suitable design of the GD source, an efficient suppression of gas species in dc-GDMS detection could be realized

Parity-related molecular signatures and breast cancer subtypes by estrogen receptor status

INTRODUCTION: Relationships of parity with breast cancer risk are complex. Parity is associated with decreased risk of postmenopausal hormone receptor–positive breast tumors, but may increase risk for basal-like breast cancers and early-onset tumors. Characterizing parity-related gene expression patterns in normal breast and breast tumor tissues may improve understanding of the biological mechanisms underlying this complex pattern of risk. METHODS: We developed a parity signature by analyzing microRNA microarray data from 130 reduction mammoplasty (RM) patients (54 nulliparous and 76 parous). This parity signature, together with published parity signatures, was evaluated in gene expression data from 150 paired tumors and adjacent benign breast tissues from the Polish Breast Cancer Study, both overall and by tumor estrogen receptor (ER) status. RESULTS: We identified 251 genes significantly upregulated by parity status in RM patients (parous versus nulliparous; false discovery rate = 0.008), including genes in immune, inflammation and wound response pathways. This parity signature was significantly enriched in normal and tumor tissues of parous breast cancer patients, specifically in ER-positive tumors. CONCLUSIONS: Our data corroborate epidemiologic data, suggesting that the etiology and pathogenesis of breast cancers vary by ER status, which may have implications for developing prevention strategies for these tumors

Choroidal thickness in school children: The Gobi Desert Children Eye Study

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Microwave-induced plasma boosted microsecond-pulse glow discharge optical emission spectrometry

A microsecond-pulse (mu s-pulse) glow discharge (GD) source boosted by a microwave-induced plasma (MIP) has been developed and studied for optical emission spectrometry (OES), The excitation processes of the tandem GD source were investigated, The analytical characteristics of the GD-OES source in the presence and absence of the MIP were compared, including the operating parameters, signal-to-background ratios (S/B) and relative standard deviation (RSD), The results show that under a relatively low discharge pressure (<180 Pa), the mu s-pulse GD can couple fairly well with the MIP and emit intense analytical lines, When the GD source is operated under a pressure higher than 200 Pa, tao emission peaks appear, independent in time, for a given resonance atomic line, because sample atoms are independently structurally excited, first by the mu s-pulse GD and then by the MIP. The time interval between the tao peaks for Zn I 213.8 nm is longer than that for Cu I 324.7 nm, which is believed to be due to the faster diffusing velocity of copper atoms, When the mu s-pulse GD lamp is operated under a gas pressure higher than 220 Pa, the ion population is so high that Cu II ionic line at 224.7 nm 'becomes' two peaks because of a possible self-absorption. The results show that the supplementary nse of an MIP can eliminate the self-absorption of ionic and atomic lines, When the mu s-pulse GD source is coupled with the MTP, S/Bs are improved by a factor of more than one order of magnitude for several analytical lines. A short-term RSD of 0.2% is achieved for the 'mu s-pulse GD+MIP' configuration compared with that of 1.0% for 'mu s-pulse GD only' mode. The experimental results show that the MIP boosted mu s-pulse GD is a promising technique for solid sample and surface analysis

Underexpression of Deleted in liver cancer 2 (DLC2) is associated with overexpression of RhoA and poor prognosis in hepatocellular carcinoma

<p>Abstract</p> <p>Background</p> <p>DLC2, a unique RhoGAP, has been recently identified as a tumor suppressor gene in hepatocellular carcinoma (HCC). However, the expression of DLC2 protein, and its relationship with RhoA in clinical hepatocellular carcinoma have not been studied. The aim of this study was to investigate the DLC2 protein expression and its correlation with expression of RhoA, as well as to evaluate the prognostic value of DLC2 for HCC patients.</p> <p>Methods</p> <p>Western blot and immunohistochemical staining were employed to detect DLC2 protein expression in 128 HCC specimens. The correlation between DLC2 protein expression and clinicopathologic outcome, and prognostic value of DLC2 for HCC patients were analyzed.</p> <p>Results</p> <p>HCC tissues revealed significantly lower level of DLC2 protein than pericarcinomatous liver tissues (PCLT). There was significant correlation between underexpression of DLC2 protein and cell differentiation. Meanwhile, underexpression of DLC2 protein was correlated with overexression of RhoA. Furthermore, HCC Patients with DLC2-negative expression showed a significantly poorer prognosis than those with DLC2-positve expression.</p> <p>Conclusion</p> <p>Our data strongly suggested that decreased DLC2 expression in HCC correlates with cell differentiation of HCC and overexpression of RhoA, underexpression of DLC2 is associated with poor prognosis in HCC patients.</p

The Effect of Chronic Antipsychotic Drug on Hypothalamic Expression of Neural Nitric Oxide Synthase and Dopamine D2 Receptor in the Male Rat

Antipsychotic-induced sexual dysfunction is a common and serious clinical side effect. It has been demonstrated that both neuronal nitric oxide (nNOS) and dopamine D2 receptor (DRD2) in the medial preoptic area (MPOA) and the paraventricular nucleus (PVN) of the hypothalamus have important roles in the regulation of sexual behaviour. We investigated the influences of 21 days’ antipsychotic drug administration on expression of nNOS and DRD2 in the rat hypothalamus. Haloperidol (0.5 mg/kg/day i.p.) significantly decreased nNOS integrated optical density in a sub-nucleus of the MPOA, medial preoptic nucleus (MPN), and decreased the nNOS integrated optical density and cell density in another sub-nucleus of the MPOA, anterodorsal preoptic nucleus (ADP). Risperidone (0.25 mg/kg) inhibited the nNOS integrated optical density in the ADP. nNOS mRNA and protein in the MPOA but not the PVN was also significantly decreased by haloperidol. Haloperidol and risperidone increased DRD2 mRNA and protein expression in both the MPOA and the PVN. Quetiapine (20 mg/kg/day i.p.) did not influence the expression of nNOS and DRD2 in either the MPOA or the PVN. These findings indicate that hypothalamic nNOS and DRD2 are affected to different extents by chronic administration of risperidone and haloperidol, but are unaffected by quetiapine. These central effects might play a role in sexual dysfunction induced by certain antipsychotic drugs