1,007 research outputs found

    Zero Liquid Discharge (ZLD) as Sustainable Technology —  Challenges and Perspectives

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    In sustainable treatment of wastewater, in addition to treatment performance, other aspects viz. energy utilization, recycling of wastewater and social issues also play vital role in evaluation of the sustainability. It is useful for achieving zero liquid discharge from industries. Soil biotechnology (SBT) is a type of biological treatment that plays major part in zero liquid discharge (ZLD) technology. ZLD is used for conversion of organic matter present in wastes into various grades of products for soil application and turns wastewater to cleaner water in the presence of selective geophagus earthworms, bacterial culture and formulated soil. SBT reduces the level of various pollutants in industrial wastewater viz. biological oxygen demand, chemical oxygen demand, ammonium nitrate, phosphates, nitrogen, suspended solids, odour, colour and other undesired organisms. This review briefly discusses the need for sustainable development in treatment of wastewater. It also provides an updated scientific literature on zero liquid discharge systems in industries including challenges and perspective

    Zero Liquid Discharge (ZLD) as Sustainable Technology — Challenges and Perspectives

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    508-514In sustainable treatment of wastewater, in addition to treatment performance, other aspects viz. energy utilization, recycling of wastewater and social issues also play vital role in evaluation of the sustainability. It is useful for achieving zero liquid discharge from industries. Soil biotechnology (SBT) is a type of biological treatment that plays major part in zero liquid discharge (ZLD) technology. ZLD is used for conversion of organic matter present in wastes into various grades of products for soil application and turns wastewater to cleaner water in the presence of selective geophagus earthworms, bacterial culture and formulated soil. SBT reduces the level of various pollutants in industrial wastewater viz. biological oxygen demand, chemical oxygen demand, ammonium nitrate, phosphates, nitrogen, suspended solids, odour, colour and other undesired organisms. This review briefly discusses the need for sustainable development in treatment of wastewater. It also provides an updated scientific literature on zero liquid discharge systems in industries including challenges and perspectives

    Common variants in CLDN2 and MORC4 genes confer disease susceptibility in patients with chronic pancreatitis

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    A recent Genome-wide Association Study (GWAS) identified association with variants in X-linked CLDN2 and MORC4 and PRSS1-PRSS2 loci with Chronic Pancreatitis (CP) in North American patients of European ancestry. We selected 9 variants from the reported GWAS and replicated the association with CP in Indian patients by genotyping 1807 unrelated Indians of Indo-European ethnicity, including 519 patients with CP and 1288 controls. The etiology of CP was idiopathic in 83.62% and alcoholic in 16.38% of 519 patients. Our study confirmed a significant association of 2 variants in CLDN2 gene (rs4409525—OR 1.71, P = 1.38 x 10-09; rs12008279—OR 1.56, P = 1.53 x 10-04) and 2 variants in MORC4 gene (rs12688220—OR 1.72, P = 9.20 x 10-09; rs6622126—OR 1.75, P = 4.04x10-05) in Indian patients with CP. We also found significant association at PRSS1-PRSS2 locus (OR 0.60; P = 9.92 x 10-06) and SAMD12-TNFRSF11B (OR 0.49, 95% CI [0.31–0.78], P = 0.0027). A variant in the gene MORC4 (rs12688220) showed significant interaction with alcohol (OR for homozygous and heterozygous risk allele -14.62 and 1.51 respectively, P = 0.0068) suggesting gene-environment interaction. A combined analysis of the genes CLDN2 and MORC4 based on an effective risk allele score revealed a higher percentage of individuals homozygous for the risk allele in CP cases with 5.09 fold enhanced risk in individuals with 7 or more effective risk alleles compared with individuals with 3 or less risk alleles (P = 1.88 x 10-14). Genetic variants in CLDN2 and MORC4 genes were associated with CP in Indian patients

    HIV-1 gp120 Induces Expression of IL-6 through a Nuclear Factor-Kappa B-Dependent Mechanism: Suppression by gp120 Specific Small Interfering RNA

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    In addition to its role in virus entry, HIV-1 gp120 has also been implicated in HIV-associated neurocognitive disorders. However, the mechanism(s) responsible for gp120-mediated neuroinflammation remain undefined. In view of increased levels of IL-6 in HIV-positive individuals with neurological manifestations, we sought to address whether gp120 is involved in IL-6 over-expression in astrocytes. Transfection of a human astrocyte cell line with a plasmid encoding gp120 resulted in increased expression of IL-6 at the levels of mRNA and protein by 51.3±2.1 and 11.6±2.2 fold respectively; this effect of gp120 on IL-6 expression was also demonstrated using primary human fetal astrocytes. A similar effect on IL-6 expression was observed when primary astrocytes were treated with gp120 protein derived from different strains of X4 and R5 tropic HIV-1. The induction of IL-6 could be abrogated by use of gp120-specific siRNA. Furthermore, this study showed that the NF-κB pathway is involved in gp120-mediated IL-6 over-expression, as IKK-2 and IKKβ inhibitors inhibited IL-6 expression by 56.5% and 60.8%, respectively. These results were also confirmed through the use of NF-κB specific siRNA. We also showed that gp120 could increase the phosphorylation of IκBα. Furthermore, gp120 transfection in the SVGA cells increased translocation of NF-κB from cytoplasm to nucleus. These results demonstrate that HIV-1 gp120-mediated over-expression of IL-6 in astrocytes is one mechanism responsible for neuroinflammation in HIV-infected individuals and this is mediated by the NF-κB pathway
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