2,820 research outputs found

    Water quality indices and abiotic characteristics of western Yamuna canal in Yamunanagar, Haryana

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    The present paper deals with the monthly variations of physico-chemical characteristics of western Yamuna canal water, Yamunanagar which is polluted with industrial effluents and domestic sewage. Three sampling points i.e. station-1: Upstream of the river; station-2: Point of influx of industrial effluents and domestic sewage; Station-3: About 6 kms downstream from station 2 were selected for the investigation. Studies revealed high values of turbidity, conductivity, free CO2, alkalinity, calcium, hardness, magnesium, chloride, orthophosphate, phosphate, sulphate and ammonia and low values of DO at station-2. The differences in various parameters were statistically significant (P<0.05) when compared from upstream and downstream stretches of the river particularly in summer. DO and BOD were found to be two important parameters which showed strong correlation with other parameters and hence can serve as good indices of river water quality. Water Quality index designated station-1 as highly polluted and station-2 and 3 as severely polluted. Thus the hydro biological conditions were not congenial/ optimum for the survival/ production of sensitive fish fauna, therefore, proper and efficient treatment of the effluents and sewage should be carried out before discharging these into the canal

    Hospital Wastewater Sludge: An Unaddressed Environmental Reservoir for Emerging and Rare Nosocomial Pathogens

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    Nosocomial infections cause significant mortality and financial losses each year. Most of these infections are caused by multidrug resistant (MDR) opportunistic pathogens and therefore are difficult to treat by standard therapies. Though hospitals are considered as ecological niches for nosocomial pathogens, environmental reservoirs for the same are still underexplored. The present study addressed this issue by systematically profiling the pathogenic diversity of hospital wastewater sludge hypothesized as an important reservoir for nosocomial pathogens within a hospital setting using Illumina Miseq Next Generation Sequencing (NGS) approach. The NGS data showed that i) nosocomial pathogens dominated the hospital sludge bacterial profile and majority of them fell in the category of either emerging or rare pathogens ii) Majority of the pathogens formed part of the low abundant microbiota represented by 3.56% of the reads iii) Nearly 14% of the reads were represented by the unculturable bacteria iv) Of the 580 species-level operational taxonomic units (OTUs) identified in this study, 166 matched with potential human pathogens v) Enterobacter cloacae (56.45%) was the most dominant species followed by  Pseudomonas putida (6.07%), Fusobacterium ulcerans (3.08%) Acidaminococcus fermentans (2.03%) respectively. Aeromonas hydrophila, Klebsiella pneumoniae and Pantoea agglomerans formed the less dominant species. This study points towards the catastrophic effect on public health and environment that may result from the co-treatment of hospital wastewater with domestic wastewater in municipal wastewater treatment plants and the use of resultant sludge in agriculture which is a common method of sludge disposal practiced in developing countries. Keywords: Hospital sludge, Next Generation Sequencing, Nosocomial Pathogens, Emerging Pathogens, Rare Pathogens &nbsp

    Clinico-Epidemiological Profile and Utility of Diagnostic Techniques in Immunocompetent Children with Cryptosporidium Diarrhoea

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    Purpose: To assess the Clinical and Epidemiological profile of children 6 months to 5 years having Cryptosporidium diarrhoea and to compare the diagnostic accuracy of rapid diagnostic test (RDT) against modified acid-fast stain technique to detect Cryptosporidium in stool. Materials and Methods: Details of demography, presenting complaints, and detailed examination of children presenting with acute or persistent diarrhoea were recorded in a predesigned proforma. Two Stool samples were collected and examined same day by rapid antigen test and microscopy for presence of antigen or oocyst of cryptosporidium. Results: Out of the total of 280 samples tested, 40 (14.3%) samples were positive for Cryptosporidium. The prevalence of Cryptosporidium in children presenting with diarrhoea in our study came out to be 14.3%. Fever, vomiting and pain abdomen were the most common presenting complaints. Epidemiological factors like providing clean water, proper feeding and hygiene, and avoidance of overcrowding can help in reducing the burden of Cryptosporidium diarrhoea. Persistent diarrhoea was more common among cryptosporidium positive cases. Rapid detection kits enhance the detection rate and are sensitive as well as specific. It could be utilised as an aid in diagnosis of Cryptosporidium diarrhoea. Conclusion: The study shows that cryptosporidial diarrhoea is not uncommon in immunocompetent children. Improvement in personal hygiene, feeding practices and access to safe and potable water can help in reducing burden of this disease. Antigen detection kits aid in early diagnosis. Keywords: Paediatric cryptosporidiosis, Persistent diarrhoea, Sanitation, RDT in diarrhoea, Abdominal pai

    DEVELOPMENT AND EVALUATION OF FREEZING RESISTANT INTRAVENOUS FLUID

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    Objectives: Hemorrhagic or hypovolemic shocks accounts for a large portion of civilian and military trauma deaths due to life-threatening blood loss which requires intravenous fluid infusion to prevent essential deficiencies of fluids. However, at low temperature (-150C) fluid bottles freeze out and can not be used in emergency. In view of that, objective of the present work is to develop a freezing resistant intravenous formulation (FRIV) and its in vivo safety and efficacy evaluation. Methods: FRIV formulations were developed using standardized ringer lactate (RL) formulation protocol, in which varying concentrations of ethanol and glycerol were added to induce desired physiochemical properties. Efficacy of FRIV was evaluated in terms of survival percentage of hemorrhagic animal models (Swiss albino strain mice). Acute toxicity studies were carried out through an infusion at dose levels (0, 20 and 40 ml/Kg b. wt.). Results: In vitro data showed that optimized FRIV (F-10) takes more time (360 ± 21 min) for freezing and less time in thawing (50 ± 4.50 min) in comparison to control which takes (110 ± 15 min) in freezing and (80 ± 7.25 min) in thawing. Formulations were found to be stable and sterile up to six months. In vivo efficacy data showed ≥ 75% survival in animals infused with FRIV as compared to control group in hemorrhagic animal models and no treatment related toxic effects of optimized formulation in terms of hematological, serum biochemistry and histopathological analysis. Conclusion: Pre-clinical safety and efficacy data of the present study indicated that developed FRIV formulation could be used for fluid recovery during the hemorrhagic shocks conditions in the combat scenario

    Economic evaluation of shortened, bedaquiline-containing treatment regimens for rifampicin-resistant tuberculosis (STREAM stage 2): a within-trial analysis of a randomised controlled trial

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    BACKGROUND: The STREAM stage 2 trial assessed two bedaquiline-containing regimens for rifampicin-resistant tuberculosis: a 9-month all-oral regimen and a 6-month regimen containing an injectable drug for the first 2 months. We did a within-trial economic evaluation of these regimens. METHODS: STREAM stage 2 was an international, phase 3, non-inferiority randomised trial in which participants with rifampicin-resistant tuberculosis were randomly assigned (1:2:2:2) to the 2011 WHO regimen (terminated early), a 9-month injectable-containing regimen (control regimen), a 9-month all-oral regimen with bedaquiline (oral regimen), or a 6-month regimen with bedaquiline and an injectable for the first 2 months (6-month regimen). We prospectively collected direct and indirect costs and health-related quality of life data from trial participants until week 76 of follow-up. Cost-effectiveness of the oral and 6-month regimens versus control was estimated in four countries (oral regimen) and two countries (6-month regimen), using health-related quality of life for cost-utility analysis and trial efficacy for cost-effectiveness analysis. This trial is registered with ISRCTN, ISRCTN18148631. FINDINGS: 300 participants were included in the economic analyses (Ethiopia, 61; India, 142; Moldova, 51; Uganda, 46). In the cost-utility analysis, the oral regimen was not cost-effective in Ethiopia, India, Moldova, and Uganda from either a provider or societal perspective. In Moldova, the oral regimen was dominant from a societal perspective. In the cost-effectiveness analysis, the oral regimen was likely to be cost-effective from a provider perspective at willingness-to-pay thresholds per additional favourable outcome of more than US4500inEthiopia,4500 in Ethiopia, 1900 in India, 3950inMoldova,and3950 in Moldova, and 7900 in Uganda, and from a societal perspective at thresholds of more than 15900inEthiopia,15 900 in Ethiopia, 3150 in India, and 4350inUganda,whileinMoldovatheoralregimenwasdominant.InEthiopiaandIndia,the6monthregimenwouldcosttuberculosisprogrammesandparticipantslessthanthecontrolregimenandwashighlylikelytobecosteffectiveinbothcostutilityanalysisandcosteffectivenessanalysis.Reducingthebedaquilinepricefrom4350 in Uganda, while in Moldova the oral regimen was dominant. In Ethiopia and India, the 6-month regimen would cost tuberculosis programmes and participants less than the control regimen and was highly likely to be cost-effective in both cost-utility analysis and cost-effectiveness analysis. Reducing the bedaquiline price from 1·81 to $1·00 per tablet made the oral regimen cost-effective in the provider-perspective cost-utility analysis in India and Moldova and dominate over the control regimen in the provider-perspective cost-effectiveness analysis in India. INTERPRETATION: At current costs, the oral bedaquiline-containing regimen for rifampicin-resistant tuberculosis is unlikely to be cost-effective in many low-income and middle-income countries. The 6-month regimen represents a cost-effective alternative if injectable use for 2 months is acceptable. FUNDING: USAID and Janssen Research & Development

    Chemoenzymatic synthesis, nanotization and anti- aspergillus activity of optically enriched fluconazole analogues

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    Despite recent advances in diagnostic and therapeutic advances in antifungal research, aspergillosis still remains a leading cause of morbidity and mortality. One strategy to address this problem is to enhance the activity spectrum of known antifungals, and we now report the first successful application of Candida antarctica lipase (CAL) for the preparation of optically enriched fluconazole analogs. Anti-Aspergillus activity was observed for an optically enriched derivative, (-)-S-2-(2’ ,4’ -difluorophenyl)-1-hexyl-amino-3-(1‴,2‴,4‴) triazol-1‴-yl-propan-2-ol, which exhibits MIC values of 15.6 μg/mL and 7.8 μg/disc in microbroth dilution and disc diffusion assays, respectively. This compound is tolerated by mammalian erythrocytes and cell lines (A549 and U87) at concentrations of up to 1000 μg/mL. When incorporated into dextran nanoparticles, the novel, optically enriched fluconazole analog exhibited improved antifungal activity against Aspergillus fumigatus (MIC = 1.63 μg/mL). These results not only demonstrate the ability of biocatalytic approaches to yield novel, optically enriched fluconazole derivatives but also suggest that enantiomerically pure fluconazole derivatives, and their nanotised counterparts, exhibiting anti-Aspergillus activity may have reduced toxicity

    Constraints on the χ_(c1) versus χ_(c2) polarizations in proton-proton collisions at √s = 8 TeV

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    The polarizations of promptly produced χ_(c1) and χ_(c2) mesons are studied using data collected by the CMS experiment at the LHC, in proton-proton collisions at √s=8  TeV. The χ_c states are reconstructed via their radiative decays χ_c → J/ψγ, with the photons being measured through conversions to e⁺e⁻, which allows the two states to be well resolved. The polarizations are measured in the helicity frame, through the analysis of the χ_(c2) to χ_(c1) yield ratio as a function of the polar or azimuthal angle of the positive muon emitted in the J/ψ → μ⁺μ⁻ decay, in three bins of J/ψ transverse momentum. While no differences are seen between the two states in terms of azimuthal decay angle distributions, they are observed to have significantly different polar anisotropies. The measurement favors a scenario where at least one of the two states is strongly polarized along the helicity quantization axis, in agreement with nonrelativistic quantum chromodynamics predictions. This is the first measurement of significantly polarized quarkonia produced at high transverse momentum
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