Is the Market Efficiency Static or Dynamic – Evidence from Colombo Stock Exchange (CSE)

The study tests the weak form efficiency of the Colombo Stock Exchange (CSE) and the consistency of the concept. In this study, daily market closing index values of (All Share Price Index) ASPI of CSE for five years, from June 2010 to June 2015, without adjustments, have been selected as the sample. Both parametric tests and non-parametric tests have been used in this study. The evidence presented in this study confirms that CSE is not weak form efficient within the sample period and is consistent with the findings of previous studies. Therefore, the fact that Efficient Market Hypothesis as a dynamic concept is debatable as studies over the past have consistently confirmed that CSE is not in weak form efficient, although the efficiency of most markets is dynamic.  </p

Community-based interventions for the prevention and control of cutaneous leishmaniasis: A systematic review

We reviewed the evidence on community-based interventions for the prevention and control of cutaneous leishmaniasis (CL). Community initiatives tailored towards awareness and mobilisation are regarded as a priority area in the Neglected Tropical Disease Roadmap 2021–2030 by the World Health Organization. We searched nine electronic databases for intervention-based studies. Two independent reviewers screened and assessed the articles for methodological quality using predefined criteria. We conducted a meta-analysis using a random effects model, along with narrative synthesis. Thirteen articles were eligible for inclusion, of which 12 were quantitative studies (quasi-experimental with control group and pre-post interventions) and one qualitative study. All articles reported on health education interventions aimed at changing people’s knowledge, attitudes, and practices (KAP) in relation to CL. Participant groups included students, mothers, housewives, volunteer health workers, and residents in general. An increased score was recorded for all outcomes across all interventions: knowledge (SMD: 1.85, 95% CI: 1.23, 2.47), attitudes (SMD: 1.36, 95% CI: 0.56, 2.15), and practices (SMD: 1.73, 95% CI: 0.99, 2.47). Whilst our findings show that educational interventions improved people’s knowledge, attitudes, and practices about CL, we argue that this approach is not sufficient for the prevention and control of this disease. Knowledge does not always translate into action, particularly where other structural barriers exist. Therefore, we recommend the design of more innovative community-based interventions with a broader focus (e.g., stigma, financial barriers, and healthcare access)

Sustainable High-Performance Hydraulic Concrete

Concrete has always been indispensable as a material for the engineering and construction of hydraulic structures (e [...]</jats:p

Effectiveness of Cutting-Edge Technology for Library Management System

With technology advancing, manual systems must be converted to user friendly automated system. Researchers have designed the Library Management System to transfer the physical view of libraries into a digital view. This project offers knowledge on creating and putting in place an LMS. In traditional library system people have to search for a particular book from shelf to shelf which is a tedious and time-consuming work. It can be more cumbersome if the library hasn’t a properly maintained library system. The manual system isn’t user-friendly not only for the borrowers but also for librarians. They have to keep an eye on each and every book lending and borrowing. And They occasionally have to arrange and classify the books. The process of creating reports and analyzing data is also highly laborious. LMS assists the librarians for all these tasks. They can simply view, update, delete, read books and articles to manage the resources. Readers don’t have to stand in long queues and no need of going around to read a book. They can read a book just by clicking a single button. The full system is designed using MERN stack, with the aid of JWT authentications and JOY dependency validations

Immunohistochemical detection of Claudin low breast cancer; which subcellular level to be assessed?

Objectives: Claudin low breast cancers are often high grade, triple negative tumours with poor prognosis.  They are identified at genetic level and are not diagnosed routinely by immunohistochemistry. The objective was to determine the best subcellular level to detect Claudin low breast cancer by immunohistochemistry, in terms of their histopathological prognostic features.Methods: This cross sectional study included all archival breast cancer tissue collected up to December 2015 in our unit. Tissue microarrays (TMA) were constructed using 23 breast cancer cores with a diameter of 2mm, in each TMA. TMAs were immunohistochemically stained for Claudin 3 expression and was scored as; no staining=0, weak staining=1, moderate staining=2 and strong staining=3, separately for membrane, cytoplasmic and nuclear staining. A score <2 was considered Claudin low and analysed against the histopathological prognostic features of the breast cancer.Results: A total of 546 breast cancers were assessed. Claudin low expression was identified at cytoplasmic, membrane and nuclear level in 74.9%, 74.5% and 42% of breast cancers respectively. Low nuclear expression of Claudin 3 was associated with high grade (p=0.028), Nottingham Prognostic Index of >3.4 (p=0.028), ER and PR negative (p<0.001) and HER 2 negative (p=0.013) tumours while low membrane staining was associated with low grade (p=0.038), HER 2 negative (p<0.001) breast cancers. Low cytoplasmic staining was associated with HER 2 negative breast cancer only (p=0.002).Conclusions: Nuclear staining for Claudin should be assessed to identify Claudin low breast cancer by immunohistochemistry as it significantly associates with most of the Claudin low breast cancer characteristics

IEA SHC Task 42 / ECES Annex 29 WG A1: Engineering and Processing of PCMs, TCMs and Sorption Materials

An overview on the recent results on the engineering and characterization of sorption materials, PCMs and TCMs investigated in the working group WG A1 "Engineering and processing of TES materials" of IEA SHC Task 42 / ECES Annex 29 (Task 4229) entitled "Compact Thermal Energy Storage" is presented

Human stomach microbiota: Effects on health and disease

The gut microbiota is a complex ecological community, consisting of trillions of microbes which include bacteria, viruses, fungi and protozoa. The stomach was previously considered as a sterile site uninhabited by microbes due to its hostile environmental conditions. Breaking this concept, Helicobacter pylori was the first pathogen reported to inhabit the stomach. Recent studies have suggested that the stomach harbours transient as well as certain commensal bacterial and fungal species. The five major microbial phyla in the stomach have been identified as Firmicutes, Bacteroidetes, Actinobacteria, Fusobacteria and Proteobacteria. The composition of gastric microbiota is dynamic and is affected by several factors.  These include age group, dietary habits, medication use, inflammation of gastric mucosa and H. pylori colonization.  Further, the role of host genetics has recently been studied in maintaining the stomach microbiota. Mutations in host genes may affect the host’s immune response towards commensal bacteria and reduce their number and diversity. The essential multiple roles of gut microorganisms include maintaining homeostasis in the gut, contributing to immune function and extraction of nutrients and energy from our diets.  Loss of the normal balance between the gut microbiota and host has been associated with several abnormal conditions and disorders such as obesity, malnutrition, inflammatory bowel diseases (IBD), neurological disorders, and cancer. In the stomach, the interaction between H. pylori and the gastric microbiota can also influence gastric dis­ease progression. Further studies should focus on addressing the role of gastric dysbiosis in health and disease. Identifying gastric microbiota is essential to understand how the gut microbiota and H. pylori affect health and disease.</p

Formation of Human Colonic Crypt Array by Application of Chemical Gradients Across a Shaped Epithelial Monolayer

Background & Aims The successful culture of intestinal organoids has greatly enhanced our understanding of intestinal stem cell physiology and enabled the generation of novel intestinal disease models. Although of tremendous value, intestinal organoid culture systems have not yet fully recapitulated the anatomy or physiology of the in vivo intestinal epithelium. The aim of this work was to re-create an intestinal epithelium with a high density of polarized crypts that respond in a physiologic manner to addition of growth factors, metabolites, or cytokines to the basal or luminal tissue surface as occurs in vivo. Methods A self-renewing monolayer of human intestinal epithelium was cultured on a collagen scaffold microfabricated with an array of crypt-like invaginations. Placement of chemical factors in either the fluid reservoir below or above the cell-covered scaffolding created a gradient of that chemical across the growing epithelial tissue possessing the in vitro crypt structures. Crypt polarization (size of the stem/proliferative and differentiated cell zones) was assessed in response to gradients of growth factors, cytokines, and bacterial metabolites. Results Chemical gradients applied to the shaped human epithelium re-created the stem/proliferative and differentiated cell zones of the in vivo intestine. Short-chain fatty acids applied as a gradient from the luminal side confirmed long-standing hypotheses that butyrate diminished stem/progenitor cell proliferation and promoted differentiation into absorptive colonocytes. A gradient of interferon-γ and tumor necrosis factor-α significantly suppressed the stem/progenitor cell proliferation, altering crypt formation. Conclusions The in vitro human colon crypt array accurately mimicked the architecture, luminal accessibility, tissue polarity, cell migration, and cellular responses of in vivo intestinal crypts

TiO2 21 nm nanoparticles as a photocatalytic antimicrobial agent against Escherichia coli, Candida albicans and Methicillin resistant Staphylococcus aureus: A comparison

 Objectives: To determine and compare the antimicrobial activity of 21 nm TiO2 nanoparticles against Escherichia colii, Candida albicans and Methicillin resistant Staphylococcus aureus (MRSA).Methods: Titanium dioxide (TiO2) 21 nm anatase nanoparticles (13.9 g/l) were suspended in miliQ (MQ) water, sonicated (35 MHz for 1 hour) and autoclaved. Sterile glass petriplates were treated with TiO2 suspension or sterile MQ(control). Overnight cultures of E.coli MRSA and C. albicans were added to TiO2 coated plates and control plates and kept at room temperature.   Viable counts were obtained by spread plate method at 0 hours and 24 hours; before and after sunlight exposure for 30 minutes.  Colony forming units (CFU) / ml was calculated to determine percentage reduction of CFU in presence of TiO2. Experiments were done in triplicates.Results: TiO2 nanoparticles demonstrated antimicrobial activity against E.coli, MRSA and C. albicans. Estimated percentage CFU reduction in E.coli (13±8.4), MRSA (12±6.6) and C. albicans (36±4.9 ) was observed at 0 hours of contact in the supernatant. The bactericidal effect was enhanced on exposure of the plates to sunlight. Estimated percentage CFU reductions are E. coli (46±7.9), MRSA (99±0.2 ) and C. albicans (99±0.4). The results for 24 hours were (95±1 ), (35±2.1 ) and (83±4 ) reduction for E. coli, MRSA and C. albicans respectively. When the 24 hour plates were exposed to sunlight (99±0.6), (99±0.6) and (99±0.2) reduction was seen for E.coli, MRSA and C. albicans respectively. Conclusion: Anatase 21 nm TiO2 nanoparticles show enhanced antimicrobial activity against the tested microbial strains following photoactivation by sunlight.  Antimicrobial activity against three different types of microbial strains has varying effects

An Integrated Microfluidic Device for Monitoring Changes in Nitric Oxide Production in Single T-Lymphocyte (Jurkat) Cells

A considerable amount of attention has been focused on the analysis of single cells in an effort to better understand cell heterogeneity in cancer and neurodegenerative diseases. Although microfluidic devices have several advantages for single cell analysis, few papers have actually demonstrated the ability of these devices to monitor chemical changes in perturbed biological systems. In this paper, a new microfluidic channel manifold is described that integrates cell transport, lysis, injection, electrophoretic separation, and fluorescence detection into a single device, making it possible to analyze individual cells at a rate of 10 cells/min in an automated fashion. The system was employed to measure nitric oxide (NO) production in single T-lymphocytes (Jurkat cells) using a fluorescent marker, 4-amino-5-methylamino-2',7'-difluorofluorescein diacetate (DAF-FM DA). The cells were also labeled with 6-carboxyfluorescein diacetate (6-CFDA) as an internal standard. The NO production by control cells was compared to that of cells stimulated using lipopolysaccharide (LPS), which is known to cause the expression of inducible nitric oxide synthase (iNOS) in immune-type cells. Statistical analysis of the resulting electropherograms from a population of cells indicated a twofold increase in NO production in the induced cells. These results compare nicely to a recently published bulk cell analysis of NO