FORMULATION AND EVALUATION OF LIQUISOLID COMPACTS OF LORNOXICAM

Objective: Objective of the present investigation was to enhance the solubility and dissolution rate of poorly water-soluble drug lornoxicam using liquisolid technique with comparative determination of in vitro release profile of liquisolid compacts and conventional formulation of lornoxicam. Methods: Formulation was prepared by a liquisolid technique using different drug concentration in a liquid vehicle and different carrier/coating ratio. Prepared liquisolid compact was evaluated for Fourier transform infrared (FTIR) spectra analysis, differential scanning calorimetry (DSC), X-ray diffraction (P-XRD), scanning electron microscopy (SEM) and in vitro dissolution study. Results: The result showed that liquisolid compacts of lornoxicam displayed significantly higher drug release rate as compared to pure drug and conventional tablet prepared. The results of both DSC and X-ray crystallography indicated loss of crystallinity of the drug upon formulated into the liquisolid compact. Conclusion: Dissolution rate of the drug from liquisolid compacts was affected by changing the drug concentration and excipient ratio. The liquisolid technique appeared to be a promising approach for improving the dissolution of poorly soluble drug lornoxicam

Utility of serum lactate dehydrogenase in the diagnosis of megaloblastic anemia

Background: Megaloblastc anemia corresponds to severe macrocytic anemia with hypersegmented neutrophils and very high serum Lactate Dehydrogenase (LDH). The present study was undertaken to evaluate the utility of serum LDH and chloroform inhibited serum LDH in the diagnosis of megaloblastic anemia and to observe if this can be used to differentiate megaloblastic anemia from iron deficiency anemia and hemolytic anemia.Methods: The present study was carried out on 75 patients of anemia categorised on bone marrow examination (into megaloblastic and non-megaloblastic anaemia) to evaluate the efficacy of total serum LDH levels and LDH isoenzyme pattern in the diagnosis of megaloblastic anemia. About 25 healthy adults were taken as controls.Results: In megaloblastic anemia, total serum LDH level was found to be increased to about nineteen folds and in hemolytic anemia it was found to increased four folds as compared to normal. On statistical analysis this increased total serum LDH level in megaloblastic anemia and hemolytic anemia as compared to control group was found to be significant.In the present study serum LDH level above 3000IU/L was associated with megaloblastic anemia and serum LDH level below 900IU/L was suggestive of iron deficiency anemia. The chloroform inhibition test was less than 25% in megaloblastic anemia and more than 25% in hemolytic anemia and these differences were found to be statistically significant (t=9.62, df=49, pLDH2) by chloroform inhibition test is an adjuvant in the diagnosis where total serum LDH levels are between 451-3000IU/L and can also differentiate megaloblastic anemia from hemolytic anemia

Bromo-butyl Rubber for Face Piece of a Respiratory Mask

Respiratory mask contains a number of components made of materials like rubber, plastics, and metals. Out of all the components, face piece is the main component exposed to the external environment. This study aims to evaluate degradation of bromo-butyl rubber. The experiments were carried out for thermal exposure, swelling study, saline exposure, etc. It is observed that the elongation at break was increased by 10 per cent when these were exposed to 100 oC. However, the tensile strength has been observed to decrease by 50 per cent when exposed to 55 oC. It is decreased to around 63 per cent when exposed to 80 oC and 100 oC. The morphological appearance of unaged sample was intact. Only samples at 120 oC aged for 48 h appeared to have developed minor cracks of <0.01 µm. There were no significant changes observed when the samples were exposed to saline (3 % NaCl) and artificial sweat solution.Defence Science Journal, 2009, 59(5), pp.505-511, DOI:http://dx.doi.org/10.14429/dsj.59.155

Search and analysis of giant radio galaxies with associated nuclei (SAGAN) -- I : New sample and multi-wavelength studies

We present the first results of a project called SAGAN, which is dedicated solely to the studies of relatively rare megaparsec-scale radio galaxies in the Universe, called giant radio galaxies (GRGs). We have identified 162 new GRGs primarily from the NVSS with sizes ranging from ~0.71 Mpc to 2.82 Mpc in the redshift range of ~0.03 - 0.95, of which 23 are hosted by quasars (giant radio quasars, GRQs). As part of the project SAGAN, we have created a database of all known GRGs, the GRG catalogue, from the literature (including our new sample); it includes 820 sources. For the first time, we present the multi-wavelength properties of the largest sample of GRGs. Our results establish that the distributions of the radio spectral index and the black hole mass of GRGs do not differ from the corresponding distributions of normal-sized radio galaxies (RGs). However, GRGs have a lower Eddington ratio (ER) than RGs. Using the mid-infrared data, we classified GRGs in terms of their accretion mode: either a high-power radiatively efficient high-excitation state, or a radiatively inefficient low-excitation state. We find that GRGs in high-excitation state statistically have larger sizes, stronger radio power, jet kinetic power, and higher ER than those in low-excitation state. Our analysis reveals a strong correlation between the ER and the scaled jet kinetic power, which suggests a disc-jet coupling. Our environmental study reveals that ~10% of all GRGs may reside at the centres of galaxy clusters, in a denser galactic environment, while the majority appears to reside in a sparse environment. We find that the probability of BCG as a GRG is quite low. We present new results for GRGs that range from black hole mass to large-scale environment properties. We discuss their formation and growth scenarios, highlighting the key physical factors that cause them to reach their gigantic size. Abridged.Comment: Accepted for publication in Astronomy & Astrophysics. 14 figures, 7 tables and 7 montages. Comments are welcome. "SAGAN Project website https://sites.google.com/site/anantasakyatta/sagan

Acute stress impairs sensorimotor gating via the neurosteroid allopregnanolone in the prefrontal cortex

Ample evidence indicates that environmental stress impairs information processing, yet the underlying mechanisms remain partially elusive. We showed that, in several rodent models of psychopathology, the neurosteroid allopregnanolone (AP) reduces the prepulse inhibition (PPI) of the startle, a well-validated index of sensorimotor gating. Since this GABAA receptor activator is synthesized in response to acute stress, we hypothesized its participation in stress-induced PPI deficits. Systemic AP administration reduced PPI in C57BL/6J mice and Long-Evans, but not Sprague-Dawley rats. These effects were reversed by isoallopregnanolone (isoAP), an endogenous AP antagonist, and the GABAA receptor antagonist bicuculline and mimicked by AP infusions in the medial prefrontal cortex (mPFC). Building on these findings, we tested AP's implication in the PPI deficits produced by several complementary regimens of acute and short-term stress (footshock, restraint, predator exposure, and sleep deprivation). PPI was reduced by acute footshock, sleep deprivation as well as the combination of restraint and predator exposure in a time- and intensity-dependent fashion. Acute stress increased AP concentrations in the mPFC, and its detrimental effects on PPI were countered by systemic and intra-mPFC administration of isoAP. These results collectively indicate that acute stress impairs PPI by increasing AP content in the mPFC. The confirmation of these mechanisms across distinct animal models and several acute stressors strongly supports the translational value of these findings and warrants future research on the role of AP in information processing

Online Databases Backbone for Teaching and Research: Case Study of Rajarambapu Institute of Technology, affiliated to Shivaji University, Kolhapur, Maharashtra (India)

The library facilities and services have changed during the pandemic from both the librarians’ and library users’ points of view. Research and academic communication disseminated via emerging online databases and resulted in creating awareness and utilization of electronic resources remotely. The present study investigates the availability, awareness, and use of online databases subscribed from direct publishers and also accessed from Shivaji University, Kolhapur, India, under the INFEED project by Rajarambapu Institute of Technology (RIT) staff members and students during the lockdown period. A mixed research approach (i.e. quantitative and qualitative) has been applied by using an online questionnaire as a data collection tool. Total 128 filled questionnaires were received with an 85.3 percent response rate, and it is found to be valid for analysis. More than 90 percent of the respondents were aware of the Online Databases. Science Direct is a highly used database by 50 percent of the users, majority i. e. 75 percent of the respondents use E-books as a source of information from an online database. The study also found some problems faced by the respondents, such as network problems, technical problems, lack of guidance, etc. Finally, the study made it very clear that most of the users are satisfied with the Online Databases provided by the institutional library

A detailed study of giant pulses from PSR B1937-1-21 using the Large European Array for Pulsars

Contains fulltext : 202558.pdf (Publisher’s version ) (Open Access

Urine Biomarkers of Risk in the Molecular Etiology of Breast Cancer

Endogenous estrogens can be bio-activated to endogenous carcinogens via formation of estrogen quinones. Estrogen-3,4-quinones react with DNA to form mutagenic depurinating estrogen-DNA adducts. The carcinogenicity of endogenous estrogens is related to unbalanced estrogen metabolism leading to excess estrogen quinones and formation of depurinating DNA adducts. The present studies were initiated to confirm that relatively high levels of depurinating estrogen-DNA adducts are present in women at high risk for breast cancer or diagnosed with the disease. These adducts may be biomarkers for early detection of breast cancer risk. The estrogen metabolites, conjugates and depurinating DNA adducts were identified and quantified by using ultraperformance liquid chromatography/tandem mass spectrometry to analyze urine samples from 40 healthy control women, 40 high-risk women and 40 women with newly diagnosed breast cancer. Estrogen metabolism was shifted from protective methoxylation and conjugation pathways in healthy control women towards activating pathways leading to formation of depurinating DNA adducts in women at high risk or with breast cancer. These results support the hypothesis that breast cancer is initiated by mutations derived from depurination of estrogen-DNA adducts. Therefore, relative levels of depurinating estrogen-DNA adducts could become biomarkers for early detection of breast cancer risk and aid in determining preventive strategies

Analytical Method Development of Saxagliptin HCl by RP-HPLC

Reversed-phase chromatography is the mainly used in chromatographic mode, it is used to separate neutral molecules in solution based on their hydrophobicity. This technique is the reverse of normal-phase chromatography in the intelligence that it involves the employ of a polar mobile phase and a non-polar stationary phase. A sensitive, accurate, rapid, cost effective and robust HPLC method was developed for the quantification of Saxagliptin Hydrochloride (SGH) with UV detector. In this method, a reversed-phase Grace C18 (250mm x 4.6ID, Particle size: 5 micron) column with a mobile phase of methanol: water (80:20; v/v) at 0.8ml/min flow rate was used to separate SGH with a detection of 212nm.The volume injected was 20 µL. The retention time of SGH was obtained as 4.196 min. Hence it can be applied for routine analysis of Saxagliptin Hydrochloride (SGH) in bulk drug. Keywords: Saxagliptin Hydrochloride (SGH), RP-HPLC, Assay, Method validation

Solubility Enhancment of Azithromycin by Solid Dispersion Method by using Polymer PVP K 90

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