Physico-chemical Properties of Chloramine-T: Part III- Conductometric Study of the Interaction of Chloramine-T with Th(IV) & Zr(IV) Solutions

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A multicomponent model of the infrared emission from Comet Halley

A model based on a mixture of coated silicates and amorphous carbon grains produces a good spectral match to the available Halley data and is consistent with the compositional and morphological information derived from interplanetary dust particle studies and Halley flyby data. The dark appearance of comets may be due to carbonaceous coatings on the dominant (by mass) silicates. The lack of a 10 micrometer feature may be due to the presence of large silicate grains. The optical properties of pure materials apparently are not representative of cometary materials. The determination of the optical properties of additional silicates and carbonaceous materials would clearly be of use

Interaction of membrane-spanning proteins with peripheral and lipid-anchored membrane proteins: perspectives from protein- lipid interactions (Review)

Studies of lipid-protein interactions in double-reconstituted systems involving both integral and peripheral or lipid- anchored proteins are reviewed. Membranes of climyristoyl phosphatidylglycerol containing either myelin proteolipid protein or cytochrome c oxidase were studied. The partner peripheral proteins bound to these membranes were myelin basic protein or cytochrome c, respectively. In addition, the interactions between the myelin proteolipid protein and avidin that was membrane-anchored by binding to N-biotinyl phosphatidylethanolamine were studied in dimyristoyl phosphatidylcholine membranes. Steric exclusion plays a significant role when sizes of the peripheral protein and transmembrane domain of the integral protein are comparable. Even so, the effects on avidin-linked lipids are different from those induced by myelin basic protein on freely diffusible lipids, both interacting with the myelin proteolipid protein. Both the former and the cytochrome c/cytochrome oxidase couple evidence a propagation of lipid perturbation out from the intramembrane protein interface that could be a basis for formation of microdomains

Cosmic ray produced Mg<SUP>28</SUP>, Si<SUP>31</SUP>, S<SUP>38</SUP>, C<SUP>l38</SUP>, Cl<SUP>34m</SUP> and other short-lived radioisotopes in wet precipitation

The concentrations of seven radioisotopes, expected to be produced in the troposphere by interactions of secondary cosmic rays with atmospheric nuclei, have been measured in "fresh" rain collections. The half-lives of these isotopes range from about half an hour to a day. The procedures developed for rapid, specific and sensitive analyses of these nuclides are discussed. Detection of two of the isotopes studied, Cl39 (half-life: 55 mins.) and Na24 (15 hrs.), has been reported earlier by Winsberg and Rodel respectively. Amongst the remaining nuclides, two: S38 (2.9 hrs.) and Cl38 (37.3 mins.) were independently and almost simultaneously detected by us and Perkins and his collaborators. Three other isotopes, Cl34m (32 mins.), Si31 (2.6 hrs.) and Mg28 (21.2 hrs.), detected in the present work have not yet been reported elsewhere. The nature of cosmic ray secondary particles responsible for the production of these short-lived radionuclides in the troposphere is discussed. Isotope production is found to vary strongly with altitude in the troposphere; it increases by a factor of two every 1.5-2 km depending on the radioisotope under question. This fact combined with the availability of several isotopes of half-lives ranging from about half an hour to a day leads to the possibility of using them as tracers for studying short-term tropospheric processes, e.g. those occurring prior to and during condensation in a precipitating cloud. The implications of the present measurements are discussed

Model atmosphere analysis of the extreme DQ white dwarf GSC2U J131147.2+292348

A new model atmosphere analysis for the peculiar DQ white dwarf discovered by Carollo et al. (2002) is presented. The effective temperature and carbon abundance have been estimated by fitting both the photometric data (UBJ,VRF,IN,JHK) and a low resolution spectrum (3500<lambda<7500 A) with a new model grid for helium-rich white dwarfs with traces of carbon (DQ stars). We estimate Teff ~ 5120 +/- 200 K and log[C/He] ~ -5.8 +/- 0.5, which make GSC2U J131147.2+292348 the coolest DQ star ever observed. This result indicates that the hypothetical transition from C2 to C2H molecules around Teff = 6000 K, which was inferred to explain the absence of DQ stars at lower temperatures, needs to be reconsidered.Comment: 4 pages, 2 figures, accepted for publication in Astronomy and Astrophysics Letter

Identification of Phytochemical Constituents of Aegle marmelos Responsible for Antimicrobial Activity against Selected Pathogenic Organisms

Antimicrobial activity and phytochemical constituents of an ethanolic extract of Aegle marmelos were investigated. The phytochemical screening of the crude extract revealed the presence of Alkaloids, Cardiac glycosides, Terpenoids, Saponins, Tannis, Flavonoids, and Steroids. The crude ethanolic extract was tested for antimicrobial activity against gram positive organisms of Bacillus subtilis (NCIM: 3471), Staphylococcus aureus (NCIM: 2079), gram negative Escherichia coli (NCIM: 2065) and Pseudomonas aeruginosa (NCIM: 2200) at different concentrations levels of 0.5, 1.0, 1.5, 2.0 and 2.5 mg/ml. At the 2.5 mg/ml concentration, gram negative Escherichia coli exhibits a zone of inhibition about 25.7mm; Pseudomonas aeruginosa 19.9mm; gram positive Staphylococcus aureus 29.0 mm; and Bacillus subtilis, a maximum zone of inhibition about 28.1 mm as compared to the control drug penicillin. Escherichia coli, Pseudomonas aeruginosa and Bacillus subtilis exhibit a maximum zone of inhibition, hence they were considered as susceptible to the plant extracts but Staphylococcus aureus doesn’t exhibit such a zone of inhibition and is therefore considered as resistant

Preparation, Characterization and In Vitro Drug Release Studies of 6-mercaptopurine Thin Film

Oral thin films of 6-mercaptopurine were fabricated from mucoadhesive polymer, chitosan and polyvinylpyrrolidone for the purpose of prolonging drug release and improving its bioavailability. All fabricated film formulations prepared were smooth and translucent, with good flexibility. The weight and thickness of all the formulations were found to be uniform. These films were also evaluated for surface pH, folding endurance, swelling percentage (% S) and in vitro disintegration time. Scanning Electron Microscopy (SEM) and Fourier Transform Infrared (FTIR) were used to evaluate the physico-chemical nature of the films. In-vitro drug release have shown enhanced release profiles for thin films compared to pure drug and the release patterns have been found to be pH dependant. The results of the study reveals that fabrication of 6-MP oral thin film by using solvent cast technology is a simple and an efficient method for drug delivery to achieve desired therapeutic compliance.Keywords: 6-mercaptopurine; In Vitro Drug Release; SEM; FTI

Development and Validation of Glimepiride and Metformin in Human Plasma by HPLC: An application study

A simple and cost effective RP-HPLC method is developed for simultaneous estimation of glimepiride (GLIM) and metformin (MET) at tablet dosage form using C-18 column (4.6 x 250mm, 5?, 100 A?) with a mobile phase composed ofmethanol: water (90:10% v/v) buffered with ortho phosphoric acid at a flow rate of1.0 mL/min (UV detection at 231 nm). The retention time of both drugs (GLIM and MET) are observed as 4.286 and 2.262 respectively. Human plasma spiking studies of both the API and the formulation at the concentration of (0.2g/mL - 1g/mL) for glimepiride and metformin (1g/mL - 5g/mL) expresses the standard correlation coefficients of 0.9998 and 0.9999 respectively for API and 0.9917 and 0.99 respectively for the tablet dosage form. The mean (%) recoveries of glimepiride and metformin are 99.98 and 99.9% respectively. The % RSD below 0.5 shows the high precision of the proposed method. Assay studies revealed that 98.05% of purity is observed for glimepiride and 99.69 for metformin in a tablet dosage form. Human plasma spiking studies revealed that a minimal quantum of glimepiride had been bound with the plasma proteins compare to metformin in the tablet dosage form. The method was validated as per the ICH guidelines