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121.
Kamath Srinivas S. Narayana B. D’Souza Renita Shiny Nayak S. Rashmi Mohan M. P. Dileep B. N. Baburajan A. Ravi P. M. Karunakara N. 《Journal of Radioanalytical and Nuclear Chemistry》2019,322(2):389-397
Tritium concentration was monitored in different water sources collected around Kaiga Nuclear Power plant, India. The concentration was in the ranges?<?1.9–27.4 Bq L?1 (GM?=?4.0 Bq L?1) for groundwater,?<?1.9–42.1 Bq L?1 (GM?=?3.5 Bq L?1) for surface water and in 12.4–42.0 Bq L?1 (GM?=?24.07 Bq L?1) for reservoir water. The concentration values observed in this study are similar to those reported for other PHWR stations of the world. The radiation dose to the public due to ingestion of Tritium through groundwater was computed to be 0.08 μSvy?1.
相似文献122.
Russian Journal of General Chemistry - A series of novel 1,2,4-oxadiazole-isoxazole linked quinazoline compounds is designed, synthesized and screened for anticancer activity on four human cancer... 相似文献
123.
124.
The influence of Mm (Mm=mischmetal) substitution and hydrogen absorption on the magnetic properties of Ho1−xMmxCo2 (x=0, 0.1, 0.2, 0.3 and 0.4) alloys have been determined through the temperature dependence of ac susceptibility and thermopower measurements. The changes in magnetic-ordering temperature of Ho1−xMmxCo2 alloys have been explained based on the dilution of the magnetic ions and weakening of 4f–3d exchange interactions. The gradual disappearance of the magnetic transition temperature upon increasing hydrogen concentration (y) has been interpreted by the lattice expansion and charge transfer between absorbed hydrogen and 3d-band of Ho1−xMmxCo2. 相似文献
125.
Vinay Kiran Narayanan Balaji Bhavesh Babulal Gabani Manjuanth Bajantri Rajesh Chandran Abhishek Dixit Nuggehally R. Srinivas Ramesh Mullangi 《Biomedical chromatography : BMC》2020,34(9):e4879
We developed and validated a simple, sensitive, selective, and reliable LC–MS/MS–ESI method for the direct quantitation of lumefantrine (LFN) enantiomers [(−)-LFN and (+)-LFN] in mice plasma as per regulatory guideline. LFN enantiomers and carbamazepine (internal standard) were extracted from mice plasma using Strata X SPE (solid-phase extraction) cartridges. Good resolution between enantiomers was achieved on a Chiralpak IA-3 column using an isocratic mobile phase (0.1% of diethyl amine in methanol), which was delivered at a flow rate of 0.8 mL/min. Detection and quantitation were performed using multiple reaction monitoring mode following the transitions m/z 530.27 → 512.30 and 237.00 → 194.00 for LFN enantiomers and the internal standard, respectively, in the positive-ionization mode. The proposed method provided accurate and reproducible results over the linearity range of 2.39–895 ng/mL for each enantiomer. The intra- and inter-day precisions were in the range of 1.03–6.14 and 6.36–8.70 and 2.03–4.88 and 5.82–11.5 for (−)-LFN and (+)-LFN, respectively. Both (−)-LFN and (+)-LFN were found to be stable under different stability conditions. The method was successfully used to delineate stereoselective pharmacokinetics of LFN enantiomers in mice after an oral administration of rac-LFN (20 mg/kg). The pharmacokinetic results indicated that the disposition of LFN enantiomers was stereoselective in mice. 相似文献
126.
Bhavesh Babulal Gabani Neeraj Kumar Saini Ravi Kumar Jairam Pavan Shrinivas Ravi Kumar Trivedi Nuggehally R. Srinivas Ramesh Mullangi 《Biomedical chromatography : BMC》2020,34(11):e4939
A selective, sensitive and rapid LC–MS/MS method has been developed and validated as per US Food and Drug Administration regulatory guidelines for the simultaneous quantitation of colchicine and febuxostat in rat plasma. Colchicine and febuxostat were extracted from the rat plasma using 10% tert-butyl methyl ether in ethyl acetate using colchicine-d6 as an internal standard (IS). The chromatographic separation of colchicine, febuxostat and the IS was achieved using a mobile phase comprising 5 mm ammonium formate and 0.025% formic acid in acetonitrile (20:80, v/v) in isocratic mode on an Eclipse XDB-C18 column. The injection volume and flow rate were 5.0 μl and 0.9 ml/min, respectively. Colchicine and febuxostat were detected by positive electrospray ionization in multiple reaction monitoring mode using transition pairs (Q1 → Q3) of m/z 400.10 → 358.10 and 317.05 → 261.00, respectively. The assay was linear in the ranges of 0.25–254 and 2.60–622 ng/ml for colchicine and febuxostat, respectively. The inter- and intra-day precision values were 0.58–13.0 and 1.03–4.88% for colchicine and febuxostat, respectively. No matrix or carryover effects were observed during the validation. Both analytes were stable on the bench-top, in the autosampler and in storage (freeze–thaw cycles and long-term storage at −80 ° C). A pharmacokinetic study in rats was performed to show the applicability of the validated method. 相似文献
127.
Kumar B. Ravi Kumar A. Kishore Reddy B. Srinivas Shashikala K. Laxminarayana E. 《Russian Journal of Organic Chemistry》2022,58(4):580-583
Russian Journal of Organic Chemistry - tert-Butyl 4-[(E)-but-1-en-3-yn-1-yl]-3-{[tert-butyl(dimethyl)silyl]oxy}-1H-indole-1-carboxylate has been synthesized with a good yield and selectivity... 相似文献
128.
Srinivas G. Ravi Kumar V. Laxma Reddy K. Praveen Kumar Y. Satyanarayana S. 《Russian Journal of General Chemistry》2018,88(12):2621-2627
Russian Journal of General Chemistry - A thiophene contained imidazo phenanthroline ligand TIP {TIP = 2-(thiophen-2-yl)-1H-imidazo-[4,5-f][1,10]phenanthroline{ and its mononuclear Ru(II)... 相似文献
129.
Chilukuri S. P. Sastry Yaramati Srinivas Pulugurtha V. Subba Rao 《Mikrochimica acta》1997,126(1-2):63-67
Three spectrophotometric methods (A-C) for the assay of cisapride (CPD) in pure and dosage forms are described. Method A is based on the oxidative coupling reaction of CPD with 3-methyl-2-benzothiazolinone hydrazone hydrochloride (MBTH) in the presence of ferric chloride to form a coloured species (max; 565 nm.) Method B is based on the oxidation of CPD with Fe (III) and subsequent chelation of Fe(II) to form a coloured complex with 1,10-phenanthroline (max: 520 nm). Method C is based on the formation of a coloured charge-transfer complex between CPD and chloranilic acid (max; 555 nm). Regression analysis of Beer-Lambert plots showed good correlation in the concentration ranges 2.0–32.0, 0.4–6.4 and 25.0–450.0 g/ml for methods A,B and C, respectively. The validity of the proposed methods was tested by analysing pharmaceutical dosage forms containing CPD and the relative standard deviations were within 1.0% 相似文献
130.
Ordered, mesoporous SBA-15 functionalized with organic and inorganic moieties exhibits efficient catalytic activity in a variety
of organic transformations. In this account, reviewing our own work, three-sets of surface-modified SBA-15 materials have
been investigated. The first-set of materials consists of SBA-15 modified with organo-acidic (propyl thiol and propyl sulfonic
acid) and basic (propyl amine and propyl adenine) moieties. The second-set of materials was prepared by grafting Mn complexes
to the organo-functionalized SBA-15. The third-set composes of nanocrystalline metal oxides supported on SBA-15. All these
catalysts have been characterized by structural and spectroscopic techniques. Catalytic activities of the first-set of solid
materials have been investigated in acid/base-catalyzed reactions viz., ring-opening of epoxides with amines (producing β-amino
alcohols), esterification, three-component-Mannich reactions and cycloaddition of CO2 to epoxides. The Mn complexes grafted on organofunctionalized SBA-15 are efficient catalysts for the chemo-, regio- and stereoselective
aerial oxidation of monoterpenes at ambient conditions. TiOx, VOx, MoOx and WOx supported on SBA-15 catalyzed biomimetic oxyhalogenation of aromatic compounds. In all these reactions, the functionalized
SBA-15 showed high selectivity. 相似文献