1. Journal Articles
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Item Use of cellulose acetate/polyphenylsulfone derivatives to fabricate ultrafiltration hollow fiber membranes for the removal of arsenic from drinking water(2019) Kumar, M.; RaoT., S.; Isloor, A.M.; Ibrahim, G.P.S.; Inamuddin; Ismail, N.; Ismail, A.F.; Asiri, A.M.Cellulose acetate (CA) and cellulose acetate phthalate (CAP) were used as additives (1 wt%, 3 wt%, and 5 wt%) to prepare polyphenylsulfone (PPSU) hollow fiber membranes. Prepared hollow fiber membranes were characterized by surface morphology using scanning electron microscopy (SEM), surface roughness by atomic force microscopy (AFM), the surface charge of the membrane was analyzed by zeta potential measurement, hydrophilicity by contact angle measurement and the functional groups by fourier transform infrared spectroscopy (FTIR). Fouling resistant nature of the prepared hollow fiber membranes was evaluated by bovine serum albumin (BSA) and molecular weight cutoff was investigated using polyethylene glycol (PEG). By total organic carbon (TOC), the percentage rejection of PEG was found to be 14,489 Da. It was found that the hollow fiber membrane prepared by the addition of 5 wt% of CAP in PPSU confirmed increased arsenic removal from water as compared to hollow fiber membrane prepared by 5 wt% of CA in PPSU. The removal percentages of arsenic with CA-5 and CAP-5 hollow fiber membrane was 34% and 41% with arsenic removal permeability was 44.42 L/m 2 h bar and 40.11 L/m 2 h bar respectively. The increased pure water permeability for CA-5 and CAP-5 hollow fiber membrane was 61.47 L/m 2 h bar and 69.60 L/m 2 h bar, respectively. � 2019 Elsevier B.V.Item The inhibition action of ethyl-2-phenyl hydrozono-3-oxobutyrate on the corrosion of 6061 Al alloy/SiCp composite in hydrochloric acid medium(2010) Kini, U.A.; Shetty, P.; Shetty, S.D.; Isloor, A.M.; Herle, R.The inhibition behavior of ethyl-2-phenyl hydrozono-3-oxobutyrate on the corrosion of 6061 Al alloy/SiCp composite in 0.1, 0.5 and 1 N hydrochloric acid solution at four different temperatures (30-60 C) has been investigated using potentiostatic polarization techniques and weight loss method. The results indicated that the corrosion inhibition efficiency and the extent of surface coverage were increased with the increase in inhibitor concentration up to a critical concentration. The adsorption of the inhibitor compound on the composite surface was found to obey Temkins' and Langmuir adsorption isotherms. The potentiostatic polarization results have revealed that oxobutyrate acts as an efficient cathodic inhibitor for the corrosion of 6061 Al alloy/SiCp composite in HCl medium. The thermodynamic parameters for the corrosion and adsorption processes were determined. 2010.Item The effect of glycine betaine additive on the PPSU/PSF ultrafiltration membrane performance(2016) Moideen, K, I.; Isloor, A.M.; Garudachari, B.; Ismail, A.F.A series of new ultrafiltration (UF) membranes were prepared by blending polyphenylsulfone and polysulfone with glycine betaine (GB) and polyethylene glycol-1000 (PEG-1000) as additive. GB of varying concentrations (0 2 wt.%) were dissolved in N-Methyl-2-pyrrolidone to prepare the membranes by phase inversion method. The membranes were characterized by Scanning Electron Microscope and dispersive X-ray analysis to study the asymmetric nature of membranes and the retention of GB in membranes, respectively. The stability tests were conducted to study the stability of additives in the membranes. The membrane hydrophilicity was determined by contact angle, porosity, water uptake, and permeability studies. The addition of GB additives enhanced the membrane performance like permeability, antifouling property, and heavy metal rejection. Also, the antifouling property improved with the addition of GB. The antifouling nature was calculated by flux recovery ratio, reversible and irreversible fouling. Polymer-enhanced UF of heavy metals like Pb2+ and Cd2+ was performed and rejection of 80.23 and 71.45%, respectively, was exhibited by the GB 1 membrane with agreeable permeability and antifouling property. 2016 Balaban Desalination Publications. All rights reserved.Item T3P mediated synthesis of some new quinoline substituted pyrazole derivatives and its antibacterial studies(2012) Chandrakantha, B.; Isloor, A.M.; Peethambar, S.K.; Shetty, P.A series of new N-(substituted)-5-phenyl-1-(quinolin-2-yl)-1H-pyrazole-4-carboxamide derivatives (5a-h) have been synthesized by condensing ethyl-3-(dimethylamino)-2-[(phenyl)carbonyl]prop-2-enoate 2 with quinoline-2-yl-hydrazine. Compound 3 is hydrolyzed into 4 which is upon further coupled with different aromatic/aliphatic amines using 50% prpopyl phosphonic anhydride (T3P) in ethyl acetate as coupling reagent to afford different quinoline substituted pyrazole carboxamide derivatives. All the newly synthesized compounds were screened for their invitro antibacterial studies against Escherichia coli, Bacillus subtilis and Pseudomonas aeruginosa. The results revealed that compounds 5d, 5f, and 5h showed good antibacterial activity towards all bacterial strains. These newly synthesized compounds were characterized by NMR, mass spectral, IR spectral study and also by C, H, N analyses.Item Synthesis, characterization, antioxidant, and anticancer studies of 6-[3-(4-chlorophenyl)-1H-pyrazol-4-yl]-3-[(2-naphthyloxy) methyl][1,2,4] triazolo[3,4-b][1,3,4]thiadiazole in HepG2 cell lines(2011) Sunil, D.; Isloor, A.M.; Shetty, P.; Satyamoorthy, K.; Prasad, A.S.B.Triazolo- thiadiazoles exhibit a variety of pharmacological properties, due to their cytotoxicity. In continuation of a previous study on triazolo-thiadiazoles, the authors have synthesized a new thiadiazole, 6-[3-(4-chlorophenyl)- 1-H-pyrazol-4-yl]-3-[(2-naphthyloxy)methyl] [1,2,4]triazolo[3,4-b][1,3,4]thiadiazole (CPNT), which was further characterized by advanced spectral techniques and elemental analysis. The compound exhibited a dose-dependent cytotoxic effect on hepatocellular carcinoma cell line, HepG2 with very low IC50 value of 0.8 ?g/ml in 24 h when compared with standard drug, doxorubicin. Incorporation of [3H] thymidine in conjunction with cell cycle analysis suggested that CPNT inhibited the growth of HepG2 cells. Flow cytometric studies revealed more percentage of cells in subG1 phase, indicating apoptosis, which was further confirmed through chromatin condensation studies by Hoechst staining. In vitro antioxidant activity of CPNT was determined by DPPH and ABTS free radical scavenging assays which revealed increasing scavenging activity with increasing concentration of the compound when compared with reference ascorbic acid. Springer Science+Business Media, LLC 2010.Item Synthesis, characterization, anticancer, and antioxidant activity of some new thiazolidin-4-ones in MCF-7 cells(2013) Isloor, A.M.; Sunil, D.; Shetty, P.; Malladi, S.; Pai, K.S.R.; Maliyakkl, N.There are limited studies centring on the potential of thiazolidin-4-ones as anticancer agents. In this study, a new series of 2-(3-substituted-1H- pyrazol-4-yl)-3-(3-substituted-5-sulfanyl-1,2,4-triazol-4-yl)-1, 3-thiazolidin-4-one (4a-o) have been synthesized by cyclo-condensation reaction of 5-substituted-4-[(3-substituted-1H-pyrazol-4-ylmethylidene)amino]-2H-1,2,4- triazole-3-thione (3a-o) and thioglycolic acid. The structures of all the synthesized compounds were confirmed by elemental analysis, spectral techniques like IR, 1H NMR, and mass spectroscopy. Few compounds exhibited dose-dependent cytotoxic effect in MTT assay in human breast cancer (MCF-7) cells. Apoptotic degradation of DNA due to action of potent thiazolidin-4-ones was analysed by agarose gel electrophoresis and visualized by ethidium bromide staining (comet assay). A concentration-dependent increase in tail length and olive tail moment was observed when treated with thiazolidin-4-ones. In vitro antioxidant studies like DPPH and ABTS-free radical scavenging assays-indicated moderate activity of thiazolidin-4-ones. 2012 Springer Science+Business Media, LLC.Item Synthesis, characterization and their anticonvulsant, anti-inflammatory studies of some novel chromeno oxadiazoles(2013) Ubaradka, S.R.; Isloor, A.M.; Shetty, P.; Shetty, P.; Isloor, N.A.In this study, a series of new 1,2,4-oxadiazole derivatives containing 3,4-dihydro-2H-chromen-2-amine moiety were synthesized by efficient microwave reaction of 2-amino-N?-hydroxychroman-3-carboxamidine and suitable aldehyde. Structures of all the synthesized compounds were confirmed by spectral studies and C, H, N analyses. Newly synthesized compounds were screened for their anticonvulsant and anti-inflammatory properties. Few of the compounds exhibited excellent anticonvulsant activity as compared to the standard drug Diazepam. Also compounds have exhibited moderate anti-inflammatory activity as compared to the standard drug Diclofenac sodium. 2012 Springer Science+Business Media, LLC.Item Synthesis, characterization and nonlinear optical properties of 2-[(E)-2-(4-ethoxyphenyl)ethenyl]-1-methylquinolinium 4-substitutedbenzenesulfonate compounds(2010) Ruanwas, P.; Kobkeatthawin, T.; Chantrapromma, S.; Fun, H.-K.; Philip, R.; Smijesh, N.; Padaki, M.; Isloor, A.M.In the present investigation, 2-[(E)-2-(4-ethoxyphenyl)ethenyl]-1-methylquinolinium 4-substituted benzenesulfonate (X = CH3 (1), X = OCH3 (2), X = Cl (3), X = Br (4)) have been synthesized and characterized by 1H NMR, UV-Vis and FT-IR spectroscopy methods. In addition compound 3 was also characterized by single crystal X-ray diffraction (XRD) and found that it crystallized out in the monoclinic space group P21 with cell parameters, a = 9.8072(9) , b = 6.4848(5) , c = 19.4405(16) , ? = 90 , ? = 103.421(5) , ? = 90 , z = 2 and V = 1202.61(17) 3. The nonlinear optical absorption of the samples has been studied at 532 nm using 5 ns laser pulses, employing the open-aperture z-scan technique. It is found that some of the samples are potential candidates for optical limiting applications. 2009 Elsevier B.V. All rights reserved.Item Synthesis, characterization and in vitro cytotoxic properties of some new Schiff and Mannich bases in Hep G2 cells(2011) Sunil, D.; Isloor, A.M.; Shetty, P.; Chandrakantha, B.; Satyamoorthy, K.A series of 5-substituted-4-amino-3-mercapto- 1,2,4-triazoles were synthesized and were treated with various 3-substituted pyrazole aldehydes to obtain a series of new Schiff bases (3a-l). Few of the selected Schiff bases were converted into Mannich bases by reaction with diphenylamine/morpholine in presence of formaldehyde in ethanol media (4a-e, 5a-e). These newly synthesized compounds were characterized by elemental analysis, IR, NMR and mass spectrometry studies. A comparative study on the cytotoxic activities of few selected Schiff and Mannich bases was done in HepG2 cells using MTT assay. Few of the screened Schiff bases, 3a, 3d, 3e, 3g and 3h showed dose dependent cytotoxic activity, 3a being the most potent with an IC50 value of 0.018 g/l comparable to the standard drug doxorubicin. Among the Mannich bases, 5b was the most active with an IC50 value of 0.034 g/l. The Schiff bases were found to be more active, when compared to Mannich bases derived from them. The morpholine derived Mannich bases were more potent than those obtained from diphenyl amine. Springer Science+Business Media, LLC 2010.Item Synthesis, characterization and biological activities of some new benzo[b]thiophene derivatives(2010) Isloor, A.M.; Kalluraya, B.; Sridhar, Pai, K.Benzo[b]thiophene molecules are found to be important tools in synthetic medicinal chemistry. They are of current interest due to their wide spectrum of pharmacological properties. In view of the biological activities of benzo[b]thiophene containing molecules, in this present research work, we propose the synthesis of some new benzo[b]thiophene derivatives such as thiadiazoles, oxadiazoles, pyrazolin & diaryl pyrazoles starting from 3-chlorobenzo[b]thiophene-2-carboxyl chloride. These newly synthesized compounds were characterized by elemental analyses, I.R, NMR and Mass spectral studies. Some of the selected compounds were screened for their antibacterial, antifungal and anti-inflammatory studies. Many of the molecules were found to be potent. 2009 Elsevier Masson SAS. All rights reserved.