Faculty Publications

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    Artificial neural networks model for the prediction of steady state phenol biodegradation in a pulsed plate bioreactor
    (2008) Shetty K, K.V.; Nandennavar, S.; Srinikethan, G.
    Background: A recent innovation in fixed film bioreactors is the pulsed plate bioreactor (PPBR) with immobilized cells. The successful development of a theoretical model for this reactor relies on the knowledge of several parameters, which may vary with the process conditions. It may also be a time-consuming and costly task because of their nonlinear nature. Artificial neural networks (ANN) offer the potential of a generic approach to the modeling of nonlinear systems. Results: A feedforward ANN based model for the prediction of steady state percentage degradation of phenol in a PPBR by immobilized cells of Nocardia hydrocarbonoxydans (NCIM 2386) during continuous biodegradation has been developed to correlate the steady state percentage degradation with the flow rate, influent phenol concentration and vibrational velocity (amplitude x frequency). The model used two hidden layers and 53 parameters (weights and biases). The network model was then compared with a Multiple Regression Analysis (MRA) model, derived from the same training data. Further these two models were used to predict the percentage degradation of phenol for blind test data. Conclusions: The performance of the ANN model was superior to that of the MRA model and was found to be an efficient data-driven tool to predict the performance of a PPBR for phenol biodegradation. © 2008 Society of Chemical Industry.
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    Biological treatment of toxic petroleum spent caustic in fluidized bed bioreactor using immobilized cells of thiobacillus RAI01
    (2008) Potumarthi, R.; Mugeraya, G.; Jetty, A.
    In the present studies, newly isolated Thiobacillus sp was used for the treatment of synthetic spent sulfide caustic in a laboratory-scale fluidized bed bioreactor. The sulfide oxidation was tested using Ca-alginate immobilized Thiobacillus sp. Initially, response surface methodology was applied for the optimization of four parameters to check the sulfide oxidation efficiency in batch mode. Further, reactor was operated in continuous mode for 51 days at different sulfide loading rates and retention times to test the sulfide oxidation and sulfate and thiosulfate formation. Sulfide conversions in the range of 90-98% were obtained at almost all sulfide loading rates and hydraulic retention times. However, increased loading rates resulted in lower sulfide oxidation capacity. All the experiments were conducted at constant pH of around 6 and temperature of 30?±?5 °C. © 2008 Humana Press.
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    6-[3-(4-Fluorophenyl)-1H-pyrazol-4-yl]-3-[(2-naphthyloxy)methyl][1,2,4]triazolo[3,4-b][1,3,4]thiadiazole as a potent antioxidant and an anticancer agent induces growth inhibition followed by apoptosis in HepG2 cells
    (2010) Dhanya, D.; Isloor, A.M.; Shetty, P.; Satyamoorthy, K.; Bharath Prasad, A.S.
    In this paper we have investigated the in vitro antioxidant property of two triazolo-thiadiazoles, 6-[3-(4-fluorophenyl)-1H-pyrazol-4-yl]-3-[(2-naphthyloxy)methyl][1,2,4]triazolo[3,4-b][1,3,4]thiadiazole (FPNT) and 6-[3-(4-chlororophenyl)-1H-pyrazol-4-yl]-3-[(phenyloxy)methyl][1,2,4]triazolo[3,4-b][1,3,4]thiadiazole (CPPT) by spectrophotometric DPPH and ABTS radical scavenging methods as well as by lipid peroxide assay. The anticancer activity along with possible mechanism of action of triazolo-thiadiazoles in Hep G2 cells was explored using MTT assay, [3H] thymidine assay, flow cytometry and chromatin condensation studies. Both FPNT and CPPT exhibited a dose dependent cytotoxic effect on hepatocellular carcinoma cell line, HepG2. The IC50 value was very low for both the compounds when compared to standard drug, doxorubicin. Incorporation of [3H] thymidine in conjunction with cell cycle analysis suggested that FPNT inhibited the growth of HepG2 cells. Flow cytometric studies revealed more percentage of cells in sub-G1 phase, indicating apoptosis, which was further confirmed through chromatin condensation studies by Hoechst staining. FPNT was found to be a potent antioxidant when compared to the standard in DPPH, ABTS radical scavenging assays and lipid peroxidation studies. © 2010 .
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    Modelling and simulation of steady-state phenol degradation in a pulsed plate bioreactor with immobilised cells of Nocardia hydrocarbonoxydans
    (2011) Shetty K, V.S.; Verma, D.K.; Srinikethan, G.
    A novel bioreactor called pulsed plate bioreactor (PPBR) with cell immobilised glass particles in the interplate spaces was used for continuous aerobic biodegradation of phenol present in wastewater. A mathematical model consisting of mass balance equations and accounting for simultaneous external film mass transfer, internal diffusion and reaction is presented to describe the steady-state degradation of phenol by Nocardia hydrocarbonoxydans (Nch.) in this bioreactor. The growth of Nch. on phenol was found to follow Haldane substrate inhibition model. The biokinetic parameters at a temperature of 30 ± 1 °C and pH at 7.0 ± 0.1 are ? m = 0.5397 h -1, K S = 6.445 mg/L and K I = 855.7 mg/L. The mathematical model was able to predict the reactor performance, with a maximum error of 2% between the predicted and experimental percentage degradations of phenol. The biofilm internal diffusion rate was found to be the slowest step in biodegradation of phenol in a PPBR. © 2010 Springer-Verlag.
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    Mixing and solid-liquid mass transfer characteristics in a three phase pulsed plate column with packed bed of solids in interplate spaces-a novel aerobic immobilized cell bioreactor
    (2011) Shetty K, V.S.; Srinikethan, G.
    Background: The pulsed plate column (PPC) with packed bed of solids in the interplate spaces finds use as a three phase aerobic bioreactor and is a potential heterogeneous catalytic reactor. Good knowledge of the extent of mixing in the liquid phase and solid-liquid mass transfer coefficient are essential for modeling, design and optimization of these columns. The present work aims at the study of liquid phase mixing and solid-liquid mass transfer characteristics in a three phase PPC. Results: Residence time distribution studies were performed. Dispersion number was found to increase with increase in liquid superficial velocities, frequency of pulsation, amplitude of pulsation and the vibrational velocities. Increase in frequency and amplitude of pulsation, and hence increase in vibrational velocity, resulted in increase of the solid-liquid mass transfer coefficient. Conclusions: The mixing behaviour in this contactor approximated a mixed flow behaviour. The three phase PPC was found to outperform many other kinds of three phase contactors in terms of solid liquid mass transfer characteristics. Empirical correlations developed can be used for the determination of solid-liquid mass transfer coefficients for three phase PPC and hence can facilitate the design, scale-up and modeling of these columns, when used as chemical or biochemical reactors. © 2011 Society of Chemical Industry.
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    Biodegradation of phenol using immobilized nocardia hydrocarbonoxydans in a pulsed plate bioreactor: Effect of packed stages, cell carrier loading, and cell acclimatization on startup and steady-state behavior
    (2013) Shetty K, K.; Yarangali, S.B.; Srinikethan, G.
    The effect of the number of stages and cell carrier loading on the steady-state and startup performance of a continuous pulsed plate bioreactor with glass beads as the cell carrier material for biodegradation of phenol in wastewater using immobilized Nocardia hydrocarbonoxydans has been studied. It was found that the performance of the pulsed plate bioreactor during startup and at steady state can be improved by an increase in cell carrier loading, number of stages, total plate stack height, and with a decrease in plate spacing. The startup time for the continuous bioreactor can be decreased by increasing the number of preacclimatization steps for the cells. The attainment of steady effluent phenol concentration can be considered as an indication of steady state of the continuous bioreactor, as when phenol concentration attained a steady value, biofilm thickness, and the attached biomass dry weight also attained a constant value. © 2013 Copyright Taylor and Francis Group, LLC.
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    Indole-3-carbinol and 1,3,4-oxadiazole hybrids: Synthesis and study of anti-proliferative and anti-microbial activity
    (CSIRO, 2015) Gokhale, N.; Panathur, N.; Udayakumar, U.; Kumsi, M.
    In the present study, molecular hybrids of indole-3-carbinol and 1,3,4-oxadiazole-2-thiols have been designed and synthesized. The thiol analogues consisted of diversely substituted benzyl and alkyl groups with different electronic properties. The structures of all the newly synthesized scaffolds and target compounds were ascertained using 1H NMR, 13C NMR, mass spectrometry, and elemental analyses. All the final compounds were screened in vitro for their anti-proliferative and anti-microbial activity. Three compounds showed excellent anti-proliferative activity with more than 70% cell growth inhibition against three cancer cell lines, HepG2 (human liver hepatocellular carcinoma), HeLa (human cervix carcinoma), and MCF-7 (human breast carcinoma). In the anti-microbial studies, compounds with electron-withdrawing fluoro or nitro substituent displayed appreciable activity similar to that of standard drugs. Also, the final compounds are non-toxic to non-cancerous Vero cell line. © 2015 CSIRO.
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    Synthesis and in vitro biological evaluation of new pyrazole chalcones and heterocyclic diamides as potential anticancer agents
    (Elsevier B.V., 2015) Sankappa Rai, U.; Isloor, A.M.; Shetty, P.; Pai, K.S.R.; Fun, H.-K.
    Synthesis and characterization of new heterocyclic pyrazole chalcones (4a-. e) and diamide (6a-. e) derivatives are described. Pyrazole chalcones were synthesized by the reaction of pyrazole aldehydes and suitable aromatic ketones. Diamides were synthesized by the reaction of phthalic acid and amines. Newly synthesized compounds were characterized by spectral studies and their biological activity was assessed in vitro using MCF-7 (human breast adenocarcinoma) and HeLa (human cervical tumor cells) cell lines. Few of the synthesized molecules inhibited the growth of the human breast cancer cell lines and human cervical tumor cell lines at low micromolar to nanomolar concentrations. © 2014 King Saud University.
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    Biosynthesis of copper nanoparticles using copper-resistant Bacillus cereus, a soil isolate
    (Elsevier Ltd, 2016) Tiwari, M.; Jain, P.; Raghu Chandrashekar, R.; Narayanan, K.; Bhat, K.U.; Udupa, N.; Rao, J.V.
    Microorganisms are useful systems for the production of biocompatible metal nanoparticles. Copper, an essential element of life, has good therapeutic potential. However, copper lacks suitable form for effective in vivo delivery, which has diminished its applicability. In this study, we produced biosynthesized copper nanoparticles (BCuNps) using a copper-resistant bacterial isolate from copper mine. The organism was able to tolerate >10 mM of copper and when analysed by 16S rRNA technique, showed 100% similarity with Bacillus cereus. BCuNps, produced by this microorganism, in cell-free filtrate, were characterized for surface plasmon resonance (SPR), particle's characteristics, spectroscopic properties and morphology. SPR peaks for BCuNps were recorded between 570–620 and 350–370 nm. BCuNps characteristics, namely particle size distribution, polydispersity index and zeta potential were found to be 11–33 nm, 0.433 and (?) 19.6 mV, respectively. Scanning electron microscope (SEM), transmission electron microscope (TEM) and atomic force microscope (AFM) analyses confirmed the uniform morphology; X-ray diffraction (XRD) spectrum revealed the crystalline nature; and Fourier transform infrared (FTIR) spectrum disclosed the presence of protein with BCuNps. A comparative evaluation of BCuNps with copper sulphate to determine their antimicrobial and cell toxicity levels was undertaken. BCuNps showed better antimicrobial effect and found to be safer against normal cell lines, such as HaCat, Vero and hFOB, than the copper sulphate control. © 2016 Elsevier Ltd
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    Synthesis and optimization of poly (N,N-diethylacrylamide) hydrogel and evaluation of its anticancer drug doxorubicin’s release behavior
    (Springer London, 2019) Havanur, S.; Farheenand, V.; JagadeeshBabu, P.E.
    A macroporous temperature-responsive poly(N,N-diethylacrylamide) (PDEA) hydrogel was synthesized and optimized through free radical polymerization. The optimized hydrogel was achieved by evaluating the swelling characteristics, physical stability and mechanical strength through altering the components namely concentration of N,N-diethylacrylamide (monomer), ammonium peroxodisulfate (initiator), N,N?-methylbisacrylamide (cross-linker) and N,N,N?,N?-tetramethylethylenediamine (accelerator). The equilibrium swelling behavior was performed gravimetrically, and the PDEA hydrogel synthesized at 36 °C exhibited a maximum swelling of 18.332 g.g ?1 . Also, the LCST of the prepared PDEA hydrogel was found to be around 29 °C. However, the results of time-controlled swelling and deswelling kinetics indicated that hydrogels are temperature sensitive. Further, characterization of the hydrogel was performed using scanning electron microscopy, differential scanning calorimetry, thermal gravimetric analysis, and Fourier transform infrared spectroscopy. The hydrogel was assessed for its cytotoxicity in MDA-MB-231 cell line by MTT assay. The release behavior of anticancer drug doxorubicin (DOX), a hydroxyl derivative of anthracycline, was studied at above and below the LCST temperature. It was found that the DOX release from the DOX-loaded hydrogels was significantly improved when the surrounding temperature of the release media was increased near to physiological temperature. The cumulative release profile of hydrogel at different temperatures was fitted to different kinetic model equations and non-Fickian diffusion release mechanism was revealed. These results suggest that PDEA has a potential application as an intelligent drug carrier. © 2018, Iran Polymer and Petrochemical Institute.