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Biomedical subjects

T Pradeep

Publications and source records attributed to T Pradeep.

At least 19 recordsLinked to original sources
PubMed2006

Investigations of the antibacterial properties of ciprofloxacin@SiO2.

The antibacterial activity of ciprofloxacin-encapsulated silica nanoshells synthesized from gold@silica core-shell nanoparticles has been investigated. The minimum inhibitory concentration of the material was found using the agar dilution method, and it showed better antibacterial activity compared to free ciprofloxacin in the case of Escherichia coli DH5, whereas the same activity was found for Lactococcus lactis MG 1363. Hydrophobicity measurements carried out in an octanol-water mixture suggested that ciprofloxacin@SiO2 is distributed almost equally in the aqueous and nonaqueous phases. The kinetics of the uptake of ciprofloxacin@SiO2 was compared with that of free ciprofloxacin. Fluorescence imaging studies carried out using fluorescein isothiocyanate@SiO2 showed that the nanoshells enter the bacterial cell. The uptake of silica shells has been probed by transmission electron microscopy also.

Anti-Bacterial Agents↗
PubMed2005

Growth of gold nanoparticles in human cells.

Gold nanoparticles of 20-100 nm diameter were synthesized within HEK-293 (human embryonic kidney), HeLa (human cervical cancer), SiHa (human cervical cancer), and SKNSH (human neuroblastoma) cells. Incubation of 1 mM tetrachloroaurate solution, prepared in phosphate buffered saline (PBS), pH 7.4, with human cells grown to approximately 80% confluency yielded systematic growth of nanoparticles over a period of 96 h. The cells, stained due to nanoparticle growth, were adherent to the bottom of the wells of the tissue culture plates, with their morphology preserved, indicating that the cell membrane was intact. Transmission electron microscopy of ultrathin sections showed the presence of nanoparticles within the cytoplasm and in the nucleus, the latter being much smaller in dimension. Scanning near field microscopic images confirmed the growth of large particles within the cytoplasm. Normal cells gave UV-visible signatures of higher intensity than the cancer cells. Differences in the cellular metabolism of cancer and noncancer cells were manifested, presumably in their ability to carry out the reduction process.

Gold↗
PubMed2005

Interaction of azide ion with hemin and cytochrome c immobilized on Au and Ag nanoparticles.

This paper presents a set of investigations on the binding of a metabolic inhibitor, azide with prosthetic heme group of biomolecules, hemin chloride (Hem) and cytochrome c (Cyt c) immobilized on Au and Ag nanoparticles. A variety of spectroscopic tools have been used to understand the chemistry occurring on the nanoparticle surface. While the nature of binding of the model system, hemin has been investigated by UV-visible, fluorescence, FTIR, and Raman spectroscopies, the azide binding has been studied in detail by MALDI-TOF MS. Hemin binding on the nanoparticle surface occurs through the carboxylic acid groups. The hemin-N(3) adduct on the nanoparticle surface has been detected by mass spectrometry and its fragments have been studied by post source decay analysis. The chemistry of hemin on the nanoparticle surface has been compared with that of the protein, Cyt c. Azide binding of Cyt c requires thermal activation due to reduced accessibility of the heme center, unlike in the case of hemin. The binding chemistry is similar for free Cyt c and Cyt c bound to the nanoparticles.

Azides↗
PubMed2005

Flow-induced transverse electrical potential across an assembly of gold nanoparticles.

We report the generation of a potential difference, of the order of tens of millivolts, induced by the flow of polar liquids over an assembly of gold nanoparticles. The device consisted of two conducting glass plates, one of which contained the gold nanoparticle multilayer assembly. The potential generated is in transverse direction to the flow and is dependent on the nature of the flowing liquid. We propose a simple theoretical model to account qualitatively for the generation of the flow-induced transverse potential.

Journal Article↗
PubMed2005

Novel cage clusters of MoS2 in the gas phase.

Laser evaporation of MoS(2) nanoflakes gives negatively charged magic number clusters of compositions Mo(13)S(25) and Mo(13)S(28), which are shown to have closed-cage structures. The clusters are stable and do not show fragmentation in the post-source decay analysis even at the highest laser powers. Computations suggest that Mo(13)S(25) has a central cavity with a diameter of 4.5 A. The nanosheets of MoS(2) could curl upon laser irradiation, explaining the cluster formation.

Disulfides↗
PubMed2005

Potential of silver nanoparticle-coated polyurethane foam as an antibacterial water filter.

Silver nanoparticles can be coated on common polyurethane (PU) foams by overnight exposure of the foams to nanoparticle solutions. Repeated washing and air-drying yields uniformly coated PU foam, which can be used as a drinking water filter where bacterial contamination of the surface water is a health risk. Nanoparticles are stable on the foam and are not washed away by water. Morphology of the foam was retained after coating. The nanoparticle binding is due to its interaction with the nitrogen atom of the PU. Online tests were conducted with a prototypical water filter. At a flow rate of 0.5 L/min, in which contact time was of the order of a second, the output count of Escherichia coli was nil when the input water had a bacterial load of 10(5) colony-forming units (CFU) per mL. Combined with the low cost and effectiveness in its applications, the technology may have large implications to developing countries.

Anti-Bacterial Agents↗
PubMed2004

Model for heat conduction in nanofluids.

A comprehensive model has been proposed to account for the large enhancement of thermal conductivity in nanofluids and its strong temperature dependence, which the classical Maxwellian theory has been unable to explain. The dependence of thermal conductivity on particle size, concentration, and temperature has been taken care of simultaneously in our treatment. While the geometrical effect of an increase in surface area with a decrease in particle size, rationalized using a stationary particle model, accounts for the conductivity enhancement, a moving particle model developed from the Stokes-Einstein formula explains the temperature effect. Predictions from the combined model agree with the experimentally observed values of conductivity enhancement of nanofluids.

Journal Article↗
PubMed2004

Concentration of CO2 over melting ice oscillates.

We report that the concentration of CO2 over melting ice oscillates as long as water and ice coexist. A phenomenological model involving melting of CO2 containing ice leading to its release, readsorption of the vapor on ice, and dissolution in water is proposed. Thermokinetics of these processes lead to nonlinearity of the dynamics. This phenomenon is also observed over impure ice contaminated with salts or in the presence of nitrogen or air. Oscillations have been observed in several other solute or ice-water systems.

Journal Article↗
PubMed2004

Ciprofloxacin-protected gold nanoparticles.

The antibacterial drug ciprofloxacin (cfH) has been used to protect gold nanoparticles of two different mean diameters, 4 and 20 nm. The protection is complete with about 65 and 585 cfH molecules covering 4 and 15 nm particles, respectively. The nature of binding has been investigated by several analytical techniques. The nitrogen atom of the NH moiety of piperazine group binds on the gold surface, as revealed by voltammetric and spectroscopic studies. The cfH-adsorbed particles are stable in the dry state as well as at room temperature, and as a result, redispersion is possible. The rate of release of the drug molecule from the nanoparticles is more in the basic medium than in pure water, and the kinetics depend on the size of the particle; faster desorption is seen in smaller particles. The bound cfH is fluorescent, and this property could be used in biological investigations. This study shows that metal nanoparticles could be useful carriers for cfH and fluoroquinolone molecules. Most of the bound molecules could be released over an extended period of time.

Adsorption↗
PubMed2003

Solvothermal synthesis of silver nanoparticles from thiolates.

A new solvothermal method for the synthesis of thiol-protected silver nanoparticles starting from silver thiolates is reported. The method has been tried with thiols of different chain length, such as octane and octadecane thiols, and the particle size was found to be nearly the same for both molecules. The synthesis was dependent on heating conditions and the best results were obtained when the temperature was between 180 and 200 degrees C. Addition of complexation agents such as acetyl acetone or triethylamine to the solvent did not change the product distribution significantly.

Journal Article↗
PubMed2003

Detection and extraction of endosulfan by metal nanoparticles.

One of the most common pesticides in the developing world, endosulfan, can be detected in ppm levels using gold nanoparticles. Endosulfan adsorbs on the nanoparticle surface and upon interaction for a long time, the nanoparticles precipitate from the solution. Interaction with silver is weak, yet adsorption occurs leading to removal of endosulfan from the solution. A multilayer assembly of gold nanoparticles prepared on a glass substrate shows excellent spectrophotometric response suggesting potential applications.

Endosulfan↗
PubMed2000

A method to study the phase transition and desorption of self-assembled monolayers on planar gold surfaces.

In-plane resistance of thin gold films (thickness approximately 1,000 A) after the formation of self-assembled monolayers has been measured as a function of temperature. We attribute the observed increase in the slope of the resistance vs temperature plot in the case of octadecanethiol and octanethiol monolayers at characteristic temperatures to phase transitions. The structural transition of 1,4-benzenedimethanethiol is also manifested similarly. Propanethiol does not show any phase transition, as expected. The observed changes in the alkanethiol monolayers are related to the decrease in the lifetime of the parallel vibrational motion of the adsorbate on the gold surface. The increase in slope is followed by a decrease which is attributed to the commencement of desorption of monolayers from the gold surface.

Journal Article↗
PubMed2000

Surface Chemical Studies on Pyrite in the Presence of Polysaccharide-Based Flotation Depressants.

The interaction of dextrin and guar gum with pyrite has been investigated through adsorption, flotation, and electrokinetic measurements. The adsorption densities of the polysaccharides onto pyrite reveal a region of higher adsorption density in the pH range 7.5-11, with a maximum around pH 10 for both polymers. The isotherms exhibit Langmuirian behavior. The adsorption density of guar gum onto pyrite is higher than that of dextrin. Electrokinetic measurements indicate a decrease in the electrophoretic mobility values in proportion to the concentration of the polymer added. Co-precipitation tests confirm polymer-ferric species interaction in the bulk solution, especially in the pH range 5.5-8.5. The pH range for higher adsorption, significant co-precipitation, and appreciable depression of pyrite encompass each other. XPS and FTIR spectroscopic studies provide evidence in support of chemical interaction between hydroxylated pyrite and the hydroxyl groups of the polymeric depressants. Copyright 2000 Academic Press.

Journal Article↗
PubMed1999

Ion/Surface Reactions at Monolayers in Solution: A Combined Surface Enhanced Raman-X-Ray Photoelectron Spectroscopic Investigation of the Chemical Modification of a 2-Mercaptobenzothiazole Monolayer on Polycrystalline Au Films.

Reaction of a methyltriphenylphosphonium (TPP) ion with a 2-mercaptobenzothiazole (MBT) monolayer on polycrystalline gold under electrochemical conditions leads to the chemical modification of the monolayer. Surface-enhanced Raman spectroscopy (SERS) has been used to study the molecular nature of the transformation. MBT, which adsorbs in the thione form on Au, gets transformed to the thiolate form upon reaction. Thermal stability of the modified monolayer is substantially lower than the corresponding pure monolayers and complete desorption of the modified monolayer occurs below 473 K. Time, potential, and solvent dependence of the reaction has been investigated. Electron transfer from the monolayer to the approaching ion in solution is suggested as the cause of the reaction. XPS investigation shows the change in the valence states of the species concerned. While the parent MBT gets oxidized, the TPP moiety gets reduced. The results suggest that modified monolayers can be made by simple electrochemical procedures and the processes are similar to the corresponding gas-phase events (1994, R. G. Cooks, T. Ast, T. Pradeep, and V. H. Wysocki, Acc. Chem. Res. 27, 316). Copyright 1999 Academic Press.

Journal Article↗
PubMed1999

Charge-Transfer Complexation of C(60) with Diphenyltetrathiafulvalene (DPTTF) Capped Gold Clusters.

4,4'-Diphenyltetrathiafulvalene (DPTTF) capped gold nanoparticles of 3- to 5-nm diameter have been prepared and their thermal stability has been investigated by variable temperature FT-IR spectroscopy. The DPTTF molecules at the cluster surface undergo charge-transfer complexation with C(60) to form Au/DPTTF.C(60). Direct evidence of complexation is observed in the x-ray photoelectron and infrared spectra of the clusters. The orientational ordering transition of C(60) in Au/DPTTF.C(60) clusters occur at a higher temperature than pure C(60) indicating increased resistance to orientational disorder due to charge transfer. Variable-temperature infrared spectroscopic studies yield complementary information. Both FT-IR and mass spectra show that some of the sites on the gold surface are occupied by the phase-transfer reagent used in the cluster preparation. Copyright 1999 Academic Press.

Journal Article↗
PubMed1999

3D Monolayers of 1,4-Benzenedimethanethiol on Au and Ag Clusters: Distinct Difference in Adsorption Geometry with the Corresponding 2D Monolayers.

Au and Ag clusters of 3-nm mean diameter were prepared with 1,4-benzenedimethanethiol (BDMT) as the capping molecule. In both the monolayer-capped clusters, BDMT adsorbs in the dithiolate form in contrast to in the 2D monolayers, where the dithiolate form exists only in the case of Ag. As a result, the molecule lies flat on the cluster surface in both Au and Ag, whereas the molecular plane is perpendicular to the surface in the 2D monolayer of Au. This difference in adsorbate structure is attributed to the evolution in the cluster surface as adsorption occurs. Transmission electron microscopy and X-ray powder diffraction suggest that no superlattice of the clusters exists. Mass spectrometry suggests the presence of the phase transfer reagent at the surface. X-ray photoelectron spectroscopy confirms the chemical similarity of the two surfaces and suggests that the thiolate at the surface is susceptible to X-ray beam induced damage. Copyright 1999 Academic Press.

Journal Article↗
PubMed1999

Self-assembled Monolayers of Two Aromatic Disulfides and a Diselenide on Polycrystalline Silver Films: An Investigation by SERS and XPS.

Self-assembled monolayers of diphenyldisufide (DDS), naphthalenedisulfide (NDS), and diphenyldiselenide (DDSe) on polycrystalline silver films have been investigated by surface enhanced Raman spectroscopy (SERS) and X-ray photoelectron spectroscopy (XPS). DDS adsorbs on Ag through a homolytic cleavage of the S-S bond and resultant thiolate at the surface decomposes upon prolonged exposure to air. The geometry of the molecule is such that the benzene ring is almost horizontal to the surface. The Raman spectrum has been assigned in the light of ab-initio molecular orbital calculations. In DDSe, the Se-Se bond is retained upon adsorption and the molecule sticks up. In contrast, NDS is highly reactive on the microscopically rough surface so that a stable monolayer could not be prepared. A temperature dependent Raman study of the DDS monolayer shows the absence of any reorientation at the surface as one would expect from the adsorption geometry. XPS study complements the SERS data and shows the presence of Ag2S on an NDS exposed surface. Copyright 1999 Academic Press.

Journal Article↗