Sunil K. Singh

Attachment of biomolecules (protein and DNA) to amino-functionalized carbon nanotubes

An efficient method for the attachment of biomolecules [e.g. bovine serum albumin (BSA) protein and deoxyribonucleic acid (DNA)] to amino-group-functionalized multiwalled carbon nanotubes (f-MWCNTs) was reported. MWCNTs were prepared by spray pyrolysis of a benzene-ferrocene solution in argon atmosphere at ∼850 °C followed by functionalization with an amino group by chemical modification of carboxylic groups introduced on the nanotube surface. This process involves a direct coupling of ethylenediamine with carboxylic groups to introduce amino groups by amide formation. The as-synthesized MWCNTs, f-MWCNTs, and amino f-MWCNTs with BSA protein and DNA were characterized by scanning and transmission electron microscopy, and Fourier transform infrared spectroscopy, which confirm the attachment of biomolecules (BSA protein and DNA) to the amino f-MWCNTs.

Light-into-heat conversion in La 2 O 3 :Er 3+ -Yb 3+ phosphor: an incandescent emission

Low-power-threshold cw laser-induced incandescence (CWLII) has been observed in La(2)O(3):Er(3+)-Yb(3+) phosphor on excitation by a 976 nm IR laser. It is suggested that incandescence originates from the extensive heating induced by the nonradiative processes taking place following the laser excitation. Other mechanisms for similar observations have also been suggested in the literature and have been discussed with the present observations. The estimated temperature for the CWLII approaches around 2650 K, and this seems to provide an effective way to rapidly attain high temperature in nano/microvolumes of phosphor. The phosphor exhibited efficient upconversion, and the ratio of the (2)H(11/2)→(4)I(15/2) and (4)S(3/2)→(4)I(15/2) band intensities of Er(3+) permits measurement of the temperature rise, from a distance.

Ionic cross-linked chitosan beads for extended release of ciprofloxacin: In vitro characterization

Chitosan beads loaded with ciprofloxacin hydrochloride were fabricated by ionic cross-linking with sodium tripolyphosphate. The beads showed an excellent water retention property. The degradation of fabricated beads was influenced by the pH of test medium. High drug load was achieved within the bead with a short curing time. Drug release was high in acidic medium (pH 1.2) vis-à-vis intestinal medium (pH 7.4). Ciprofloxacin hydrochloride release increased with an increasing concentration of ciprofloxacin and decreasing proportion of chitosan. Drug release followed both first-order and Higuchis root time kinetics showing non-Fickian release mechanism.

Magnetic-field-induced optical bistability in multifunctional Gd 2 O 3 :Er 3+ ∕Yb 3+ upconversion nanophosphor

The effect of an external magnetic field (0-1 T) on the upconversion emission (lambda(exc)=976 nm) of Gd(2)O(3):Er(3+)Yb(3+) nanocrystalline phosphor has been studied. Optical bistability (hysteresis behavior in the intensity of the optical emission) for different transitions of the Er(3+) ion has been observed for a complete cycle of the magnetic field between 0 and 1 T. The phosphor shows paramagnetic behavior, consistent with the presence of Gd(3+) ions, at room temperature. Interaction between induced magnetization in the Gd(2)O(3) host and the intrinsic magnetic moment of the nanosized clusters of Er(3+) and Yb(3+) ion pairs is proposed to be responsible for the hysteresis behavior.

Self-assembled aliphatic chain extended polyurethane nanobiohybrids: emerging hemocompatible biomaterials for sustained drug delivery.

Novel polyurethanes (PUs) have been synthesized using an aliphatic diisocyanate and aliphatic chain extenders with varying chain length. Nanocomposites of PUs have been prepared by dispersing 2-D nanoclay in poly-ol followed by prepolymerization and subsequent chain extension using various chain extenders. Systematic improvement in toughness and adequate enhancement in stiffness in the presence of nanoclay has been observed for PUs with longer chain extenders, and these new classes of nanocomposites exhibit no toughness-stiffness trade-off. Bottom-up self-assembly starting from the molecular level to micron-scale crystallite has been revealed through electronic structure calculation, X-ray diffraction, small-angle neutron scattering, atomic force microscopy and optical images. The role of hydrogen bonding has been revealed for this type of supramolecular assembly, and in the presence of organically modified nanoclay hydrogen bonding contributes to the formation of bigger clusters of nanocomposites. Controlled biodegradation of PU and its nanocomposites has been investigated in enzymatic media. Biocompatibility of these novel nanocomposites has been extensively verified through platelet adhesion, aggregation and hemolysis assay. Sustained drug delivery by biocompatible pristine PU and its nanocomposites has been demonstrated either by controlling the crystallite size of the polyurethane through alteration of the aliphatic chain length of the extender or by incorporating disc-like nanoclay, creating a tortuous path that results in delayed diffusion. Hence, the developed nanohybrids are potential biomaterials for tissue engineering and drug delivery.

Negative regulation of fibrin polymerization and clot formation by nanoparticles of silver

Thrombolytic therapy in acute stroke has reduced ischemia; however, it is also associated with increased incidence of intracerebral hemorrhage and expanding stroke. Platelets and fibrin are the major components of thrombi. Since fibrin is available in large concentration at lesion sites and in all types of thrombi, it is an obvious target for majority of antithrombotic therapies. Previously we have demonstrated innate antiplatelet properties with nanosilver. It can effectively prevent platelet activation in response to physiological agonists, under both in vitro as well as ex vivo conditions, and immobilize and stabilize proteins. Here we report for the first time that nanosilver can significantly retard fibrin polymerization kinetics both in pure and plasma-incorporated systems and hence can impede thrombus formation. We also discuss the conformational changes ensued upon fibrinogen following interaction with nanosilver. Together with its inherent antiplatelet and antibacterial properties, capacity to inhibit fibrin polymerization can open up possibilities of newer biomedical application and research potential involving silver nanoparticles.

Effect of Silver Nanoparticles on Growth of Eukaryotic Green Algae

Silver nanoparticles, endowed with powerful antimicrobial property, are the most widely used nanomaterial in consumer products, with associated risk of their easy access to environment and freshwater ecosystems by surface runoff. Although toxic effects of nanosilver on bacterial, fungal and mammalian cells have been documented, its impact on algal growth remains unknown. Pithophora oedogonia and Chara vulgaris are predominant members of photosynthetic eukaryotic algae, which form major component of global aquatic ecosystem. Here we report for the first time that nanosilver has significant adverse effects on growth and morphology of these filamentous green algae in a dose-dependent manner. Exposure of algal thalli to increasing concentrations of silver nanoparticles resulted in progressive depletion in algal chlorophyll content, chromosome instability and mitotic disturbance, associated with morphological malformations in algal filaments. SEM micrographs revealed dramatic alterations in cell wall in nanoparticle-treated algae, characterized with cell wall rupture and degradation in Pithophora. Although these observations underscore severe deleterious effects of nanosilver on aquatic environment, the information can also be exploited as a bioengineering strategy to control unwanted and persistent growth of noxious algal weeds that clog the municipal water supply and water channels and produce fouling of water bodies.

Long acting ophthalmic formulation of indomethacin: Evaluation of alginate gel systems

Different types of in situ gelling systems of indomethacin, in sodium alginate vehicle, were prepared and evaluated for their pharmaceutical properties including viscosity, sterility and drug content uniformity. The gelling efficacy of the prepared systems was evaluated by using an in house fabricated gelation cell. The in vitro release kinetics of the prepared systems was determined in simulated tear. The gelling time and the nature of the gel formed were dependent on the concentration of sodium alginate present in the systems. The drug release from these systems was extended up to 8 h and predominately followed zero-order kinetics.

Enhanced Red Upconversion Emission, Magnetoluminescent Behavior, and Bioimaging Application of NaSc0.75Er0.02Yb0.18Gd0.05F4@AuNPs Nanoparticles

The present study reports significant enhancement in the red upconversion emission of Er(3+) in NaSc0.8Er0.02Yb0.18F4 upconversion nanoparticles (UCNPs), via a two step process, (i) codoping of Gd(3+) ion at Sc(3+) site and (ii) attaching gold nanoparticles (AuNPs) at the surface of these codoped nanostructures, and further probes the use of these Gd:UCNPs@AuNPs for bioimaging application. The Gd(3+) codoping tailors the particle size (reduces) of UCNPs and bring out Er(3+)-Yb(3+) ion pair in close proximity, which promotes the cross relaxation mechanism and boosts the population in red emitting level (4)F9/2. Further, attachment of AuNPs on the surface of UCNPs gives 2-fold advantages, that is, reduction in green band (through resonance energy transfer with efficiency 31.54%) and enhancement in red band (through plasmonic effect). It gives red to green (R/G) ratio nearly 20:1 (almost single band red UC), which is quite promising for imaging application. In addition to this, codoping of Gd(3+) enhances the magnetic moment appreciably and the obtained magnetic moment for NaSc0.75Er0.02Yb0.18Gd0.05F4 UCNPs (∼1.7 emu/g) is close to the reported values for bioseparation in case of NPs. This shows the potential of the material for multimodal (optical and magnetic both) imaging application. These magnetoluminescence particles were found safe up to 1 mg/mL dose as assessed by cytotoxicity measurement in human cervical cancer (HeLa) and lung cancer (A549) cells. Ultrafine nanoparticles, transparent, and stable colloidal solution and the unique red UC emission endow these NPs as optical probe for imaging applications.

New Perspective in Garnet Phosphor: Low Temperature Synthesis, Nanostructures, and Observation of Multimodal Luminescence

Herein, we report a new concept for garnet materials in terms of the synthesis of nanocrystalline structure at low temperatures and its multimodal luminescence processes. Terbium- and ytterbium-ion-codoped yttrium gallium garnet nanophosphors have been synthesized via solution combustion technique; nearly pure phase nanophosphor samples were obtained. The synthesized nanophosphor shows efficient multimodal upconversion (UC), downshifting (DS), and quantum cutting (QC)/downconversion (DC) luminescence, which is a new paradigm in garnet material. The garnet nanophosphor shows strong green emission through DS and UC processes both. Furthermore, cooperative energy transfer (CET) has been described in detail, and a possible mechanism for the QC process is also proposed. A UV/blue photon absorbed by Tb(3+) ion splits into two near-infrared photons (wavelength range 900-1040 nm), emitted by a Yb(3+) ion pair, with an efficiency of more than 100%. The Yb(3+) concentration dependent ET from Tb(3+) to Yb(3+) has been verified using time domain analysis. An ET efficiency as high as 28% and a corresponding QC efficiency of about 128% (for 15 mol % of Yb(3+) concentration) have been attained. Such a multimode emitting nanophosphor could be very useful in display devices and for enhancing the conversion efficiency of next generation solar cells via spectral modification etc.