M. Eswaramoorthy

Intrinsically Fluorescent Carbon Nanospheres as a Nuclear Targeting Vector: Delivery of Membrane-Impermeable Molecule to Modulate Gene Expression In Vivo

In this report, we demonstrate glucose-derived carbon nanospheres to be an emerging class of intracellular carriers. The surfaces of these spheres are highly functionalized and do not need any further modification. Besides, the intrinsic fluorescence property of carbon nanospheres helps in tracking their cellular localization without any additional fluorescent tags. The spheres are found to target the nucleus of the mammalian cells, causing no toxicity. Interestingly, the in vivo experiments show that these nanospheres have an important ability to cross the blood-brain barrier and localize in the brain besides getting localized in the liver and the spleen. There is also evidence to show that they are continuously being removed from these tissues over time. Furthermore, these nanospheres were used as a carrier for the membrane-impermeable molecule CTPB (N-(4-chloro-3-trifluoromethylphenyl)-2-ethoxybenzamide), the only known small-molecule activator of histone acetyltransferase (HAT) p300. Biochemical analyses such as Western blotting, immunohistochemistry, and gene expression analysis show the induction of the hyperacetylation of histone acetyltransferase (HAT) p300 (autoacetylation) as well as histones both in vitro and in vivo and the activation of HAT-dependent transcription upon CTPB delivery. These results establish an alternative path for the activation of gene expression mediated by the induction of HAT activity instead of histone deacetylase (HDAC) inhibition.

A study of micropores in single-walled carbon nanotubes by the adsorption of gases and vapors

Adsorption of N2, benzene and methanol have been studied on as-prepared single-walled carbon nanotubes (SWNT) as well as SWNTs treated with HCl and HNO3. These nanotubes are good microporous materials with total surface areas well above 400 m2/g and internal surface areas of 300 m2/g or higher. Benzene molecules are shown to be adsorbed within the pores of the SWNTs.

Light-Harvesting Hybrid Assemblies

Light-harvesting hybrids have gained much importance as they are considered as potential mimics for photosynthetic systems. In this Concept article we introduce the design concepts involved in the building up of light-harvesting hybrids; these resemble the well-studied organic-based assemblies for energy transfer. We have structured this article into three parts based on the strategies adopted in the synthesis of hybrid assemblies, as covalent, semicovalent, and noncovalent procedures. Furthermore, the properties and structural features of the hybrids and analogous organic assemblies are compared. We also emphasize the challenges involved in the processability of these hybrid materials for device applications and present our views and results to address this issue through the design of soft-hybrids by a solution-state, noncovalent, self-assembly process.

Highly pure solid-state white-light emission from solution-processable soft-hybrids.

Highly pure and solution processable white-light-emitting hybrids are presented. These soft-hybrids are designed by an organic-inorganic supramolecular co-assembly in water. White-light emission is achieved by partial energy transfer (ET) between donor and acceptor molecules anchored on the inorganic component. The unique and remarkable processability feature of these hybrids is demonstrated by painting/writing onto large glass and flexible plastic substrates.

Water-solubilized aminoclay–metal nanoparticle composites and their novel properties

Nanoparticles of metals such as Au, Ag, Pd and Pt embedded in exfoliated sheets of aminoclays of the type R8Si8Mg6O16(OH)4, where R = CH2CH2NH2 are entirely water soluble. These sheets of the composite come to the organic-aqueous interface on addition of alkane thiols to the aqueous layer.

A Novel Activator of CBP/p300 Acetyltransferases Promotes Neurogenesis and Extends Memory Duration in Adult Mice

Although the brain functions of specific acetyltransferases such as the CREB-binding protein (CBP) and p300 have been well documented using mutant transgenic mice models, studies based on their direct pharmacological activation are still missing due to the lack of cell-permeable activators. Here we present a small-molecule (TTK21) activator of the histone acetyltransferases CBP/p300, which, when conjugated to glucose-based carbon nanosphere (CSP), passed the blood–brain barrier, induced no toxicity, and reached different parts of the brain. After intraperitoneal administration in mice, CSP-TTK21 significantly acetylated histones in the hippocampus and frontal cortex. Remarkably, CSP-TTK21 treatment promoted the formation of long and highly branched doublecortin-positive neurons in the subgranular zone of the dentate gyrus and reduced BrdU incorporation, suggesting that CBP/p300 activation favors maturation and differentiation of adult neuronal progenitors. In addition, mRNA levels of the neuroD1 differentiation marker and BDNF, a neurotrophin required for the terminal differentiation of newly generated neurons, were both increased in the hippocampus concomitantly with an enrichment of acetylated-histone on their proximal promoter. Finally, we found that CBP/p300 activation during a spatial training, while not improving retention of a recent memory, resulted in a significant extension of memory duration. This report is the first evidence for CBP/p300-mediated histone acetylation in the brain by an activator molecule, which has beneficial implications for the brain functions of adult neurogenesis and long-term memory. We propose that direct stimulation of acetyltransferase function could be useful in terms of therapeutic options for brain diseases.

Mixing Does the Magic: A Rapid Synthesis of High Surface Area Noble Metal Nanosponges Showing Broadband Nonlinear Optical Response

Here we report an instantaneous formation of high surface area metal nanosponges through a one-step inexpensive method in a completely green solvent, water. Merely by optimizing the concentration of the precursors and the reducing agent, we were able to generate a three-dimensional porous structure made up of nanowire networks. This is a general process, involves a simple, room temperature reduction of metal salts with sodium borohydride, and is therefore scalable to any amount. Further, these nanoporous metals because of their network structures show optical limiting behavior of a true broadband nature that would find applications in optoelectronic nanodevices.

pH-Sensitive breathing of clay within the polyelectrolyte matrix.

Stimuli-responsive organic-inorganic hybrid spheres were synthesized by coating the colloidal polystyrene spheres with polyelectrolyte-protected aminoclay, Mg phyllo(organo)silicate layers in a layer-by-layer method. The clay layers are sandwiched between the polyelectrolyte layers. The aminoclay swells in water due to protonation of amino groups, and the degree of swelling depends on the pH of the medium. As a result, the hybrid spheres undergo a size change up to 60% as the pH is changed from 9 to 4. The stimuli-responsive property of the hybrid spheres was used for the release of ibuprofen and eosin at different pH.

Synthesis, structure and properties of homogeneous BC4N nanotubes

BCN nanotube brushes have been obtained by the high temperature reaction of amorphous carbon nanotube (a-CNT) brushes with a mixture of boric acid and urea. The a-CNT brushes themselves were obtained by the pyrolysis of glucose in a polycarbonate membrane. The BCN nanotubes have been characterized by EELS, XPS, electron microscopy, Raman spectroscopy and other techniques. The composition of these nanotubes is found to be BC4N. The nanotubes, which are stable up to 900 °C, are insulating and nonmagnetic. They exhibit a selective uptake of CO2 up to 23.5 wt%. In order to understand the structure and properties, we have carried out first-principles density functional theory based calculations on (6,0), (6,6) and (8,0) nanotubes with the composition BC4N. While (8,0) BC4N nanotubes exhibit a semiconducting gap, the (6,0) BC4N nanotube remains metallic if ordered BN bonds are present in all the six-membered rings. The (6,6) BC4N nanotubes, however, exhibit a small semiconducting gap unlike the carbon nanotubes. The most stable structure is predicted to be the one where BN3 and NB3 units connected by a B–N bond are present in the graphite matrix, the structure with ordered B–N bonds in the six-membered rings of graphite being less stable. In the former structure, (6,0) nanotubes also exhibit a gap. The calculations predict BC4N nanotubes to be overall nonmagnetic, as is indeed observed.

Aminoclay: a functional layered material with multifaceted applications

Layered silicates provide an interesting avenue to novel materials. There has been a growing interest in recent years for the development of functional materials using tailor made clays. This review highlights one such tailor made, water dispersible aminopropyl functionalized magnesium phyllosilicate (aminoclay) of the type R8Si8Mg6O16(OH)4, (where R = –CH2CH2NH2) and its multiple applications in catalysis, biology, fuel cells and light-harvesting hybrids.