Raman Imaging: An Impending Approach Towards Cancer Diagnosis

In accordance with the recent studies, Raman spectroscopy is well experimented as a highly sensitive analytical and imaging technique in biomedical research, mainly for various disease diagnosis including cancer. In comparison with other imaging modalities, Raman spectroscopy facilitate numerous assistances owing to its low background signal, immense spatial resolution, high chemical specificity, multiplexing capability, excellent photo stability and non-invasive detection capability. In cancer diagnosis Raman imaging intervened as a promising investigative tool to provide molecular level information to differentiate the cancerous vs non-cancerous cells, tissues and even in body fluids. Anciently, spontaneous Raman scattering is very feeble due to its low signal intensity and long acquisition time but new advanced techniques like coherent Raman scattering (CRS) and surface enhanced Raman scattering (SERS) gradually superseded these issues. So, the present review focuses on the recent developments and applications of Raman spectroscopy-based imaging techniques for cancer diagnosis.     

Scanning tunneling microscopy/spectroscopy on Au nanoparticles assembled using lauryl amine (LAM) and octadecane thiol (ODT)

In this report, we demonstrate scanning tunneling microscopy and spectroscopy on thin films of lauryl amine (LAM) and octadecane thiol (ODT) protected gold nanoparticles. We show that the zero current in the I-V curves (measure of Coulomb blockade (CB) of the nanoparticles) depends on the properties of the spacer molecule. In both the cases the gap voltage and the tunneling current at which the images are obtained are quite different which is further confirmed from the fitting performed based on the orthodox theory. The values for the capacitance and charging energy obtained from the fitting for ODT capped particles are comparable to the values obtained using spherical capacitor model. In contrast, values of these parameters were found to differ for LAM capped nanoparticles. While imaging, ODT capped nanoparticles were observed to drag along the scan direction leading to ordering of particles. Images of LAM capped gold nanoparticles show local ordering in self-assembly of particles although no evidence of large scale ordering in spatial Fourier transform was seen. These observations suggest that nanoparticles with larger CB would be imaged nonevasively in contrast to small CB systems for which tip induced effects will be dominant. In both the systems the current was found to rise faster than theoretical curves based on the orthodox theory suggesting that mechanism of charge transfer in this case may involve field emission rather than tunneling through a rectangular barrier. An attempt has been made to explain charge transfer based on Fowler-Nordheim (F-N) plots of the I-V curves.     

Self‐Assembly of DNA–Oligo(p‐phenylene‐ethynylene) Hybrid Amphiphiles into Surface‐Engineered Vesicles with Enhanced Emission

Surface‐addressable nanostructures of linearly π‐conjugated molecules play a crucial role in the emerging field of nanoelectronics. Herein, by using DNA as the hydrophilic segment, we demonstrate a solid‐phase “click” chemistry approach for the synthesis of a series of DNA–chromophore hybrid amphiphiles and report their reversible self‐assembly into surface‐engineered vesicles with enhanced emission. DNA‐directed surface addressability of the vesicles was demonstrated through the integration of gold nanoparticles onto the surface of the vesicles by sequence‐specific DNA hybridization. This system could be converted to a supramolecular light‐harvesting antenna by integrating suitable FRET acceptors onto the surface of the nanostructures. The general nature of the synthesis, surface addressability, and biocompatibility of the resulting nanostructures offer great promises for nanoelectronics, energy, and biomedical applications.     

Design and synthesis of highly stable poly(tetrafluoroethylene)-zirconium phosphate (PTFE-ZrP) ion-exchange membrane for vanadium redox flow battery (VRFB)

Vanadium redox flow battery (VRFB) is a promising technology for large-scale renewable energy storage. Design of ion-exchange membrane (IEM) with desired properties like low-cost, mechanically chemically stable, low vanadium ion permeability and high proton conductivity is one of the major challenges. Here, we report the design and synthesis of novel poly(tetrafluoroethylene)-zirconium phosphate (PTFE-ZrP) asymmetric IEM using a simple brush coating method. XRD results confirmed the presence of α-ZrP crystalline phase onto the top layer of the membrane. Excellent mechanical strength was observed with burst pressure of 3.22 × 10⁵ N m^?2. Oxidative stability of membrane in Fenton’s reagent was much better than Nafion-115. Vanadium ion (V⁴⁺) permeability of the membrane was more than three times lower than that of Nafion-115. Single-cell VRFB with PTFE-ZrP membrane showed ～80% energy efficiency below 30 mA cm^?2. Very high columbic efficiency ～100% of VRFB with PTFE-ZrP membrane confirmed little contamination of electrolyte due to cross-mixing.     

Kinetic studies on saponification of ethyl acetate using an innovative conductivity‐monitoring instrument with a pulsating sensor

An innovative conductometric measurement technique using a nonconventional but high‐performance (high‐precision, high‐resolution, rapid response features for online graphic display) in house–built pulsating conductivity monitoring instrument has been deployed to study the kinetic behavior during the reaction of ethyl acetate and NaOH. A laboratory‐made constant temperature reaction bath with the facility of continuous stirring of solution for homogeneous mixing was used to carry out experiments at desired solution temperatures. Rate constants of the saponification reaction in the temperature range at various temperatures (30–55°C) were determined, and the results were compared with the reported values. Although the reported data exhibit wide scatter, our data are in agreement with some of the literature data. From these data, thermodynamic parameters such as activation energy, activation enthalpy, activation entropy, and activation free energy have been evaluated. With the introduction of this novel conductometric measurement technique, the determination of rate constants at various solution temperatures becomes much simpler and faster. © 2011 Wiley Periodicals, Inc. Int J Chem Kinet 43: 648–656, 2011     

Imaging the neural circuitry and chemical control of aggressive motivation

Background  

With the advent of functional magnetic resonance imaging (fMRI) in awake animals it is possible to resolve patterns of neuronal activity across the entire brain with high spatial and temporal resolution. Synchronized changes in neuronal activity across multiple brain areas can be viewed as functional neuroanatomical circuits coordinating the thoughts, memories and emotions for particular behaviors. To this end, fMRI in conscious rats combined with 3D computational analysis was used to identifying the putative distributed neural circuit involved in aggressive motivation and how this circuit is affected by drugs that block aggressive behavior.     

Probing decoherence with electromagnetically induced transparency in superconductive quantum circuits

Superconductive quantum circuits comprise quantized energy levels that may be coupled via microwave electromagnetic fields. Described in this way, one may draw a close analogy to atoms with internal (electronic) levels coupled by laser light fields. In this Letter, we present a superconductive analog to electromagnetically induced transparency that utilizes superconductive quantum circuit designs of present day experimental consideration. We discuss how a superconductive analog to electromagnetically induced transparency can be used to establish macroscopic coherence in such systems and, thereby, be utilized as a sensitive probe of decoherence.     

Test by NMR of the phase coherence of electromagnetically induced transparency

Electromagnetically induced transparency is an effect observed in atomic systems, originating from quantum interference, in which electromagnetic transitions to and from a certain quantum state become suppressed. This dark state is also characterized by a quantum phase, relative to other states, which theoretically should stop evolving, but remain phase coherent, during transparency. We test this theoretical prediction using techniques developed for liquid-state nuclear magnetic resonance quantum computation, applied to a spin-7/2 nuclear spin system. A sequence of quantum operations is applied to create the dark state, and during transparency its phase evolution is measured relative to a reference state using Ramsey interferometry. Experimental measurements of the fringe visibility are in excellent agreement with theoretical expectations, taking into account measured decoherence rates.     

Gold nanosheets via reduction of aqueous chloroaurate ions by anthracene anions bound to a liquid-liquid interface

Anthracene anions bound to a liquid-liquid interface and charged by photochemically reduced Keggin ions when exposed to aqueous chloroaurate ions result in the formation of high concentration of thin, gold nanosheets at the interface.