A millimeter wavelength radiation source using a dual gratingresonator

A novel means of producing coherent radiation by passing an electron through a dual-grating resonator is presented, The observed radiation is in accordance with the Smith-Purcell dispersion relation for a single grating. Feedback is provided by a second grating. Experiments carried out at beam energies from 30-55 keV produced radiation at wavelengths from 6 to 0.75 mm. Power measurement were used to clarify the grating beam interaction, Indications are that operation could be easily extended to shorter wavelengths to provide an inexpensive and compact radiation source in the far-infrared     

The selectivity of electrosynthesised polymer membranes depends on the electrode dimensions: implications for biosensor applications

A biosensor selectivity coefficient defined for poly(o-phenylenediamine) electrosynthesised onto Pt microdisks and cylinders was unexpectedly found to change as the scale of the electrodes decreased, mainly due to enhanced permeability of a ubiquitous interference species in biological systems, ascorbic acid.     

Zeeman studies of the 0.839eV emission in SI GaAs:Cr

The multi-structured zero phonon transitions of the 0.839eV emission observed in SI GaAs:Cr have been investigated by Zeeman measurements. Magnetic splittings for the directions [111], [110] and [100] as well as angular dependence studies in the (110) plane show that the centre has a symmetry axis along [111] with a small orthorhombic distortion. The emissions cannot be due to the isolated [100] Jahn-Teller distorted Cr²⁺ ions observed in magnetic resonance but to [111] centres such as the (Cr²⁺-donor) pairs as suggested by White.     

Impact of a conformationally restricted receptor on the BF2 chelated azadipyrromethene fluorosensing platform

Conformational control of the receptor-fluorophore orientation of BF2 chelated azadipyrromethene sensors reveals two photophysically different modes of analyte triggered fluorescence switching both of which exhibit large off-on fluorescence intensity responses to the light input-output of the sensors in the visible red spectral region.     

In vitro demonstration of the heavy-atom effect for photodynamic therapy

Photodynamic therapy (PDT) is an emerging treatment modality for a range of disease classes, both cancerous and noncancerous. This has brought about an active pursuit of new PDT agents that can be optimized for the unique set of photophysical characteristics that are required for a successful clinical agent. We now describe a totally new class of PDT agent, the BF2-chelated 3,5-diaryl-1H-pyrrol-2-yl-3,5-diarylpyrrol-2-ylideneamines (tetraarylazadipyrromethenes). Optimized synthetic procedures have been developed to facilitate the generation of an array of specifically substituted derivatives to demonstrate how control of key therapeutic parameters such as wavelength of maximum absorbance and singlet-oxygen generation can be achieved. Photosensitizer absorption maxima can be varied within the body's therapeutic window between 650 and 700 nm, with high extinction coefficients ranging from 75,000 to 85,000 M(-1) cm(-1). Photosensitizer singlet-oxygen generation level was modulated by the exploitation of the heavy-atom effect. An array of photosensitizers with and without bromine atom substituents gave rise to a series of compounds with varying singlet-oxygen generation profiles. X-ray structural evidence indicates that the substitution of the bromine atoms has not caused a planarity distortion of the photosensitizer. Comparative singlet-oxygen production levels of each photosensitizer versus two standards demonstrated a modulating effect on singlet-oxygen generation depending upon substituent patterns about the photosensitizer. Confocal laser scanning microscopy imaging of 18a in HeLa cervical carcinoma cells proved that the photosensitizer was exclusively localized to the cellular cytoplasm. In vitro light-induced toxicity assays in HeLa cervical carcinoma and MRC5-SV40 transformed fibroblast cancer cell lines confirmed that the heavy-atom effect is viable in a live cellular system and that it can be exploited to modulate assay efficacy. Direct comparison of the efficacy of the photosensitizers 18b and 19b, which only differ in molecular structure by the presence of two bromine atoms, illustrated an increase in efficacy of more than a 1000-fold in both cell lines. All photosensitizers have very low to nondeterminable dark toxicity in our assay system.     

An Integrated Approach toward NanoBRET Tracers for Analysis of GPCR Ligand Engagement

Gaining insight into the pharmacology of ligand engagement with G-protein coupled receptors (GPCRs) under biologically relevant conditions is vital to both drug discovery and basic research. NanoLuc-based bioluminescence resonance energy transfer (NanoBRET) monitoring competitive binding between fluorescent tracers and unmodified test compounds has emerged as a robust and sensitive method to quantify ligand engagement with specific GPCRs genetically fused to NanoLuc luciferase or the luminogenic HiBiT peptide. However, development of fluorescent tracers is often challenging and remains the principal bottleneck for this approach. One way to alleviate the burden of developing a specific tracer for each receptor is using promiscuous tracers, which is made possible by the intrinsic specificity of BRET. Here, we devised an integrated tracer discovery workflow that couples machine learning-guided in silico screening for scaffolds displaying promiscuous binding to GPCRs with a blend of synthetic strategies to rapidly generate multiple tracer candidates. Subsequently, these candidates were evaluated for binding in a NanoBRET ligand-engagement screen across a library of HiBiT-tagged GPCRs. Employing this workflow, we generated several promiscuous fluorescent tracers that can effectively engage multiple GPCRs, demonstrating the efficiency of this approach. We believe that this workflow has the potential to accelerate discovery of NanoBRET fluorescent tracers for GPCRs and other target classes.     

Design variations of a polymer–enzyme composite biosensor for glucose: Enhanced analyte sensitivity without increased oxygen dependence

The glucose sensitivity and oxygen dependence of a variety of implantable biosensors based on glucose oxidase (GOx), incorporating an electrosynthesized poly-o-phenylenediamine (PPD) permselective barrier on 125-μm diameter Pt disks (Pt_D) and cylinders (Pt_C, 1-mm length), were measured and compared. Full glucose calibrations and experimental monitoring of solution oxygen concentration allowed us to determine apparent Michaelis–Menten parameters for glucose and oxygen. In the linear region of glucose response, the most sensitive biosensor design studied was Pt_D/PPD/GOx (enzyme deposited over polymer) that was 20 times more sensitive than the more widely used Pt_C/GOx/PPD (enzyme immobilized before polymer deposition) configuration. The oxygen dependence, quantified as K_M(O₂), of both active and less active designs was surprisingly similar, a finding that could be rationalized in terms of an increase in K_M(G) with increased enzyme loading. The Pt_D/PPD/GOx design will now enable us to explore glucose concentration dynamics in smaller and layered brain regions with good sensitivity and minimal interference from fluctuations in tissue pO₂.     

New rapid method to determine radon and thoron from a single counting sequence using a field portable alpha particle scintillometer

Measurement of soil-gas radon (Rn) concentration is an important parameter in estimating soil Rn potential for a building site. Typically, field methods for grab samples (as contrasted with continuous flow systems) using a protable alpha-scintillometer only considered²²²Rn (T _1/2= 3.8 d) and ignored²²⁰Rn (T _1/2=55 s). Now the calculation permits the determination of the concentrations of both isotopes with a single series of readings. A sample is collected and within 1 minute is introduced into the counting system. A series of 1 minute counts begins immediately and continues for 10 minutes. If high²²⁰Rn concentrations are present, there will be a rapid decay followed by a steady ingrowth of²²²Rn progeny. If very little²²⁰Rn is present, the ingrowth will be seen immediately. In either case, a non-linear least square fitting program from Statgraphics is used to obtain both concentrations at time zero. When inexact timings ranging from 1 to 30 seconds were imposed on the measured data, the method proved to be very robust; the biases did not exceed 15 percent.     

Observation of the effect of DAP separation on electron-hole pair ODMR signals in GaS

ODMR investigations of electron-hole pairs localized at donor-acceptor pairs with separations ranging from close to distant are reported. The resonances change from a triplet exciton spectrum to a single resonance at $\text{g}{}_{\mathrm{ex}}\text{=}\text{g}{}_{\mathrm{e}}\text{+}\text{g}{}_{\mathrm{h}}\text{2}$ corresponding to reduced exchange coupling.     

Optically detected electron resonance in phosphorus-doped ZnTe

Samples of ZnTe showing near gap edge luminescence predominantly due to exciton recombination at shallow neutral acceptors and donor- acceptor pair recombination have been investigated using optically detected magnetic resonance (ODMR). Emission polarization changes at 2.318 eV were observed due to magnetic resonance of electrons at g_e = + 0.401 ± 0.004. The observations are consistent with the donor trapped electron resonance resulting from microwave induced changes in donor-acceptor pair photoluminescence.