Inverse polarography with stationary amalgam anodes: Basic principles and technique

A new method of electrochemical analysis has been devised in which the metallic ions present in an electrolyte are discharged into a mercury cathode. The amalgam electrode so formed is then combined with a standard reference electrode in a suitable dissolution medium and the cell thus produced is allowed to supply current against an opposing voltage set up on a potentiometer. By decreasing the potentiometer voltage in stages a curve of current against potential can be constructed for the dissolution of the amalgam anode; in this curve each metal gives rise to a characteristic wave from the height of which the amount of metal originally present can be derived. Although the method is not so universally applicable as the conventional polarographic technique with the dropping mercury cathode, it possesses advantages in sensitivity and simplicity in suitable cases and may form a useful complementary method of analysis.     

STUDIES OF ADHESION OF METAL PARTICLES TO SILICA PARTICLES BASED ON ZETA POTENTIAL MEASUREMENTS

The zeta-potentials of silica, copper, platinum and gold particles have been measured as a function of pH. The isoelectric points were found to be at pH 3.0, 5.8, 3.0 and 3.5, respectively. In the pH range 3.0 to 5.8 copper and silica particles are oppositely charged and accordingly the coating of silica with copper particles could be demonstrated. In the case of gold and platinum the sign of the charge is such that direct adhesion to silica particles cannot be expected and this was also demonstrated in the case of platinum.     

Applications of inverse gas chromatography in the study of liquid crystalline stationary phases

We describe measurements on a number of low-molar-mass and polymeric liquid crystals that contain the same mesogenic groups. Transition temperatures for the mesophases have been measured and the supercooled region of hexyloxycyanobiphenyl studied, revealing some differences from the stable mesophase. Activity coefficients and interaction parameters for a range of probes have been measured and allow us to determine the nature and origin of the thermodynamic interactions in the systems. A discussion of how this fundamental information can be used in designing more efficient stationary phases for analytical gas chromatography is also presented.     

<Emphasis Type="Italic">N</Emphasis>-arachidonoyl glycine,an abundant endogenous lipid,potently drives directed cellular migration through GPR18, the putative abnormal cannabidiol receptor

Background  

Microglia provide continuous immune surveillance of the CNS and upon activation rapidly change phenotype to express receptors that respond to chemoattractants during CNS damage or infection. These activated microglia undergo directed migration towards affected tissue. Importantly, the molecular species of chemoattractant encountered determines if microglia respond with pro- or anti-inflammatory behaviour, yet the signaling molecules that trigger migration remain poorly understood. The endogenous cannabinoid system regulates microglial migration via CB₂ receptors and an as yet unidentified GPCR termed the 'abnormal cannabidiol' (Abn-CBD) receptor. Abn-CBD is a synthetic isomer of the phytocannabinoid cannabidiol (CBD) and is inactive at CB₁ or CB₂ receptors, but functions as a selective agonist at this G_i/o-coupled GPCR. N-arachidonoyl glycine (NAGly) is an endogenous metabolite of the endocannabinoid anandamide and acts as an efficacious agonist at GPR18. Here, we investigate the relationship between NAGly, Abn-CBD, the unidentified 'Abn-CBD' receptor, GPR18, and BV-2 microglial migration.     

Nanofibrillar Peptide Hydrogels for the Immobilization of Biocatalysts for Chemical Transformations

Enzymes are attractive, “green” alternatives to chemical catalysts within the industrial sector, but their robustness to environmental conditions needs optimizing. Here, an enzyme is tagged chemically and recombinantly with a self‐assembling peptide that allows the conjugate to spontaneously assemble with pure peptide to form β‐sheet‐rich nanofibers decorated with tethered enzyme. Above a critical concentration, these fibers entangle and form a 3D hydrogel. The immobilized enzyme catalyzes chemical transformations and critically its stability is increased significantly where it retains activity after exposure to high temperatures (90 °C) and long storage times (up to 12 months).