Hg-supported phospholipid monolayer as rapid screening device for low molecular weight narcotic compounds in water.

This study positions the fabricated Pt/Hg-supported phospholipid sensor element in the context of more conventional biomembrane-based screening platforms. The technology has been used together with immobilised artificial membrane (IAM) chromatography and COSMOmic simulation methods to screen the interaction of a series of low molecular weight narcotic organic compounds in water with phosphatidylcholine (PC) membranes. For these chemicals it is shown that toxicity to aquatic species is related to compound hydrophobicity which is associated with compound accumulation in the phospholipid membrane as modelled by IAM chromatography measurements and COSMOmic simulations.

Predicting the phospholipophilicity of monoprotic positively charged amines.

The sorption affinity of eighty-six charged amine structures to phospholipid monolayers (log K) was determined using immobilized artificial membrane high-performance liquid chromatography (IAM-HPLC). The amine compounds covered the most prevalent types of polar groups, widely ranged in structural complexity, and included forty-seven pharmaceuticals, as well as several narcotics and pesticides. Amine type specific corrective increments were used to align log K data with bilayer membrane sorption coefficients (K(IAM)).

Phospholipophilicity of CxHyN(+) amines: chromatographic descriptors and molecular simulations for understanding partitioning into membranes.

Using immobilized artificial membrane high-performance liquid chromatography (IAM-HPLC) the sorption affinity of 70 charged amine structures to phospholipids was determined. The amines contained only 1 charged moiety and no other polar groups, the rest of the molecule being aliphatic and/or aromatic hydrocarbon groups. We systematically evaluated the influence of the amine type (1°, 2°, 3° amines and quaternary ammonium), alkyl chain branching, phenyl ring positioning, charge positioning (terminal vs.

Silver and cesium diffusion dynamics at the β-SiC Σ5 grain boundary investigated with density functional theory molecular dynamics and metadynamics.

The diffusion and release of silver-110m, a strong γ-radiation emitter, through silicon carbide in coated nuclear fuel particles has remained an unsolved topic since it was first observed 40 years ago. The challenge remains to explain why, contrary to other elements, silver is capable of escaping the ceramic diffusion barriers. The current work investigates the underlying differences in the diffusion of silver and cesium along a symmetric tilt Σ5 grain boundary of β-SiC through accelerated density functional theory molecular dynamics simulations.

Dimensionality transformation through paddlewheel reconfiguration in a flexible and porous Zn-based metal-organic framework.

The reaction between Zn and a pyrene-based ligand decorated with benzoate fragments (H(4)TBAPy) yields a 2D layered porous network with the metal coordination based on a paddlewheel motif. Upon desolvation, the structure undergoes a significant and reversible structural adjustment with a corresponding reduction in crystallinity. The combination of computationally assisted structure determination and experimental data analysis of the desolvated phase revealed a structural change in the metal coordination geometry from square-pyramidal to tetrahedral.