The Effect of Copper Salts on Bioactive Compounds and Ultrastructure of Wheat Plants

Abiotic stress agents, among them metal stress, can cause oxidative damage to plant cells. In defense, plants can increase the production of secondary metabolites in order to mitigate the harmful effects caused by them. The purpose of this work was to evaluate the effect of two types of copper salts (CuSO₄ and Cu(NO₃)₂), added in two different amounts in soil (150 mg/kg, respectively 300 mg/kg), on assimilating pigments, total polyphenols, antioxidant activity and the elemental composition of wheat. The obtained results were compared with those from control plants grown in the same conditions but without copper salts. The amount of assimilating pigments, total polyphenols, and antioxidant activity respectively increases or decreases in the plants treated with copper salts compared to the control depending on the stage of development of the plant. No significant damage induced in the leaves of the wheat plants treated with the selected salts was observed following the TEM analysis. In six-week-old plants it was observed by EDX analysis that the salts are transformed into nanoparticles. The bioactive compounds, elemental composition and their interaction is influenced by concentration of metal’s salt, type of salt and exposure period.     

Posetic Cluster Expansion for Substitution-Reaction Networks and Application to Methylated Cyclobutanes

Substitution-reaction networks frequently arise in chemistry and are naturally identifiable as “partially ordered sets” (or posets). The direction of the reaction identifies the partial ordering of the set of the member molecular species, for which various properties may be developed in light of the partial ordering. Here some general characteristics of such posets are noted, and a chemically appealing posetic cluster-expansion analysis of molecular properties is described and illustrated for methyl substitutions on cyclobutane. The results for computed energies and a few further selected properties are compared to alternative posetic approaches.     

Bilayer vesicles of amphiphilic cyclodextrins: host membranes that recognize guest molecules

A family of amphiphilic cyclodextrins (6, 7) has been prepared through 6-S-alkylation (alkyl=n-dodecyl and n-hexadecyl) of the primary side and 2-O-PEGylation of the secondary side of alpha-, beta-, and gamma-cyclodextrins (PEG=poly(ethylene glycol)). These cyclodextrins form nonionic bilayer vesicles in aqueous solution. The bilayer vesicles were characterized by transmission electron microscopy, dynamic light scattering, dye encapsulation, and capillary electrophoresis. The molecular packing of the amphiphilic cyclodextrins was investigated by using small-angle X-ray diffraction of bilayers deposited on glass and pressure-area isotherms obtained from Langmuir monolayers on the air-water interface. The bilayer thickness is dependent on the chain length, whereas the average molecular surface area scales with the cyclodextrin ring size. The alkyl chains of the cyclodextrins in the bilayer are deeply interdigitated. Molecular recognition of a hydrophobic anion (adamantane carboxylate) by the cyclodextrin vesicles was investigated by using capillary electrophoresis, thereby exploiting the increase in electrophoretic mobility that occurs when the hydrophobic anions bind to the nonionic cyclodextrin vesicles. It was found that in spite of the presence of oligo(ethylene glycol) substituents, the beta-cyclodextrin vesicles retain their characteristic affinity for adamantane carboxylate (association constant K(a)=7.1 x 10(3) M(-1)), whereas gamma-cyclodextrin vesicles have less affinity (K(a)=3.2 x 10(3) M(-1)), and alpha-cyclodextrin or non-cyclodextrin, nonionic vesicles have very little affinity (K(a) approximately 100 M(-1)). Specific binding of the adamantane carboxylate to beta-cyclodextrin vesicles was also evident in competition experiments with beta-cyclodextrin in solution. Hence, the cyclodextrin vesicles can function as host bilayer membranes that recognize small guest molecules by specific noncovalent interaction.     

The kinetics and mechanism of the oxidation of DL ethionine and thiourea by potassium ferrate

The kinetics of the reaction between ethionine and thiourea were investigated under pseudo and non-pseudo-first-order conditions. Ethionine was oxidized to the sulfoxide within 500 s and thiourea was oxidized to urea within 10 s. Above a pH of ca. 8.5 the reaction was first-order in the concentration of the organosulfur compound, the hydrogen ions and the ferrate ions, whereas, below this pH, the kinetics were independent of the hydrogen ion concentration. A possible mechanism for both compounds is initial protonation of the ferrate ion followed by the two electron rate-determining step of addition of oxygen to the organosulfur compound. The kinetic parameters for ethionine compare favorably with those for similar compounds, whereas thiourea tends to be more active. The rate constant for the rate-determining step is 4.1 × 10² M^–1 s^–1 for ethionine and 4.1 × 10³ M^–1 s^–1 for thiourea.     

An Iterative Modification of Shepard–Bernoulli Operator

We introduce an iterative modification of the combined Shepard operator of Bernoulli type, introduced in C?tina? (Calcolo 44:189–202, 2007), that is free from artificial setup of parameters, and corresponds to successive scaling.     

The influence of the nanofiller on thermal properties of thermoplastic polyurethane elastomers

Pure Fe₃O₄ and Mn-doped Fe₃O₄ nanoparticles were synthesized by simple wet chemical reduction technique using nontoxic precursors. Manganese doping of two concentrations, 10 and 15%, were employed. All the three synthesized nanoparticles were characterized by stoichiometry, crystal structure, and surface morphology. Thermal studies on as-synthesized nanoparticles of pure ferrite (Fe₃O₄) and manganese (Mn) doped ferrites were carried out. The thermal analysis of the three as-synthesized nanoparticles was done by thermogravimetric (TG), differential thermogravimetric, and differential thermal analysis techniques. All the thermal analyses were done in nitrogen atmosphere in the temperature range of 308–1233 K. All the thermocurves were recorded for three heating rates of 10, 15, and 20 K min^?1. The TG curves showed three steps thermal decomposition for Fe₃O₄ and two steps thermal decompositions for Mn-doped Fe₃O₄ nanoparticles. The kinetic parameters of the three as-synthesized nanoparticles were evaluated from the thermocurves employing Kissinger–Akahira–Sunose (KAS) method. The thermocurves and evaluated kinetic parameters are discussed in this paper.     

DISTRIBUTION OF TEMOPORFIN, A NEW PHOTOSENSITIZER FOR THE PHOTODYNAMIC THERAPY OF CANCER, IN A MURINE TUMOR MODEL

Abstract— The biodistribution of temoporfin (tetra[ m -hydroxyphenyl]chlorin, m -THPC), a recently developed photosensitizer, was investigated in BALB/c mice. The drug was administered intravenously (0.35-0.75 μmol/kg) to tumor-free mice or to mice implanted with the Colo 26 colorectal carcinoma. Blood and tissue samples were collected for up to 96 h post-dose. Drug concentrations were determined by HPLC coupled to photometric detection at 423 nm. Concentrations in blood and liver fell relatively rapidly such that blood concentrations at later time points were below the limit of detection. Tumor concentrations rose at first and then remained constant from 24 h. Temoporfin concentrations in some tissues, notably heart and skeletal muscle, declined only slowly when compared to blood. The tumor: tissue ratios for those organs that showed a more rapid decline in temoporfin concentrations were higher at later times, whereas in tissues such as muscle the ratio remained relatively constant. The organs with the highest tumor: tissue ratios were small intestine (8.6), liver (6.9) and skeletal muscle (5.0).     

Water‐Soluble Triarylborane Chromophores for One‐ and Two‐Photon Excited Fluorescence Imaging of Mitochondria in Cells

Three water‐soluble tetracationic quadrupolar chromophores comprising two three‐coordinate boron π‐acceptor groups bridged by thiophene‐containing moieties were synthesised for biological imaging applications. Compound 3 containing the bulkier 5‐(3,5‐Me₂C₆H₂)‐2,2′‐(C₄H₂S)₂‐5′‐(3,5‐Me₂C₆H₂) bridge is stable over a long period of time, exhibits a high fluorescence quantum yield and strong one‐ and two‐photon absorption (TPA), and has a TPA cross section of 268 GM at 800 nm in water. Confocal laser scanning fluorescence microscopy studies in live cells indicated localisation of the chromophore at the mitochondria; moreover, cytotoxicity measurements proved biocompatibility. Thus, chromophore 3 has excellent potential for one‐ and two‐photon‐excited fluorescence imaging of mitochondrial function in cells.