Level-set techniques for microwave medical imaging

Microwave tomographic imaging is showing significant promise as a new technique for the early detection of breast cancer. Its physical basis is the contrast between the dielectric properties of the healthy breast tissue and the malignant tumors at microwave frequencies. We propose and analyze a novel shape-reconstruction technique for the early detection of breast cancer from microwave data which is based on a level-set technique. The advantages of this method compared to more traditional pixel-based approaches are well-defined boundaries and the incorporation of an intrinsic regularization in form of a-priori assumptions about the general anatomical structure of breast that reduces the dimensionality of the inverse problem and thereby stabilizes the reconstruction. Our goal is not only to detect the tumors but to simultaneously determine their approximate locations, sizes and permittivity values. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim)     

Evaluation of the Use of Elicitors for the Production of Antioxidant Compounds in Liquid Cultures of Ganoderma curtisii from Costa Rica

The use of substances or conditions as elicitors can significantly increase the production of secondary metabolites. In this research, the effects of different elicitors on the production of antioxidant secondary metabolites were evaluated in a strain of Ganoderma sp. The elicitors tested were pH changes in different growth phases of the fungus (pH 3, 5.5 and 8), different concentrations of peptone as a nitrogen source (1 g/L and 10 g/L), and the addition of chemical agents to the culture medium (ethanol, growth regulators, and salts). The alkaline pH during the stationary phase and the high availability of nitrogen were effective elicitors, producing cultures with higher antioxidant activity (37.87 g/L and 43.13 g/L dry biomass) although there were no significant differences with other treatments.     

Enantioselective 1,3-Dipolar Cycloaddition Using (Z)-α-Amidonitroalkenes as a Key Step to the Access to Chiral cis-3,4-Diaminopyrrolidines

The enantioselective 1,3-dipolar cycloaddition between imino esters and (Z)-nitroalkenes bearing a masked amino group in the β-position was studied using several chiral ligands and silver salts. The optimized reaction conditions were directly applied to the study of the scope of the reaction. The determination of the absolute configuration was evaluated using NMR experiments and electronic circular dichroism (ECD). The reduction and hydrolysis of both groups was performed to generate in an excellent enantiomeric ratio the corresponding cis-2,3-diaminoprolinate.     

PET Imaging of the Neuropeptide Y System: A Systematic Review

Neuropeptide Y (NPY) is a vastly studied biological peptide with numerous physiological functions that activate the NPY receptor family (Y₁, Y₂, Y₄ and Y₅). Moreover, these receptors are correlated with the pathophysiology of several diseases such as feeding disorders, anxiety, metabolic diseases, neurodegenerative diseases, some types of cancers and others. In order to deepen the knowledge of NPY receptors’ functions and molecular mechanisms, neuroimaging techniques such as positron emission tomography (PET) have been used. The development of new radiotracers for the different NPY receptors and their subsequent PET studies have led to significant insights into molecular mechanisms involving NPY receptors. This article provides a systematic review of the imaging biomarkers that have been developed as PET tracers in order to study the NPY receptor family.     

General electrochemical Minisci alkylation of N-heteroarenes with alkyl halides

Herein, we report, a general, facile and environmentally friendly Minisci-type alkylation of N-heteroarenes under simple and straightforward electrochemical conditions using widely available alkyl halides as radical precursors. Primary, secondary and tertiary alkyl radicals have been shown to be efficiently generated and coupled with a large variety of N-heteroarenes. The method presents a very high functional group tolerance, including various heterocyclic-based natural products, which highlights the robustness of the methodology. This applicability has been further proved in the synthesis of various interesting biologically valuable building blocks. In addition, we have proposed a mechanism based on different proofs and pieces of electrochemical evidence.

Herein, we report, a general, facile and environmentally friendly Minisci-type alkylation of N-heteroarenes under simple and straightforward electrochemical conditions using widely available alkyl halides as radical precursors.     

Self-Assembled Binaphthyl-Bridged Amphiphilic AABB Phthalocyanines: Nanostructures for Efficient Antimicrobial Photodynamic Therapy

Herein, the photodynamic activity of phthalocyanine (pc)-assembled nanoparticles against bacterial strains is demonstrated. The photosensitizers (PS) studied in this work are two chiral Zn^IIPcs ( PS-1 and PS-2 ), with an AABB geometry (where A and B refer to differently substituted isoindole constituents). They contain differently functionalized, chiral binaphthyloxy-linked A isoindole units, which determine the hydrophobicity of the system, and cationic methyl pyridinium moieties in the other two isoindoles to embody hydrophilicity. Both compounds have the ability to self-assemble into nanoparticles in aqueous media and have proved efficient in the photo-inactivation of Staphylococcus aureus and Escherichia coli, selected as models of Gram-positive and Gram-negative bacteria. The average size of the nanoparticles was determined by substitution at the binaphthyl core and, in turn, influences the toxicity of the PS. Thus, PS-1 , presenting a nonsubstituted binaphthyl core, forms larger nanoparticles with a larger cationic surface than the octyl-functionalized PS-2 . Although both PSs present similar structure and photophysical features, the self-assembled nanostructures of PS-1 are more effective at killing both types of strain, showing an outstanding photo-inactivation capacity with the Gram-negative E. coli.     

Determination of pesticides in dried minor tropical fruits from Colombia using the Quick,Easy, Cheap,Effective, Rugged,and Safe method‐gas chromatography–tandem mass spectrometry

The AOAC 2007.1 quick, easy, cheap, effective, rugged, and safe official method, together with gas chromatography coupled to a triple quadrupole mass spectrometer was applied for the analysis of 38 multiclass pesticides from dried fruits typically cultivated and exported from Colombia: uchuva (Physalis peruviana), lulo (Solanum quitoense), guanabana (Anona muricata), and pitahaya (Hylocereus undatus). The whole method was validated in terms of matrix‐matched calibration, matrix effect, and recovery using atrazine‐d₅ as internal standard, triphenylphosphate for quality control of the injection, and a proper mixture of analytes protectants. Matrix‐matched calibration data were found satisfactory for all pesticides and dried fruits, reporting R² values above 0.99. Matrix effect values evidenced the existence of such effect in most cases. The applied procedure gave satisfactory recovery percentages (70–120%) and relative standard deviation values (< 20%) for 92% of the 456 combinations pesticide/fruit studied (spiked levels of 25, 200, and 400 µg/kg). Finally, 20 real dried fruit samples were analyzed and residues of tebuconazole were found in two samples of uchuva at a concentration below the lowest calibration level of the method for one of them and at 10.8 ± 1.6 µg/kg for the other, being below or similar to the general maximum residue level established for monitoring purposes in food applications.     

Optimal time allocation in active retirement

Central European Journal of Operations Research - We set up a lifecycle model of a retired scholar who chooses optimally the time devoted to different activities including physical activity,...     

Applying the voltammetry of microparticles to assess the metal ion excess following a precipitation reaction: the determination of arsenic

Journal of Solid State Electrochemistry - Here we demonstrate that the metal ion excess after precipitating a sparingly soluble metal salt can be conveniently determined by a secondary...     

Ultrathin Films of Porous Metal–Organic Polyhedra for Gas Separation

Ultrathin films of a robust Rh^II-based porous metal–organic polyhedra (MOP) have been obtained. Homogeneous and compact monolayer films (ca. 2.5 nm thick) were first formed at the air–water interface, deposited onto different substrates and characterized using spectroscopic methods, scanning transmission electron microscopy and atomic force microscopy. As a proof of concept, the gas separation performance of MOP-supported membranes has also been evaluated. Selective MOP ultrathin films (thickness ca. 60 nm) exhibit remarkable CO₂ permeance and CO₂/N₂ selectivity, demonstrating the great combined potential of MOP and Langmuir-based techniques in separation technologies.