An Analytical Approach for the Design of Class-E Resonant DC-DC Converters

We present a new approach to design resonant dc-dc converters, that allows us to achieve both a more accurate implementation and a simpler architecture, by reducing the number of required passive components. The approach is applied to a class-E topology, and it is based on the analytic solution of the system of differential equations regulating the converter evolution. Our technique is also capable of taking into account the most important circuit nonidealities. This represents an important breakthrough with respect to the state of the art, where class-E circuit analysis is based on strong simplifying assumptions, and the final circuit design is achieved by means of numerical simulations after many time-consuming parametric sweeps. The developed methodology is dimensionless, and the achieved design curves can be denormalized to easily get the desired circuit design. Measurements on two different prototypes confirm an extremely high adherence to the developed mathematical approach.We present a new approach to design resonant dc-dc converters, that allows us to achieve both a more accurate implementation and a simpler architecture, by reducing the number of required passive components. The approach is applied to a class-E topology, and it is based on the analytic solution of the system of differential equations regulating the converter evolution. Our technique is also capable of taking into account the most important circuit nonidealities. This represents an important breakthrough with respect to the state of the art, where class-E circuit analysis is based on strong simplifying assumptions, and the final circuit design is achieved by means of numerical simulations after many time-consuming parametric sweeps. The developed methodology is dimensionless, and the achieved design curves can be denormalized to easily get the desired circuit design. Measurements on two different prototypes confirm an extremely high adherence to the developed mathematical approach

Design of epidermal growth factor immobilization on 3D biocompatible scaffolds to promote tissue repair and regeneration

Exogenous application of human epidermal growth factor (hEGF) stimulates epidermal wound healing. The aim of this study was to develop bioconjugates based on hEGF mimicking the protein in its native state and thus suitable for tissue engineering applications, in particular for treating skin-related disorders as burns. Ribonuclease A (RNase A) was used to investigate a number of different activated-agarose carriers: cyanogen bromide (CNBr)-activated-agarose and glyoxyl-agarose showed to preserve the appropriate orientation of the protein for receptor binding. EGF was immobilized on these carriers and immobilization yield was evaluated (100% and 12%, respectively). A peptide mapping of unbound protein regions was carried out by LC–MS to take evidence of the residues involved in the immobilization and, consequently, the flexibility and surface accessibility of immobilized EGF. To assess cell proliferative activities, 10, 25, 50, and 100 ng/mL of each immobilized EGF sample were seeded on fibroblast cells and incubated for 24, 48 and 72 h. The immobilized growth factor showed significantly high cell proliferative activity at 50 and 100 ng/mL compared to control and soluble EGF. Although both of the immobilized samples show dose-dependency when seeded with high number of fibroblast cells, CNBr-agarose-EGF showed a significantly high activity at 100 ng/mL and 72 h incubation, compared to glyoxyl-agarose-EGF

Batch and Flow Synthesis of Nucleosides by Enzymatic Transglycosylation

Enzymatic methods for the preparation of high-value products have clearly shown their potential in many areas, including nucleic acid chemistry. Enzymes of nucleic acid metabolism such as nucleoside phosphorylases (NPs, EC 2.4.2) can be conveniently used as biocatalysts in the synthesis of nucleoside analogues. These enzymes catalyze the reversible cleavage of the glycosidic bond of (deoxy)ribonucleosides in the presence of inorganic phosphate (Pi) to generate the nucleobase and \u3b1-D-(deoxy)ribose-1-phosphate (phosphorolysis). If a second nucleobase is added to the reaction medium, the formation of a new nucleoside can result (transglycosylation). Because of its broad substrate specificity [1,2], a purine nucleoside phosphorylase from Aeromonas hydrophila (AhPNP) was exploited to catalyze the \u201cone-pot, one-enzyme\u201d transglycosylation of 7-methylguanosine iodide with a series of 6-substituted purines, resulting in a moderate to high conversion (18-65%) of the bases into a 22-compound library of 6-substituted purine ribonucleosides [2]. Successively, AhPNP was covalently immobilized [3,4] in a pre-packed column containing aminopropyl silica particles. The resulting AhPNP-IMER (Immobilized Enzyme Reactor) was coupled on-line to a HPLC apparatus containing a semi-preparative chromatographic column. In such a system, \u201cone-enzyme\u201d transglycosylation and product purification were run in a single platform, affording a set of 6-modified purine ribonucleosides at a mg scale [4]. Using this \u201cflow-based\u201d approach, the synthesis of adenine nucleosides through a \u201ctwo-enzyme\u201d transglycosylation was carried out by connecting the AhPNP-IMER to uridine phosphorylase from Clostridium perfringens, immobilized on a silica monolithic column (CpUP-IMER)

HPLC determination of urinary 2,4- and 2,6-toluendiamines as potential degradation products of polyurethane breast implants

A reversed-phase HPLC method has been developed for the urinary determination of mutagenic 2,4- and 2,6-toluendiamines. These amines are degradation products of polyurethane, a material used to cover textured silicone breast implants. FMOC-Cl was used as fluorescent derivatising agent in order to obtain a limit of detection of 15 ng/ml in urine. Pre-treatment of urine samples was by liquid/liquid extraction and urine specimens of patients after surgery were analysed

Anti- and prooxidant activity of water soluble components of some common diet vegetables and the effect of thermal treatment

The pro-antioxidant activity of carrot, cauliflower, celery, eggplant, garlic, mushroom, onio, white cabbage, white potato, tomato, yellow bell pepper, and zucchini, was investigated. Juices obtained by centrifugation of vegetables were treated at different temperatures (2, 25, 102°C) and assessed for antioxidant activity (AA) using a model system beta carotene-linoleic acid. Antioxidant activity of vegetable juices showed a linear correlation with time. The equations of all straight lines obtained showed positive slope values indicating either an increase in antioxidant activity or a decrease in prooxidant activity during the reaction. Negative intercept values were found when the juices showed prooxidant activity at least during the first phase of the reaction. Mushroom and white cabbage always showed more than 80ª, while cauliflower, celery, and eggpland showed such high AA only after boiling. Tomato and yellow bell pepper were always prooxidant. Cluster analysis allowed the the vegetables to be divided into five groups according to their anti- and prooxidant behavior as a function of thermal treatment and reaction time. Vegetable juice components were separated on Bakerbond C18 solid phase extraction cartridge according to their polarity, and the AA of the bound and unbound fractions of each vegetable was also tested