ABSTRACT
Starch-legume protein composites were obtained by extrusion of pea flour and pea starch-protein blend at various specific mechanical energies (100-2000â¯kJ/kg) and a temperature low enough to avoid expansion. The morphology of these composites displayed protein aggregates dispersed in a starch matrix, revealed by microscopy. Image analysis was used to determine the median width of protein aggregates (D50), their total perimeter and surface, from which a protein/starch interface index (Ii) was derived. The mechanical properties of composites were determined by a three-point bending test. The pea flour composites had a higher interface index Ii (1.8-3.1) with lower median particle width D50 (8-18⯵m) and a more brittle behaviour than the blend composites that had a lower Ii (1-1.1) and higher D50 (22-31⯵m). For both materials, rupture stress and strain were negatively correlated with Ii. This result suggested that there was a poor interfacial adhesion between the pea starch and proteins.
Subject(s)
Pea Proteins/chemistry , Pisum sativum/chemistry , Starch/chemistry , Color , Materials Testing , Particle Size , Surface Properties , TemperatureABSTRACT
El estudio del equilibrio ácido-base (EAB), su regulación y su interpretación ha sido objeto de debate desde los inicios del siglo XX. Las interpretaciones más empleadas y aceptadas están basadas en el concepto de pH introducido por Sorensen en 1909 y en la ecuación de Henderson-Hasselbalch en 1916. Desde entonces se han desarrollado nuevos conceptos destinados a completar y facilitar el entendimiento de los trastornos del EAB. A comienzo de los años 80 Peter Stewart puso en duda la interpretación clásica de las alteraciones del EAB y desarrolló un nuevo método. Esta innovadora visión de Stewart parece más apropiada para el estudio de los trastornos complejos del EAB que presentan los pacientes críticamente enfermos. El objetivo de este manuscrito es revisar y actualizar los conceptos básicos de la regulación del EAB, los métodos empleados para su evaluación, sus limitaciones y aplicaciones (AU)
The study of acid-base equilibrium, its regulation and its interpretation have been a source of debate since the beginning of 20th century. Most accepted and commonly used analyses are based on pH, a notion first introduced by Sorensen in 1909, and on the Henderson-Hasselbalch equation (1916). Since then new concepts have been development in order to complete and make easier the understanding of acid-base disorders. In the early 1980's Peter Stewart brought the traditional interpretation of acid-base disturbances into question and proposed a new method. This innovative approach seems more suitable for studying acid-base abnormalities in critically ill patients. The aim of this paper is to update acid-base concepts, methods, limitations and applications (AU)
Subject(s)
Humans , Male , Female , Acid-Base Equilibrium , Acid-Base Equilibrium/physiology , Bicarbonates/therapeutic use , Acidosis/etiology , Hypoalbuminemia/drug therapy , Metabolic Diseases/drug therapy , Hydrogen-Ion Concentration , Glomerular Filtration Rate , Electrolytes/metabolism , Electrolytes/therapeutic useABSTRACT
The study of acid-base equilibrium, its regulation and its interpretation have been a source of debate since the beginning of 20th century. Most accepted and commonly used analyses are based on pH, a notion first introduced by Sorensen in 1909, and on the Henderson-Hasselbalch equation (1916). Since then new concepts have been development in order to complete and make easier the understanding of acid-base disorders. In the early 1980's Peter Stewart brought the traditional interpretation of acid-base disturbances into question and proposed a new method. This innovative approach seems more suitable for studying acid-base abnormalities in critically ill patients. The aim of this paper is to update acid-base concepts, methods, limitations and applications.
Subject(s)
Acid-Base Equilibrium , Critical Illness , HumansABSTRACT
The foaming properties, foaming capacity and foam stability, of soluble complexes of pectin and a globular protein, napin, have been investigated with a "Foamscan" apparatus. Complementary, we also used SANS with a recent method consisting in an analogy between the SANS by foams and the neutron reflectivity of films to measure in situ film thickness of foams. The effect of ionic strength, of protein concentration and of charge density of the pectin has been analysed. Whereas the foam stability is improved for samples containing soluble complexes, no effect has been noticed on the foam film thickness, which is almost around 315Å whatever the samples. These results let us specify the role of each specie in the mixture: free proteins contribute to the foaming capacity, provided the initial free protein content in the bulk is sufficient to allow the foam formation, and soluble complexes slow down the drainage by their presence in the Plateau borders, which finally results in the stabilisation of foams.
Subject(s)
2S Albumins, Plant/chemistry , Pectins/chemistry , Osmolar Concentration , Static ElectricitySubject(s)
Anesthetics, Local/adverse effects , Myoclonus/chemically induced , Prilocaine/adverse effects , Anesthetics, Local/administration & dosage , Female , Follow-Up Studies , Humans , Injections, Spinal , Intraoperative Complications/chemically induced , Middle Aged , Myoclonus/physiopathology , Prilocaine/administration & dosage , Spinal Cord/physiopathologyABSTRACT
The binding of a cationic surfactant (hexadecyltrimethylammonium bromide, CTAB) to a negatively charged natural polysaccharide (pectin) at air-solution interfaces was investigated on single interfaces and in foams, versus the linear charge densities of the polysaccharide. Besides classical methods to investigate polymer/surfactant systems, we applied, for the first time concerning these systems, the analogy between the small angle neutron scattering by foams and the neutron reflectivity of films to measure in situ film thicknesses of foams. CTAB/pectin foam films are much thicker than the pure surfactant foam film but similar for high- and low-charged pectin/CTAB systems despite the difference in structure of complexes at interfaces. The improvement of the foam properties of CTAB bound to pectin is shown to be directly related to the formation of pectin-CTAB complexes at the air-water interface. However, in opposition to surface activity, there is no specific behavior for the highly charged pectin: foam properties depend mainly upon the bulk charge concentration, while the interfacial behavior is mainly governed by the charge density of pectin. For the highly charged pectin, specific cooperative effects between neighboring charged sites along the chain are thought to be involved in the higher surface activity of pectin/CTAB complexes. A more general behavior can be obtained at lower charge density either by using a low-charged pectin or by neutralizing the highly charged pectin in decreasing pH.
Subject(s)
Polysaccharides/chemistry , Surface-Active Agents/chemistry , Air , Carbohydrate Sequence , Cetrimonium , Cetrimonium Compounds/chemistry , Hydrogen-Ion Concentration , Models, Chemical , Molecular Sequence Data , Neutrons , Pectins/chemistry , Polymers/chemistry , Scattering, Radiation , Solubility , Surface Properties , Water/chemistryABSTRACT
This paper presents a novel, semiautomatic method for microscopic identification of multicomponent samples, which allows the identification, location, and percentage quantity of each component to be determined. The method involves applying discriminant analysis to a sequence of multichannel fluorescence microscopy images via a supervised learning approach; by selecting groups of pixels that are representative for each component type in a "known" sample, a computer is "taught" how to recognize the behavior (i.e., fluorescence emission) of the various components when illuminated under different spectral conditions. The identity, quantity, and location of these components in "unknown" samples (i.e., samples with the same component types but in different ratios or distributions) can then be investigated. The technique therefore enables semiautomatic quantitative fluorescence microscopy and has potential as a quality control tool. This work demonstrates the application of the technique to artificial and natural samples and critically discusses its quality, potential, and limitations.