RESUMO
Studies on the effect of urea on micelle formation and structure of n-octyl-beta-D-thioglucoside (OTG) and N-decanoyl-N-methylglucamide (MEGA-10) were carried out by using the steady-state and time-resolved fluorescence techniques, together with combined static and dynamic light scattering measurements. A similar increase in the critical micelle concentration with the urea addition was observed for both surfactants. This behavior was attributed to a rise in the solubility of hydrocarbon tails and the increase of solvation of the headgroup of the surfactants in the presence of urea. Structural studies mainly based on the analysis of the hydrodynamic radius and aggregation number of micelles revealed that urea induces changes much more significant on micelles of OTG. Particularly, it was found that, whereas the surface area per headgroup of OTG increases with the urea concentration, it does decrease in the case of MEGA-10. This fact suggests that different action mechanisms operate for both surfactants. Accordingly, investigations on the micellar microstructure based on the study of microenvironmental properties such as micropolarity and microviscosity also indicated a more pronounced effect in the case of OTG. Although changes were not observed in the hydrophobic inner region of both micellar systems, a significant increase of polarity and viscosity in the micellar interface of OTG suggests a direct participation of urea in the micellar solvation layer. The differences between the observed behaviors for both micellar systems were interpreted on the basis of two features: the weaker hydration and greater rigidity of the OTG headgroup as compared with MEGA-10.
RESUMO
Synthesis, characterization and spectroscopic investigation of maslinic acid labeled with fluorescent 7-amino-4-methylcoumarin is reported. It was found that the coumarin-maslinic derivative (MaCo) forms an excellent fluorescence resonance energy transfer (FRET) pair with the tryptophan (Trp) residue of human serum albumin (HSA). This feature allowed for monitoring HSA conformational alterations by measuring the distance between donor (Trp) and acceptor (MaCo) through Förster energy transfer mechanism. Displacement experiments confirmed that MaCo binds to subdomain IIA of HSA with independence of temperature. It was observed that, in the temperature range 35-45⯰C, the fluorescence emission maximum of HSA-MaCo complex decreased, whereas in the range 45⯰C-65⯰C, an increment was detected. The concomitant change in the polarity of environment surrounding Trp was confirmed by red edge excitation shift experiments. Thermal denaturation of HSA was followed by time-resolved fluorescence spectroscopy. Average lifetime of Trp residue decreased with temperature due to the increment of solvent collisions and changes in the solvent exposure of Trp. To discriminate the importance of each effect, lifetime of N-Acetyl-L-tryptophanamide (NATA) at different temperatures was measured. Circular dichroism (CD) studies confirmed the loss of secondary structure of HSA with increasing temperature and showed a different trend in the conformational transformation below and above 45⯰C, in agreement with steady-state and time-resolved fluorescence experiments.
Assuntos
Cumarínicos/química , Transferência Ressonante de Energia de Fluorescência , Temperatura Alta , Albumina Sérica Humana/química , Dicroísmo Circular , Humanos , Concentração de Íons de Hidrogênio , Estrutura Secundária de Proteína , Espectrometria de FluorescênciaRESUMO
Liquid lipid nanocapsules (LLN) represent a promising new generation of drug-delivery systems. They can carry hydrophobic drugs in their oily core, but the composition and structure of the surrounding protective shell determine their capacity to survive in the circulatory system and to achieve their goal: penetrate tumor cells. Here, we present a study of LLN covered by the protein human serum albumin (HSA) and loaded with curcumin as a hydrophobic model drug. A cross-linking procedure was performed to further strengthen the protective protein layer. Physicochemical properties and release kinetics of the nanocapsules were investigated, and cellular uptake and killing capacity were evaluated on the human breast-cancer line MCF-7. The nanocapsules exhibited a half maximal inhibitory concentration (IC50) capacity similar to that of free curcumin, but avoiding problems associated with excipients, and displayed an outstanding uptake performance, entering cells massively in less than 1â¯min.
Assuntos
Neoplasias da Mama/metabolismo , Endocitose , Lipídeos/química , Nanocápsulas/química , Albumina Sérica/metabolismo , Neoplasias da Mama/patologia , Proliferação de Células/efeitos dos fármacos , Sobrevivência Celular/efeitos dos fármacos , Cumarínicos/química , Curcumina/farmacologia , Curcumina/uso terapêutico , Liberação Controlada de Fármacos , Feminino , Humanos , Células MCF-7 , Nanocápsulas/ultraestrutura , Tiazóis/químicaRESUMO
A statistical mechanics approach is applied to predict the critical parameters of coagulation in the secondary minimum for charged colloidal suspensions. This method is based on the solution of the reference hypernetted chain (RHNC) integral equation, and it is intended to estimate only the locus of the critical point instead of the full computation of the "gas-liquid" coexistence. We have used an extrapolation procedure due to the lack of solution of the integral equation in the vicinity of the critical point. Knowing that the osmotic isothermal compressibility of the colloidal system should ideally diverge in the critical point, we work out the critical salt concentration for which the inverse of the compressibility should be zero. This extrapolation procedure is more rapid than that previously proposed by Morales and co-workers [Morales, V.; Anta, J. A.; Lago, S. Langmuir 2003, 19, 475], and it is shown to give equivalent results. We also present experimental results about secondary minimum coagulation for polystyrene latexes and use our method to reproduce the experimental trends. The comparison between theory and experiment is quite good for all colloidal diameters studied.
Assuntos
Coloides/química , Modelos Estatísticos , Soluções/química , Suspensões/químicaRESUMO
The influence of NaCl addition and temperature on the self-assembly, hydration, and structures of N-decanoyl-N-methylglucamide (MEGA-10) in dilute solution has been investigated by using several experimental techniques, including tensiometry, steady-state fluorescence, density, viscosity, and static and dynamic light scattering. Tensiometry and fluorescence probe studies, by using pyrene as a probe, were used to obtain the critical micelle concentration (cmc) upon the electrolyte addition. The mean micellar aggregation numbers (N(agg)) as a function of the salt addition were obtained by both static light scattering and static quenching methods. The N(agg) values estimated by both methods were found to be in good agreement. It was found that the increase in the micelle size, produced by the addition of NaCl, is due to the increase in the aggregation number and in the amount of water non-specifically associated to the micelle. On the other hand, we have observed that the aggregation number remains invariant in the temperature range studied, whereas the hydrodynamic radius slightly decreases. The effect of electrolyte addition and temperature on the properties of MEGA-10 micelles is much less pronounced than those observed in the traditionally used POE-based surfactants.
Assuntos
Ácidos Graxos/química , Glucosamina/análogos & derivados , Micelas , Cloreto de Sódio/química , Tensoativos/química , Eletrólitos/química , Glucosamina/químicaRESUMO
This report investigates the effect of sodium chloride (NaCl) on the micellization, surface activity, and the evolution in the shape and size of n-octyl beta-D-thioglucopyranoside (OTG) aggregates. By using surface tension measurements, information was obtained on both changes in the critical micelle concentration and adsorption behavior in the air-liquid interface with the electrolyte concentration. These data were used to obtain the thermodynamic properties of micellization along with the corresponding adsorption parameters in the air-liquid interface. From extended static and dynamic light scattering measurements, the micelle molecular weight, the mean aggregation number, and the second virial coefficient, the apparent diffusion coefficient and the mean hydrodynamic radius of micelles in a range of NaCl concentrations were obtained. The light scattering data have shown that when the surfactant concentration is lower to 4.5 g/L, only spherical micelles are formed. However, an increase in the surfactant concentration induces an increase in micellar size, suggesting a rodlike growth of the micelles. This deviation of micelle geometry from spherical to rodlike is supported both by the ratio between the hydrodynamic radius and the radius of gyration and by the angular dependence of light scattering. On the other hand, the studies performed in the presence of high NaCl concentration (0.2 and 0.5 M) provide strong support for the view that the micelles may overlap together to form an entangled network above certain crossover concentration.
RESUMO
The immunological agglutination reactions of physically absorbed F(ab')2 molecules onto anionic and cationic latex particles have been investigated by means of optical absorbance measurements. These measurements have been conducted under different conditions to determine the most influential factors. Surface F(ab')2 and BSA densities, particle concentration in the reaction medium and polyethylene glycol concentration are some of these factors. Sensitized cationic and anionic latexes differ considerably with respect to their colloidal stability and reactivity. As a general rule, the sensitized cationic latex has a relatively higher colloidal stability and hence, it provides reagents with a better optical response. Less than 0.025 microgram/ml of C-reactive protein has been detected using this particle enhanced optical immunoassay.
Assuntos
Fragmentos Fab das Imunoglobulinas/química , Látex/química , Adsorção , Animais , Proteína C-Reativa/imunologia , Coloides , Imunoensaio , Coelhos , Espalhamento de Radiação , SonicaçãoRESUMO
In previous publications we have discussed the stabilization mechanism of hydration forces as applied to the development of latex agglutination tests. We describe here how we have obtained stable and reactive IgG-latex conjugates in a high-ionic-strength reaction buffer. To this end we have made agglutination tests with polystyrene beads sensitized with IgG, measuring the immunoaggregation reaction with human C-reactive protein in a stopped-flow nephelometer. The results are compared to those obtained with a F(ab')2-latex conjugate with similar antibody molecule coverage. Adsorption isotherms of F(ab')2 and IgG on latex at pH 7.2 were obtained to study the affinity of these antibodies for the surface. The results of the electrokinetic characterization of the antibody-latex conjugates agree satisfactorily with those obtained from stability studies. This research throws light upon the use of hydration forces as a new approach to stabilizing immunoassay reagents that are colloidally unstable in physiological reaction buffers.
Assuntos
Fragmentos Fab das Imunoglobulinas/imunologia , Imunoglobulina G/imunologia , Testes de Fixação do Látex , Adsorção , Proteína C-Reativa/imunologia , Coloides , Humanos , PoliestirenosRESUMO
This work is based on the well-established immunoassay principle of agglutination of latex particles covered by immunoproteins. In our experiments, positively charged particles act as carriers for the F(ab')2 fragment, obtained from rabbit polyclonal IgG, active against C-reactive protein (CRP). The presence of the antigen CRP in the immunolatex system causes agglutination and the aim of the present study was to compare different optical techniques (turbidimetry, nephelometry, angular anisotropy and photon correlation spectroscopy) capable of detecting the agglutination. The sensitivity and detection limit largely depend on the optical method. We have analyzed for each optical technique the following aspects: sensitivity, reproducibility, detection limit, reaction time, amount of sample wasted and availability of the required detection device. The results presented in this paper show that both angular anisotropy and photon correlation spectroscopy offer lower detection limits, and use little reagent, but have longer assay times than the classical optical techniques of turbidimetry and nephelometry.
Assuntos
Proteína C-Reativa/análise , Testes de Fixação do Látex/métodos , Óptica e Fotônica , Animais , Anisotropia , Testes de Fixação do Látex/estatística & dados numéricos , Luz , Nefelometria e Turbidimetria , Coelhos , Espalhamento de Radiação , Sensibilidade e Especificidade , EspectrofotometriaRESUMO
The effect of formamide on the micellization of tetradecyltrimethylammonium bromide has been investigated by conductance and fluorescence probe experiments. The critical micelle concentration and the degree of counterion dissociation of micelles were obtained from conductance measurements in the temperature range of 20 to 40 degrees C. It was found that these two parameters increase with both temperature and formamide content in the solvent system. The thermodynamic parameters of micellization were estimated using the equilibrium model of micelle formation. The standard free energy of micellization was found to be negative in all cases and becomes less negative as the formamide content in the mixed solvent increases, but it is roughly independent of temperature. Although the entropic contribution was found to be larger than the enthalpy one, in particular at lower temperatures, an enthalpy-entropy compensation effect was observed for all systems. Micellar aggregation numbers were determined by the static quenching method, using pyrene as a probe and cetylpyridinium chloride as a quencher. The observed decrease in the micelle aggregation number, which is controlled by the increase in the surface area per headgroup, was attributed to an enhanced solvation in formamide rich solvent mixtures. Changes in the pyrene 1:3 ratio index, indicating a more polar environment, are consistent with an increased micellar solvation. Fluorescence polarization of both coumarin 6 and fluorescein are indicative of a decrease in microviscosity with cosolvent addition. The data on fluorescence anisotropy of coumarin 6 were analyzed using the wobbling in cone model. Data indicated the formation of micelles with a less ordered structure as the formamide increases in the solvent system.
RESUMO
The latex agglutination immunoassay technique uses polymer colloids as carriers for antibodies or antigens to enhance the immunological reaction. In this work, the interaction of a lipopolysaccharide (LPS) of Brucella Melitensis with two conventional latexes has been studied. Some experiments on the physical adsorption of the LPS onto these polystyrene beads have been performed and several complexes with different coverage degrees were obtained by modifying the incubation conditions. Regarding the application in the development of diagnostic test systems, it is advisable to study the latex-LPS complexes from an electrokinetic and colloidal stability point of view. The complexes were electrokinetically characterized by measuring the electrophoretic mobility under different redispersion conditions. The colloidal stability was determined by simple turbidity measurements. Experimental and theoretical data have been employed to study the molecular disposition of the LPS in the latex particle surface to compare with the outer membrane of bacterial cells. Latex complexes covered by different LPS amounts showed high colloidal stability and adequate immunoreactivity that remains for a long time period.
Assuntos
Brucella melitensis/química , Imunoensaio/métodos , Látex/química , Lipopolissacarídeos/química , Microesferas , Adsorção , Testes de Aglutinação , Animais , Anticorpos/sangue , Ensaio de Imunoadsorção Enzimática , Humanos , Látex/classificação , Substâncias Macromoleculares/química , Estrutura Molecular , Tamanho da Partícula , Poliestirenos/química , Poliestirenos/classificaçãoRESUMO
Albumins, in the form of nanoparticles, are increasingly used as drug carriers in the medical field, and the size effect of these nanomaterials is of major importance since it may affect their bioavailability and the in vivo behaviour after intravenous injection. This research provides a comprehensive study on the preparation of BSA nanoparticles, based on a simple coacervation method, with suitable size, size distribution, and surface charge for drug-delivery applications. Numerous experimental variables were examined in order to characterize their impact on nanoparticle size, distribution, electrophoretic mobility, and yield. Particle size was controlled by adjusting self-assembly phenomena of the protein molecules, which was affected by preparation conditions including BSA content, pH, and ionic strength (a parameter that strongly influences nanoparticle formation but surprisingly has not been previously studied in detail). Small particles with a narrow size distribution were obtained under experimental conditions where the repulsion between BSA molecules was high, i.e. at pH values far from the isoelectric point of the protein and low salt concentration. Changes in temperature, volume, and rate of addition of the dehydrating agent (ethanol) also affect nanoparticle characteristics, as they influence the nucleation rate and particle growth. The effect of these experimental conditions on the quantity of protein still dissolved in the aqueous phase after desolvation (i.e. the yield of BSA nanoparticles) was also studied. Nanoparticles surface charge was modulated with the extension of cross-linking. Finally, long-term colloidal stability of samples was evaluated after 2 months of storage.
Assuntos
Nanopartículas/química , Soroalbumina Bovina/química , Animais , BovinosRESUMO
Mixed micelles of n-octyl-ß-D-thioglucoside (OTG) and octaethylene-glycol monododecyl ether (C(12)E(8)), two non-ionic surfactants belonging to the alkyl glucosides and polyoxyethylene alkyl ether families, respectively, were investigated by using light scattering and fluorescence probe techniques. From the determination of the critical micelle concentration (cmc), by the well-established pyrene 1:3 ratio method, it was found that the mixed system behaves ideally, the micellization process being clearly controlled by the ethoxylated surfactant. The micellar hydrodynamic radius as a function of temperature, composition and concentration was obtained by dynamic light scattering measurements. It was observed that the micellar size increases with temperature, this growth being more pronounced as the relative proportion of the ethoxylated surfactant was increased. The behavior of the micellar size with the total surfactant concentration was also found to be dependent on temperature and composition. The clouding temperature, characteristic of the ethoxylated surfactants, was increased with the addition of the sugar surfactant. Lastly, possible structural changes in the micellar palisade layer were examined by steady-state fluorescence anisotropy in conjunction with time-resolved fluorescence studies with the hydrophobic probe coumarin 6 (C6). The obtained results indicate that the participation of the ethoxylated surfactant induces a slightly more polar palisade layer, whereas the probe carries out a faster rotational reorientation as a result of a less compact environment. All these observations were attributed to the different structure of the head groups of both surfactants and, as a consequence, to their different hydration.
Assuntos
Polietilenoglicóis/química , Tensoativos/química , Tioglucosídeos/química , Fluorescência , Luz , Micelas , Espalhamento de RadiaçãoRESUMO
Adhesion forces between different protein layers adsorbed on different substrates in aqueous media have been measured by means of an atomic force microscope using the colloid probe technique. The effects of the loading force, the salt concentration and pH of the medium, and the electrolyte type on the strength, the pull-off distance, and the separation energy of such adhesion forces have been analyzed in depth. Two very different proteins (bovine serum albumin and apoferritin) and two dissimilar substrates (silica and polystyrene) were used in the experiments. The results clearly point out a very important contribution of the electrostatic interactions in the adhesion between protein layers.
Assuntos
Soroalbumina Bovina/química , Adesividade , Animais , Cloreto de Cálcio , Bovinos , Concentração de Íons de Hidrogênio , Microscopia de Força Atômica , Cloreto de SódioRESUMO
Silica is a very interesting system that has been thoroughly studied in the last decades. One of the most outstanding characteristics of silica suspensions is their stability in solutions at high salt concentrations. In addition to that, measurements of direct-interaction forces between silica surfaces, obtained by different authors by means of surface force apparatus or atomic force microscope (AFM), reveal the existence of a strong repulsive interaction at short distances (below 2 nm) that decays exponentially. These results cannot be explained in terms of the classical Derjaguin, Landau, Verwey, and Overbeek (DLVO) theory, which only considers two types of forces: the electrical double-layer repulsion and the London-van der Waals attraction. Although there is a controversy about the origin of the short-range repulsive force, the existence of a structured layer of water molecules at the silica surface is the most accepted explanation for it. The overlap of structured water layers of different surfaces leads to repulsive forces, which are known as hydration forces. This assumption is based on the very hydrophilic nature of silica. Different theories have been developed in order to reproduce the exponentially decaying behavior (as a function of the separation distance) of the hydration forces. Different mechanisms for the formation of the structured water layer around the silica surfaces are considered by each theory. By the aid of an AFM and the colloid probe technique, the interaction forces between silica surfaces have been measured directly at different pH values and salt concentrations. The results confirm the presence of the short-range repulsion at any experimental condition (even at high salt concentration). A comparison between the experimental data and theoretical fits obtained from different theories has been performed in order to elucidate the nature of this non-DLVO repulsive force.
RESUMO
The atomic force microscope, together with the colloid probe technique, has become a very useful instrument to measure interaction forces between two surfaces. Its potential has been exploited in this work to study the interaction between protein (apoferritin) layers adsorbed on silica surfaces and to analyze the effect of the medium conditions (pH, salt concentration, salt type) on such interactions. It has been observed that the interaction at low salt concentrations is dominated by electrical double layer (at large distances) and steric forces (at short distances), the latter being due to compression of the protein layers. The DLVO theory fits these experimental data quite well. However, a non-DLVO repulsive interaction, prior to contact of the protein layers, is observed at high salt concentration above the isoelectric point of the protein. This behavior could be explained if the presence of hydration forces in the system is assumed. The inclusion of a hydration term in the DLVO theory (extended DLVO theory) gives rise to a better agreement between the theoretical fits and the experimental results. These results seem to suggest that the hydration forces play a very important role in the stability of the proteins in the physiological media.
Assuntos
Apoferritinas/química , Dióxido de Silício , Animais , Cavalos , Concentração de Íons de Hidrogênio , Cinética , Modelos Teóricos , Baço/química , Propriedades de Superfície , TermodinâmicaRESUMO
Protein coated particles present an anomalous colloidal stability at high ionic strength when the classical theory (DLVO) predicts aggregation. This observed deviation from DLVO behaviour appears for electrolyte concentrations above some critical bulk value. As we have suggested in previous publications the existence of an additional short-range repulsive 'hydration force' due to specific hydrated cation adsorption could explain this anomalous stability. The overlap of the hydration layers when two particles approach should provoke this repulsive force. New evidence of this mechanism has been observed when electrophoretic mobilities of protein-carrying latex particles were measured at various concentrations of sodium and calcium chloride. In the latter case a sign reversal of zeta-potential was found, probably due to the specific adsorption of Ca(2+) ions on protein molecules. The adsorption increases with the medium pH. These results have been analyzed following the treatment proposed by Ohshima and co-workers for large charged colloidal particles coated with a layer of protein. This study shows an increase in the positive fixed-charge density on the protein caused by the adsorption of cations.
RESUMO
Colloidal particles coated with antibodies are currently used in diagnostic test systems for the detection of antigens in biological fluids. Immobilization is usually carried out by physical adsorption. Covalent coupling of antibodies to particles, however, offers certain advantages. The present research deals with the study of these possible advantages. A sulphonated polystyrene latex has been used to prepare an immunolatex with physically adsorbed antibodies, while a functionalized latex with chloromethyl groups on the surface has been used for the partly covalent coupling of the antibody (F(ab')2 fragments). The immunoreactivity was studied by measuring the variations in scattered light intensity after mixing a solution of CRP antigen and the sensitized latex. The influence on the immunoresponse of the scattering angle (5, 10, and 20 deg), protein coverage and storage time have been studied for both systems.
Assuntos
Fragmentos Fab das Imunoglobulinas/imunologia , Testes de Fixação do Látex , Adsorção , Proteína C-Reativa/química , Proteína C-Reativa/imunologia , Fragmentos Fab das Imunoglobulinas/química , Luz , Microesferas , Poliestirenos/química , Espalhamento de Radiação , Dodecilsulfato de Sódio , Fatores de TempoRESUMO
Latex particles coated with IgG, currently used for immunoassay tests, are not colloidally stable under physiological conditions. Post-treatment of sensitized polystyrene microspheres with different substances (BSA, surfactants) to increase colloidal stability has been often used to solve this problem. We propose the possibility of stabilizing the antibody-latex conjugates by hydration forces at high ionic strength. On the other hand. immobilization of the proteins may be performed either by physical adsorption or by covalent binding to functionalized surface groups. In this second part of these series we have studied the immunoreactivity of IgG antibody partly covalently bound and physically adsorbed, and the results were compared to those obtained with F(ab')2 fragments in Part I.
Assuntos
Imunoglobulina G/imunologia , Testes de Fixação do Látex , Adsorção , Proteína C-Reativa/química , Proteína C-Reativa/imunologia , Coloides , Fragmentos Fab das Imunoglobulinas/química , Fragmentos Fab das Imunoglobulinas/imunologia , Imunoglobulina G/química , Microesferas , Nefelometria e Turbidimetria , Fatores de TempoRESUMO
The aim of the present work is to study the role of the different forces involved in the agglutination of immuno gamma-globulin (IgG) covered latex particles due to antigen-antibody reaction. An experimental investigation on the adsorption of IgG molecules on three latexes with different surface charge densities is described. Photon correlation spectroscopy was used to determine the hydrodynamic layer thickness of the IgG molecules adsorbed on the latexes. In order to get an insight into the forces acting between two antibody-covered particles approaching each other, the colloidal stability and immunoreactivity of these biocomplexes were studied. They can be stabilized by electrostatic or hydration forces. The immunological agglutination of IgG-immobilized latex particles due to the addition of the antigen was quantified through scattered light intensity measurements. The immunoresponse increases with ionic strength of the medium until a maximum value is achieved. Above this maximum, the immunoreactivity decreases.