Biomedical subjects

Elena Junquera

Publications and source records attributed to Elena Junquera.

10 recordsLinked to original sources

PubMed2006

Cationic prevesicle and vesicle nanoaggregates: an experimental and theoretical study.

The formation of spontaneous mixed prevesicles and vesicles consisting of a cationic double-chain surfactant, didecyldimethylammonium bromide (di-C(10)DMAB), and a cationic single-chain alkyltrimethylammonium bromide with 10 and/or 14 carbon atoms (decyltrimethylammonium bromide, C(10)TAB, and/or tetradecyltrimethylammonium bromide, C(14)TAB) has been investigated by means of a series of (i) highly precise experimental techniques, such as conductometry, transmission electronic microscopies (TEM and cryo-TEM), laser Doppler electrophoresis (LDE), and steady-state fluorescence spectroscopy and (ii) theoretical models, such as the DLVO theory and two of its main further modifications, Inoues's and Sogami's models. Two new potentials, based on the combination of DLVO or Inoue potentials with that of Sogami, have been proposed and checked. This theoretical analysis has been carried out not only for the aggregates studied in this work but also for other di-C(m)DMAB + C(n)TAB (m = 10, 12 and n = 10, 12, 14) systems previously reported by us. In respect to the experimental study, special emphasis has been devoted to the prevesicle domain. We have confirmed the existence of two critical aggregation concentrations in the very diluted concentration domain, where the conductivity plot shows a zigzag pattern: the so-called mixed critical aggregate concentration, CAC* and the mixed critical vesicle concentration, CVC*. Contrarily, only CVC* is detected. The pre-CAC* nanoaggregates, with a variety of sizes and shapes, do not show a clear aggregation pattern, but even at such low concentrations a small number of nanoaggregates with a clear and ordered aggregation pattern has been visualized. In the postvesicle domain, the aggregates (vesicles) are unilamellar and spherical with a medium polidispersity and a net averaged surface density charge of around 14 x 10(-3) (pure vesicles) and 24 x 10(-3) C m(-2) (mixed vesicles). The hydrophobicities of the lipidic bilayer and the surface of the vesicles resemble those of media with dielectric constants of around 30 and 75, respectively. Finally, theoretical predictions confirm the stability of the pure and mixed vesicles studied in this work and in other works previously reported.

Algorithms↗

PubMed2006

Electrochemical, microscopic, and spectroscopic characterization of prevesicle nanostructures and vesicles on mixed cationic surfactant systems.

Several experimental techniques (conductivity, zeta potential, transmission electronic microscopy, and steady-state fluorescence spectroscopy) have been used to study the formation of mixed colloidal aggregates consisting of a cationic double-chain surfactant, di-dodecyldimethylammonium bromide (di-C12DMAB), and a single-chain alkyltrimethylammonium bromide with 10 and/or 14 carbon atoms (decyltrimethylammonium bromide, C10TAB, and/or tetradecyltrimethylammonium bromide, C14TAB). Special interest has been devoted to the prevesicle domain, within which the formation of aggregated nanostructures was first reported in our laboratory. For that purpose, studies have been carried out on the very dilute region by means of conductivity experiments, confirming the existence of two critical aggregation concentrations in that concentration domain: the so-called mixed critical aggregate concentration, CAC, and the mixed critical vesicle concentration, CVC. By carrying out TEM experiments on negatively stained samples, we were surprised to find a number of aggregates without a clear aggregation pattern and with a variety of sizes and shapes at concentrations below CAC, where only monomers were expected. However, the nanoaggregates found at concentrations between CAC and CVC, also by TEM microscopy, show a clear and ordered "fingerprint"-like aggregation pattern similar to the liquid-crystalline phases reported for DNA-liposome complexes and/or DNA packed with viral capsids. Finally, at total surfactant concentrations above CVC, the aggregates were confirmed, by means of cryo-TEM micrographs and zeta potential measurements, to be essentially unilamellar spherical vesicles with a medium polydispersity and a net-averaged surface density charge of around 12 x 10(-3) C m(-2). The fluorescence emission of two probes, TNS (anionic) and PRODAN (nonionic), allows for the analysis of the micropolarity and microviscosity of the different microenvironments present in aqueous surfactant solutions where the above-mentioned vesicle and prevesicle aggregates are present.

Journal Article↗

PubMed2006

Spectrofluorimetric characterization of mixed nanoaggregates comprising a double-chain cationic surfactant and a cationic or non-ionic single-chain surfactant.

A series of mixed vesicle and pre-vesicle nanoaggregates, comprising a cationic double-chain surfactant (di-decyldimethylammonium bromide, di-C(10)DMAB, or di-dodecyldimethylammonium bromide, di-C(12)DMAB), and a cationic (dodecylethyldimethylammonium bromide, C(12)EDMAB) or non-ionic (octyl-beta-D-glucopyranoside, OBG) single-chain surfactant have been characterized by means of steady-state fluorescence spectroscopy. For that purpose, the fluorescent emission of two probes, one anionic (TNS) and the other non-ionic (PRODAN), which is known to be sensitive to the polarity, rigidity, and/or microviscosity of the environment within which the probes are housed, has been measured in the presence of the above-mentioned mixed aggregates. The results of this analysis yield interesting information about the characteristics of the vesicle surface and bilayer, as well as about the existence of clusters and/or nanoaggregates prior to the formation of vesicles.

Journal Article↗

PubMed2005

Self-organization of the ternary didecyldimethylammonium bromide/octyl-beta-D-glucopyranoside/water system.

The spontaneous and thermodynamically stable mixed vesicles constituted by a double-chain cationic surfactant with 10 carbon atoms hydrophobic tail, didecyldimethylammonium bromide (di-C(10)DMAB), and a nonionic single-chain surfactant, octyl-beta-d-glucopyranoside (OBG), have been characterized in aqueous media by means of a series of experimental techniques, as well as a theoretical approach. Conductivity data allow for the determination of the concentrations at which the monomer-to-vesicle (CVC) and/or vesicle-to-micelle (CMC) transitions occur. Electrophoretic mobilities, obtained from laser-doppler-electrophoresis experiments, permit the determination of zeta-potentials and, from them, the surface charge density of the vesicle aggregates. Cryogenic transmission electron microscopy (cryo-TEM) provides pictures of the vesicles, their size and shape being, thus, determined. Finally, the sensitivity of the emission spectra of some fluorescent probes, such as the cationic TNS and the nonionic PRODAN, to the polarity of the environment, allow for a complete study of different pre- and post-vesicle microdomains, of variable rigidity and micropolarity. This, in turn, yield interesting information about the vesicle surface and bilayer, as well as, about the existence of clusters and/or nanoaggregates prior to the formation of vesicles, as was proposed by us in a previous paper.

2-Naphthylamine↗

PubMed2005

Aggregation phenomena on the ternary ionic-nonionic surfactant system: didodecyldimethylammonium bromide/octyl-beta-D-glucopyranoside/water. Mixed microaggregates, vesicles, and micelles.

The formation of a variety of mixed colloidal aggregates has been investigated on a ternary ionic-nonionic system constituted by (i) a double-chain cationic surfactant with a 12-carbon atom hydrophobic tail, didodecyldimethylammonium bromide (di-C(12)DMAB), (ii) a nonionic single-chain surfactant, octyl-beta-D-glucopyranoside (OBG), and (iii) water. The study has been carried out by means of conductivity, zeta-potential, transmission electron microscopy (TEM), and cryogenic transmission electron microscopy (cryo-TEM) experiments on the highly diluted, very diluted, and moderately diluted regions. The formation of mixed microaggregates, prior to the appearance of mixed vesicles, has been undoubtly confirmed by conductivity, TEM, and zeta-potential results. The concentrations at which these mixed colloidal aggregates form, i.e., the mixed critical microaggregate concentration (CAC), the mixed critical vesicle concentration (CVC), and the mixed critical micelle concentration (CMC), have been determined from conductivity data, while the zeta-potential experiments allow for the characterization of the aggregate/solution interface. The shape and size of the microaggregates and vesicles have been evaluated from TEM and cryo-TEM micrographs, respectively. All of the experimental evidence has been also analyzed in terms of the theoretical packing parameter, P.

Cryoelectron Microscopy↗

PubMed2004

Mixed vesicle formation on a ternary surfactant system: didodecyldimethylammonium bromide/dodecylethyldimethylammonium bromide/water.

The formation of mixed aggregates has been investigated on a ternary system consisting of two cationic surfactants with similar polar heads and two and/or one 12 carbon atom hydrophobic tail, respectively, didodecyldimethylammonium bromide and dodecylethyldimethylammonium bromide and water. The study has been carried out by means of conductivity, zeta potential, and cryogenic transmission electronic microscopy (cryo-TEM) experiments on the very diluted region. A variety of mixed aggregates, microaggregates, vesicles, and micelles has been found, depending on system composition and total surfactant concentration. Mixed critical microaggregate concentration and mixed critical vesicle concentration have been determined from conductivity data. Furthermore, zeta potential and cryo-TEM experiments allow for the characterization of the aggregates/solution interface and of the shape and size of the aggregates. This experimental evidence has also been analyzed in terms of the theoretical packing parameter, P.

Electric Conductivity↗

PubMed2004

Mixed micelles formed by n-octyl-beta-D-glucopyranoside and tetradecyltrimethylammonium bromide in aqueous media.

Speed of sound, density, conductivity, and fluorescence spectroscopy experiments were run to analyze the mixed aggregation process of a nonionic-cationic surfactant system in aqueous media at 298.15 K. The mixed system comprises a nonionic surfactant, n-octyl-beta-D-glucopyranoside (OBG), and a cationic surfactant, tetradecyltrimethylammonium bromide (C14TAB), with 8 and 14 carbon atoms on the hydrophobic tails, respectively. From these data, the total and partial critical micellar concentrations, the total and partial aggregation numbers, apparent molar volumes and isentropic compressibilities, hydration numbers, and the corresponding changes in the latest properties due to the mixed aggregation process were determined. Pure and mixed micelles were analyzed from a geometrical point of view by determining the packing parameter of the aggregates. Furthermore, the experimental characterization of both the monomeric and micellar phases was completed with a theoretical study of the mixed micellization phenomena studied herein, by means of some of the most relevant theoretical models.

Electric Conductivity↗

PubMed2004

Mixed micellization of a nonionic-cationic surfactant system constituted by n-octyl-beta-D-glucopyranoside/dodecyltrimethylammonium bromide/H2O. An electrochemical, thermodynamic, and spectroscopic study.

The mixed micelles constituted by a nonionic surfactant widely used in the biochemical field, n-octyl-beta-D-glucopyranoside, and a cationic surfactant with 12 carbon atoms on the hydrophobic tail, dodecyltrimethylammonium bromide, have been studied in aqueous solution, at 298.15 K, by means of conductivity, speed of sound, density, and fluorescence spectroscopy experiments. From these data, the monomeric and micellar phases of the mixed aggregates were fully analyzed through the determination of the total and partial critical micellar concentrations, the dissociation degree of the mixed micelle, the total and partial aggregation numbers, the apparent molar volumes and isentropic compressibilities, the hydration numbers, and the corresponding changes in these thermodynamic properties due to the mixed aggregation process. The experimental findings have been compared with those obtained with several theoretical models, some of them modified in this work to take into account the specific characteristics of the aggregates studied herein.

Electrochemistry↗

PubMed2004

Conductometric and spectrofluorimetric characterization of the mixed micelles constituted by dodecyltrimethylammonium bromide and a tricyclic antidepressant drug in aqueous solution.

Conductivity and static fluorescence measurements have been carried out at 25 degrees C to study the monomeric and micellar phases of aqueous solutions of mixed micelles constituted by a conventional cationic surfactant, dodecyltrimethylammonium bromide (D(12)TAB), and a tricyclic antidepressant drug, amitriptyline hydrochloride (AMYTP), with aggregation properties. From conductivity data, the total mixed critical micelle concentration and the dissociation degree of the mixed micelle have been obtained, while fluorescence experiments allow for the determination of the total aggregation number, and the micropolarity of micellar inside. Furthermore, the partial contribution of each surfactant to the mixed micellization process, through their critical micelle concentrations and their aggregation numbers have been determined, as well. The solubilization of the drug in the mixed micelles has been also studied through the mass action model, by determining the association constant between the micelles and the drug. From these results, the use of the micelles studied in this work as potential models for vectors of antidepressant drugs of the amitriptyline family has been discussed. The theoretical aspects of the mixed micellization process have been also analyzed.

Amitriptyline↗

PubMed1996

Thermodynamics of alpha-Cyclodextrin-p-Nitrophenyl Glycoside Complexes. A Simple System To Understand the Energetics of Carbohydrate Interactions in Water.

Thermodynamic studies of the binding of a series of p-nitrophenyl glycosides (PNPGly) of varying stereochemistry to alpha-cyclodextrin (alpha-CD) were performed at three different temperatures (25, 35, and 42 degrees C) using a microcalorimetric technique. The system p-nitrophenol (PNP) at pH = 3 and alpha-CD was also studied for the sake of comparison. All these complexes were found to be enthalpy driven with a favorable enthalpic term clearly dominant over an unfavorable entropic term. A clear enthalpy-entropy compensation effect was observed at all the temperatures, with a slope close to unity (alpha = 1.02) and an intercept TDeltaS degrees (o) = 2.91 kcal mol(-)(1). This thermodynamic pattern is in agreement with those usually found for lectin-carbohydrate associations and for the binding processes of several host-guest systems. This pattern is explained in terms of the contribution of primarily two driving forces: the van der Waals interactions between the host and the guest, and the solvation/desolvation processes which accompany the association reaction. The presence of the carbohydrate molecule in the PNP ring causes a slight destabilization of the complex at 25 degrees C with respect to the alpha-CD-PNP (pH = 3) complex, although a different behavior has been observed depending on the axial/equatorial configuration of the glycoside and the temperature. This behavior is modulated by the stereochemistry of the glycoside. Differences were observed between the deoxy-derivatives (LAra and LFuc) and those derivatives with a hydroxymethyl group (Glc, Gal, Man). DeltaC(p) degrees values were obtained from the dependency of DeltaH degrees on temperature (=( partial differentialDeltaH degrees / partial differentialT)(p)). These values are small and negative except for alphaMan complex. For the latter complex, discrepancy between the calorimetric and the calculated van't Hoff enthalpies was observed. Parallels are drawn between the thermodynamics of our model and those proposed for carbohydrate-protein associations.

Journal Article↗