Patricia Losada-Pérez

The critical behavior of the refractive index near liquid-liquid critical points.

The nature of the critical behavior in the refractive index n is revisited in the framework of the complete scaling formulation. A comparison is made with the critical behavior of n as derived from the Lorentz-Lorenz equation. Analogue anomalies to those predicted for the dielectric constant ε, namely, a leading |t|(2β) singularity in the coexistence-curve diameter in the two-phase region and a |t|(1-α) along the critical isopleth in the one phase region, are expected in both cases. However, significant differences as regards the amplitudes of both singularities are obtained from the two approaches. Analysis of some literature data along coexistence in the two-phase region and along the critical isopleth in the one-phase region provide evidence of an intrinsic effect, independent of the density, in the critical anomalies of n. This effect is governed by the shift of the critical temperature with an electric field, which is supposed to take smaller values at optical frequencies than at low frequencies in the Hz to MHz range.

The Heat-Transfer Method: A Versatile Low-Cost, Label-Free, Fast, and User-Friendly Readout Platform for Biosensor Applications

In recent years, biosensors have become increasingly important in various scientific domains including medicine, biology, and pharmacology, resulting in an increased demand for fast and effective readout techniques. In this Spotlight on Applications, we report on the recently developed heat-transfer method (HTM) and illustrate the use of the technique by zooming in on four established bio(mimetic) sensor applications: (i) mutation analysis in DNA sequences, (ii) cancer cell identification through surface-imprinted polymers, (iii) detection of neurotransmitters with molecularly imprinted polymers, and (iv) phase-transition analysis in lipid vesicle layers. The methodology is based on changes in heat-transfer resistance at a functionalized solid-liquid interface. To this extent, the device applies a temperature gradient over this interface and monitors the temperature underneath and above the functionalized chip in time. The heat-transfer resistance can be obtained by dividing this temperature gradient by the power needed to achieve a programmed temperature. The low-cost, fast, label-free and user-friendly nature of the technology in combination with a high degree of specificity, selectivity, and sensitivity makes HTM a promising sensor technology.

Interactions of Aqueous Imidazolium-Based Ionic Liquid Mixtures with Solid-Supported Phospholipid Vesicles

Despite the environmentally friendly reputation of ionic liquids (ILs), their safety has been recently questioned given their potential as cytotoxic agents. The fundamental mechanisms underlying the interactions between ILs and cells are less studied and by far not completely understood. Biomimetic films are here important biophysical model systems to elucidate fundamental aspects and mechanisms relevant for a large range of biological interaction ranging from signaling to drug reception or toxicity. Here we use dissipative quartz crystal microbalance QCM-D to examine the effect of aqueous imidazolium-based ionic liquid mixtures on solid-supported biomimetic membranes. Specifically, we assess in real time the effect of the cation chain length and the anion nature on a supported vesicle layer of the model phospholipid DMPC. Results indicate that interactions are mainly driven by the hydrophobic components of the IL, which significantly distort the layer and promote vesicle rupture. Our analyses evidence the gradual decrease of the main phase transition temperature upon increasing IL concentration, reflecting increased disorder by weakening of lipid chain interactions. The degree of rupture is significant for ILs with long hydrophobic cation chains and large hydrophobic anions whose behavior is reminiscent of that of antimicrobial peptides.

Array formatting of the heat-transfer method (HTM) for the detection of small organic molecules by molecularly imprinted polymers.

In this work we present the first steps towards a molecularly imprinted polymer (MIP)-based biomimetic sensor array for the detection of small organic molecules via the heat-transfer method (HTM). HTM relies on the change in thermal resistance upon binding of the target molecule to the MIP-type receptor. A flow-through sensor cell was developed, which is segmented into four quadrants with a volume of 2.5 μL each, allowing four measurements to be done simultaneously on a single substrate. Verification measurements were conducted, in which all quadrants received a uniform treatment and all four channels exhibited a similar response. Subsequently, measurements were performed in quadrants, which were functionalized with different MIP particles. Each of these quadrants was exposed to the same buffer solution, spiked with different molecules, according to the MIP under analysis. With the flow cell design we could discriminate between similar small organic molecules and observed no significant cross-selectivity. Therefore, the MIP array sensor platform with HTM as a readout technique, has the potential to become a low-cost analysis tool for bioanalytical applications.

Effect of cholesterol on the phase behavior of solid-supported lipid vesicle layers.

The interest in solid-supported biomimetic membranes stems from their utility in nanotechnology and biosensing. In particular, supported lipid vesicles (SLVs) have become popular in both fundamental biophysical studies and pharmaceutical screening applications. It is thus essential to gain information on the structural properties and phase behavior of SLVs. Here we report on a study on the influence of cholesterol on the phase behavior of SLVs of saturated phospholipids by using quartz crystal microbalance with dissipation monitoring, a label-free and nonintrusive surface-sensitive technique. Two complementary approaches have been used, a Voigt-based viscoelastic model yielding shear viscosity temperature profiles and the first-order derivative of the frequency (mass-sensitive) shifts. Anomalies in the shear viscosity and extrema in the first-order derivative frequency curves stand as a token of the main phase transition and provide information on its gradual suppression upon addition of cholesterol. This method proves convenient for its small sample volume needed, its short temperature equilibration time and the non-necessity of external labels. This work can be regarded as a starting point for further studies on more rare lipid systems and different geometries, such as tethered SLVs or biologically relevant vesicles produced by living cells.

Phase Transitions of Binary Lipid Mixtures: A Combined Study by Adiabatic Scanning Calorimetry and Quartz Crystal Microbalance with Dissipation Monitoring

The phase transitions of binary lipid mixtures are studied by a combination of Peltier-element-based adiabatic scanning calorimetry (pASC) and quartz crystal microbalance with dissipation monitoring (QCM-D). pASC, a novel type of calorimeter, provides valuable and unambiguous information on the heat capacity and the enthalpy, whereas QCM-D is proposed as a genuine way of determining phase diagrams by analysing the temperature dependence of the viscosity. Two binary mixtures of phospholipids with the same polar head and differing in the alkyl chain length, DMPC

Critical behavior of static properties for nitrobenzene-alkane mixtures.

We present experimental data of the isobaric heat capacity per unit volume C(p,x)V(-1) for mixtures containing nitrobenzene and an alkane (C(N)H(2N+2), with N ranging from 6 to 15) upon approaching their liquid-liquid critical points along a path of constant composition. Values for the critical amplitude A(+) have been determined. They have been combined with the previously reported ones for the leading term of the coexistence-curve width to obtain, with the aid of well-known universal relations, the critical amplitudes of the correlation length and of the osmotic susceptibility. The trends of all these critical parameters, which exhibit anomalous behavior in the low N region, are discussed in terms of particular microscopic phenomena characterizing NB-C(N)H(2N+2) mixtures. The work is completed with an analysis of the analog of the Yang-Yang anomaly in liquid-liquid criticality: the behavior of the partial molar heat capacities of the two liquid components is found to illustrate previously uncovered asymmetry effects.

Thermodynamic consistency near the liquid-liquid critical point.

The thermodynamic consistency of the isobaric heat capacity per unit volume at constant composition C(p,x) and the density rho near the liquid-liquid critical point is studied in detail. To this end, C(p,x)(T), rho(T), and the slope of the critical line (dT/dp)(c) for five binary mixtures composed by 1-nitropropane and an alkane were analyzed. Both C(p,x)(T) and rho(T) data were measured along various quasicritical isopleths with a view to evaluate the effect of the uncertainty in the critical composition value on the corresponding critical amplitudes. By adopting the traditionally employed strategies for data treatment, consistency within 0.01 K MPa(-1) (or 8%) is attained, thereby largely improving the majority of previous results. From temperature range shrinking fits and fits in which higher-order terms in the theoretical expressions for C(p,x)(T) and rho(T) are included, we conclude that discrepancies come mainly from inherent difficulties in determining the critical anomaly of rho accurately: specifically, to get full consistency, higher-order terms in rho(T) are needed; however, the various contributions at play cannot be separated unambiguously. As a consequence, the use of C(p,x)(T) and (dT/dp)(c) for predicting the behavior of rho(T) at near criticality appears to be the best choice at the actual experimental resolution levels. Furthermore, the reasonably good thermodynamic consistency being encountered confirms that previous arguments appealing to the inadequacy of the theoretical expression relating C(p,x) and rho for describing data in the experimentally accessible region must be fairly rejected.

Melittin disruption of raft and non-raft-forming biomimetic membranes: A study by quartz crystal microbalance with dissipation monitoring

In this work we examine the role of lateral phase separation in cholesterol-containing biomimetic membranes on the disrupting action of melittin using a label-free surface-sensitive technique, quartz crystal microbalance with dissipation monitoring (QCM-D). Melittin disruption mechanisms depend strongly on the geometry of the lipid layer; however, despite the interplay between layer geometry/thickness and melittin activity, results indicate that the presence of lipid heterogeneity and lateral phase separation greatly influences the disrupting efficiency of melittin. In homogeneous non-raft forming membranes with high cholesterol content, melittin spontaneous activity is strongly delayed compared to heterogeneous raft-forming systems with the same amount of cholesterol. These results confirm the importance of lateral phase separation as a determinant factor in peptide activity. The information provided can be used for the design of more efficient antimicrobial peptides and the possibility of using a label-free approach for tailored-membranes and interactions with other types of peptides, such as amyloid peptides.

Temperature, concentration, and frequency dependence of the dielectric constant near the critical point of the binary liquid mixture nitrobenzene-tetradecane

Detailed results are reported for the dielectric constant epsilon as a function of temperature, concentration, and frequency near the upper critical point of the binary liquid mixture nitrobenzene-tetradecane. The data have been analyzed in the context of the recently developed concept of complete scaling. It is shown that the amplitude of the low frequency critical Maxwell-Wagner relaxation (with a relaxation frequency around 10 kHz) along the critical isopleth is consistent with the predictions of a droplet model for the critical fluctuations. The temperature dependence of epsilon in the homogeneous phase can be well described with a combination of a (1-alpha) power law term (with alpha the heat capacity critical exponent) and a linear term in reduced temperature with the Ising value for alpha. For the proper description of the temperature dependence of the difference Deltaepsilon between the two coexisting phases below the critical temperature, it turned out that good fits with the Ising value for the order parameter exponent beta required the addition of a corrections-to-scaling contribution or a linear term in reduced temperature. Good fits to the dielectric diameter epsilon(d) require a (1-alpha) power law term, a 2beta power law term (in the past considered as spurious), and a linear term in reduced temperature, consistent with complete scaling.