Biomedical subjects

Charles Maldarelli

Publications and source records attributed to Charles Maldarelli.

5 recordsLinked to original sources

PubMed2006

Effects of functional groups on surface pressure-area isotherms of hydrophilic silicone polymers.

Organic/inorganic hybrid silicone polymers are increasingly used in cosmetics, inks and paints, and fabric care applications owing to their special Si-O bond characteristics. Because of the presence of organic as well as inorganic groups, they show the properties of both, and the presence of hydrophobic as well as hydrophilic character makes them behave like a hybrid polymer. Though they are widely used, the utilization of hydrophilically modified silicones on a large scale has mainly been empirical due to lack of fundamental knowledge about variation in their properties with systematic change in their structure. The choice of moieties for hydrophilic modification of silicones in most of the earlier works has been nonionic based on ethylene oxide and propylene oxide groups, however, very little is known about their ionic counterparts. The current work focuses on understanding the behavior of functionally grafted silicone polymers with respect to the variation in the hydrophilic part of the grafting chain. Hydrophilically grafted silicone polymers form monolayers at the air-water interface, which are stabilized by interactions of functional groups with water. The present work examined the effects of functional group modifications on the conformational behavior of chains at the interface. It was observed that the shape of the chain depends on the available area at the interface (or surface pressure), and there are conformational changes with an increase in the number of molecules per unit area. While a poly(dimethylsiloxanes) (PDMS) chain may undergo stretched to helix transition as predicted earlier, this may not be the case for hydrophilically grafted chains. On the basis of the shape of the surface pressure-area isotherm and correlation with the scaling theory, a gradation in hydrophilicity of functional groups and hence modified silicone chains at the air-water interface is predicted.

Journal Article↗

PubMed2006

Arraying of intact liposomes into chemically functionalized microwells.

Here, we describe a protocol to bind individual, intact phospholipid bilayer liposomes, which are on the order of 1 microm in diameter, in microwells etched in a regular array on a silicon oxide substrate. The diameter of the wells is on the order of the liposome diameter, so only one liposome is located in each well. The background of the silicon oxide surface is functionalized with a PEG oligomer using the contact printing of a PEG silane to present a surface that resists the adsorption of proteins, lipid material, and liposomes. The interiors of the wells are functionalized with an aminosilane to facilitate the conjugation of biotin, which is then bound to Neutravidin. The avidin-coated well interiors bind the liposomes whose surfaces contain biotinylated lipids. The specific binding of the liposomes to the surface using the biotin-avidin linkage, together with the resistant nature of the background and the physical confinement of the wells, allows the liposomes to remain intact and to not unravel, rupture, and fuse onto the surface. We demonstrate this intact arraying using confocal laser scanning microscopy of fluorophores specifically tagging the microwells, the lipid bilayer, and the aqueous interior of the liposome.

Avidin↗

PubMed2005

Molecular dynamics study of the influence of surfactant structure on surfactant-facilitated spreading of droplets on solid surfaces.

The spreading of a partially wetting aqueous drop in air on a hydrophobic surface can be facilitated by the adsorption of surfactants from the drop phase onto the air/aqueous and aqueous/hydrophobic solid interfaces of the drop. At the contact line at which these interfaces meet, conventional surfactants with a linear alkyl hydrophobic chain attached to a polar group adsorb onto the surfaces, forming monolayers which remain distinct as they merge at the contact juncture. The adsorption causes a decrease in the interfacial tensions and reduction in the contact angle but the angle remains above zero so the drop is still nonwetting. Trisiloxane surfactants with a T-shaped geometry in which the hydrophobic group is composed of a trisiloxane oligomer with a polar group attached at the center of the chain can give rise to a zero contact angle at the contact line and complete wetting (superspreading). Experimental evidence suggests the adsorption of the T-shaped molecule, in addition to significantly decreasing the tensions of the interfaces (relative to the conventional surfactants), promotes the formation of a precursor film consisting of a surfactant bilayer at the contact line which facilitates the spreading. The aim of this study is to use molecular dynamics to examine if the T-shaped structure can promote spreading by the formation of a bilayer and to contrast this case with that of the linear chain surfactant where complex assembly does not occur. The simulation models the solvent as a monatomic liquid, the substrate as a particle lattice, and the surfactants as united atom structures, with all interactions given by Lennard-Jones potentials. We start with a base case in which the solvent partially wets a substrate comprised of a lattice of particles. We demonstrate that adsorbed T-shaped surfactant monolayers can, when the interaction between the solvent and the hydrophile particles is strong enough, assemble into a bilayer, allowing the drop to extend to a thin planar film. In the case of the flexible linear chain surfactant, there is no interaction between the monolayers on the two interfaces in the case of a strong hydrophile-solvent interaction and less coordination for a weaker interaction. In either case, the monolayers remain distinct, as the surfactant only marginally improves wetting.

Models, Molecular↗

PubMed2003

Measurement of the kinetic rate constants for the adsorption of superspreading trisiloxanes to an air/aqueous interface and the relevance of these measurements to the mechanism of superspreading.

Super-spreading trisiloxane surfactants are a class of amphiphiles which consist of nonpolar trisiloxane headgroups ((CH3)3-Si-O)2-Si(CH3)(CH2)3-) and polar parts composed of between four and eight ethylene oxides (ethoxylates, -OCH2CH2-). Millimeter-sized aqueous drops of trisiloxane solutions at concentrations well above the critical aggregate concentration spread rapidly on very hydrophobic surfaces, completely wetting out at equilibrium. The wetting out can be understood as a consequence of the ability of the trisiloxanes at the advancing perimeter of the drop to adsorb at the air/aqueous and aqueous/hydrophobic solid interfaces and to reduce considerably the tensions of these interfaces, creating a positive spreading coefficient. The rapid spreading can be due to maintaining a positive spreading coefficient at the perimeter as the drop spreads. However, the air/aqueous and solid/aqueous interfaces at the perimeter are depleted of surfactant by interfacial expansion as the drop spreads. The spreading coefficient can remain positive if the rate of surfactant adsorption onto the solid and fluid surfaces from the spreading aqueous film at the perimeter exceeds the diluting effect due to the area expansion. This task is made more difficult by the fact that the reservoir of surfactant in the film is continually depleted by adsorption to the expanding interfaces. If the adsorption cannot keep pace with the area expansion at the perimeter, and the surface concentrations become reduced at the contact line, a negative spreading coefficient which retards the drop movement can develop. In this case, however, a Marangoni mechanism can account for the rapid spreading if the surface concentrations at the drop apex are assumed to remain high compared to the perimeter so that the drop is pulled out by the higher tension at the perimeter than at the apex. To maintain a high apex concentration, surfactant adsorption must exceed the rate of interfacial dilation at the apex due to the outward flow. This is conceivable because, unlike that at the contact line, the surfactant reservoir in the liquid at the drop center is not continually depleted by adsorption onto an expanding solid surface. In an effort to understand the rapid spreading, we measure the kinetic rate constants for adsorption of unaggregated trisiloxane surfactant from the sublayer to the air/aqueous surface. The kinetic rate of adsorption, computed assuming the bulk concentration of monomer to be uniform and undepleted, represents the fastest that surfactant monomer can adsorb onto the air/aqueous surface in the absence of direct adsorption of aggregates. The kinetic constants are obtained by measuring the dynamic tension relaxation as trisiloxanes adsorb onto a clean pendant bubble interface. We find that the rate of kinetic adsorption is only of the same order as the area expansion rates observed in superspreading, and therefore the unaggregated flux cannot maintain very high surface concentrations at the air/aqueous interface, either at the apex or at the perimeter. Hence in order to maintain either a positive spreading coefficient or a Marangoni gradient, the surfactant adsorptive flux needs to be augmented, and the direct adsorption of aggregates (which in the case of the trisiloxanes are bilayers and vesicles) is suggested as one possibility.

Journal Article↗

PubMed2002

Fluorescence evidence that a phase transition causes the induction time in the reduction in dynamic tension during surfactant adsorption to a clean air/water interface and a kinetic-diffusive transport model for the phase-induced induction.

An aqueous soluble surfactant adsorbing from solution onto an initially clean air/water interface often exhibits an induction period in the surface tension relaxation in which, as the adsorption begins, the tension remains near the clean interface value for an extended period of time before decreasing rapidly to the equilibrium value. In this study, using a model nonionic soluble surfactant, C14E6(CH3(CH2)13-(OCH2CH2)6-OH), we present direct fluorescence evidence that this induction is due to a first-order phase transition from a gaseous (G) to a liquid expanded (LE) phase that the assembling monolayer undergoes at constant surface pressure. An open channel flow cell is initially filled with water, and onto its air/water interface is spread an insoluble amphiphilic dye that fluoresces upon irradiation in the LE phase and whose fluorescence is quenched in the G phase. An aqueous solution of C14E(6) is then allowed to flow through the channel. We observe the immediate appearance of bright islands of the LE phase growing in a dark (G) background, confirming the presence of the G/LE phase transition. These islands eventually occupy the entire surface, after which the interface remains uniformly bright. We correlate this phase transition to the induction period by simultaneously measuring the tension of the interface of the open channel, and verifying that as the islands grow the tension remains at the clean value until the bright LE phase occupies the entire surface, whereupon the tension rapidly decreases. We further develop a phase transition surfactant transport model for the induction period in which surfactant diffuses toward and kinetically adsorbs onto the surface, and then rapidly equilibrates between the G and LE phases. For our model surfactant C14E6, we independently measure the surface concentration of the nucleating LE phase, the LE phase surfactant equation of state, the kinetic rate constants for adsorption into the LE phase, and the bulk diffusion coefficient. Using these measurements, we predict induction times for adsorption onto a clean surface without convection. We also measure these induction times in tension relaxation for adsorption onto a pendant bubble using axisymmetric shape analysis, and demonstrate agreement with the simulations with no adjustable constants.

Journal Article↗