Investigating the effect of particle size on pulmonary surfactant phase behavior.

We study the impact of the addition of particles of a range of sizes on the phase transition behavior of lung surfactant under compression. Charged particles ranging from micro- to nanoscale are deposited on lung surfactant films in a Langmuir trough. Surface area versus surface pressure isotherms and fluorescent microscope observations are utilized to determine changes in the phase transition behavior. We find that the deposition of particles close to 20 nm in diameter significantly impacts the coexistence of the liquid-condensed phase and liquid-expanded phase. This includes morphological changes of the liquid-condensed domains and the elimination of the squeeze-out phase in isotherms. Finally, a drastic increase of the domain fraction of the liquid-condensed phase can be observed for the deposition of 20-nm particles. As the particle size is increased, we observe a return to normal phase behavior. The net result is the observation of a critical particle size that may impact the functionality of the lung surfactant during respiration.

Measurement of monolayer viscosity using noncontact microrheology.

Microrheological studies of phospholipid monolayers, bilayers, and other Langmuir monolayer systems are traditionally performed by observing the thermal fluctuations of tracers attached to the membrane or interface. Measurements of this type obtain surface moduli that are orders of magnitude different from those obtained using macroscopic or active techniques. These large discrepancies can result from uncertainties in the tracer's coupling to the monolayer or the local disruption of the monolayer by the tracer. To avoid such problems, we perform a microrheological experiment with the tracer particle placed at a known depth beneath the monolayer; this avoids the issues mentioned at the cost of generating a weaker, purely hydrodynamic coupling between the tracer and the monolayer. We calculate the appropriate response functions for this submerged particle microrheology and demonstrate the technique on three model monolayer systems.

Particle size effects on collapse in monolayers.

We report on the impact of differently sized particles on the collapse of a Langmuir monolayer. We use an SDS-DODAB monolayer because it is known to collapse reversibly under compression and expansion cycles. Particles with diameters of 1 µm, 0.5 µm, 0.1 µm, and 20 nm are deposited on the SDS-DODAB monolayer. We find a critical particle size range of 0.1 to 0.5 µm that produces a transition from reversible to irreversible collapse. The nature of the collapse is determined through optical observations and surface pressure measurements. In addition, although 20 nm particles do not cause irreversible collapse in the monolayer, they significantly decrease the collapse pressure relative to the other systems. Therefore, we observe three distinct collapse behaviors-reversible, irreversible, and reversible at a reduced surface pressure.

Tracking giant folds in a monolayer.

The collapse dynamics of giant folds in a catanionic monolayer at the air-water interface are examined. A monolayer of dioctadecyldimethylammonium bromide (DODAB) and sodium dodecyl sulfate (SDS) in a 1:1 ratio is the system of study that previously was found to fold upon compression in a Langmuir trough. Carboxylate-coated polystyrene beads (1 microm diameter) are deposited and bound to the monolayer. Displacement of the beads is measured with epifluorescence microscopy and particle image velocimetry, yielding a measurement of the velocity of the monolayer around the fold. Reversibility is confirmed by measuring the amount of monolayer material entering and leaving the fold. Material near folds are found to have a maximum relative velocity on the order of 0.1 mm/s, and fold depths are found to be on the order of 1 mm. The folds exhibit regular unfolding behavior, which can be explained qualitatively by a simple mechanical model.