No abstract

Meibum is the primary component of the tear film lipid layer. Thought to play a role in tear film stabilization, understanding the physical properties of meibum and how they change with disease will be valuable in identifying dry eye treatment targets. Grazing incidence X-ray diffraction and X-ray reflectivity were applied to meibum films at an air-water interface to identify molecular organization. At room temperature, interfacial meibum films formed two coexisting scattering phases with rectangular lattices and next-nearest neighbor tilts, similar to the Ov phase previously identified in fatty acids. The intensity of the diffraction peaks increased with compression, although the lattice spacing and molecular tilt angle remained constant. Reflectivity measurements at surface pressures of 18 mN/m and above revealed multilayers with d-spacings of 50 Å, suggesting that vertical organization rather than lateral was predominantly affected by meibum-film compression.

No abstract

The colloidal stability of Stöber silica dispersed in acetone (99.7 wt %) was investigated and compared to the results obtained in water using electrophoresis and coagulation experiments with NaI, CaI2, and Bu4NI. A critical coagulation concentration (cc) of 19.6 mM NaI in acetone was observed whereas Bu4NI acetone solutions up to 145 mM had no effect on the stability of the silica organosols. In NaI and Bu4NI acetone solutions, the magnitude of the electrophoretic mobilities of the silica organosols decreased with increasing electrolyte concentration. From 0.11 to 13.5 mM NaI the electrophoretic mobilities decreased from -3.3 × 10 -8 to -0.39 × 10 -8 m 2 V -1 s -1 ; from 3.9 to 39 mM Bu4NI the mobilities decreased from -2.8 × 10 -8 to -0.91 × 10 -8 m 2 V -1 s -1 . Results using a single-site dissociation model were compared with experimental -potentials for silica in NaI acetone solutions and showed adequate agreement when ∆pH was assumed to be 2. Experimental coagulation concentrations for NaI and Bu4NI did not agree with simple DLVO theory. The discrepancy was believed to be due to the presence of a steric barrier consisting of a silicic acid gel network. CaI2 additions to the silica acetone solutions influenced the electrostatic potential of the particles and caused coagulation. At 0.06 and 1 mM CaI2, the electrophoretic mobilities of the particles were -2.9 × 10 -8 and +2.3 × 10 -8 m 2 V -1 s -1 , respectively. The charge reversal led to the restabilization of the particles as evidenced by two cc values 0.045 mM (cc1) and 2.75 mM (cc2).

More than two-fold RT differences were found for the higher viscosity, more muco-adhesive formulations compared to saline. However, other formulations provided RTs close to saline, suggesting that RT is influenced by factors other than simple viscosity. Future studies should examine the interplay of spreading characteristics, pseudoplasticity and muco-adhesion relative to RT to determine the individual and cumulative effects on formulation retention.

HSPM is an effective tool that is suitable for biophysical and morphological evaluation of meibum. Morphological properties and melting characteristics of human meibum were found to be similar to those of mice. Abnormal meibum of many dry eye patients contained large quantities of nonlipid, protein-like inclusions, which were routinely absent in meibum of normal controls.

A model tear film lipid layer composed of a binary mixture of cholesteryl myristate (CM) and 1,2-dipalmitoyl- sn-glycero-3-phosphocholine (DPPC) was characterized using surface tension measurements, Brewster angle microscopy (BAM) and interfacial stress rheology (ISR). Isotherms showed that films containing >or=90 mol % CM have a 17-fold greater % area loss between the first and second compressions than the films with less CM. BAM images clearly showed that CM films did not expand after compression, and solid-like regions extending 1-2 mm were observed at low pressures (1 mN/m). Lipid films with or=50 mol % CM became elastic at higher surface pressures. Increasing CM content reduced the surface pressure at which the mixed film became elastic. Lysozyme adsorption into a CM film increased the compressibility and resulted in a more expanded film. Lysozyme increased the ductility of the CM/DPPC films with no film breakdown occurring up to the highest pressure measured (40 mN/m). In summary, CM increased the elasticity of the lipid films, but also caused them to become brittle and incapable of expansion following compression. Lysozyme adsorption increased the ductility and decreased the isotherm hysteresis for CM/DPPC films.

Interactions between amphiphilic block copolymers and lipids are of medical interest for applications such as drug delivery and the restoration of damaged cell membranes. A series of monodisperse poly(ethylene oxide)-poly(butylene oxide) (EOBO) block copolymers were obtained with two ratios of hydrophilic/hydrophobic block lengths. We have explored the surface activity of EOBO at a clean interface and under 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) monolayers as a simple cell membrane model. At the same subphase concentration, EOBO achieved higher equilibrium surface pressures under DPPC compared to a bare interface, and the surface activity was improved with longer poly(butylene oxide) blocks. Further investigation of the DPPC/EOBO monolayers showed that combined films exhibited similar surface rheology compared to pure DPPC at the same surface pressures. DPPC/EOBO phase separation was observed in fluorescently doped monolayers, and within the liquid-expanded liquid-condensed coexistence region for DPPC, EOBO did not drastically alter the liquid-condensed domain shapes. Grazing incidence X-ray diffraction (GIXD) and X-ray reflectivity (XRR) quantitatively confirmed that the lattice spacings and tilt of DPPC in lipid-rich regions of the monolayer were nearly equivalent to those of a pure DPPC monolayer at the same surface pressures.