Journal
SOFT MATTER
Volume 10, Issue 30, Pages 5579-5588Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4sm00758a
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Funding
- Collaborative Study Grant by Rohto Pharmaceutical Co. Ltd., Osaka, Japan
- Ministry of Education, Culture, Sports, Science and Technology of Japan [25462728]
- Grants-in-Aid for Scientific Research [25462728] Funding Source: KAKEN
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The surface properties of human meibomian lipids (MGS), the major constituent of the tear film (TF) lipid layer, are of key importance for TF stability. The dynamic interfacial properties of films by MGS from normal eyes (nMGS) and eyes with meibomian gland dysfunction (dMGS) were studied using a Langmuir surface balance. The behavior of the samples during dynamic area changes was evaluated by surface pressure-area isotherms and isocycles. The surface dilatational rheology of the films was examined in the frequency range 10(-5) to 1 Hz by the stress-relaxation method. A significant difference was found, with dMGS showing slow viscosity-dominated relaxation at 10(-4) to 10(-3) Hz, whereas nMGS remained predominantly elastic over the whole range. A Cole-Cole plot revealed two characteristic processes contributing to the relaxation, fast (on the scale of characteristic time tau < 5 s) and slow (tau > 100 s), the latter prevailing in dMGS films. Brewster angle microscopy revealed better spreading of nMGS at the air-water interface, whereas dMGS layers were non-uniform and patchy. The distinctions in the interfacial properties of the films in vitro correlated with the accelerated degradation of meibum layer pattern at the air-tear interface and with the decreased stability of TF in vivo. These results, and also recent findings on the modest capability of meibum to suppress the evaporation of the aqueous subphase, suggest the need for a re-evaluation of the role of MGS. The probable key function of meibomian lipids might be to form viscoelastic films capable of opposing dilation of the air-tear interface. The impact of temperature on the meibum surface properties is discussed in terms of its possible effect on the normal structure of the film.
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