Abstract

Recent clinical findings suggest that mucomimetic polymers (MMP) can alter not only the texture of the aqueous tear but also the spreading and structure of the tear film (TF) lipid layer, thereby allowing for their synchronized performance in vivo. Thus, we aimed to evaluate in vitro (i) the capability of pharmaceutically applicable MMP to ensure the formation of post-evaporative ferning patterns (a characteristic feature of the “healthy” tear colloid) and (ii) the MMP interactions with human meibum films accessed in the course of blink-like deformations via Langmuir surface balance and Brewster angle microscopy (BAM). Four MMP were used- hyaluronic acid (HA), cross-linked hyaluronic acid (CHA), carboxymethyl cellulose (CMC) and gellan gum (GG)- at the concentrations of 0.0001%, 0.001%, 0.01%, 0.05% and 0.1%. Significant differences were observed in the MMP fern formation capability: CHA (≥0.001%) > HA (≥0.01%) = CMC (≥0.01%) > GG (≥0.05%). All MMP affected the spreading of meibum, with BAM micrographs revealing thickening of the films. CHA was particularly efficient, showing concentration-dependent enhancement of tear ferning and of meibomian layer structure, surfactant properties and viscoelasticity. Thus, endogenous and exogenous MMP may play key roles for the concerted action of the TF layers at the ocular surface, revealing novel routes for TF-oriented therapeutic applications.

Highlights

  • Tear film (TF) represents a composite wetting film composed by tear film lipid layer (TFLL) at the air/tear surface and underlying aqueous tear (AT) situated over the glycocalyx of the corneal epithelium [1,2]

  • This is because TFLL, a maze of 236 lipid species distributed among nine molecular classes [4], is built primarily (>95%) by the meibomian gland secretion (MGS, or meibum): a composite lipid-rich mixture that may contain up to 22 wt% non-lipid components [5,6,7]

  • It can be seen that among all the polymers studied, only gellan gum (GG) is not capable to form fine-structured ferning patterns by itself, and it is not able to enhance the inherent capability of tears to do so

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Summary

Introduction

Tear film (TF) represents a composite wetting film composed by tear film lipid layer (TFLL) at the air/tear surface and underlying aqueous tear (AT) situated over the glycocalyx of the corneal epithelium [1,2]. Tear film lipid layer has received a lot of attention as it was found that more than 80% of the dry eye sufferers report symptoms of meibomian gland dysfunction (MGD), a condition associated with qualitative and quantitative abnormalities in the TFLL [3]. This is because TFLL, a maze of 236 lipid species distributed among nine molecular classes [4], is built primarily (>95%) by the meibomian gland secretion (MGS, or meibum): a composite lipid-rich mixture that may contain up to 22 wt% non-lipid components (proteins, salts, polysachharides) [5,6,7].

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