724
Views
7
CrossRef citations to date
0
Altmetric
Articles; Pharmaceutical Biotechnology

Effect of hydrophilic polymers on the wettability, static and dynamic, of solid substrate covered by confluent monolayer of air-damaged SIRC cells

, , &
Pages 390-394 | Received 20 Mar 2014, Accepted 08 Dec 2014, Published online: 13 Jan 2015
 

Abstract

The aim of this study was to evaluate the possible implementation of hydrophilic polymers as recovery agents in air-damaged corneal cells. The sessile bubble technique was implemented to measure the wetting properties of four selected polymers: hydroxyethyl cellulose (HEC), sodium chondroitin sulphate (SCS), hydroxypropyl-methylcellulose (HPMC) and poloxamer F127 (PO12), at equilibrium conditions and in the case of advancing and receding contact angle. For testing the wetting properties of the polymers, glass slides covered with a confluent monolayer of Statens Seruminstitut rabbit cornea (SIRC) cells were used. HEC showed best properties for a broad concentration range, as the polymer showed capability to maintain low values of the static (equilibrium) contact angle (average static contact angle – 36.07˚, compared to average static compact angles of HPMC – 38.44˚, PO12 – 38.92˚ and SCS – 37.85˚), i.e. better wettability. Sessile bubble technique provides quick, relatively simple and reliable approach for testing surface properties of the listed polymers. The nature of the surface damage produced by the exposition of SIRC cells was used as a plausible model of evaporative dry eye syndrome, and thus the results may have clinical implementation.

Acknowledgements

We would like to express our deep gratitude to Dr. Norihiko Yokoi from the department of Ophthalmology of Kyoto Prefectural University of Japan for being our mentor and leader in the field of dry eye research. The contribution of Yana Néncheva and Nataly Nedelcheva, for their assistance in data collection is also acknowledged.

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

The study was supported by a Collaborative Study [grant number 1970] by Rohto Pharmaceutical Co., Osaka, Japan.