Liquid crystals are considered to be an intermediate state between liquids and solids. They are associated with solids because of their anisotropy, birefringence, structure and mechanical stability, while their flowability correlate them with liquids. According to their origin, they are divided into thermotropic and lyotropic liquid crystals. Lyotropic ones exist in several forms: lamellar, cubic and hexagonal Lamellar liquid crystals represent the innovative dermal delivery system, mainly because of their structure, which is similar to that of the intercellular lipids of the stratum corneum of the skin.
For the purposes of this thesis, the influence of lecithin-based lamellar liquid crystals on the skin’s barrier function, more precisely on transepidermal water loss and hydration, was evaluated in vitro on a porcine skin model embedded in Franz diffusion cells. Influence of eight liquid crystal systems with different quantitative compositions (while the proportion of the aqueous phase was rising, the ratio of the oil phase to the emulsifiers was constant) on the studied parameters was determined. First, as a part of the preliminary tests, we determined the time of the skin’s pre-hydration in Franz diffusion cells to determine basal values, the amount of time the liquid crystals were exposed to the skin, and time points to assess the effect of liquid crystals after removal from the skin. Transepidermal water loss was determined using the Tewameter® TM 300. Afterwards, the hydration was determined at the same time points using the Corneometer® CM 825. The values measured before the application of the liquid crystals (basal values) were compared with the final values, i.e. 30 minutes and 90 minutes after the liquid crystals had been removed.
Following skin application, the liquid crystals improved the barrier function as seen in decreased transepidermal water loss and increased hydration. The maximum decrease in TEWL was 18,6 %, 30 minutes after, and 22,3 %, 90 min after the liquid crystal system had been removed from the skin. The maximum increase in hydration was 158,3 %, 30 minutes after, and 165,5 %, 90 min after the liquid crystal had been removed from the skin. The improvement of skin barrier function, especially hydration, correlates with quantitative composition of liquid crystals, namely the proportion of oil phase and emulsifier mixture, contributing to formation of semipermeable film on the skin surface. Moreover, the effect was time dependent.
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