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. 2021 Sep 8;13(9):1422.
doi: 10.3390/pharmaceutics13091422.

Spontaneously Self-Assembled Microgel Film as Co-Delivery System for Skincare Applications

Affiliations

Spontaneously Self-Assembled Microgel Film as Co-Delivery System for Skincare Applications

Garbine Aguirre et al. Pharmaceutics. .

Abstract

Nowadays, the design of innovative delivery systems is driving new product developments in the field of skincare. In this regard, serving as potential candidates for on-demand drug delivery and fulfilling advanced mechanical and optical properties together with surface protection, spontaneously self-assembled microgel films can be proposed as ideal smart skincare systems. Currently, the high encapsulation of more than one drug simultaneously in a film is a very challenging task. Herein, different ratios (1:1, 3:1, 9:1) of different mixtures of hydrophilic/hydrophobic UVA/UVB-absorbers working together in synergy and used for skin protection were encapsulated efficiently into spontaneously self-assembled microgel films. In addition, in vitro release profiles show a controlled release of the different active molecules regulated by the pH and temperature of the medium. The analysis of the release mechanisms by the Peppas-Sahlin model indicated a superposition of diffusion-controlled and swelling-controlled releases. Finally, the distribution of active molecule mixtures into the film was studied by confocal Raman microscopy imaging corroborating the release profiles obtained.

Keywords: co-delivery; cosmetic active molecules; self-assembled microgel film.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Release kinetics as a function of pH for different mixtures at 25 °C. ■ DBBH at pH 6, □ DBBH at pH 4.4, ● Benzophenone-4 at pH 6, ○ Benzophenone at pH 4.4, ▲ Salicylic acid at pH 6, Δ Salicylic acid at pH 4.4.
Figure 2
Figure 2
Release kinetics as a function of temperature for different mixtures at pH 6. ■ DBBH at 25 °C, □ DBBH at 37 °C, ● Benzophenone-4 at 25 °C, ○ Benzophenone at 37 °C, ▲ Salicylic acid at 25 °C, Δ Salicylic acid at 37 °C.
Figure 3
Figure 3
Cross-sectional from the top (image top) to the bulk (image bottom) (50 × 50 µm2) (a) and 2D surface (75 × 75 µm2) (b) confocal images of different mixtures.

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