Abstract

Non-ionic emulsifiers are commonly found in existing pharmaceutical and cosmetic formulations and have been widely employed to enhance the penetration and permeation of active ingredients into the skin. With the potential of disrupting skin barrier function and increasing fluidity of stratum corneum (SC) lipids, we herein examined the effects of two kinds of non-ionic emulsifiers on intercellular lipids of skin, using confocal Raman spectroscopy (CRS) with lipid signals on skin CRS spectrum. Non-ionic emulsifiers of polyethylene glycol alkyl ethers and sorbitan fatty acid esters were studied to obtain a deep understanding of the mechanism between non-ionic emulsifiers and SC lipids. Emulsifier solutions and dispersions were prepared and applied onto excised porcine skin. Water and sodium laureth sulfate solution (SLS) served as controls. SC lipid signals were analysed by CRS regarding lipid content, conformation and lateral packing order. Polyethylene glycol (PEG) sorbitan esters revealed no alteration of intercellular lipid properties while PEG-20 ethers appeared to have the most significant effects on reducing lipid content and interrupting lipid organization. In general, the polyoxyethylene chain and alkyl chain of PEG derivative emulsifiers might indicate their ability of interaction with SC components. HLB values remained critical for complete explanation of emulsifier effects on skin lipids. With this study, it is possible to characterize the molecular effects of non-ionic emulsifiers on skin lipids and further deepen the understanding of enhancing substance penetration with reduced skin barrier properties and increased lipid fluidity.

Highlights

  • Skin represents the largest organ of the human organism and forms the outermost barrier film that protects the human body from external environment impacts and exogenous irritations and corrosions

  • It is evident that most of the Polyethylene glycol (PEG) ethers cause a reduction of lipid content (Figure 3a) while all the polysorbate emulsifiers show no effects on stratum corneum (SC) lipid content (Figure 3b)

  • Regarding the PEG-10 alkyl ethers, O10 shows a relatively smaller difference compared to S10 and C10 which both indicate a greater reduction of skin lipid content

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Summary

Introduction

Skin represents the largest organ of the human organism and forms the outermost barrier film that protects the human body from external environment impacts and exogenous irritations and corrosions. Stratum corneum (SC) is the uppermost layer of the skin, composed of a highly ordered, multilamellar lipid matrix with embedded flattened, keratin-filled corneocytes [1,2]. It has been well accepted that intercellular lipids in SC play an important role in maintaining skin barrier function and keeping the skin in a proper hydration state [5]. The removal and organizational alteration of intercellular lipids would disrupt the barrier function from multiple aspects and deteriorate into some chronic skin diseases [6,7]. With the importance of assuring the solid structures and ordered properties of skin lipids, it is essential to monitor the molecular lipid interactions with exposed substances and maintain the protective barrier state for further optimization of dermatological treatments

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