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Several applications, ranging from standard cosmetic to advanced drug delivery, involve the interaction of different formulations, generally creams or lotions based on emulsions, with biological systems, for example skin. Drug release through the skin, usually referred to as Transdermal Drug Delivery (TDD), requires penetration through the skin barrier, which is a highly organized system composed of several layers with different properties and morphology. TDD can be considered as good alternative to traditional oral or parenteral delivery, which are more painful for the patients. However, standard methods for transdermal studies, such as microscopy, spectroscopy and the well-established Franz cell diffusion chamber, can only capture few aspects of the drug penetration process and do not allow a complete view of the interactions between single components. For the same reasons, although many works have been aimed at improving drug transport by optimization of the carriers (vesicles, nanoparticles, and emulsion droplets), a full understanding of possible enhancer effects is currently lacking. Dimensions, shape or amount of the ingredients in the formulation are considered possible parameters involved in this improvement. Here, an innovative methodology to investigate penetration of different compounds through the skin, by time-lapse confocal microscopy and images analysis is presented. In particular, diffusion of fluorescent molecules in solutions or emulsions is investigated and the corresponding diffusion coefficients are estimated. Based on the formulations properties and their affinity with the medium in which they diffuse, a different behavior is observed. In particular, emulsion microstructure seems to play an important role, enhancing the penetration compared to pure solutions. In addition, the possibility to use soft materials, such as Bicontinuous Emulsion Gels (BEGs), tunable as desired to mimic skin morphology and/or properties are presented as a valid alternative to skin biopsies in penetration studies. The easy preparation and low cost of these materials are some of the main advantages of the proposed approach. To this aim, gelatin is used to mimic hydrophilic properties of skin cells, while cross-linked oil is used for the lipid matrix. A complete characterization of the gelatin gel and its structure-related mechanisms are investigated by Confocal Laser Scanning Microscopy (CLSM), Nuclear Magnetic Resonance (NMR) and birefringence imaging.

Skin is a complex structured system primarily involved in Transdermal Drug Delivery (TDD). The outer stratum corneum represents the main barrier to the entrance of external molecules. Nowadays, none of the recognized methods, used for the investigation of penetration processes, is able to give a complete overview of the transport mechanisms involved. Standard protocols are based on the use of human or animal skin samples, which are difficult and expensive to obtain. Here, we present a novel experimental setup to investigate TDD by using Confocal Laser Scanning Microscopy and image analysis. The methodology is based on diffusion experiments of fluorescent-labelled fluids (water, oil, and oil-in-water emulsions), in a model matrix. Using an agarose gel as model for a proof of concept, different penetration efficiencies were observed, suggesting an important role of both chemical composition and fluid microstructure on the transport mechanism. An adequate model system should be used to better mimic the stratum corneum morphology and properties. To this aim, several bicontinuous emulsion gels, obtained from an emulsification process, were preliminary formulated and suggested as model systems to mimic the stratum corneum. In this work, we define the key directions for the development of an innovative approach to study the penetration of formulations through the skin.

Phospholipids, which are amphiphilic biomolecules composed of a polar head group and two nonpolar fatty acid tails, play a central role in cellular and body functions. The most common phospholipid is phosphatidylcholine (PC), which is also widespread used as a surfactant in colloidal systems, such as oil-in-water (O/W) emulsions, for several applications ranging from food to cosmetics. In these systems, PC tends to arrange at the interface between polar and nonpolar phases. Specific identification of these molecules at the interface is still an ambitious task. In this work, we propose immunofluorescence and confocal microscopy as valuable tools for the localization of PC at the interface of O/W emulsions, where phospholipids are used as surfactants. The protocol required the use of a primary antibody (TEPC-15), specific for choline, and a secondary fluorescently-labelled antibody, which selectively binds to the primary antibody. By using this approach, we were able to visualize choline-based phospholipids in cell membranes, lipid-based emulsions and in PC films and to estimate molecule concentration by image analysis techniques. We also investigated the interference of proteins on the staining procedure. We attributed this interference to possible molecular interactions close to the interface, which were found to depend on protein concentration. This innovative approach can have a relevant impact in a wide range of interfacial engineering applications, such as tuning emulsion microstructure and stability.

Gelatin gels are increasingly involved in many industrial applications due to several advantages including cost efficiency and biocompatibility. Generally, their production requires the use of aqueous solvents, which cause significant swelling, due to the ability of solvent molecules to penetrate through the gel microstructure and increase its volume. Since swelling mechanisms and their effect on the gel structure are not fully understood, further investigations are required. In this work, we combine macroscopic measurements of the swelling ratio (SR) with Nuclear Magnetic Resonance (NMR) and Confocal Laser Scanning Microscopy (CLSM) to investigate changes in the gelatin structure as a function of both polymer concentration and swelling time. SR values increase as a function of time until a maximum is reached and then show a slight drop for all the gelatin concentrations after 24 h swelling time, probably due to a network relaxation process. NMR allows determination of mass transport and molecular dynamics of water inside the gelatin pores, while CLSM is used to visualize the penetration of tracers (polystyrene microbeads) with a diameter much larger than the gel pores. Structural parameters, such as average pore size and tortuosity, are estimated. In particular, the pore size decreases for higher polymer concentration and increases during swelling, until reaching a maximum, and then dropping at longer times. The penetration of tracers provides evidence of the heterogeneity of the gel structure and shows that single microcarriers can be loaded in gelatin gels upon swelling.

Interaction of microstructured fluids with skin is ubiquitous in everyday life, from the use of cosmetics, lotions, and drugs, to personal care with detergents or soaps. The formulation of microstructured fluids is crucial for the control of the transdermal transport. In biomedical applications transdermal delivery is an efficient approach, alternative to traditional routes like oral and parenteral administration, for local release of drugs. Poor skin permeability, mainly due to its outer layer, which acts as the first barrier against the entry of external compounds, greatly limits the applicability of transdermal delivery. In this review, we focus on recent studies on the improvement of skin transport efficiency by using microemulsions (ME). Quantitative techniques, which are able to investigate both skin morphology and penetration processes, are also reviewed. ME are increasingly used as transdermal systems due to their low preparation cost, stability and high bioavailability. ME may act as penetration enhancers for many active principles, but ME microstructure should be chosen appropriately considering several factors such as ratio and type of ingredients and physic-chemical properties of the active components. ME microstructure is strongly affected by the flow conditions applied during processing, or during spreading and rubbing onto skin. Although the role played by ME microstructure has been generally recognized, the skin transport mechanisms associated with different ME microstructures are still to be elucidated and further investigations are required to fully exploit the potential of ME in transdermal delivery.