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Water-In-Oil Nano-Emulsions Prepared by Spontaneous Emulsification: New Insights on the Formulation Process

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Water-In-Oil Nano-Emulsions Prepared by Spontaneous Emulsification: New Insights on the Formulation Process pharmaceutics Article Water-in-Oil Nano-Emulsions Prepared by Spontaneous Emulsification: New Insights on the Formulation Process Salman Akram 1,†, Nicolas Anton 1,2,†, Ziad Omran 3,* and Thierry Vandamme 1,2,* 1 Faculty of Pharmacy, Université de Strasbourg, CNRS, CAMB UMR 7199, F-67000 Strasbourg, France; [email protected] (S.A.); [email protected] (N.A.) 2 INSERM, Regenerative Nanomedicine UMR 1260, Centre de Recherche en Biomédecine de Strasbourg (CRBS), Université de Strasbourg, F-67000 Strasbourg, France 3 Pharmacy Program, Department of Pharmaceutical Sciences, Batterjee Medical College, Jeddah 21442, Saudi Arabia * Correspondence: [email protected] (Z.O.); [email protected] (T.V.) † These authors contributed equally to this work. Abstract: Nano-emulsions consist of stable suspensions of nano-scaled droplets that have huge loading capacities and are formulated with safe compounds. For these reasons, a large number of studies have described the potential uses of nano-emulsions, focusing on various aspects such as formulation processes, loading capabilities, and surface modifications. These studies typically concern direct nano-emulsions (i.e., oil-in-water), whereas studies on reverse nano-emulsions (i.e., water-in-oil) remain anecdotal. However, reverse nano-emulsion technology is very promising (e.g., as an alternative to liposome technology) for the development of drug delivery systems that encapsulate hydrophilic compounds within double droplets. The spontaneous emulsification process has the added advantages of optimization of the energetic yield, potential for industrial scale-up, Citation: Akram, S.; Anton, N.; improved loading capabilities, and preservation of fragile compounds targeted for encapsulation. In Omran, Z.; Vandamme, T. this study, we propose a detailed investigation of the processes and formulation parameters involved Water-in-Oil Nano-Emulsions in the spontaneous nano-emulsification that produces water-in-oil nano-emulsions. The following Prepared by Spontaneous Emulsification: New Insights on the details were addressed: (i) the order of mixing of the different compounds (method A and method Formulation Process. Pharmaceutics B), (ii) mixing rates, (iii) amount of surfactants, (iv) type and mixture of surfactants, (v) amount of 2021, 13, 1030. https://doi.org/ dispersed phase, and (vi) influence of the nature of the oil. The results emphasized the effects of the 10.3390/pharmaceutics13071030 formulation parameters (e.g., the volume fraction of the dispersed phase, nature or concentration of surfactant, or nature of the oil) on the nature and properties of the nano-emulsions formed. Academic Editor: Masahiro Goto Keywords: nano-emulsion; water-in-oil; spontaneous emulsification; low-energy method; surfactant Received: 27 May 2021 Accepted: 3 July 2021 Published: 7 July 2021 1. Introduction Publisher’s Note: MDPI stays neutral Nano-medicine has emerged in the past few decades as an important field of research with regard to jurisdictional claims in due to its advantages over conventional therapeutic options [1,2]. Nano-emulsions (NEs) published maps and institutional affil- are one of the most important drug vehicles in nano-medicine, as they offer the possibility iations. of high-efficiency delivery of lipophilic drugs loaded within the oily core of the droplets [3]. Anecdotally, hydrophilic molecules can also be encapsulated in water-in-oil NEs by direct entrapment in the oil nano-droplets [4–6], or by the use of complex double structures such as nano double emulsions [7–9]. The choices of oil and type and grade of surfactant, with a Copyright: © 2021 by the authors. focus on the intended administration route, allow the production of NEs that are nontoxic Licensee MDPI, Basel, Switzerland. and nonirritating, with improved drug bioavailability [10,11]. However, these choices can This article is an open access article also determine many other NE properties, and therefore, their applications, including the distributed under the terms and NE physical stability and loading properties [12–16]. conditions of the Creative Commons Attribution (CC BY) license (https:// One important consideration is that even when NEs are thermodynamically unstable, creativecommons.org/licenses/by/ the droplet suspension is kinetically stable, regardless of the sense of the emulsion, i.e., 4.0/). direct or reverse [17]. The Gibbs free energy DG of this type of droplet suspension is Pharmaceutics 2021, 13, 1030. https://doi.org/10.3390/pharmaceutics13071030 https://www.mdpi.com/journal/pharmaceutics Pharmaceutics 2021, 13, 1030 2 of 12 theoretically very high, since it relies on the interface increase DA, which is as high as the droplet size is small [18]. However, although the DG of a NE is much greater than that of a microscale emulsion, the NEs, in practice, appear significantly more stable or are “kinetically stable” for steric stabilization reasons [18,19]. Conversely, gravitational separation, sedimentation or creaming, is negligible with these Brownian droplets. In addition, Ostwald ripening induces only a small evolution of NEs, making the suspension highly stable over months [20–22]. NEs can be formed in several ways, classified mainly as high-energy and low-energy methods [19,23]. The most popular high-energy methods are high-pressure homogeniza- tion, micro-fluidization, and ultrasonication [18,19], whereas the low-energy methods, also known as transitional nano-emulsification methods [24,25], are mainly described as phase-inversion temperature methods and spontaneous emulsification. The advantages of low-energy over high-energy methods lie in the gain in energy yields, which is beneficial for industrial scale-up as well as in the fact that a low-energy process is itself soft, and prevents the potential denaturation or destruction of fragile molecules like proteins and peptides [26]. Our overall research objective is to encapsulate hydrophilic therapeutic agents in lipid droplets as a strategy for increasing their bioavailability after oral administration or for fabricating preparations for topical application. In the present study, our focus was on the formulation of water-in-oil (w/o) NEs by low-energy methods. As a preamble to the formulation of double emulsions (i.e., w/o NEs dispersed in an aqueous phase), a better understanding and optimization of the formulation of w/o low-energy NEs is provided. Spontaneous nano-emulsification methods and processes are well documented regarding oil-in-water (o/w) NEs, whereas the literature reports on the formulation of reverse w/o NEs by spontaneous methods still remain anecdotal, despite the great potential of these NEs. A recent report [27] has provided a general description of this spontaneous w/o emulsification process, also called the emulsion inversion point (EIP), and showed that surfactant interactions with the phases strongly affect the emulsification. The efficiency of the formulation of w/o or o/w NEs was shown to depend on (i) the properties of the surfactants used (i.e., the hydrophilic-lipophilic balance [HLB] of the surfactant mixture), and (ii) the order of mixing of the different phases. Two methods were proposed and compared: in this reference, method A, where oil is slowly poured into the (water + surfactant) mixture, and method B, where water is slowly poured into the (oil + surfactant) mixture. Interestingly, for the formulation of o/w NEs, using a mixture of Tween 80 and Span 80 in different amounts to change the HLBs, methods A and B were roughly comparable and showed only a slight variation for specific HLB values. By contrast, the two methods showed clear differences in the formulation of w/o NEs, as method B only worked for lower HLBs, whereas method A was successful for a large range of HLB values. However, this previous study [27] focused primarily on investigations into o/w NEs and only showed the feasibility of formulating reverse w/o NEs. In the present study, our objective was to conduct a more in-depth investigation of the spontaneous formulation process of NEs as a preliminary step for the fabrication of complex carriers for hydrophilic or both hydrophilic and lipophilic active ingredients. Based on the pioneering study discussed above [27], we proposed to compare method A and method B, but with a focus on w/o NEs and a deeper examination of the formulation and process parameters. We studied the impact of the process parameters, e.g., flow rate of the dropping phase and mixing rate of the suspension, as well as the impact of the phase ratio, surfactant ratio, surfactant mixture composition, and nature of the oils for both methods. Our aim in taking this approach was to identify the factors and the experimental conditions that substantially affect the process, as a way to clarify how to optimize the spontaneous w/o nano-emulsification. No literature with this focus has been published to date, making the present study an important step forward as a starting point for future innovations. Pharmaceutics 2021, 13, x 3 of 12 the spontaneous w/o nano-emulsification. No literature with this focus has been pub- Pharmaceutics 2021, 13, 1030 3 of 12 lished to date, making the present study an important step forward as a starting point for future innovations. 2. Materials and2. MaterialsMethodology and Methodology 2.1. Materials 2.1. Materials ® The model oil Thechosen model for oilthe chosenexperiments for the was experiments Labrafac® was WL Labrafac1349 (GattefosséWL 1349 S.A., (Gattefoss é S.A., Saint-Priest, France).Saint-Priest, This oil France).
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