Person:
Guzmán Solís, Eduardo

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First Name
Eduardo
Last Name
Guzmán Solís
Affiliation
Universidad Complutense de Madrid
Faculty / Institute
Ciencias Químicas
Department
Química Física
Area
Química Física
Identifiers
UCM identifierORCIDScopus Author IDWeb of Science ResearcherIDDialnet IDGoogle Scholar ID

Search Results

Now showing 1 - 10 of 40
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    The journey of tuning chitosan properties in colloidal systems: Interactions with surfactants in the bulk and on the alumina surface
    (Chemical Engineering Journal, 2022) Matusiak, Jakub; Grządka, Elzbieta; Maciołek, Urszula; Godek, Ewelina; Guzmán Solís, Eduardo
    The specific physico-chemical properties of chitosan (Ch), a biopolymer isolated from chitin, and its impact on the stability of colloidal dispersity have focused the interest of science and industry. However, in some cases chitosan alone is not enough to provide high stability to dispersions, making it necessary to add surfactant to the chitosan/oxide system, leading to superior stabilizing properties due to the association of polymer and surfactant molecules to form complexes that can modify the ability of bare chitosan for adsorbing on colloidal materials. This study explores the interactions between chitosan and alumina in the presence of three different anionic surfactants: the hydrocarbon SDS (sodium dodecyl sulfate), the fluorocarbon FS-91 (Capstone® FS-91), and the silicone A-Si (Silphos A-100). Different analytical methods evidenced chitosan adsorption on the alumina surface, forming hybrid organic–inorganic materials. This process can be enhanced by adding surfactant, with SDS leading to a strong increase of chitosan adsorption. Elemental mapping and scanning electron microscope imaging have provided a confirmation of the co-adsorption of polymer and surfactant on the alumina surface. The latter emerges as a very important finding because the results have shown that small quantities of surfactant (as low as 0.002% v/v) can strongly influence the adsorption and stability of multicomponent colloidal systems. This allows decreasing the chitosan amount required for the enhancement of the colloidal stability in relation to dispersions without added surfactants, providing the basis for reducing the production costs of colloidal dispersion, which opens new opportunities to chemical industry
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    A closer physico-chemical look to the Layer-by-Layer electrostatic self-assembly of polyelectrolyte multilayers
    (Advances in Colloid and Interface Science, 2020) Guzmán Solís, Eduardo; González Rubio, Ramón; Ortega Gómez, Francisco
    The fabrication of polyelectrolyte multilayer films (PEMs) using the Layer-by-Layer (LbL) method is one of the most versatile approaches for manufacturing functional surfaces. This is the result of the possibility to control the assembly process of the LbL films almost at will, by changing the nature of the assembled materials (building blocks), the assembly conditions (pH, ionic strength, temperature, etc.) or even by changing some other operational parameters which may impact in the structure and physico-chemical properties of the obtained multi-layered films. Therefore, the understanding of the impact of the above mentioned parameters on the assembly process of LbL materials plays a critical role in the potential use of the LbL method for the fabrication of new functional materials with technological interest. This review tries to provide a broad physico-chemical perspective to the study of the fabrication process of PEMs by the LbL method, which allows one to take advantage of the many possibilities offered for this approach on the fabrication of new functional nanomaterials
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    Aqueous dispersions of oleic acid nanodroplets for thymol encapsulation
    (Colloids and Surfaces A, 2024) Paula Gutiérrez-González; Peña Fernández, Laura Luisa; Alejandro Lucia; Ortega Gómez, Francisco; González Rubio, Ramón; Guzmán Solís, Eduardo
    This study focuses on the use of oleic acid to disperse thymol as nanodroplets, stabilized by a mixture of alkylpolyglucoside and lecithin, in an aqueous environment. This approach aims to develop innovative platforms for the encapsulation and release of poorly water-soluble molecules such as thymol, useful for drug delivery and insecticide systems. The results highlight the critical role of controlling the content and concentration of the oil phase (thymol-oleic acid mixture) in achieving optimal thymol dispersion and nanodispersion stability. The interplay between the ability of oleic acid to inhibit thymol crystallization and the maximum dispersible oil amount is crucial. It affects the dispersion of thymol within the nanodroplets and influences coalescence and Ostwald ripening phenomena. The balance between oleic acid and thymol content is key: while oleic acid stabilizes dispersions, higher thymol content increases droplet size, potentially triggering destabilization. The uneven distribution of thymol within the droplets, revealed by fluorescence spectroscopy, suggests that up to three different chemical environments exist. This investigation may pave the way for the development of efficient platforms to improve access to biologically relevant, poorly soluble molecules.
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    Unravelling the orientation of the inositol-biphosphate ring and its dependence on phosphatidylinositol 4,5-bisphosphate cluster formation in model membranes
    (Journal Colloid and Interface Science, 2023) Santamaria, Andreas; Javier Carrascosa-Tejedor; Guzmán Solís, Eduardo; Zaccai, Nathan R.; Maestro, Armando
    Hypothesis Inositol phospholipids are well known to form clusters in the cytoplasmic leaflet of the plasma membrane that are responsible for the interaction and recruitment of proteins involved in key biological processes like endocytosis, ion channel activation and secondary messenger production. Although their phosphorylated inositol ring headgroup plays an important role in protein binding, its orientation with respect to the plane of the membrane and its lateral packing density has not been previously described experimentally. Experiments Here, we study phosphatidylinositol 4,5-bisphosphate (PIP2) planar model membranes in the form of Langmuir monolayers by surface pressure-area isotherms, Brewster angle microscopy and neutron reflectometry to elucidate the relation between lateral (in-plane) and perpendicular (out-of-plane) molecular organization of PIP2. Findings Different surface areas were explored through monolayer compression, allowing us to correlate the formation of transient PIP2 clusters with the change in orientation of the inositol-biphosphate headgroup, which was experimentally determined by neutron reflectometry.
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    Probing the effect of the capping polyelectrolyte on the internal structure of Layer-by-Layer decorated nanoliposomes
    (Journal Colloid and Interface Science, 2023) Mateos-Maroto, Ana; Rubio, José ; Prévost, Sylvain; Maestro, Armando; González Rubio, Ramón; Ortega Gómez, Francisco; Guzmán Solís, Eduardo
    Hypothesis The internal organization of polyelectrolyte layers deposited on colloidal templates plays a very important role for the potential applications of these systems as capsules for drug delivery purposes. Experiments The mutual arrangement of oppositely charged polyelectrolyte layers upon their deposition on positively charged liposomes has been studied by combining up three different scattering techniques and Electronic Spin Resonance, which has provided information about the inter-layer interactions and their effect on the final structure of the capsules. Findings The sequential deposition of oppositely charged polyelectrolytes on the external leaflet of positively charged liposomes allows modulating the organization of the obtained supramolecular structures, impacting the packing and rigidity of the obtained capsules due to the change of the ionic cross-linking of the multi-layered film as a result of the specific charge of the last deposited layer. The possibility to modulate the properties of the LbL capsules by tuning the characteristics of the last deposited layers offers a very interesting route for the design of materials for encapsulation purposes with their properties controlled almost at will by changing the number of deposited layers and their chemistry.
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    Dilution-controlled deposition of mixtures of a synthetic polycation and a natural origin polyelectrolyte with anionic surfactants on negatively charged surfaces
    (Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2024) Puente-Santamaría, Ana; Monge-Corredor, Julia; Ortega Gómez, Francisco; González Rubio, Ramón; Guzmán Solís, Eduardo
    The cosmetics industry is constantly seeking sustainable and environmentally friendly ingredients for hair care formulations to replace those traditionally derived from the petrochemical industry. In this context, the substitution of traditional cationic polyelectrolytes, such as poly(diallyldimethylammonium chloride, PDADMAC), by others of natural origin, such as chitosan, is a key challenge to achieve new formulations with a higher degree of naturality and more environmentally friendly without compromising product efficacy. This work investigates the effect of dilution on the phase separation of concentrated binary mixtures of two anionic surfactants (sodium laureth sulfate, SLES, and sodium dodecyl sulfate, SDS) with PDADMAC or chitosan. PDADMAC is a polycation of petrochemical origin, whereas chitosan is obtained from natural resources. Also, how this phase separation affects the formation of conditioning deposits on surfaces that mimic the charge and wettability of damaged hair fibers has been studied. The results show that for polymers of similar molecular weight, the substitution of PDADMAC by a highly charged chitosan is a promising alternative. The deposition is greatly enhanced for model wash formulations containing chitosan after minimal dilution. The results obtained here may pave the way to an important line of research toward improving the sustainability profile of hair care formulations without compromising consumer satisfaction.
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    Ionic strength effect in the equilibrium and rheological behavior of an amphiphilic triblock copolymer at the air/solution interface
    (Colloids and Interface, 2024) Carbone, Carlo; Guzmán Solís, Eduardo; Maldonado-Valderrama, Julia; González Rubio, Ramón; Ortega Gómez, Francisco
    This study investigates the effect of an inert salt (NaCl) on the equilibrium interfacial tension and dilatational modulus of Pluronic F-68 copolymer, a triblock copolymer consisting of two terminal blocks of poly(ethylene oxide) and a less hydrophilic central block of poly(propylene oxide). Interfacial tension measurements were carried out using a surface force balance and a drop shape tensiometer, while rheological measurements were carried out in two different frequency ranges. This involved the use of the oscillatory barrier/droplet method and electrocapillary wave measurements, complemented by an appropriate theoretical framework. This work aimed to elucidate the influence of NaCl on the interfacial behavior of Gibbs monolayers of Pluronic F-68. In addition, this study highlights some of the technical and theoretical limitations associated with obtaining reliable dilatational rheological data at high frequencies (<1 kHz) using electrocapillary wave measurements. The results provide valuable insights into the interplay between salt presence and interfacial properties of Pluronic F-68 and highlight the challenges of obtaining accurate dilatational rheological data under specific measurement conditions.
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    Anomalous Colloidal Motion under Strong Confinement
    (Small, 2023) Abelenda Núñez, Irene; Ortega Gómez, Francisco; González Rubio, Ramón; Guzmán Solís, Eduardo
    Diffusion of biological macromolecules in the cytoplasm is a paradigm of colloidal diffusion in an environment characterized by a strong restriction of the accessible volume. This makes of the understanding of the physical rules governing colloidal diffusion under conditions mimicking the reduction in accessible volume occurring in the cell cytoplasm, a problem of a paramount importance. This work aims to study how the thermal motion of spherical colloidal beads in the inner cavity of giant unilamellar vesicles (GUVs) is modified by strong confinement conditions, and the viscoelastic character of the medium. Using single particle tracking, it is found that both the confinement and the environmental viscoelasticity lead to the emergence of anomalous motion pathways for colloidal microbeads encapsulated in the aqueous inner cavity of GUVs. This anomalous diffusion is strongly dependent on the ratio between the volume of the colloidal particle and that of the GUV under consideration as well as on the viscosity of the particle's liquid environment. Therefore, the results evidence that the reduction of the free volume accessible to colloidal motion pushes the diffusion far from a standard Brownian pathway as a result of the change in the hydrodynamic boundary conditions driving the particle motion
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    Fluid interfaces as models for the study of lipid-based films with biophysical relevance
    (Coatings, 2023) Argudo, Pablo G.; Maestro, Armando; Guzmán Solís, Eduardo
    This comprehensive review aims to provide a deep insight into the fascinating field of biophysics in living organisms through the study of model fluid interfaces that mimic specific lipid-based structures with biophysical relevance. By delving into the study of these physiological fluid interfaces, we can unravel crucial aspects of their behavior, lateral organization, and functions. Through specific examples, we will uncover the intricate dynamics at play and shed light on potential pathogenic conditions that may result from alterations in these interfaces. A deeper understanding of these aspects can lead to the emergence of novel technologies and medical advances, potentially leading to the development of innovative treatments and diagnostic tools.
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    Physico-chemical challenges on the self-assembly of natural and bio-based ingredients on hair surfaces: towards sustainable haircare formulations
    (Green Chemistry, 2023) Luengo, Gustavo S.; Leonforte, Fabien; Greaves, Andrew; González Rubio, Ramón; Guzmán Solís, Eduardo
    Polymers and surfactants are used in many technological and industrial applications such as the manufacture of functional materials and coatings, personal care and pharmaceutical products, food science, paints, anti-icing fluids, tertiary oil recovery and the paper industry. Polymer–surfactant mixtures are particularly important in shampoos and conditioners. However, as in almost every other industry over the past five or more decades, the performance of hair care formulations has been significantly improved by the use of petrochemical-derived ingredients. As a result, cosmetic formulations, and hair care formulations in particular, have been based primarily on polymers and surfactants that are neither renewable, nor derived from environmentally friendly processes, nor have a positive environmental impact. This contrasts with the extensive use of natural and renewable products, mainly plant extracts, in cosmetics in ancient times. Therefore, the substitution of currently used ingredients with others of natural origin has been a top priority for the cosmetic industry over the last two decades, and in order to achieve greater consumer acceptance, it is crucial to maintain and, where possible, improve the technical performance of such products. This paper describes the complexities and challenges of developing greener shampoo and conditioner ingredients and formulations to meet current and future needs, and outlines a methodological approach based on model hair surfaces and a selection of appropriate experimental and numerical techniques to achieve our goals. Some encouraging technical routes using biosurfactants, biopolymers and bio-based polymers are presented, along with the significant opportunity to obtain a wide range of green ingredients through molecular design and well-controlled biotechnological processes. Similar concerns apply to other cosmetic products such as waxes, fragrances, bleaching agents, etc.