Mixing phase behavior of trilaurin and monounsaturated triacylglycerols based on palmitic and oleic fatty acids

Differential scanning calorimetry and X-ray diffraction were used to examine the mixing phase behavior of LLL (trilaurinor 1,2,3-trilauroyl-glycerol) and POP (1,3-dipalmitoyl-2-oleoyl-glycerol), PPO (1,2-dipalmitoyl-3-oleoyl-rac-glycerol), orthe 50POP/50PPO blend able to form a molecular compound. This research aims to provide an insight into the molecularinteractions ruling the physical behavior of fat blends of lauric (i.e., coconut oil) and non-lauric lipids (cocoa butter, palmoil, etc.). The results showed eutectic behavior and no mutual solubility of triacylglycerols in stable LLL/POP and LLL/PPO mixtures. Applying high-rate cooling treatments had a positive effect on miscibility, but the high incompatibility ofthe components due to differences in length and degree of unsaturation of fatty acids was still evident in metastable polymorphs.In ternary LLL/(50POP/50PPO) mixtures, on the other hand, molecular compound β-2L crystals formed by POPand PPO showed to favor the solubility of LLL as compared to the binary systems. Accordingly, promoting the presence oftriacylglycerols forming molecular compound in specific fat blends may help reducing eutectic or incompatible interactionsamong triacylglycerol molecules in the solid state. These lead to phase separation and are a major cause of the restrictedapplicability of lauric oils in the confectionery and chocolate industries

An insight into the solid-state miscibility of triacylglycerol crystals

The crystallization properties of triacylglycerols (TAGs) strongly determine the functional properties of natural lipids. The polymorphic and mixing phase behavior of TAG molecules have long been, and still are, a hot topic of research with special relevance for the cosmetic, pharmaceutical, and food industry. To avoid the difficulties arising from the study of whole real fats, studies at the molecular level on mixtures of a limited number of TAGs has become an indispensable tool to identify the underlying causes of the physical properties in lipid systems. In particular, phase diagrams of binary mixtures of TAGs exhibiting a different degree of heterogeneity (monoacid or mixed fatty acids; molecular symmetry; the presence of cis or trans double bonds) have resulted in a significant breakthrough in our knowledge about structure-interaction-function relationships. The present work aims to provide an overview of the main reports regarding binary and ternary TAG systems, from the early studies to the most recent developments

Polymorphism and crystallization behaviour of triacylglycerols. From pure components to mixtures rich in oleic acid

[eng] Quality attributes of food products such as visual appearance, melting behavior, or shelf-life are strongly determined by the crystallization behavior of natural fats and oils within. In turn, this behavior depends on the polymorphism and the sort of mixing states (eutectic phase, solid solution phase, molecular compound formation) displayed by their major triacylglycerol components. Therefore, it becomes essential that studies regarding lipid crystallization cover from pure molecular components and their mixtures to real fats and oils. In connection with the above, this thesis focuses on gaining further fundamental knowledge about the polymorphism and crystalline behavior of lipid systems with varying degrees of complexity. Thus, the first stage of the research involved a study of pure triacylglycerols based on palmitic, lauric, and oleic acids (P, L, and O, respectively), which are typical of natural fats and oils such as lard and palm, olive, and coconut oils. During the second stage, binary and ternary mixtures including these triacylglycerols were examined to obtain an insight into their solid-state miscibility properties. Concretely, the mixtures were composed of a fully saturated triacylglycerol and one or two saturated-unsaturated triacylglycerols able to form a molecular compound. Despite the presumable crucial role of interactions including triacylglycerols forming molecular compound in the physical behavior of natural lipids and their blends, the phase behavior of triacylglycerol mixtures with such configuration is barely known. Finally, the third stage consisted of a more applied investigation of the crystalline and thermal properties of blends including natural fats. More specifically, binary blends of cocoa butter and shea butter stearin. Regarding the investigation of pure TAGs, calorimetric and X-ray diffraction techniques were used to examine the polymorphic occurrence and transformation behavior of PPP, LLL, OPO, and PPO during the application of dynamic thermal treatments at varying cooling and heating rates. The results showed that the polymorphic occurrence on cooling, as well as the sequence and type of transformations during heating, were influenced by the rate of the thermal treatments applied. However, it was also found that the extent of the kinetic influence depended on the intrinsic properties of triacylglycerols such as the length of the fatty acid chains or the characteristic polymorphism. The mixtures under examination during the phase behavior studies included the binary systems PPP/POP, PPP/PPO, PPP/OPO, LLL/POP, and LLL/PPO, and the ternary systems PPP/POP/OPO, PPP/POP/PPO, and LLL/POP/PPO (keeping an equimolecular ratio of POP/OPO or POP/PPO to favor molecular compound formation). Eutectic behavior with partial miscibility was observed under metastable and stable conditions. Furthermore, the results obtained for stable binary mixtures showed that the degree of miscibility was primarily influenced by the oleic acid content of the unsaturated component, as well as the differences in the size of the triacylglycerols within the mixture. From the solid-state miscibility observed in ternary systems containing LLL or PPP, it was concluded that third components may affect the mixing interactions associated with molecular compound formation. In addition, the results suggested that the ternary interactions studied may help to explain the crystallization behavior of edible lipids like palm oil and be useful in fat structuring applications. As a case study of real fat blends, combinations of cocoa butter and shea butter stearin at varying proportions were examined through calorimetric, X-ray diffraction, spectroscopic, and microscopic techniques. These made possible to characterize the effect of composition on the polymorphic crystallization and transformation properties, the melting profile, and the microstructural development. The results obtained for some of the parameters under study suggested that specific combinations might be considered for its application in chocolate-type confectionery products.[spa] Atributos de calidad de productos alimentarios con base lipídica, como la apariencia visual, el perfil de fusión o la vida útil, están determinados por el comportamiento cristalino de las grasas, polimorfismo y del estado de mezcla (fases eutécticas, fase de solución sólida, formación de compuesto molecular) de sus triacilgliceroles mayoritarios. Por tanto, los estudios en cristalografía de lípidos deben abarcar desde componentes moleculares puros y sus mezclas hasta grasas y aceites reales. En línea con esto, la presente tesis se centra en el estudio del polimorfismo y comportamiento cristalino de sistemas lipídicos atendiendo a los diferentes grados de complejidad. Por un lado, se ha investigado la cristalización y transformación polimórfica bajo condiciones dinámicas de temperatura de triacilgliceroles basados en ácidos palmítico, láurico y oleico (P, L y O, respectivamente), comunes en la manteca y los aceites de palma, oliva y coco. Además, se han estudiado mezclas binarias y ternarias incluyendo estos triacilgliceroles para determinar sus propiedades de miscibilidad en estado sólido. Específicamente, las mezclas han consistido en un triacilglicerol trisaturado y uno o dos triacilgliceroles con cierto grado de insaturación capaces de formar un compuesto molecular. A pesar del rol fundamental de las interacciones entre triacilgliceroles capaces de formar un compuesto molecular y otros componentes en las propiedades físicas de lípidos naturales y sus combinaciones, el comportamiento de fase de mezclas de triacilgliceroles con esta configuración apenas se ha investigado con anterioridad. Por último, esta tesis también recoge un estudio de carácter más aplicado sobre las propiedades térmicas y cristalinas de mezclas de grasas naturales. Más concretamente, de mezclas binarias de manteca de cacao y estearina de karité. El interés de este estudio reside en la importancia a nivel económico de los productos relacionados con el chocolate y en la necesidad de encontrar nuevas mezclas lipídicas que permitan satisfacer la creciente demanda global de manteca de cacao u obtener nuevas funcionalidades en los productos finales

Solid phase behavior of mixture systems based on tripalmitoyl glycerol and monounsaturated triacylglycerols forming a molecular compound

Differential scanning calorimetry and X-ray diffraction were used to investigate the mixing behavior of triacylglycerol (TAG) mixtures of PPP/PPO (tripalmitoyl glycerol/1,2-dipalmitoyl-3-oleoyl-rac-glycerol) and PPP/MCPOP/PPO (where MCPOP/PPO is the equimolecular blend of 1,3-dipalmitoyl-2-oleoyl-glycerol and PPO forming a molecular compound) under metastable and stable conditions. During cooling and reheating treatments at moderate rates, the eutectic properties of the two systems examined were mainly governed by the crystallization, transformation, and melting behavior of structurally similar β′ forms. In addition, steric and kinetic effects determined the formation of solid solutions with up to 10% and 20% of mixed-acid components in PPP/PPO and PPP/MCPOP/PPO mixtures, respectively. These values increased to 30% and 35% when thermodynamically stable β crystalline phases were obtained. In PPP/MCPOP/PPO mixtures, the diffraction data suggested that POP and PPO acted as a single component by dissolving in similar amounts in the solid solution phases and forming molecular compound crystals in eutectic compositions. This fundamental research shows the important role of specific combinations of mixed-acid TAGs and their interaction with high-melting components on the solidification behavior of edible lipids

Mixing phase behavior of tripalmitin and oleic-rich molecular compound-forming triacylglycerols

The binary phase behavior of triacylglycerol (TAG) mixtures constituted by PPP (tripalmitin) and either POP (1,3-dipalmitoyl-2-oleoyl-glycerol), OPO (1,3-dioleoyl-2-palmitoyl-glycerol), or MCPOP/OPO (molecular compound formed by POP/OPO at a 1:1 concentration ratio) was determined by differential scanning calorimetry (DSC), synchrotron (SR-) and laboratory-scale X-ray diffraction (XRD). Steric hindrance due to saturated-unsaturated acyl chain interactions and differences in the thermal stability of TAGs seemed to dictate the independent polymorphic crystallization and transformation observed under kinetic conditions, as well as the very asymmetric eutectic-type phase diagrams obtained from the study of thermodynamically stabilized PPP/POP, PPP/OPO, and PPP/MCPOP/OPO mixtures. Moreover, the solid integration determined for MCPOP/OPO in the βPPP crystalline phase (20-25%), halfway between that of OPO (<5%) and POP (30-35%), showed the ability of molecular compounds to tune the thermophysical properties of fat systems. This highlights the impact that molecular compound-forming TAGs may have on the efficient industrial separation of lipids, and suggest their potential applicability in the development of edible fat blends with tailored functionalities

In situ analyses of crystallization behavior of 1,2,3‑tripalmitoyl glycerol under static and dynamic thermal conditionsIn situ analyses of crystallization behavior of 1,2,3‑tripalmitoyl glycerol under static and dynamic thermal conditions

The crystallization behavior of 1,2,3-tripalmitoyl glycerol or PPP using differential scanning calorimetry (DSC), thermooptical polarized light microscopy and in situ synchrotron radiation X-ray diffraction (SR-XRD) techniques was precisely examined under static isothermal and dynamic thermal treatments, and the results were compared with preceding studies. PPP was rapidly (15 °C min−1) cooled to target temperatures (from 40 to 59 °C) to determine the precise moment at which crystallization was initiated. Once crystallization ceased, polymorphic transformation and melting were analyzed during subsequent heating. α form was crystallized during isotherms from 40 to 46 °C, temperature at which it coexisted with β′ phase. The latter was solely formed from 47 to 53 °C, and polymorphic crystallization was directed to obtain exclusively most stable β at 54 °C and higher temperatures. Nucleation time values for the α, β′ and β polymorphs exhibited exponential growth type, and a good correlation was found between data obtained by DSC and SR-XRD. Dynamic experiments were based on the use of high (15 °C min−1), intermediate (2 °C min−1) and low (0.5 and 0.1 °C min−1) cooling and heating rates.Thermo-optical polarized light microscopy experiments also provided valuable information on microstructural changesoccurring during polymorphic modifications. Less stable forms predominated at high cooling rates, whereas lower velocities leaded the polymorphic crystallization to obtain more stable forms

Report of in vitro antileishmanial properties of Iberian macroalgae

Here is reported the anti Leishmania infantum activity of 48 hexane, CH2Cl2 and MeOH extracts from 16 macroalgae collected on the Iberian Coast. Seven hexane and CH2Cl2Cystoseira baccata, Cystoseira barbata, Cystoseira tamariscifolia, Cystoseira usneoides, Dictyota spiralis and Plocamium cartilagineum extracts were active towards promastigotes (IC50 29.8-101.8 μg/mL) inducing strong morphological alterations in the parasites. Hexane extracts of C. baccata and C. barbata were also active against intracellular amastigotes (IC50 5.1 and 6.8 μg/mL, respectively). Fatty acids, triacylglycerols, carotenoids, steroids and meroterpenoids were detected by nuclear magnetic resonance (NMR), and gas chromatography in the Cystoseira extracts. These results suggest that Cystoseira macroalgae contain compounds with antileishmanial activity, which could be explored as scaffolds to the development of novel sources of antiparasitic derivatives.FCT: IF/00049/2012/ IF/00743/2015; 00743/2015info:eu-repo/semantics/publishedVersio

Report of <i>in vitro</i> antileishmanial properties of Iberian macroalgae

<p>Here is reported the anti <i>Leishmania infantum</i> activity of 48 hexane, CH₂Cl₂ and MeOH extracts from 16 macroalgae collected on the Iberian Coast. Seven hexane and CH₂Cl₂ <i>Cystoseira baccata, Cystoseira barbata, Cystoseira tamariscifolia, Cystoseira usneoides, Dictyota spiralis</i> and <i>Plocamium cartilagineum</i> extracts were active towards promastigotes (IC₅₀ 29.8–101.8 μg/mL) inducing strong morphological alterations in the parasites. Hexane extracts of <i>C. baccata</i> and <i>C. barbata</i> were also active against intracellular amastigotes (IC₅₀ 5.1 and 6.8 μg/mL, respectively). Fatty acids, triacylglycerols, carotenoids, steroids and meroterpenoids were detected by nuclear magnetic resonance (NMR), and gas chromatography in the <i>Cystoseira</i> extracts. These results suggest that <i>Cystoseira</i> macroalgae contain compounds with antileishmanial activity, which could be explored as scaffolds to the development of novel sources of antiparasitic derivatives.</p

Cystoseira algae (Fucaceae): update on their chemical entities and biological activities

Cystoseira (Sargassaceae) is a genus of marine brown algae composed of about 40 species, which is distributed along the Eastern Atlantic and Mediterranean coasts. The biological potential of the Cystoseira genus has been investigated and several activities have been reported. Chemically, this genus contains a wide variety of secondary metabolites, such as terpenoids, steroids, phlorotannins and phenolic compounds. Additionally, other chemical components as, for instance, carbohydrates, triacylglycerolsgatty acids, pigments as well as vitamins have been identified in the studied species. Some of the isolated compounds were associated with the reported pharmacological properties, as for example antioxidant, anti-inflammatory, cytotoxicity, anticancer, cholinesterase inhibition, anti-diabetic, activities but also antibacterial, antifungal and anti-parasitic activities. In this review, we provide a comprehensive overview of the compounds isolated and identified after 1995 from the different species of Cystoseira, compiling more than 200 compounds isolated, together with their therapeutic potential. (C) 2017 Elsevier Ltd. All rights reserved.Portuguese Foundation for Science and Technology (FCT) CCMAR/Multi/04326/2013]Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)Conselho Nacional de Desenvolvimento Cientffico e Tecnologico (CNPq)info:eu-repo/semantics/publishedVersio