Determinación de hidrocarburos alifáticos saturados en aceites vegetales

The aim of this work is to inform about the development of a simple and reliable off-line method for the determination of saturated hydrocarbons (SH) in vegetable oils. SH can be used as markers for fuel or for mineral oil contamination in edible oils and fats. The method consists of the isolation of the fraction by LC on deactivated silver-silica gel and subsequent on-column GC-FID analysis. This stationary phase was prepared avoiding any kind of activation. The method was developed and validated through the participation in both a proficiency test organized by the Joint Research Centre of the European Commission, and a collaborative trial carried out with trained Spanish laboratories according to the standard ISO 5725. Results showed acceptable repeatability and reproducibility values, and Horrat index, being this protocol in use with satisfactory results ever since. The method’s LOQ is 15 mg.kg–1 and its LOD 5 mg.kg–1, which make it suitable to quantify the 50 mg.kg–1 limit established by the EU, and to detect mineral oil content within the 10–500 mg.kg–1 range. Although other procedures with lower LOD have been developed throughout the years, the use of just regular laboratory equipment such as GC-FID makes the proposed method appropriate for application on a routine basis.El objetivo de este trabajo es el de dar cuenta del desarrollo de un método sencillo y fiable para la determinación de hidrocarburos saturados (HS) en aceites vegetales. Los HS pueden utilizarse como marcadores de contaminación de aceites y grasas comestibles con fuel-oil y aceites minerales El procedimiento consiste en el aislamiento de la fracción correspondiente por cromatografía en columna de gel de sílice argentada sin activar y posterior análisis mediante GC (on-column)-FID. El método se desarrolló y validó mediante la participación en una prueba de competencia organizada por el Joint Research Centre de la Comisión Europea, además de con un ensayo colaborativo llevado a cabo por laboratorios españoles de acuerdo con la norma ISO 5725. Los resultados mostraron valores de repetibilidad y de reproducibilidad aceptables, así como del índice de Horrat, por lo que dicho protocolo se está utilizando con resultados muy satisfactorios. El límite de detección (LDD) es de 5 mg.kg–1, y su límite de cuantificación (LDQ) de 15 mg.kg–1, lo que lo hacen muy adecuado para evaluaciones alrededor del límite de 50 mg.kg–1 establecido por la Unión Europea (UE). Asimismo es fiable para determinar el contenido de aceite mineral en el intervalo entre 10 y 500 mg.kg–1. Si bien se han desarrollado otros procedimientos con menor LDD a lo largo de los años, el uso de equipos habituales de laboratorio tales como GC-FID ha hecho que el método propuesto sea el de elección para su aplicación en cualquier laboratorio de forma rutinaria

Glyceridic and Unsaponifiable Components of Microencapsulated Sacha Inchi (Plukenetia huayllabambana L. And Plukenetia volubilis L.) Edible Oils

Sacha inchi (Plukenetia huayllabambana L. and Plukenetia volubilis L.) edible oils were microencapsulated and the lipid fraction of the microparticles was characterized. Hi-cap®, Capsule®, Arabic gum, and the binary combination of Arabic gum + maltodextrin and the ternary combination of Arabic gum + maltodextrin + whey protein isolate, were used as coating materials for the encapsulation process using spray-drying. The surface and the total oils obtained from the microparticles were evaluated in terms of fatty acid composition, minor glyceride polar compounds, polymers, oxidized triglycerides, diglycerides, monoglycerides, and free fatty acids, along with their unsaponifiable components, sterols, and tocopherols. Differences between the original oils and the microencapsulated ones were determined. The most remarkable results included the presence of polymers when there were none in the original oils, the slight loss in ¿3-fatty acids, up to 6%, the loss in tocopherols, in some of the cases around 30%, the maintaining of the phytosterol in their initial levels and the presence of cholesterol in the oils encapsulated with whey protein isolate

Marcadores de la calidad y la genuinidad de aceites de sacha inchi extra virgen comerciales

This work tackles the study of the quality and authenticity of oils labeled and commercialized as extra virgin sacha inchi oil. Major and minor components as triglycerides, fatty acid methyl esters, tocopherols, sterols and hydrocarbons are determined as well as other physicochemical parameters (density, viscosity, acidity and peroxide value). The results showed that some of the commercialized oils do not fulfill the basic requirement established in the regulation such as the content of α-linolenic acid, higher than 44.7 or 55.0% in the cases of P. volubilis and P. huayllabambana, respectively. The calculated stigmasterol/campesterol ratio for genuine sacha inchi oils should be around 4, however not all commercial oils analyzed comply with this requirement. The presence of the flavons sesamin and sesamolin indicates the addition of compounds from sesame oils. Finally, some of the commercial oils showed to contain trans fatty acids although this was not accompanied by the sterene hydrocarbon presence.En este trabajo se aborda el estudio de la calidad y la genuinidad de los aceites etiquetados y comercializados como sacha inchi extra virgen. Se estudian los componentes mayoritarios como los triglicéridos y los ésteres metílicos de ácidos grasos, componentes menores insaponificables (tocoferoles, esteroles e hidrocarburos) así como otros parámetros fisicoquímicos (densidad, viscosidad, acidez, peróxidos y estabilidad). Los resultados mostraron que algunos de los aceites comercializados no cumplían con el requisito básico establecido en la normativa de tener un contenido en α-linolénico superior a 44,7 o 55,0% determinado para P. volubilis o P. huayllabambana respectivamente. La relación estigmasterol/campesterol medida en aceites de sacha inchi genuinos es de alrededor de 4, y no todos los aceites comerciales analizados cumplían con este requisito. La presencia de las flavonas sesamina y sesamolina indica la adición de compuestos procedentes de aceites de sésamo. Por último, algunos de los aceites comerciales estudiados, contenían ácidos grasos trans aunque no se detectó en ellos la presencia de hidrocarburos esteroideos

Determination of fatty acids ethyl esters in virgin olive oils: proposals to enhance the EU official method

Fatty acids ethyl esters (FAEEs) are markers for virgin olive oils obtained from olives of poor quality or not adequately stored before being processed. FAEEs can also be considered as indirect markers in detecting the illegal treatment of soft deodorization that can be applied to slightly defective olive oils, as they are difficult to be removed from the oils at the conditions reached during this technological process. The official FAEEs determination (EU Reg. 61/2011) suffers some drawbacks in terms of amount of solvents and long time of analysis, linked with the preparative procedure to isolate these compounds. The aim of this work is to study the application of an HPLC-UV as a rapid alternative approach to the traditional liquid chromatography applied in the preparative phase. After the set up of the most appropriate working conditions (eg. mobile phase, flow, injection volume), some validation parameters (eg. precision, accuracy, LOD and LOQ, recovery) have been evaluated, in order to check the effectiveness of the proposed method. Moreover, considering the GC-FID step, the use of a PTV (programmed temperature vaporizer) injector as an alternative of the on-column one was evaluated. This work is developed in the context of the project OLEUM \u201cAdvanced solutions for assuring authenticity and quality of olive oil at global scale\u201c, funded by the European Commission within the Horizon 2020 Programme (2014\u20132020, GA no. 635690). The information expressed in this abstract reflects the authors\u2019 views; the EC is not liable for the information contained therein

Large-scale evaluation of shotgun triacylglycerol profiling for the fast detection of olive oil adulteration

Fast and effective analytical screening tools providing new suitable authenticity markers and applicable to a large number of samples are required to efficiently control the global olive oil (OO) production, and allow the rapid detection of low levels of adulterants even with fatty acid composition similar to OO. The present study aims to develop authentication models for the comprehensive detection of illegal blends of OO with adulterants including different types of high linoleic (HL) and high oleic (HO) vegetable oils at low concentrations (2–10%) based on shotgun triacylglycerol (TAG) profile obtained by Flow Injection Analysis-Heated Electrospray Ionisation-High Resolution Mass Spectrometry (FIA-HESI-HRMS) at a large-scale experimental design. The sample set covers a large natural variability of both OO and adulterants, resulting in more than one thousand samples analysed. A combined PLS-DA binary modelling based on shotgun TAG profiling proved to be a fit for purpose screening tool in terms of efficiency and applicability. The external validation resulted in the correct classification of the 86.8% of the adulterated samples (diagnostic sensitivity = 0.87), and the 81.1% of the genuine samples (diagnostic specificity = 0.81), with an 85.1% overall correct classification (efficiency = 0.85)

Characterization of Glyceridic and Unsaponifiable Compounds of Sacha Inchi ( Plukenetia huayllabambana

This work deals with the characterization of the main glyceridic and unsaponifiable components of oils obtained from Sacha inchi (Plukenetia huayllabambana L.) seed ecotypes collected during two harvests in the Department of Amazonas in Peru. The seed-oil yield was 30.3-41.2%; standing out are the high percentages of the ¿3- and ¿6-fatty acids series whose ranges lie within those of the present Regulation for Sacha inchi oils. Triacylglycerols with even equivalent carbon number (ECN; 36-42) were the main components. Minor glyceridic polar compounds such as oxidized triglycerides, diglycerides, monoglycerides, and free fatty acids were determined by high-performance size exclusion chromatography. The low campesterol/stigmasterol ratio (1:6), unusual in the majority of vegetable oils, stands out. Regarding aliphatic hydrocarbons, these oils showed a particular profile for the saturated series of odd and even carbon atom numbers. According to our results Sacha inchi P. huayllabambana oils can be offered as a good alternative to P. volubilis, the species mainly commercialized for this vegetable oil

Stepwise strategy based on 1H-NMR fingerprinting in combination with chemometrics to determine the content of vegetable oils in olive oil mixtures

1H NMR fingerprinting of edible oils and a set of multivariate classification and regression models organised in a decision tree is proposed as a stepwise strategy to assure the authenticity and traceability of olive oils and their declared blends with other vegetable oils (VOs). Oils of the ‘virgin olive oil’ and ‘olive oil’ categories and their mixtures with the most common VOs, i.e. sunflower, high oleic sunflower, hazelnut, avocado, soybean, corn, refined palm olein and desterolized high oleic sunflower oils, were studied. Partial least squares (PLS) discriminant analysis provided stable and robust binary classification models to identify the olive oil type and the VO in the blend. PLS regression afforded models with excellent precisions and acceptable accuracies to determine the percentage of VO in the mixture. The satisfactory performance of this approach, tested with blind samples, confirm its potential to support regulations and control bodies

Interlinkages: Governance for Sustainability Chapter 8

The Earth functions as a system: atmosphere, land, water, biodiversity and human society are all linked in a complex web of interactions and feedbacks. Environment and development challenges are interlinked across thematic, institutional and geographic boundaries through social and environmental processes. The state of knowledge on these interlinkages and implications for human well-being are highlighted in the following messages: Environmental change and development challenges are caused by the same sets of drivers. They include population change, economic processes, scientific and technological innovations, distribution patterns, and cultural, social, political and institutional processes