GC Method Research Articles

Analysis of unsaturated fatty acid content in blenderized enteral by spray drying method

Blenderized enteral formula is a liquid food that contains nutrients and is easily contaminated with bacteria. The drying process by using spray drying is one of the methods used to produce blenderized enteral formula powder and reduce bacterial contamination. However, it affects the fat content. This study aimed to analyze the differences in unsaturated fatty acids content in the blenderized enteral formula before and after spray drying. The design of this study was quasi-experimental using an enteral blenderized formula that was replicated 3 times and then dried using spray drying. The unsaturated fatty acid levels before and after drying were analyzed using the GC method. The differences between them were analyzed by paired T-Test and Wilcoxon. The results showed that the average unsaturated fatty acids levels before and after drying were: 0.190 and 0.370% (p = 0.055) for monounsaturated fatty acid, 0.070 and 0.100% (p = 0.109) for polyunsaturated fatty acid; 0.003 and 0.002% (p = 0.157) for omega 3, and 0.050 and 0.090% (p = 0.109) for omega 6. Statistical analysis showed that there was no significant difference in fat profile before and after drying. The conclusion showed that the spray drying method did not affect the unsaturated fatty acid levels of the blenderized enteral formula.

Effect of Seedling Rates on Crop Yield and Methane Emissions from Rice Paddies

Agricultural strategies are urgently needed to mitigate greenhouse gas emissions without reducing crop yield. Seedling rate per hill will affect the quantity and quality of tillers, which may affect rice yield and CH4 emissions. Therefore, it is hypothesized that high yields with low yield-scaled CH4 emissions could be achieved with optimal seedling rate per hill. A field experiment was conducted with three densities (low seedling rate, LSR; moderate seedling rate, MSR; and high seedling rate, HSR) for two consecutive rice seasons. The CH4 fluxes were determined by the static chamber–GC method. The results showed no significant differences in rice yields, seasonal CH4 emissions, or yield-scaled CH4 emissions between the three treatments. For early rice, the HSR tended to achieve high yield without increasing yield-scaled CH4 emissions. As for late rice, the MSR showed similar rice yield, and tended to have lower yield-scaled CH4 emissions in comparison with the HSR. The results suggest that choosing an appropriate seedling rate per hill to increase grain yield while maintaining lower or comparable yield-scaled CH4 emissions can be a promising option to reduce CH4 emissions from rice paddies.

Development of hydro-distillation extraction and macroporous resin enrichment method for GC–MS chemical profiling of volatile components in the dried root of Gentiana dahurica Fisch

The dried root of Gentiana dahurica Fisch. has an intensive flavour, which suggests the presence of volatile compounds. Thus, this study aimed to develop an effective extraction method for GC–MS profiling of volatile compounds of G. dahurica. Hydro-distillation and subsequent resin enrichment (HDRE) was developed and applied to the analysis of G. dahurica in comparison with simultaneous distillation and extraction (SDE), and ultrasonic assisted dichloromethane extraction (uDCM). The major components were azulene (33.83%), 1-hexanoic acid (14.19%) and octanoic acid (11.39%) in the HDRE; octanoic acid (17.24%), nonanoic acid (13.29%) and 2,4-di-t-butylphenol (12.73%) in the SDE; and α-amyrin (25.05%), β-amyrin acetate (15.11%) and β-amyrone (4.61%) in the uDCM. Moreover, the HDRE extract was shown to have certain antimicrobial activity against four bacterial strains. Thus, the HDRE method is a promising sample preparation method for GC-MS chemical profiling of volatile components of the dried roots of medicinal plants.

Dual-Column Stopped-Flow GC Method for Quantification of Permanent Gases, Water, and Organic Acids from a Single Injection.

Analysis of permanent gases and organic acids is typically performed with separate methods due to challenges in achieving sufficient resolution when using GC columns that are chemically compatible with acids. We developed a method to analyze samples containing high levels of water, organic acids, oxygenates, and permanent gases (CO, CO2, and C2H4) using a single injection. Resolution is achieved using two columns: (1) an HP-FFAP column resistant to water and acids, which separates compounds based on hydrogen-bonding affinity, and (2) a GS-CarbonPLOT column capable of separating permanent gases. We employed a column isolation methodology using rotary valves to allow a heart cut of permanent gases, which coelute off the HP-FFAP column, to be trapped on the CarbonPLOT column. After separation and analysis of water, organic acids, and oxygenates via the HP-FFAP column, flow is resumed on the CarbonPLOT column, and the permanent gases are separated independently. By utilizing the unique combination of columns and the stopped-flow sequence, we achieved separation and quantification of the wide array of compounds occurring during lactic acid dehydration to acrylic acid from a single injection without the need for a sophisticated flow modulator or multiple GCs or detector arrays. This GC apparatus serves as an economical in-line analysis method for our catalytic studies and is applicable to a wide array of samples relevant to biobased fuels and chemicals.

Novel multiple extraction thermal desorption approach prior to gas chromatography for the determination of residual solvents applied to modified cellulose

In this work, multiple extraction thermal desorption (METD), as a sample introduction method for GC, was developed. This technique was used for the determination of residual solvents (RS) in modified cellulose, because it is practically impossible to dissolve or distribute it uniformly in water and common organic solvents. Moreover, METD facilitates the optimization of the desorption time and it is more sensitive to quantify trace level volatiles in insoluble material, compared to direct dynamic desorption (DDD). In addition, METD provides diagnostic information about the sample-sorbent interaction. Three solvents (methanol, ethanol and tert-butanol) were determined in two types of modified cellulose (dialdehyde cellulose (DAC) and DAC-ethylenediamine (DAC-EDA)). It was shown that good linearity over a wide concentration range was achieved. The limits of detection (LOD) and limits of quantification (LOQ) for the different solvents ranged from 0.1 to 0.3 μg and from 0.3 to 0.9 μg per tube, respectively. Accuracy of the METD method was verified by using an alternative method based on the decomposition of the modified celluloses by Trichoderma reesei cellulase, followed by headspace-trap-GC (HS-trap-GC). The results obtained from the two validated methods were found to be similar (relative deviation < 17.0 %). However, the developed METD-GC method is preferable for the analysis of RS in modified cellulose since it does not require sample pretreatment and possesses higher sensitivity.

A study on source identification of contaminated soil with total petroleum hydrocarbons (aromatic and aliphatic) in the Ahvaz oil field.

The oil industry in Khuzestan province (Southwest Iran) is one of the main reasons contributing to the pollution of the environment in this area. TPH, including both aromatic and aliphatic compounds, are important parameters in creating pollution. The present study aimed to investigate the source of soil contamination by TPH in the Ahvaz oil field in 2022. The soil samples were collected from four oil centers (an oil exploitation unit, an oil desalination unit, an oil rig, and a pump oil center). An area outside the oil field was determined as a control area. Ten samples with three replicates were taken from each area according to the standard methods. Aromatic and aliphatic compounds were measured by HPLC and GC methods. The positive matrix factorization (PMF) model and isomeric ratios were used to determine the source apportionment of aromatic compounds in soil samples. The effects range low and effects range median indices were also used to assess the level of ecological risk of petroleum compounds in the soil samples. The results showed that Benzo.b.fluoranthene had the highest concentration with an average of 5667.7 ug/kg in soil samples in the Ahvaz oil field. The highest average was found in samples from the pump oil center area at 7329.48 ug/kg, while the lowest was found in control samples at 1919.4 ug/kg-1. The highest level of aliphatic components was also found in the pump oil center, with a total of 3649 (mg. Kg-1). The results of source apportionment of petroleum compounds in soil samples showed that oil activities accounted for 51.5% of the measured PAHs in soil. 38.3% of other measured compounds had anthropogenic origins, and only 10.1% of these compounds were of biotic origin. The results of the isomeric ratios also indicated the local petroleum and pyrogenic origin of PAH compounds, which is consistent with the PMF results. The analysis of ecological risk indices resulting from the release of PAHs in the environment showed that, except for fluoranthene, other PAHs in the oil exploitation unit area were above the effects range median level (ERM) and at high risk. The results of the study showed that soil pollution by total petroleum hydrocarbons (TPH), both aromatic and aliphatic, is at a high level, and is mainly caused by human activities, particularly oil activities.

Development and validation of HPLC and GC methods for quantification of cannabinoids and terpenes extracted by ultrasound assisted extraction technique

Cannabis exhibits a wide array of therapeutic effects due to its diverse and potent compounds. High-performance liquid chromatography (HPLC) and gas chromatography-mass spectrometry (GC-MS) are the primary techniques used to quantify and qualify cannabinoids and terpenes in cannabis. This paper rigorously validates HPLC and GC-MS methods for quantifying cannabinoids and terpenes in cannabis plants. Cannabinoids and terpenes were extracted using an optimised ultrasound assisted extraction (UAE) method. The HPLC and GC-MS methods were validated by assessing linearity, limit of detection (LOD), limit of quantification (LOQ), recovery, precision (inter-day and intra-day), accuracy (inter-day and intra-day), and matrix effect for 12 cannabinoids and 30 terpenes using appropriate standards. The HPLC and GC results fell within acceptable ranges (for HPLC, recovery between 73-121%, precision, accuracy and matrix effect all were below 10%; and for GC, recovery between 79-91%, precision, accuracy and matrix effect all were below 10%) demonstrating the accuracy and reliability of the validated method. The findings of this study can be used effectively to measure these important compounds in cannabis samples, facilitating quality control and standardisation of cannabis-based products for therapeutic applications.

Chemical Transformations of Benzyl Alcohol Caused by Atomic Chlorine.

Atomic chlorine present in the polluted troposphere can form potentially carcinogenic compounds as a result of a reaction with a natural product. This paper examines the stability of benzyl alcohol-a natural product commonly found in cosmetics-in interaction with atomic chlorine, which is becoming ever more present in the Earth's atmosphere as a result of its pollution. Research shows that atomic chlorine generated in the gas phase easily penetrates the liquid phase of benzyl alcohol, resulting in the formation of hydrochloric acid. The resulting HCl initiates further transformations of benzyl alcohol. Our study presents the amounts of the reaction products. The quantitative analysis was made using the GC method, and all the products were identified using the GC-MS method. The products include dichloromethyl benzene, 2-chlorobenzyl alcohol, and 3-chlorobenzyl alcohol, which are harmful, but are formed in very small amounts. The harmful substance occurring in a much higher amount is benzyl chloride-that is a product of acidification of benzyl alcohol by HCl.

Use of Endoscopic Ultrasound Elastography to Differentiate between Gastrointestinal Stromal Tumor and Leiomyoma Localized in the Upper Gastrointestinal Tract.

Gastrointestinal stromal tumors (GISTs) have malignant potential. Distinction of GISTs from leiomyoma is important to the decision of follow-up or treatment for upper gastrointestinal tract subepithelial lesions (SELs). There are few studies on the evaluation of gastrointestinal SELs with endoscopic ultrasound (EUS) elastography. To evaluate the efficiency of strain ratio (SR) measurement and Giovannini's classification (Gc) by EUS elastography in differentiating GISTs from leiomyomas. Twenty-three lesions with histopathological diagnoses of 13 GISTs and 10 leiomyomas were evaluated. The lesions' SR values were obtained from EUS reports retrospectively. Giovannini's classification was performed according to the elastography images recorded in the system. The effectiveness of SR and Gc in the distinction between GIST and leiomyomas was evaluated. Twelve of the GISTs and 3 of the leiomyomas were with scores 4 and 5 according to Gc (p = 0.006). Gastrointestinal stromal tumors had a higher SR than leiomyomas (p = 0.001). For the diagnosis of GISTs, sensitivity/specificity/diagnostic accuracy were 92.3%/80%/87% for SR alone, 92.3%/70%/82.6% for Gc alone, and 84.6%/80%/82.6% for the use of both SR and Gc. This is the first study in which semi-quantitative (SR) and qualitative (Gc) methods were evaluated together for the distinction of GISTs and leiomyomas. The sensitivity of SR alone for diagnosing GIST is higher than that of Gc alone or the combination of both methods. Although SR alone does not diagnose GIST, it can be used as an auxiliary method in biopsy and follow-up decisions. Erdem RE, Bektaş M, Ellik ZM, et al. Use of Endoscopic Ultrasound Elastography to Differentiate between Gastrointestinal Stromal Tumor and Leiomyoma Localized in the Upper Gastrointestinal Tract. Euroasian J Hepato-Gastroenterol 2024;14(1):20-23.

Exploring molecular composition of upgraded pyrolysis bio-oil using GC×GC-(EI/PI)-TOF MS with different column set-ups

Bio-oils produced from the pyrolysis of lignocellulosic biomass are rich in oxygen, which causes instability and corrosion problems. Therefore, dedicated post-pyrolysis treatments such as hydrotreatment are required to increase the H/C ratio of the products to be used as fuel or chemicals. Here, a characterization method based on two-dimensional gas chromatography (GC×GC) was developed to highlight the evolution of the volatile fraction during hydrotreatment. Six samples obtained at different times of the hydrotreatment were analyzed. In this way, information on catalyst deactivation was obtained. The combination of information from normal and reversed phase GC×GC analysis provides a detailed characterization of the hydrotreated bio-oils. Furthermore, the use of soft photoionization (PI), in addition to conventional electron impact ionization (EI), yields a better understanding of the compound structures present in the sample. Identification and semi-quantification of the sample components indicate that the concentration of paraffins, cycloalkanes, and monoaromatics have largely decreased during hydrotreatment, while the concentration of oxygenated species and polycyclic aromatic hydrocarbons have increased. Using complementary GC methods highlights changes in the molecular composition of volatile species that correlate with catalyst performance. This approach can be used to follow the decrease in hydrodeoxygenation activity as a function of time on stream to estimate the catalyst aging during the hydrotreating process.

The Chemical Profiles and Antioxidant Properties of Live Fruit or Vegetable Vinegars Available on the Polish Food Market.

Live vinegar is a product formed through a two-step fermentation process of a sugar substrate that has not been subjected to filtration or pasteurization. This is considered to preserve all nutrients and biologically active microorganisms, making it a product with a valuable composition and beneficial properties. Therefore, the purpose of this study was to analyze the chemical composition and antioxidant properties of the selected vinegars available on the Polish food market. The material in the study consisted of four live (naturally turbid, unfiltered, unpasteurized) fruit or vegetable vinegars: apple, pear, rhubarb, and lemon. Spectrophotometric, HPLC, and GC methods were used. Among the vinegars tested, lemon vinegar had the highest vitamin C content-15.95 mg/100 mL. Apple vinegar proved to be the best source of polyphenols and flavonoids (TPC-191.97 mg GAE/L, TFC-70.22 mg RE/L). All of the vinegars contained dihydroxybenzoic acid, 4-hydroxybenzoic acid, caffeic acid, 2-hydroxycinnamic acid, and myricetin. The acetic acid content of the tested vinegars ranged from 29.180 to 38.125 mM/L. The pH values ranged from 3.14 to 3.41. In conclusion, the most promising nutraceutical with potentially beneficial health-promoting properties seems to be apple vinegar.

Chemical composition, antioxidant, antimicrobial and antibiofilm activities of essential oil from the Moroccan endemic Plant, Calendula maroccana (Ball) B. D. Jacks.

The chemical characterization of the essential oil of the endemic Moroccan species, Calendula maroccana, was achieved by GC and GC-MS methods. The antioxidant, antimicrobial and antibiofilm activities of this essential oil were also studied. Eighty-one compounds were identified in the essential oil, representing 94.82% of the total. Sesquiterpenes predominate in the essential oil; 2-Methoxy-4-vinylphenol (16.13%), δ-amorphene (13.56%), α-cedrene (6.23%), γ-curcumene (5.10%) and α-bisabolol (4.94%) were the main constituents. The antioxidant potential was evaluated by DPPH, FRAP and ABTS assays: the essential oil exhibited antioxidant effectiveness with IC50 values of 0.92, 0.3 and 1.7 mg/mL, respectively. Moreover, the essential oil showed potent antimicrobial activity as revealed by inhibition zone values against selected clinically important pathogenic microorganisms. Inhibition zone values of 15.33 ± 0.19, 23 ± 0.05 and 15.33 ± 0.33 mm were observed against Staphylococcus aureus, Candida albicans and C. tropicalis, respectively. The maximal and minimal inhibition concentration values were in the range of 0.25 ± 0.17 - 4.68 ± 0.10 mg/mL for bacteria and 0.06 ± 0.03 - 0.12 ± 0.14 mg/mL, for Candida. The essential oil showed potent anti-biofilm activity with dual actions, inhibiting (69 - 88%) and eradicating (75 - 92%) the biofilms formed by the three tested bacteria strains. Based on these results, this essential oil can be considered as a natural antioxidant, antibacterial and antibiofilm agent that could be applied in phytotherapy, pharmaceutical and food sectors.

Comparison of methods for DMSP measurements in dinoflagellate cultures

AbstractA comparison of three analytical methods (the indirect GC‐FPD and MIMS, and direct LC‐MS/MS) for dimethylsulfoniopropionate (DMSP) measurements was conducted to assess their accuracy and reliability. The three methods showed a linear response but are distinguished by their linearity range, the largest being for MIMS. All three methods showed good precision on Alexandrium minutum samples (2–12%). The variability between the three methods when comparing analyses of A. minutum replicates was 11%, with the DMSP measurements by LC‐MS/MS being the highest. This result also confirms that indirect DMSP measurement after hydrolysis for GC or MIMS methods does not lead to an overestimation of DMSP values in A. minutum. A special focus was made on the more recent LC‐MS/MS method including further assays in sample preparation and storage from cultures of the dinoflagellate A. minutum. Dinoflagellate cells should be harvested by gentle filtration (&lt; 5 cm Hg) or slow centrifugation (500 × g) to retrieve the largest DMSP pool. For the LC‐MS/MS method, MeOH used for cell extraction should be added prior to freezing (to prevent DMSP degradation). Samples will then be stable in frozen storage for at least 2 months. Finally, direct and indirect methods are complementary for identifying the exact DMSP fraction among dimethylsulfide‐producing compounds that compose total and particulate DMSP pools issued from newly screened organisms or environmental samples.

Novel Injectable Hydrogel Formulations and Gas Chromatography Analysis of the Residual Crosslinker in Formulations Intended for Pharmaceutical and Cosmetic Applications.

Novel hyaluronic acid (HA) crosslinked with pentaerythritol tetra-acrylate (PT) injectable hydrogels was invented. These injectable hydrogel/dermal filler formulations were synthesised using HA and the acrylate PT as a crosslinker under basic pH conditions using thermal crosslinking methods (oven heating), which provides a simple, safe, and eco-friendly method for crosslinking in 4 h under 45 °C. Fourier-transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM) analyses were conducted to represent the difference between the formulations in terms of peak formation and pore size, respectively. The crosslinking was partial as is considered to be typical for dermal injectable fillers. The rheological properties of these formulations showed that these novel dermal injectables are highly promising, and the newly developed fillers could be used with better results for dermal anti-wrinkle corrections, shaping, and volumising reasons. Furthermore, crosslinker (PT) residual analysis was carried out to state the formulations that are valid and acceptable for intradermal usage. The results from the GC method validation revealed it was a suitable method for this study. The GC analysis of all five injectable hydrogel/filler formulations demonstrated the formulations HA-PT 1, 2, 3 and 4 were formulated using (0.05-0.1)% w/w PT containing residual PT monomers within the safe limits that were determined to be below (0.008% w/w). This work has shown the development of a novel injectable hydrogel/filler formulation for pharmaceutical and cosmetic applications can be prepared in a more sustainable and simple way using pentaerythritol tetra-acrylate as a crosslinker agent, which holds great promise for the industry's future advancement.

Matcha Green Tea: Chemical Composition, Phenolic Acids, Caffeine and Fatty Acid Profile.

Matcha-Japanese powdered tea-is a variety of green tea (Camellia sinensis L.), one of the most popular beverages in the world. Due to the unique way it is grown, it contains high concentrations of health-promoting phytochemicals. The aim of this study was to determine the basic nutritional and phenolic composition of dry matcha green tea powder. The fibre content was determined according to the enzymatic-gravimetric method. Crude protein was measured by the Kjeldahl method. The total fat content was measured by the Soxhlet method, and the fatty acid profile was defined by the GC method. The determination of the phenolic acid and caffeine content was performed using high-performance liquid chromatography. The total fibre content of matcha was 56.1 g/100 g, with 52.8 g/100 g (94.1% of total fibre) of insoluble dietary fibre and 3.3 g/100 g of soluble fibre (5.9% of total fibre). The total protein content was 17.3 g/100 g. The total fat content in dry matcha was 7.285 g/100 g, comprising varying proportions of individual fatty acids, the highest ones being those of linoleic acid and α-linolenic acid. The caffeine content of matcha tea was 2213.492 µg/g. With regard to phenolic acids, the highest content was estimated for gallic acid (252.3755 µg/g). Matcha showed a particularly high content of total dietary fibre, with a predominance of the insoluble fraction. Matcha was found to be a valuable source of plant protein and unsaturated fatty acids, mostly of the omega-3 fatty acid family.

An insight into recent updates on analytical techniques for bioactive alkaloids.

Alkaloids represent a wide class of naturally existing nitrogen-containing organic compounds having diverse biological activities. They are primary bioactive substances extracted from diverse plant parts. Due to their diverse biological activities, they are frequently used as medicines. The alkaloids have diverse pharmacological impacts on the human body; alkaloids are used for prevention, treatment, and reduction of discomfort associated with chronic illnesses. As most alkaloids exist in plants in complex form, combined with numerous other natural plant components, it is essential to recognize and characterize these molecules using different analytical techniques. We aimed to review the literature on the methods and protocols for the analysis of naturally occurring alkaloids. We carried out a literature survey using the PubMed, Scopus, and Google Scholar databases and other relevant published materials. The keywords used in the searches were "alkaloids," "analytical methods," "HPLC method," "GC method," "electrochemical methods," and "bioanalytical methods," in various combinations. In this article, several classes of alkaloids are presented, along with their biological activities. Moreover, it includes a thorough explanation of chromatographic techniques, hyphenated techniques, electrochemical techniques, and current trending analytical methods utilized for the isolation, identification, and comprehensive characterization of alkaloids. The various analytical techniques play an important role in the identification as well as the characterization of various alkaloids from plants, plasma samples, and urine samples. The hyphenation of various chromatographic techniques with mass spectrometry and NMR spectroscopy plays a crucial role in the characterization of unknown compounds.

Development of novel methods based on GC-HRMS and LC-HRMS for the determination of non-phthalate plasticizers in soil

Non-phthalate plasticizers (NPPs) are a suitable alternative to phthalates, which are harmful compounds for human, animal health, and the environment. In this study, 28 commercial non-phthalate plasticizers (NPPs) from different families, including adipates, citrates, phosphates, sebacates, trimellitates, benzoates and cyclohexanoates, were determined. Two novel methods for determining these alternative compounds in soil were developed using gas chromatography coupled to high-resolution mass spectrometry (GC-HRMS-Q-Orbitrap) and liquid chromatography coupled to high-resolution mass spectrometry (LC-HRMS-Q-Orbitrap). Solid-liquid extraction (SLE) with ethyl acetate or acetonitrile, along with water as extraction solvents, were employed. In most cases, the GC method exhibited recoveries ranging from 84.9 % to 110.8 % at 20, 40 and 200 μg/kg, while the LC method achieved recoveries between 73.1 % and 115.4 % at 10, 20, 40 and 200 μg/kg. Most of the relative standard deviation (RSD) values were below 20 % for both methods. The validated methods were then applied to analyse soil samples collected from four different areas in Almeria. The results indicated that the compounds detected most frequently at high concentrations were 1-hydroxycyclohexyl phenyl ketone (HCPK) using GC, in the range 29.1–67.4 μg/kg and 2,2,4-trimethyl-1,3-pentanediol diisobutyrate (TXIB) using LC, in the range 39.9–51.5 μg/kg. Additionally, suspect and unknown analysis were carried out, and other plasticizers as phthalates, were also detected, in addition to other substances present in the analysed samples. All the soils exhibited the presence of a few plasticizers, either phthalic and/or non-phthalic.

Compositions based on enrichment of cotton and sunflower oil with pomegranate seed oil

Oil was extracted from the seeds of pomegranate “Qayyum” variety in a Soxhlet extractor with extraction gasoline. By enriching the separated oil with sunflower and cottonseed oils, 6 different oil compositions were prepared in the proportions of 85:15, 90:10 and 95:5. The fatty acid composition of the prepared oil compositions was studied by the GC method. GC analysis of the composition of the prepared oil compositions showed that only punicic acid was detected in the conjugated α-linolenic acids. As the amount of pomegranate oil increases, the content of punicic acid in oil compositions increases. The amount of linoleic acid is the highest in the 95:5 composition of the oil, and decreases as the amount of pomegranate oil increases. Conjugated α-linolenic acids are not detected in cottonseed oil, and punicic acid is detected in compositions prepared with the addition of pomegranate oil, and its amount increases as the amount of pomegranate oil increases. Prepared oil compositions can be used in the preparation of various medicinal products and biologically active food additives depending on the acid content.

Potential Anti-Cancer Effects of Extra Virgin Olive Oil and Its Phenolic Extracts on Hepatocellular Carcinoma Cells

In this study, three types of Extra Virgin olive oils (EVOO) grown in different regions of Türkiye (Kilis Yaglik, Ayvalik, Izmir Sofralik) and their phenolic extracts (EVOOP) were evaluated for their anti-cancer activity in hepatocellular carcinoma (HCC) cells (Hep40) and a complete profiling of the fatty acid, sterol and polyphenol content of these olive oils was performed by HPLC and GC method. It was shown that genetic diversity and differences in growing conditions of the olive oils studied significantly modified the phenolic composition. The biophenol content was found as 655.4 mg/kg, 508.75 mg/kg and 197.86 mg/kg in Kilis Yaglik, Izmir Sofralik and Ayvalık respectively. The highest content of oleocanthal was found in İzmir Sofralik EVOO (142.00 mg/kg) and its anti-proliferative effect was found to be high. The highest amount of hydroxytyrosol was found in Kilis Yaglik (42.14 mg/kg) and the highest amount of tyrosol was found in Izmir Sofralik (43.86 mg/kg). It was shown that there was a significant difference in the responses of polyphenols in Hep40 cells. The direct use of olive oil in Hep40 cells and the comparison with EVOOPs were evaluated for the first time in this study. The evaluation of the anti-cancer effect of EVOOs and EVOOPs was tested by MTT and the IC50 value of Ayvalik EVOO was found to be the lowest at %12.84. In EVOOPs, Izmir Sofralik was the most effective in Hep40 cells with an IC50 value of 35.40 µg/mL.

Determination of the Nutritive Value of Ceylon Almond (Terminalia catappa) and Butterfly Pea (Clitoria ternatea) Seeds from Sabaragamuwa Region of Sri Lanka

Aims: The Global population is increasing at an accelerated rate while food security is moving in towards a negative direction. Therefore, identification and utilization of underutilized food resources are important to attain sustainability. The present study focused on seeds of two underutilized plants namely; Ceylon almond (Terminalia catappa) and Butterfly pea (Clitoria ternatea) as a source of edible oil production and to evaluate nutritional factors of the seed meal for potential application as a food/feed source.&#x0D; Methodology: The moisture content of the seeds was determined according to the method of AOAC 925.09. The fat content of the seeds was evaluated through the Soxhlet method followed by FAME determination through GC method. The crude protein content of the defatted seed meal was analyzed according to the method of AOAC 991.20 and AOAC 2011.14 procedures was followed to determine the mineral content of the seed meal using ICP-OES.&#x0D; Results: The study revealed that both of the seeds contained high levels of moisture content and Terminalia catappa seed exhibited the highest moisture content (30.0%). The seeds of Terminalia catappa contained 18.08% of fat and major fatty acid was palmitic. The crude protein content of defatted seeds of T. catappa was 35.11% and it had a high level of potassium (K) according to the ICP-OES analysis. Clitoria ternatea seed oil contained the least amount of fat (10.8%) and the major fatty acid was oleic (50.87%); an unsaturated fatty acid. The seed meal of it contained 50.16% of crude protein and major minerals were potassium, magnesium, and calcium.&#x0D; Conclusion: The C. ternatea seed meal is an excellent source of protein. However, seeds contain relatively low level of fat compared to T. catappa seeds. Both seed meals are good source of minerals.