Search

Copyright of Shipin Kexue/ Food Science is the property of Food Science Editorial Department and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Objectives: Edible oils, derived from a plant source, play a vital role in providing nutrition. A quality edible oil has a flavor, range of physicochemical parameters. Several quality parameters like saponification value, acid value, peroxidase value and iodine value will be helpful in estimating the quality of edible vegetable oils. The present study was intended to evaluate the quality difference between cooked and uncooked oils. Materials and Methods: Utilizing various edible oil samples from major brands in india e.g sunflower oil, soybean oil, canola oil, almond oil, coconut oil and, olive oil saponification value and acid value was determined. All the oil samples were thoroughly characterized by calculating their saponification value and acid value using the standard procedure of association of official analytical chemist (AOCS) and American oil chemist society. Results: In comparision to uncooked oils, cooked oils had significantly higher sapnification values. The acid values were also increased in cooked oils compared to uncooked oils. Widely used sunflower oil had a two fold significant increase in saponification value and five fold significant increase in acid value after cooking. Similar changes were not observed in olive oil. Conclusion: Taken together, results of our study indicate that widely used sunflower oil might not be appropraiate for domestic usage. Further, our results also indicate that olive oil might be a better choice for domestic cooking. Further studies are required for a large scale validation of the present results there by brining in regulation/public health policy on usage of cooked oils by various small scale food vendors. [ABSTRACT FROM AUTHOR]

BACKGROUND: Phthalates have been widely used as plasticizers in various industries and are widely focused on in the international community as a result of their reproductive toxicity. Exposure of Chinese residents to phthalates via edible vegetable oil occurs often. In the present study, gas chromatography–mass spectrometry was used to detect the two main phthalates bis(2‐ethylhexyl) phthalate (DEHP) and dibutyl phthalate (DBP) in four major edible vegetable oil sources: an edible oil blend, soybean oil, peanut oil and rapeseed oil (a total of 1016 samples), as collected throughout China. Furthermore, cumulative risk assessment was used to estimate the reproductive health risk to Chinese residents caused by the phthalates that come from edible vegetable oils. RESULTS: Both phthalates were detected in four major edible vegetable oil sources. The phthalate with the highest detection rate was DBP (13.48%), followed by DEHP (7.78%). The results of the cumulative risk assessment showed that the hazard indices of these two phthalates in edible vegetable oils were less than 1, except in soybean oil. Nevertheless, the two phthalates had the lowest detection rates in soybean oil, which were 1.94% (DEHP) and 5.16% (DBP). In China, contamination levels of phthalates in the soils where oil crops are cultivated have a great influence on the phthalate concentrations in edible vegetable oils. CONCLUSION: It is recommended that Chinese residents who are consuming soybean oil choose well‐known brands and regularly change their brand of consumption. The phthalates in edible vegetable oils pose a relatively small reproductive health risk to Chinese residents. © 2019 Society of Chemical Industry [ABSTRACT FROM AUTHOR]

Copyright of Food Research & Development is the property of Food Research & Development Editorial Department and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Pleasant flavor and nutritional benefits of vegetable oils lead to an increase in their consumption amount. In addition, due to being apparently similar to commercially qualified vegetable oils (QVOs), used frying oil (UFO) is added into it to seek high profit by the unscrupulous traders. Thus, the authenticity assurance of commercial oil and fat products remains a challenge to scientists both in terms of its health and commercial perspectives. This work focused on using low field nuclear magnetic resonance (LF-NMR) to discriminate the adulteration of commercial corn, peanut, rapeseed, and soybean oils with two kinds of UFOs. The differences between the transverse relaxation distributions ( T distributions) of qualified oil and UFO were in the appearance of the third peak (A), which could be assigned to polymer products that were produced during the deep-fat frying process and the shift of T value of the peaks. In addition, the A peak area accounted for the whole area of peaks linearly increasing along with the increase in adulteration proportion. Based on the changes of peak area, a simple linear equation was built and the determination coefficients ( R) were all higher than 0.93. Therefore, as a rapid, convenient, and nondestructive method, LF-NMR application could be used to detect adulteration of vegetable oils with UFO. [ABSTRACT FROM AUTHOR]

[Display omitted] • Raman spectroscopy was an efficient way to distinguish waste cooking oils from edible oils. • PCA of Raman spectra was used to distinguish waste cooking oils from edible oils. • Peaks at 969, and 1302 cm−1 were crucial to distinguish waste cooking oils from edible oils. • Peaks for waste cooking oil at 969, 1267 and 1302 cm−1 were highly correlated with repeated heating. Raman spectra were used to distinguish waste cooking oil from edible vegetable oils. Signals at 869, 969, 1302 and 1080 cm−1 were found to be crucial to distinguish waste cooking oil from five edible oils using PCA. When waste cooking oil was added to soybean or olive oil, PCA could separate adulterated and pure oils, when the adulteration proportions reached 10% and 20%, respectively. Peaks at 969 (R2 > 0.951), 1267 (R2 = 0.987) and 1302 (R2 > 0.984) cm−1 responded linearly to adulteration. Heating assays and 1H NMR analysis revealed that differences between the Raman spectra of waste cooking oil and edible oils at 969 and 1267 cm−1 were directly related to heat treatment. This work highlights the potential for Raman spectroscopy to detect waste cooking oil. [ABSTRACT FROM AUTHOR]

A total of 470 edible vegetable oil samples including peanut, soybean, rapeseed, sesame seed, corn, blend, and others collected from eight provinces of China were analyzed for the concentrations of beauvericin (BEA), enniatin A (ENA), A1 (ENA1), B (ENB), and B1 (ENB1) by ultraperformance liquid chromatography/electrospray ionization tandem mass spectrometry (UPLC/ESI-MS/MS). Concentrations of BEA, ENB, and ENB1 (average = 5.59 μg/kg, 5.16 μg/kg, and 4.61 μg/kg) in all positive samples were higher than those for ENA and ENA1 (average = 0.85 μg/kg and 1.88 μg/kg). Frequencies of BEA and ENNs in all analyzed samples were all higher than 50% with the exception of ENA1 (36.6%, 172/470). Levels of BEA and ENNs in all analyzed samples varied based on their sample types and geographical distributions (Kruskal–Wallis test, p < 0.05). The soybean and peanut oil samples were found to be more easily contaminated by BEA and ENNs than other oil samples. Concentrations of BEA and ENNs in samples obtained from Heilongjiang, Shandong and Guizhou were higher than those found in samples from other provinces. Besides, frequencies of mycotoxin co-contaminations were high and their co-contamination types also varied by oil types. BEA-ENA-ENA1-ENB-ENB1 was the most commonly found toxin combination type, almost in one third of the analyzed samples (30%, 141/470). Overall, these results indicate that co-occurrence of BEA and ENNs in analyzed Chinese edible vegetable oil samples is highly common, and it is vital to monitor them, both simultaneously and on a widespread level. [ABSTRACT FROM AUTHOR]