Determination of mixtures in vegetable oils and milk fat by analysis of sterol fraction by gas chromatography

1997 ◽  
Vol 74 (2) ◽  
pp. 131-135 ◽  
Author(s):  
L. Alonso ◽  
J. Fontecha ◽  
L. Lozada ◽  
M. Juárez
2018 ◽  
Vol 10 (11) ◽  
pp. 1379-1384 ◽  
Author(s):  
Zahra Ramezani ◽  
Iman Saeedi ◽  
Payman Hashemi

A recently prepared nanoporous G(1)-dendrimer supported SBA-15 solid phase microextraction fiber was successfully applied to the HS-SPME of solvent residues such as hexane, benzene, and toluene in edible vegetable oils followed by GC-FID.


2022 ◽  
Vol 34 (2) ◽  
pp. 429-431
Author(s):  
A.I. Kozhushkevich ◽  
E.S. Kozeicheva ◽  
A.M. Lebedev ◽  
V.V. Ovcharenko ◽  
A.M. Kalantaenko

Due to the increasing globalization of food markets, there are evolving new challenges for maintaing food safety. The current problem is the development of analytical methods for 3-monochloropropanediol ester and glycidol ester, which are food contaminants of concern for the scientific community. The levels of 3-monochloropropanediol ester and glycidol ester in certain food products are controlled by the European legislation. However, the maximum allowed concentrations and uptake limits for various food products are permanently revised. Therefore, we aimed to determine 3-monochloropropanediol ester and glycidol ester in various food products, which may contain vegetable oils. We analyzed food samples obtained from local food shops, predominantly low-priced products, which are more likely to contain vegetable oils, and adulterated milk fat. The levels of 3-monochloropropanediol ester and glycidol ester were determined indirectly by analyzing free 3-monochloropropanediol and glycidol ester obtained by hydrolysis and derivatized with phenylboronic acid. Samples were analyzed by GC-MS/MS on a triple-quad mass spectrometer.


Author(s):  
Harmita Harmita ◽  
Umar Mansur ◽  
Stephanie Stephanie

 Objective: Docosahexaenoic acid (DHA) is important for the development of infant’s nervous and visual system because it is a major fatty acid in brain and retina phospholipids. However, the benefit of adding DHA in infant formulas is still controversial. The over intake of DHA should be considered because of its side effect. The aim of this study was to get a valid analysis method of DHA using gas chromatography (GC) to determine the concentration of DHA in infant formula.Method: The milk fat was extracted in chloroform-methanol (1:2), continued with methylated in methanol-toluene (4:1) with acetyl chloride, and finally, injected to GC.Result: The GC conditions were as follows: Injector temperature was 230°C, detector temperature was 250°C, oven temperature was programmed to increase from 130°C to 230°C by 2°C/min and held for 20 min, helium flow rate was 2.00 ml/min, and split ratio was 1:3. This method had passed the precision and recovery evaluation. The result of DHA determination in five infant formula samples was 27.49±0.62 mg/100 g, 31.14±0.43 mg/100 g, 11.83±0.38 mg/100 g, 19.34±0.58 mg/100 g, and 45.87±0.42 mg/100 g.Conclusion: The method was valid and successfully applied to determine of DHA in infant formula.


2015 ◽  
Vol 98 (6) ◽  
pp. 1645-1654 ◽  
Author(s):  
Haixiang Zhao ◽  
Yongli Wang ◽  
Xiuli Xu ◽  
Heling Ren ◽  
Li Li ◽  
...  

Abstract A simple and accurate authentication method for the detection of adulterated vegetable oils that contain waste cooking oil (WCO) was developed. This method is based on the determination of cholesterol, β-sitosterol, and campesterol in vegetable oils and WCO by GC/MS without any derivatization. A total of 148 samples involving 12 types of vegetable oil and WCO were analyzed. According to the results, the contents and ratios of cholesterol, β-sitosterol, and campesterol were found to be criteria for detecting vegetable oils adulterated with WCO. This method could accurately detect adulterated vegetable oils containing 5% refined WCO. The developed method has been successfully applied to multilaboratory analysis of 81 oil samples. Seventy-five samples were analyzed correctly, and only six adulterated samples could not be detected. This method could not yet be used for detection of vegetable oils adulterated with WCO that are used for frying non-animal foods. It provides a quick method for detecting adulterated edible vegetable oils containing WCO.


2000 ◽  
Vol 67 (3) ◽  
pp. 437-441 ◽  
Author(s):  
MARÍA J. FRAGA ◽  
JAVIER FONTECHA ◽  
LUCIDIA LOZADA ◽  
ISABEL MARTÍNEZ-CASTRO ◽  
MANUELA JUÁREZ

The sterol fraction of milk is of nutritional interest because high levels of cholesterol in plasma (modulated by the cholesterol ingested) are associated with an increasing risk of cardiovascular disease. In addition, some sterols (ergosterol and 7-dehydrocholesterol) are provitamins (D2 and D3 respectively). At the same time, through the study of the sterol fraction, vegetable fats can be detected in milk and dairy products. Sterols are a minor fraction of total milk fat, the main sterol being cholesterol (3 mg/g fat, equivalent to 100 mg/l cows' milk). Small quantities of other sterols (7-dehydrocholesterol, 22-dehydrocholesterol, ergosterol, fucosterol, lanosterol, lathosterol, 24-methylenecholesterol) and several phytosterols have been reported in cows' milk (Walstra & Jennes, 1984). International Dairy Federation (1992) states that in the sterol profile of genuine milk fat there may appear, in addition to the peak of 7-dehydrocholesterol which ranges from 0·7 to 4% of total sterols, < 1% of minor sterols with retention times corresponding to phytosterols.Values for the cholesterol content of goats' milk vary considerably, from 211 mg/l (Pantulu et al. 1975) to 125 mg/l (Lu, 1993), partly owing to the use of different analysis techniques. Some of these values were obtained using non-specific colorimetric methods, which are inaccurate in the presence of cholesterol precursors or phytosterols (Clark et al. 1983; Haugh & Harzer, 1984). Some minor peaks have been assumed to be sterols but have not been identified (García-Olmedo & Barrera, 1985).Conventional methods of sample preparation for sterol analysis prior to gas chromatography (GC), which involve saponification of fat with or without isolation of the sterol fraction by thin layer chromatography, are tedious and time-consuming. Transesterification with KOH–methanol has been successfully used as a rapid alternative for obtaining the unsaponifiable fraction.This paper describes the identification of sterols (cholesterol and other minor sterols) in goats' milk fat using an alkali-catalysed transesterification procedure prior to GC and GC–mass spectrometry (GC–MS) analysis.


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