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1.
Determination of Double Bond Positions and Geometry of Methyl Linoleate Isomers with Dimethyl Disulfide Adducts by GC/MS
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The dimethyl disulfide (DMDS) adduct method is one of the convenient and effective methods for determining double bond positions of unsaturated fatty acid methyl esters (FAME) except conjugated FAME. When analyzed using gas chromatography/electron ionization‐mass spectrometry (GC/EI‐MS), unsaturated FAME with DMDS added to the double bonds yields high intensity MS spectra of characteristic ions. The MS spectra of characteristic ions can then be used to easily confirm double bond positions. Here we explore the GC/EI‐MS analysis of the DMDS adducts of methyl linoleate geometrical isomers isolated by high performance liquid chromatography (HPLC) with a silver nitrate column. For C18:2‐c9, c12 and C18:2‐t9, t12, DMDS randomly formed adducts with double bonds at either carbon 9–10 or carbon 12–13, but not both at the same time due to steric hindrance. For C18:2‐c9, t12 and C18:2‐t9, c12, however, DMDS only formed adducts with the double bond in the cis configuration. Consequently, when analyzing fatty acids with methylene interrupted double bonds, with one double bond in the cis and one in the trans configuration, double bond positions cannot be completely confirmed. 相似文献
2.
Position and configuration isomers of conjugated linoleic acid (CLA), from 7, 9‐ through 12, 14‐C18:2, were synthesized by directed sequential isomerizations of a mixture of rumenic (cis‐9, trans‐11 C18:2) and trans‐10, cis‐12 C18:2 acids. Indeed, the synthesized conjugated fatty acids cover the range of unsaturated systems as found in milk fat CLA. The two‐step sequence consisted in initial sigmatropic rearrangement of cis/trans CLA isomers at 200 °C for 13 h under inert atmosphere (Helium, He), followed by selenium‐catalyzed geometrical isomerization of double bonds at 120 °C for 20 h under He. Product analysis was achieved by gas‐liquid chromatography using a 120 m polar capillary column coated with 70% cyanoalkylpolysiloxane equivalent polymer. Migration of conjugated systems was geometrically controlled as follows: the cis‐Cn, trans‐Cn+2 double bond system was rearranged through a pericyclic [1, 5] sigmatropic mechanism into a trans‐Cn‐1, cis‐Cn+1 unsaturated system, while the trans‐Cn, cis‐Cn+2 double bond system was rearranged through a similar pericyclic mechanism into a cis‐Cn+1, trans‐Cn+3 unsaturated system. Selenium‐catalyzed geometrical isomerization under mild conditions then allowed cis/trans double bond configuration transitions, resulting in the formation of all cis, all trans, cis‐trans and trans‐cis isomers. A sequential combination of the two reactions resulted in a facile controlled synthesis of CLA isomers, useful for the chromatographic identification of milk fat CLA, as well as for the preparation of CLA standard mixture. 相似文献
3.
Antti Aro Truus Kosmeijer-Schuil Peter van de Bovenkamp Paul Hulshof Peter Zock Martijn B. Katan 《Journal of the American Oil Chemists' Society》1998,75(8):977-985
Trans fatty acids in foods are usually analyzed by gas-liquid chromatography (GLC) of fatty acid methyl esters (FAME). However,
this method may produce erroneously low values because of insufficient separation between cis and trans isomers. Separation can be optimized by preceding silver-ion thin-layer chromatography (Ag-TLC), but this is laborious. We
have developed an efficient method for the separation of 18-carbon trans fatty acid isomers by combining GLC of FAME with GLC of fatty acid 4,4-dimethyloxazoline (DMOX) derivatives. We validated
this method against conventional GLC of FAME, with and without preceding Ag-TLC. Fatty acid isomers were identified by comparison
with standards, based on retention times and mass spectrometry. Analysis of DMOX derivatives allowed the 13t, 14t, and 15t isomers to be separated from the cis isomers. The combination of the GLC analyses of FAME and DMOX derivatives gave results comparable with those obtained by
GLC of FAME after preceding Ag-TLC, while saving about 100 h of manpower per 25 samples. It allowed the identification and
quantitation of 11 trans and 8 cis isomers and resulted in 25% higher values for total C18:1
trans, compared with the analysis of FAME alone. The combination of DMOX and FAME analyses, as applied to the analysis of 14 foods
that contained ruminant fat and partially hydrogenated vegetable and fish oils, indicated that the most common isomers were
11t in ruminant fats, 9t in partially hydrogenated fish fats, and either 9t or 10t in partially hydrogenated vegetable fats. The combination of GLC analyses of FAME and DMOX derivatives of fatty acids improves
the quantitation of 18-carbon fatty acid isomers and may replace the laborious and time-consuming Ag-TLC. 相似文献
4.
Diana Nikolova Daniela Antonova Ilko Marekov Boryana Nikolova‐Damyanova 《European Journal of Lipid Science and Technology》2006,108(3):212-217
Preparative silver nitrate thin‐layer chromatography of fatty acid methyl esters and gas chromatography‐mass spectrometry of 4,4‐dimethyloxazoline derivatives were applied in combination to analyze the cis,cis octadecadienoic (18:2) fraction in commercial samples of bovine butter fat in Bulgaria. The main component, 9,12–18:2 was accompanied by a series of bis‐methylene‐interrupted isomers, cis,cis‐5,9‐; 6,10‐; 9,13‐ and 11,15–18:2, which were unambiguously identified by their specific mass spectra. The latter are characterized by the presence of very intensive diagnostic fragments which help to correctly locate the position of the double bond system in the carbon chain. The cis,cis‐5,9–18:2 isomer was found for the first time in butter fat, and the 6,10–18:2 isomer has not been described as yet. 相似文献
5.
Milk fat is a complex mixture of geometric and positional isomers of monounsaturated and polyunsaturated, including short-,
long- and branch-chain fatty acids (FAs). There has been partial success to resolve this mixture of FAs using different GC
temperature programs, or a combination of GC isothermal and temperature programs. To overcome the problem associated with
overlapping isomers prior silver-ion separation was recommended. However, this procedure is time consuming and not practical
for routine analysis. In addition, previous methods focused mainly on the trans and cis isomers of 18:1. The present method takes advantage of differences in the relative elution times between different types
of FAs. The method involved analyzing each milk fat using the same highly polar 100-m capillary column and GC instrument,
and conducting two separations using temperature programs that plateau at 175 and 150 °C. The relative shift among the geometric
and positional isomers at these two temperature settings was enough to permit identification of most of the trans and cis 16:1, 18:1 and 20:1, the c/t-18:2 and the c/c/t-18:3 isomers found in milk fat. The identity of these FAs was confirmed by prior separation of the total fatty acid methyl
esters (FAMEs) of milk fat using Ag+-SPE columns, and comparing the fractions to the total milk fat. The Ag+-SPE technique was modified to obtain pure saturated, trans- and cis-monounsaturated and diunsaturated FAMEs. By combining the results from these two separate GC analyses, knowing the elution
order, it was possible to determine most of the geometric and positional isomers of 16:1, 18:1, 20:1, 18:2 and 18:3 without
a prior silver-ion separation. Only few minor FAs could not be resolved, notable the conjugated linoleic acid isomers that
still required the complimentary Ag+-HPLC separation. The two GC temperature programs have been successfully used to routinely analyze most FA isomers in total
milk and beef fats in about 200 min without the use of prior silver-ion separations. 相似文献
6.
Preparation, separation, and confirmation of the eight geometrical cis/trans conjugated linoleic acid isomers 8,10-through 11,13–18∶2 总被引:1,自引:0,他引:1
Klaus Eulitz Martin P. Yurawecz Najibullah Sehat Jan Fritsche John A. G. Roach Magdi M. Mossoba John K. G. Kramer Richard O. Adlof Yuoh Ku 《Lipids》1999,34(8):873-877
Conjugated linoleic acid (CLA) mixtures were isomerized with p-toluenesulfinic acid or I2 catalyst. The resultant mixtures of the eight cis/trans geometric isomers of 8,10-, 9,11-, 10,12-, and 11,13-octadecadienoic (18∶2) acid methyl esters were separated by silver ion-high-performance
liquid chromatography (Ag+-HPLC) and gas chromatography (GC). Ag+-HPLC allowed the separation of all positional CLA isomers and geometric cis/trans CLA isomers except 10,12–18∶2. However, one of the 8,10 isomers (8cis, 10trans-18∶2) coeluted with the 9trans,11cis18∶2 isomer. There were differences in the elution order of the pairs of geometric CLA isomers resolved by Ag+-HPLC. For the 8,10 and 9,11 CLA isomers, cis,trans eluted before trans,cis, whereas the opposite elution pattern was observed for the 11,13–18∶2 geometric isomers (trans,cis before cis,trans). All eight cis/trans CLA isomers were separated by GC on long polar capillary columns only when their relative concentrations were about equal.
Large differences in the relative concentration of the CLA isomers found in natural products obscured the resolution and identification
of a number of minor CLA isomers. In such cases, GC-mass spectrometry of the dimethyloxazoline derivatives was used to identify
and confirm coeluting CLA isomers. For the same positional isomer, the cis,trans consistently eluted before the trans,cis CLA isomers by GC. High resolution mass spectrometry (MS) selected ion recording (SIR) of the molecular ions of the 18∶1
18∶2, and 18∶3 fatty acid methyl esters served as an independent and highly sensitive method to confirm CLA methyl ester peak
assignments in GC chromatograms obtained from food samples by flame-ionization detection. The high-resolution MS data were
used to correct for the nonselectivity of the flame-ionization detector. 相似文献
7.
Linoleic acid was heated at 200°C under helium. Analysis of degradation products by GC on a long polar open tubular capillary
column showed the presence of CLA isomers. The identified mono trans CLA isomers were cis-9, trans-11, trans-9, cis-11, trans-10, cis-12, cis-10, trans-12, trans-8, cis-10, and cis-11, trans-13 18:2 acids. Oils containing different levels of linoleic acid (peanut, sesame seed, and safflower seed oils) were also
heat treated, resulting in similar CLA distributions. Elution order was confirmed using cis-9, trans-11 and trans-10, cis-12 acid methyl esters standards and their respective configuration isomers (trans-9, cis-11, cis-10, trans-12), obtained after mild selenium-catalyzed isomerization. These results indicated that two conjugated mono trans isomers of 18:2 acid, cis-8, trans-10 and trans-11, cis-13 18:2 were absent from the series, thus strongly suggesting that some constraints were preventing their formation. By heating
pure methyl rumenate (cis-9, trans-11 18:2) under similar conditions, isomerization resulted principally in a nearly equimolar mixture of methyl rumenate and
trans-8, cis-10 18:2. Similarly, the methyl ester of trans-10, cis-12 18:2 acid was partially transformed into cis-11, trans-13 18:2 acid. Respective geometrical isomers were also formed in trace amounts. A concerted pericyclic isomerization mechanism,
a [1,5] sigmatropic rearrangement, is proposed that limits the conjugated system to isomerization from a cis-trans acid to a trans-cis acid, and vice versa. This mechanism is consistent with undetected cis-8, trans-10 and trans-11, cis-13 18:2 isomers in heated oils containing linoleic acid. 相似文献
8.
The distribution of hydroperoxide isomers generated by photo-oxidation of natural lipids impregnated on the surface of dried
seaweed previously exposed to visible light and without added photosensitizer were studied. The surface of dried seaweed was
impregnated with linoleic acid methyl ester, and the sample was divided into two parts. One part was exposed to light from
a 100-W tungsten bulb (4500 lux) in a low-temperature room (5°C). The other part was kept in the dark as a control. Positional
isomers of the hydroperoxides generated from the impregnated linoleic acid methyl ester were separated individually by HPLC
and further identified by MS. The dried seaweed kept in the dark contained four hydroperoxide isomers, namely, 13-hydroperoxy-cis-9, trans-11-octadecadienoate, 13-hydroperoxy-trans-9, trans-11-octadecadienoate, 9-hydroperoxy-trans-10,cis-12-octadecadienoate, and 9-hydroperoxy-trans-10, trans-12-octadecadienoate. For the dried seaweed exposed to light, the oxidized lipids contained not only the same four isomers,
but also 12-hydroperoxy-cis-9, trans-13-octadecadienoate and 10-hydroperoxy-trans-8,cis-12-octadecadienoate. When fresh seaweed was dried in the sunlight, the formation of 12-cis,trans- and 10-cis,trans-hydroperoxides of naturally occurring methyl linoleate was verified. Dried seaweed was then impregnated with eicosapentaenoic
acid ethyl ester and exposed to light. Light exposure also generated certain hydroperoxide isomers attributable to singlet
oxygen oxidation, namely, 6-hydroperoxy-trans-4,cis-8, cis-11,cis-14,cis-17-ethyl and 17-hydroperoxy-cis-5,cis-8,cis-11, cis-14,trans-18-ethyl eicosapentaenoate. When dried sea-weed without any impregnated lipids was exposed to the light for 24 h in a cold
room (5°C), characteristic isomers, including both the 20-carbon FA isomers 6-OOH and 17-OOH as well as the 18-carbon FA isomers
10-OOH and 12-OOH, were detected in the light-exposed sample but were not found in the control. These results clearly show
that singlet oxygen oxidation of lipids occurred in the seaweed exposed to light. We concluded that this lipid oxidation was
catalyzed by chlorophyll as a photosensitizer in seaweed. 相似文献
9.
In order to measure exactly the trans-fatty acids content in food materials, a preparative group separation of cis- and trans-isomers of unsaturated fatty acid methyl esters (FAMEs) was achieved by an isocratic reversed-phase HPLC (RP-HPLC) method.
The trans-isomers of 16:1, 18:1, 18:2, 18:3, 20:1 and 22:1 FAMEs were readily separated from the corresponding cis-isomers by a COSMOSIL Cholester C18 column (4.6 mm I.D. × 250 mm, Nacalai Tesque) or a TSKgel ODS-100Z column (4.6 mm I.D. × 250 mm,
TOSOH), using acetonitrile as the mobile phase. This method was applied for determining the trans-18:1 fatty acid content in partially hydrogenated rapeseed oil. The methyl esters of cis- and trans-18:1 isomers of the oil were collected as two separate fractions by the developed RP-HPLC method. Each fraction was analyzed
by gas chromatography (GC) for both qualitative and quantitative information on its positional isomers. By a combination of
RP-HPLC and GC methods, a nearly complete separation of cis- and trans-18:1 positional isomers was achieved and the trans-18:1 fatty acid content was able to be evaluated more precisely than is possible by the direct GC method. The reproducibility
of cis- and trans-18:1 isomers fractionated by the RP-HPLC method was better than 98%. These results suggested that the preparative RP-HPLC
method developed in this study could be a powerful tool for trans-fatty acid analysis in edible oils and food products as an alternative to silver-ion chromatography. 相似文献
10.
Preparation of Dimethyl Disulfide Adducts from the Mono‐Trans Octadecadienoic Acid Methyl Esters
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The dimethyl disulfide (DMDS) adduct method is one of the more effective methods for determining double bond positions of dienoic acid. The DMDS method can be simply used to obtain the characteristic ions in which cleavage occurs between the methylthio group‐added double‐bond carbons as can be seen in the mass spectrum obtained using gas chromatography/electron ionization‐mass spectrometry. In the case of the methylene‐interrupted di‐cis type and di‐trans type dienoic acid, the DMDS addition reaction only occurs at one double‐bond position, and cannot occur at the remaining double‐bond position due to steric hindrance. As a result, two types of adducts are produced in the addition reaction. However, in the case of the methylene‐interrupted mono‐trans (mono‐cis) type dienoic acid, the DMDS addition reaction only occurs at the cis‐double bond. As a result, one type of adduct is produced in the addition reaction. In this report, we investigate the cause of the reaction selectivity by focusing on the addition reaction time. 相似文献
11.
Svein A. Mjøs 《European Journal of Lipid Science and Technology》2008,110(6):547-553
A polyethylene glycol (PEG) stationary phase was evaluated for the separation of mono‐trans isomers of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) methyl esters. The resolution patterns were compared to patterns achieved with previously applied conditions on a cyanopropyl phase. There were no overlaps between all‐cis EPA/DHA and their mono‐trans isomers on the PEG phase. Because of overlap between 22:0 and 22:1 isomers, the PEG column is not a good choice for analyses of EPA trans isomers in crude fish oils. However, if the saturated and monounsaturated fatty acids are not present in significant amounts, PEG can be a better choice than cyanopropyl columns. 相似文献
12.
Robert O. Dunn Helen L. Ngo Michael J. Haas 《Journal of the American Oil Chemists' Society》2015,92(6):853-869
Biodiesel is an alternative diesel fuel derived mainly from the transesterification of plant oils with methanol or ethanol. This fuel is generally made from commodity oils such as canola, palm or soybean and has a number of properties that make it compatible in compression‐ignition engines. Despite its many advantages, biodiesel has poor cold flow properties that may impact its deployment during cooler months in moderate temperature climates. This work is a study on the use of skeletally branched‐chain‐fatty acid methyl esters (BC‐FAME) as additives and diluents to decrease the cloud point (CP) and pour point (PP) of biodiesel. Two BC‐FAME, methyl iso‐oleate and methyl iso‐stearate isomers (Me iso‐C18:1 and Me iso‐C18:0), were tested in mixtures with fatty acid methyl esters (FAME) of canola, palm and soybean oil (CaME, PME and SME). Results showed that mixing linear FAME with up to 2 mass% BC‐FAME did not greatly affect CP, PP or kinematic viscosity (ν) relative to the unmixed biodiesel fuels. In contrast, higher concentrations of BC‐FAME, namely between 17 and 39 mass%, significantly improved CP and PP without raising ν in excess of limits in the biodiesel fuel standard specification ASTM D 6751. Furthermore, it is shown that biodiesel/Me iso‐C18:0 mixtures matched or exceeded the performance of biodiesel/Me iso‐C18:1 mixtures in terms of decreasing CP and PP under certain conditions. This was taken as evidence that additives or diluents with chemical structures based on long‐chain saturated chains may be more effective at reducing the cold flow properties of mixtures with biodiesel than structures based on long‐chain unsaturated chains. 相似文献
13.
Individual trans 18:1 Isomers are Metabolised Differently and Have Distinct Effects on Lipogenesis in 3T3‐L1 Adipocytes
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P. Vahmani W. J. Meadus T. D. Turner P. Duff D. C. Rolland C. Mapiye M. E. R. Dugan 《Lipids》2015,50(2):195-204
The objective of this research was to study the metabolism of individual trans fatty acids (FAs) that can be found in ruminant fat or partially hydrogenated vegetable oils (PHVO) and determine their effects on FA composition and lipogenic gene expression in adipocytes. Differentiated 3T3‐L1 adipocytes were treated with 200 µM of either trans‐9‐18:1, trans‐11‐18:1, trans‐13‐18:1, cis‐9‐18:1 or BSA vehicle control for 120 h. Trans‐9‐18:1 increased total cell FA content (µmole/well) compared to other FA treatments, which was mainly related to the accumulation of trans‐9‐18:1 in the cells. Adipocytes were able to desaturate a significant proportion of absorbed trans‐11‐18:1 and trans‐13‐18:1 (~20 and 30 % respectively) to cis‐9,trans‐11‐18:2 and cis‐9,trans‐13‐18:2, whereas trans‐9‐18:1 was mostly incorporated intact resulting in a greater lipophilic index (i.e. decreased mean FA fluidity) of adipocytes. Trans‐9‐18:1 up‐regulated (P < 0.05) the expression of lipogenic genes including acetyl‐CoA carboxylase (1.65 fold), FA synthase (1.45 fold), FA elongase‐5 (1.52 fold) and stearoyl‐CoA desaturase‐1 (1.49 fold), compared to the control, whereas trans‐11‐18:1 and trans‐13‐18:1 did not affect the expression of these genes compared to control. Our results suggest that the metabolism and lipogenic properties of trans‐11‐18:1 and trans‐13‐18:1, typically the most abundant trans FA in beef from cattle fed forage‐based diets, are similar and are different from those of trans‐9‐18:1, the predominant trans FA in PHVO. 相似文献
14.
Mikhail Vyssotski Kirill Lagutin Andrew MacKenzie Yutaka Itabashi 《Journal of the American Oil Chemists' Society》2015,92(3):383-391
γ‐Stearidonic acid, 18:4n‐6, a potential product of β‐oxidation of arachidonic acid (20:4n‐6), was only recently positively identified in a living organism—a thermophilic cyanobacterium Tolypothrix sp., albeit at low levels, whilst some indirect evidence suggests its wider presence, e.g. in a unicellular marine alga. We have prepared 18:4n‐6 using an iodolactonisation chain‐shortening approach from 22:5n‐6 and obtained its 1H‐, 13C‐, COSY‐ and HSQC NMR spectra, with 18:5n‐3 spectra also recorded for a comparison. The GC and GC‐MS behaviour of its methyl ester was also studied. Like another Δ3 polyunsaturated acid, octadecapentaenoic (18:5n‐3), 18:4n‐6 rapidly yields 2‐trans isomer upon formation of dimethyloxazoline derivative. On a polar ionic liquid phase (SLB‐IL100, 200 °C) the methyl ester could be mistaken for 18:3n‐3, while on methylsilicone phase (BP1, 210 °C) it eluted ahead of 18:3n‐6 and 18:4n‐3, suggesting that when present it may be easily misidentified during GC analysis of fatty acids. 相似文献
15.
Pilar Luna Manuela Juárez Miguel Angel de la Fuente 《European Journal of Lipid Science and Technology》2007,109(12):1160-1166
The fatty acid composition of 39 mature human milk samples from four Spanish women collected between 2 and 18 weeks during lactation was studied by gas chromatography. The conjugated linoleic acid (CLA) isomer profile was also determined by silver‐ion HPLC (Ag+‐HPLC) with three columns in series. The major fatty acid fraction in milk lipids throughout lactation was represented by the monounsaturated fatty acids, with oleic acid being the predominant compound (36–49% of total fatty acids). The saturated fatty acid fraction represented more than 35% of the total fatty acids, and polyunsaturated fatty acids ranged on average between 10 and 13%. Mean values of total CLA varied from 0.12 to 0.15% of total fatty acids. The complex mixture of CLA isomers was separated by Ag+‐HPLC. Rumenic acid (RA, cis‐9 trans‐11 C18:2) was the major isomer, representing more than 60% of total CLA. Trans‐9 trans‐11 and 7‐9 (cis‐trans + trans‐cis) C18:2 were the main CLA isomers after RA. Very small amounts of 8‐10 and 10‐12 C18:2 (cis‐trans + trans‐cis) isomers were detected, as were different proportions of cis‐11 trans‐13 and trans‐11 cis‐13 C18:2. Although most of the isomers were present in all samples, their concentrations varied considerably. 相似文献
16.
Application of Silver Ion High-Performance Liquid Chromatography for Quantitative Analysis of Selected n-3 and n-6 PUFA in Oil Supplements
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The aim of this study was to develop a simple method for simultaneous determination of selected cis/cis PUFA–LNA (18:2), ALA (18:3), GLA (18:3), EPA (20:5), and DHA (22:6) by silver ion high‐performance liquid chromatography coupled to a diode array detector (Ag‐HPLC‐DAD). The separation was performed on three Luna SCX Silver Loaded columns connected in series maintained at 10 °C with isocratic elution by 1 % acetonitrile in n‐hexane. The applied chromatographic system allowed a baseline separation of standard mixture of n‐3 and n‐6 fatty acid methyl esters containing LNA, DHA, and EPA and partial separation of ALA and GLA positional isomers. The method was validated by means of linearity, precision, stability, and recovery. Limits of detection (LOD) for considered PUFA standard solutions ranged from 0.27 to 0.43 mg L?1. The developed method was used to evaluate of n‐3 and n‐6 fatty acids contents in plant and fish softgel oil capsules, results were compared with reference GC‐FID based method. 相似文献
17.
Jan Fritsche Sonja Fritsche M. B. Solomon M. M. Mossoba M. P. Yurawecz K. Morehouse Y. Ku 《European Journal of Lipid Science and Technology》2000,102(11):667-672
The amounts of 14 conjugated linoleic acid (CLA) isomers (t12t14, t11t13, t10t12, t9t11, t8t10, t7t9, t6t8; 12,14 c/t, t11c13, c11t13, t10c12, 9,11 c/t, t8c10, t7c9‐18:2) in 20 beef samples were determined by triple‐column silver‐ion high‐performance liquid chromatography (Ag+‐HPLC). Quantitation was performed using an external CLA reference standard consisting of cis9,trans11‐18:2,trans9,trans11‐18:2 and cis9,cis11‐18: 2. Linearity was checked as being r > 0.9999 between 0.02 × 10‐3 to 2 mg/ml. The determination limit (5‐fold signal/noise ratio) of the CLA reference was estimated to be 0.25, 0.50, 1.0 ng/injection for the cis/trans, trans,trans and cis,cis isomers, respectively. As expected, cis9,trans11‐18:2 was the predominant isomer (1.95 ± 0.54 mg/g fat) in beef, followed by trans7,cis9‐18:2 (0.19 ± 0.04 mg/g fat); cis,cis isomers were below the determination limit in most beef samples. Total CLA amounts determined by Ag+‐HPLC were compared to total CLAs determined by gas chromatography (GC, 100 m CPSilTM 88 column). The amounts obtained by GC were generally higher than those determined by Ag+ ‐HPLC due to co‐eluting compounds. 相似文献
18.
Amélie Desmarais Jean-Louis Sébédio Khaled Belkacemi Joseph Arul Paul Angers 《Journal of the American Oil Chemists' Society》2020,97(6):615-624
Cyclic fatty acid monomers (CFAM) are formed at low levels in edible oils during thermal processing operations such as frying or refining, and inevitably become part of the diet. These proatherogenic agents may increase the levels of oxidative stress markers, and induce hepatomegaly and steatosis. However, the kinetics involved in their formation is not well known. The objective of the present study was to evaluate the effects of cis and trans isomers on cyclization reactions involved in the thermal transformation of alpha-linolenic acid (ALA). Geometrical isomers of ALA were obtained from all-cis ALA by nitric acid treatment. Mono-trans isomers were concentrated using silver nitrate-silica gel chromatography. All-cis ALA, isomerized ALA, and a fraction at 85% mono-trans isomers were heat treated at 275 °C in hexadecane for periods up to 24 hours, and the formation of geometrical isomers and CFAM was monitored by GC. The results show that mono-trans isomers at carbon 9 and carbon 15 form CFAM at an accelerated rate, compared to the corresponding cis isomers, resulting in the formation of higher levels of CFAM over shorter time periods. The validation of the kinetic model was performed by solving simultaneously and nonlinearly fitting the system of coupled differential equations with experimental data. Good agreement was found between the experimental data and the predicted values. This work suggests that the use of polyunsaturated vegetable oils over extended periods for thermal processing of food may result in the formation of CFAM, in particular, if mono-trans isomers are present in the oil. 相似文献
19.
Non-conjugated cis/trans 18:2 in Beef Fat are Mainly Δ-9 Desaturation Products of trans-18:1 Isomers
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Human liver cells (HepG2) were cultured with individual trans (t) 18:1 including t6‐, t12‐, t13‐, t14‐, t15‐ and t16‐18:1, and retention times of their Δ‐9 desaturation products were determined using 100‐m biscyanopropyl‐polysiloxane and SLB‐IL111 columns. Corresponding peaks were found in beef adipose tissues known to have different delta‐9 desaturase activities. Further lines of evidence indicating the presence of Δ‐9 desaturation products of t‐18:1 isomers in beef fat were developed by analysis of fatty acid methyl esters (FAME) fractionated using Ag+‐TLC, and by GC/MS. Some of the Δ‐9 desaturation products of t‐18:1 have been previously identified in ruminant fat (c9, t12‐ and c9, t13‐18:2). Some of the Δ‐9 desaturation products of t‐18:1 (c9, t14‐ and c9, t15‐18:2) have been previously tentatively identified as different fatty acids, and for the first time we provide evidence of the presence of c9, t16‐18:2, and where t6, c9‐18:2 may elute during analysis of FAME from beef fat. 相似文献
20.
Taina I. Hmlinen Susanna Sundberg Marjukka Mkinen Seppo Kaltia Tapio Hase Anu Hopia 《European Journal of Lipid Science and Technology》2001,103(9):588-593
The aim of this study was to investigate whether hydroperoxides are formed in the autoxidation of conjugated linoleic acid (CLA) methyl ester both in the presence and absence of α‐tocopherol. The existence of hydroperoxide protons was confirmed by D2O exchange and by chemoselective reduction of the hydroperoxide groups into hydroxyl groups using NaBH4. These experiments were followed by nuclear magnetic resonance (NMR) spectroscopy. The 13C and 1HNMR spectra of a mixture of 9‐hydroper‐oxy‐10‐trans,12‐cis‐octadecadienoic acid methyl ester (9‐OOH) and 13‐hydroperoxy‐9‐cis, 11‐trans‐octadecadienoic acid methyl ester (13‐OOH), which are formed during the autoxidation of methyl linoleate, were studied in detail to allow the comparison between the two linoleate hydroperoxides and the CLA methyl ester hydroperoxides. The 13CNMR spectra of samples enriched with one of the two linoleate hydroperoxide isomers were assigned using 2D NMR techniques, namely Correlated Spectroscopy (COSY), gradient Heteronuclear Multiple Bond Correlation (gHMBC), and gradient Heteronuclear Single Quantum Correlation (gHSQC). The 13C and 1H NMR experiments performed in this study show that hydroperoxides are formed during the autoxidation of CLA methyl ester both in the presence and absence of α‐tocopherol and that the major isomers of CLA methyl ester hydroperoxides have a conjugated monohydroperoxydiene structure similar to that in linoleate hydroperoxides. 相似文献