Trioleine

Another type of reaction that has been studied is that of the oxidation of a double bond. In the case of triolein, Mittelmann and Palmer [309] found that, on a dilute permanganate substrate, the area at constant him pressure hrst increased and then decreased. The increase was attributed to the reaction... 

Ammonium sulfate triolein, oleic acid, androsten-3,17-dione, xanthanonic acid, cholesterol-propionate, N-methy Ipheny lalanine, D-glucose fluorescence after heating to 150 — 180 °C, exposure to tert-butyl hypochlorite [203]... 

Natural fats are glycerol esters of fatty acids known as triglycerides. Unsaturated fats are generally liquids (oils) at room temperature, while triglycerides rich in saturated fatty acids are generally solids. View tristearin and triolein. Which one of these is saturated and which is unsaturated Are die double bonds in the unsaturated fat cis or transl... 

Steroids, e.g. cholesterol, triolein, androsterone sugars, e.g. fructose, glucose, ribose amino acids, pyrimidines, purines, alkaloids 110-150°C, 2-12 h Conversion to fluorescent derivatives by heating. [5]... 

Multivesicular Liposomes Kim and his colleages described a method for the preparation of cell size liposomes with high encapsulation efficiency the so-called multivesicular liposomes (Kim et al., 1983). The lipid phase consists of a combination of amphiphatic lipids and a small amount of triglycerides (triolein or trioctanoin) dissolved in chloroform-diethyl ether (1 1). The aqueous phase is slowly added to the organic phase and after vigorous shaking a water-ip-lipid emulsion is formed (Fig. 2A-B). Via a narrow Pasteur pipet the emulsion is subsequently added to a sucrose solution. 

Table 2. Catalytic activity of the immobilized lipase in the transesterification reaction of triolein with methanol (18 hours of reaction, 40°C, trioleimmethanol molar ratio 1 3).

W.E. Neff, W.C. Byrdwell, Characterization of model triacylglycerol (triolein, trilinolein and trilinolenin) autoxidation products via high performance liquid chromatography coupled with atmospheric pressure chemical ionization mass spectrometry, Journal of Chromatography A, 818, 169 186 (1998). 

Metges, C. C., Kempe, K. and Wolfram, G. (1994) Enrichment of selected serum fatty acids after a small oral dosage of (1 C 13)triolein and (8 C 13)triolein in human volunteers analyzed hy gas chromatography combustion isotope ratio mass spectrometry. Biological Mass Spectrometry 23,295 301. 

Vitamin A. To overcome the difficulty of identification, vitamin A can be used as a label. The changes in the blood vitamin A curve following the administration of vitamin A in oil provide similar information to that given by the chylomicrograph. In malabsorption due to enteropathy the curve is depressed and delayed, and in pancreatic lipase deficiency it is markedly flattened. The use of vitamin A in oil and in aqueous dispersion is similar in principle to the use of labeled triolein and oleic acid (B4, G3, L4). 

K2. Kaplan, E., Edidin, B. D., Fruin, R. C., and Baker, L. A., Intestinal absorption of iodine 131 labelled triolein and oleic acid in normal subjects and in steatorrhea. Gastroenterology 34, 901-909 (1958). 

L7. Lubran, M., and Pearson, J. D., A screening test for steatorrhea using 131-1 labelled triolein. J. Clin. Pathol. 11, 165-169 (1958). 

Chiou chose glyceryl trioleate (triolein) as model lipid because of its similarity to triglycerides which are abundant in organisms [109], Triolein is also a bulk lipid and the good correlation with the bioconcentration factor is restricted to neutral compounds of moderate hydrophobicity. No attempts were made to measure partitioning of ionogenic compounds with the glyceryl trioleate-water partition system. 

PESs by the end of the exposure. Differences in exposure concentrations did not affect the sampling rates of PESs, which indicate that these devices obey first-order uptake kinetics. The sampling rate of " C-2,2 ,5,5 -TCB by PESs (4.8 L d ) was similar to that observed for 1 mL triolein SPMDs, with the same surface area. 

Table 1.1 compares key aspects and performance characteristics of selected passive samplers, including the triolein-containing SPMD. Of the eight devices examined, only a few appear to have overlapping functions. Clearly, no one device can provide the desired data for all exposure scenarios. 

Figure 1.1 A standard lipid-containing SPMD with three molecular welds near each end. Note the low interfacial tension causes intimate contact (i.e., the presence of a lipid film on the membrane interior surface) between the triolein and the membrane even where air bubbles exist. Reprinted with permission from the American Petroleum Institute (Huckins et al., 2002a).

The layflat-LDPE tubing used for making SPMDs was 2.6 cm wide and had a wall thickness of about 75 pm. The A of the 0.5 mL triolein SPMDs used in these flow-through tests was about 200 cm with an AV (lipid -I- membrane) ratio of about 80 cm The A of the 1 mL triolein SPMDs used in the static exposures was about 360 cm (i.e., = 72 cm ). The surface area of the 1 mL lipid... 

Einally, LDPE SPMDs with grass carp lipid were exposed for 21 d to 14C-2,2, 5,5 -TCB, 14c-3,3, 4,4 -TCB, i c-mirex and i c-fenvalerate, whereas SPMDs with triolein or lecithin were exposed to only " C-2,2, 5,5 -TCB. After 21 d, the largest mass fraction of these test chemicals ( " C-mirex was an exception) was in the triolein. The C-2,2, 5,5 -TCB log triolein-water partition coefficient was 6.01, whereas the " C-2,2, 5,5 -TCB partition coefficients for the grass carp lipid-water and lecithin-water systems were 30% and 35% lower, respectively. Comparison of these data to literature log AlowS of 2,2, 5,5 -TCB showed that the partition coefficients for the grass-carp lipid and the lecithin were not significantly different from median values reported for the log ATow of " C-2,2, 5,5 -TCB. However, the partition coefficient of 2,2, 5,5 -TCB in triolein and water in direct... 

Petty and Orazio (1996) developed an interesting variation in SPMD liquid phases. The approach consisted of both LDPE and silastic ffibes containing silicone fluid (50 cSt or 3200 MW) with 3% by weight PX-21 activated carbon. The presence of the activated carbon enhanced retention of planar molecules such as PAHs and the silicone fluid remains liquid at temperatures below freezing. However, the partition coefficients of HOCs for this type of silicone fluid are much lower than for triolein. 

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