1983
DOI: 10.1016/s0021-9673(01)87931-0
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Rapid method for the determination of fatty acid profiles from fats and oils using trimethylsulphonium hydroxide for transesterification

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Cited by 236 publications
(138 citation statements)
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“…The released FAs were transformed into trimethylsilyl ether derivatives using N,O-bis-trimethylsilyl-trifluoroacetamide. In a second method, lipids were transesterified by treatment with trimethylsulfoniumhydroxide in methanol modified from Butte (1983). Quantification of saponified whole-cell core lipid concentrations were measured by gas chromatography-flame ionization detector (Supplementary methods S1.1, Table 1, Supplementary Figure 2).…”
Section: Lipid Analysismentioning
confidence: 99%
“…The released FAs were transformed into trimethylsilyl ether derivatives using N,O-bis-trimethylsilyl-trifluoroacetamide. In a second method, lipids were transesterified by treatment with trimethylsulfoniumhydroxide in methanol modified from Butte (1983). Quantification of saponified whole-cell core lipid concentrations were measured by gas chromatography-flame ionization detector (Supplementary methods S1.1, Table 1, Supplementary Figure 2).…”
Section: Lipid Analysismentioning
confidence: 99%
“…The organic phase was collected and evaporated to dryness. The dried extract was suspended with chloroform and fatty acid methyl esters (FAME) were obtained by transesterification with trimethylsulfoniumhydroxide (Butte, 1983). FAME were separated using a 100 m CP-Sil-88 capillary column (Varian-Chrompack, Darmstadt, Germany), installed in a HP 5890 series II gas chromatograph with a flameionisation detector (Hewlett Packard, Munich, Germany).…”
Section: Fatty Acid Analysismentioning
confidence: 99%
“…The application of chemical ionisation as opposed to electron impact ionisation allowed the analysis of a large number of chemically defined metabolites from the complex biological matrix [14]. Owing to the hypothesis-generating nature of the screening experiment and in order to avoid the introduction of contaminants, no antioxidant or chelate forming additives were used and a single step method of extraction/methylation [9][10][11] was used, that minimized the number of sample handling steps. Larger samples sizes and improved technologies will lead to a more complete understanding of the resulting molecular pattern in the future.…”
Section: Discussionmentioning
confidence: 99%
“…A one step extraction/methylation method using trimethylsulphonium hydroxide (TMSH) [9][10][11] as agent for methylation and protection from further metabolic activity in the sample was used as follows: Ten milligrams of frozen tissue were ground with 5 mm stainless steel balls using liquid nitrogen cooling (MM301 Mixer Mill,RetschH, Haan, Germany) for 30 seconds to a fine powder. For blank samples, all steps were performed identically in parallel to the patient samples, but without tissue.…”
Section: Sample Preparation and Derivatisation For Metabolite Analysismentioning
confidence: 99%
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