1973
DOI: 10.1016/0009-8981(73)90144-7
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A method for determination of free fatty acids in serum

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Cited by 55 publications
(10 citation statements)
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“…An advantage of this methodology is that it requires no prior protein removal, relying instead on solidphase extraction, which reduces processing time to 10 min per two samples and a GC runtime of 7 min per sample. Finally, standard methodologies were used to measure both plasma albumin (Doumas and Biggs 1972) and the nonesterified fatty acids (NEFA; Mikać-Dević et al 1973). …”
Section: Biochemical Laboratory Proceduresmentioning
confidence: 99%
“…An advantage of this methodology is that it requires no prior protein removal, relying instead on solidphase extraction, which reduces processing time to 10 min per two samples and a GC runtime of 7 min per sample. Finally, standard methodologies were used to measure both plasma albumin (Doumas and Biggs 1972) and the nonesterified fatty acids (NEFA; Mikać-Dević et al 1973). …”
Section: Biochemical Laboratory Proceduresmentioning
confidence: 99%
“…The higher triglyceride level was then chosen in this series to ensure substrate saturation (see Results, Table I). During recirculating perfusions, 1-ml samples were withdrawn from the reservoir and the amount of free fatty acid was analyzed using the Mikac-Devic spectrophotometric method (31). The amount of free fatty acid in the medium before perfusion was subtracted and the results were corrected for the sample volumes.…”
Section: Lung Perfusion Systemmentioning
confidence: 99%
“…Glucagon was assayed using 30K antiserum [10]. A colorometric method was used to measure non-esterified fatty acid concentrations [11]. Enzymatic methods were used to determine lactate,/3-hydroxybutyrate and glycerol concentrations [12].…”
Section: Methodsmentioning
confidence: 99%