Abstract

A simple and rapid method was developed for determining glycerol in plasma or whole blood in a sample of 0.1 ml. The method was a fluorometric adaptation of existing spectrophotometric methods with enzymatic conversion of glycerol when reduced diphosphopyridine nucleotide is formed in proportion to the glycerol concentration in the sample. The method requires only capillary samples and is therefore suitable for repeated registration of glycerol during experimental conditions.

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