Abstract

Non-esterified fatty acids (NEFA) can significantly interfere with the radioimmunoassay of PGE and PGF 2α using commercially available anti-sera. PGB 1 antigen-antibody binding is 50% inhibited by 110 pg of PGB 1, 48 ng of PGE 1, 3.5 μg of PGF 2α, or 9.0 μg linoleic, 14 μg arachidonic, 22 μg δ-linoleic, 40 μg palmitoleic or 45 μg oleic acids. PGF 2α antigen-antibody binding is 50% inhibited by 270 pg of PGF 2α, 70 ng of PGE 1, or 4.2 μg arachidonic, 14 μg δ-linolenic, 22 μg linoleic, 70 μg palmitoleic or 110 μg oleic acids. Physiological levels of NEFA, such as the quantities found in small volumes of plasma, are sufficient to prohibit accurate prostaglandin measurements. Chromatography on small columns of silicic acid proved to be an effective technique for separation of NEFA and prostaglandin from lipid extracts, however, the results of this study suggest that the interference produced by the presence of NEFA in the measurement of prostaglandin from certain physiological fluids may be avoided if the prostaglandins are not extracted prior to radioimmunoassay.

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