High-performance liquid chromatographic analysis of serum short-chain fatty acids by direct derivatization

The application of direct derivatization in conjunction with high-performance liquid chromatography is described for the analysis of short-chain fatty acids in serum. The method is based on the reaction of these acids with acidic 2-nitrophenylhydrazine hydrochloride, without complicated isolation st...

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Published in:Journal of chromatography Vol. 421; no. 1; p. 33
Main Authors: Miwa, H, Yamamoto, M
Format: Journal Article
Language:English
Published: Netherlands 1987
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Abstract The application of direct derivatization in conjunction with high-performance liquid chromatography is described for the analysis of short-chain fatty acids in serum. The method is based on the reaction of these acids with acidic 2-nitrophenylhydrazine hydrochloride, without complicated isolation steps, which produces their non-volatile hydrazine derivatives. The hydrazides of fourteen saturated and unsaturated, straight and branched, short-chain fatty acids were separated from other acid hydrazides and interfering components by a simple solvent extraction, and were eluted isocratically on a reversed-phase C8 column within 24 min. UV detection demonstrated that the detection limits for the acids were 200-400 fmol per injection with linearity over the range from 400 fmol to 5 nmol per injection. Analytical recoveries ranged from 96.8% to 103.1% and coefficients of variation ranged from 0.9% to 3.8%. The present method is simple, accurate and adequate for the analysis of short-chain fatty acids in biological fluids and tissues of patients suffering from organic acidemias.
AbstractList The application of direct derivatization in conjunction with high-performance liquid chromatography is described for the analysis of short-chain fatty acids in serum. The method is based on the reaction of these acids with acidic 2-nitrophenylhydrazine hydrochloride, without complicated isolation steps, which produces their non-volatile hydrazine derivatives. The hydrazides of fourteen saturated and unsaturated, straight and branched, short-chain fatty acids were separated from other acid hydrazides and interfering components by a simple solvent extraction, and were eluted isocratically on a reversed-phase C8 column within 24 min. UV detection demonstrated that the detection limits for the acids were 200-400 fmol per injection with linearity over the range from 400 fmol to 5 nmol per injection. Analytical recoveries ranged from 96.8% to 103.1% and coefficients of variation ranged from 0.9% to 3.8%. The present method is simple, accurate and adequate for the analysis of short-chain fatty acids in biological fluids and tissues of patients suffering from organic acidemias.
Author Miwa, H
Yamamoto, M
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/3429573$$D View this record in MEDLINE/PubMed
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Snippet The application of direct derivatization in conjunction with high-performance liquid chromatography is described for the analysis of short-chain fatty acids in...
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StartPage 33
SubjectTerms Chromatography, High Pressure Liquid
Fatty Acids - blood
Humans
Indicators and Reagents
Spectrophotometry, Ultraviolet
Title High-performance liquid chromatographic analysis of serum short-chain fatty acids by direct derivatization
URI https://www.ncbi.nlm.nih.gov/pubmed/3429573
Volume 421
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