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 |
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Language: | English |
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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. |
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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 |
Author_xml | – sequence: 1 givenname: H surname: Miwa fullname: Miwa, H organization: Faculty of Pharmaceutical Sciences, Fukuoka University, Jonan-ku, Japan – sequence: 2 givenname: M surname: Yamamoto fullname: Yamamoto, M |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/3429573$$D View this record in MEDLINE/PubMed |
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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 |
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