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A simplified method for the quantitation of short-chain fatty acids in human stool.
Eberhart, B Loye; Wilson, Annette S; O'Keefe, Stephen J D; Ramaboli, Matsepo C; Nesengani, Lucky T.
Afiliação
  • Eberhart BL; University of Pittsburgh, United States of America Department of Medicine, Division of Gastroenterology, Hepatology, and Nutrition, 200 Lothrop Street, Room W1111/2, Biomedical Science Tower, Pittsburgh, PA, 15213, USA. Electronic address: eberhart.bl@pitt.edu.
  • Wilson AS; University of Pittsburgh, United States of America Department of Medicine, Division of Gastroenterology, Hepatology, and Nutrition, 200 Lothrop Street, Room W1111/2, Biomedical Science Tower, Pittsburgh, PA, 15213, USA. Electronic address: aswilson@pitt.edu.
  • O'Keefe SJD; University of Pittsburgh, United States of America Department of Medicine, Division of Gastroenterology, Hepatology, and Nutrition, 200 Lothrop Street, Room W1111/2, Biomedical Science Tower, Pittsburgh, PA, 15213, USA. Electronic address: sjokeefe@pitt.edu.
  • Ramaboli MC; Stellenbosch University, South Africa Department of Internal Medicine, Room 3055, Clinical Building, Faculty of Medicine & Health Sciences, Francie Van Zjil Drive, Tygerberg, 7505, USA. Electronic address: matsepor@sun.ac.za.
  • Nesengani LT; Stellenbosch University, South Africa Department of Internal Medicine, Room 3055, Clinical Building, Faculty of Medicine & Health Sciences, Francie Van Zjil Drive, Tygerberg, 7505, USA. Electronic address: ltnesengani@sun.ac.za.
Anal Biochem ; 612: 114016, 2021 01 01.
Article em En | MEDLINE | ID: mdl-33188741
A one-vial extraction method for the quantitation of short-chain fatty acids (SCFAs) in human stool was developed. Samples were extracted with an acidified aqueous internal standard solution, sodium sulfate, and diethyl ether, followed by analysis with GC-FID. Accuracy, in terms of relative recovery, was typically between 90 and 110% for most analytes; without internal standard, the accuracy was about 5-34%; the linear dynamic range (LDR) was 0.05-50 µmol per gram; the limit of detection (LOD) was less than or equal to 0.05 µmol per gram; and the (lower) limit of quantitation (LOQ) was 1 µmol per gram. The method is suitable for quantitating acetic acid, propanoic acid, isobutyric acid, butyric acid, isovaleric acid, valeric acid, isohexanoic acid, hexanoic acid, and heptanoic acid. It is not suitable for the quantitation of formic acid. Application to human biological research was tested by the measurement of SCFA in heathy humans. This confirmed that the method performed adequately, and even better than expected, with values up to 150 µmol per gram.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ácidos Graxos Voláteis / Fezes / Ionização de Chama / Cromatografia Gasosa-Espectrometria de Massas Limite: Humans País/Região como assunto: Africa Idioma: En Revista: Anal Biochem Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ácidos Graxos Voláteis / Fezes / Ionização de Chama / Cromatografia Gasosa-Espectrometria de Massas Limite: Humans País/Região como assunto: Africa Idioma: En Revista: Anal Biochem Ano de publicação: 2021 Tipo de documento: Article