A simple and accurate HPLC method for fecal bile acid profile in healthy and cirrhotic subjects: validation by GC-MS and LC-MS[S]

We have developed a simple and accurate HPLC method for measurement of fecal bile acids using phenacyl derivatives of unconjugated bile acids, and applied it to the measurement of fecal bile acids in cirrhotic patients. The HPLC method has the following steps: 1) lyophilization of the stool sample;...

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Published inJournal of lipid research Vol. 55; no. 5; pp. 978 - 990
Main Authors Kakiyama, Genta, Muto, Akina, Takei, Hajime, Nittono, Hiroshi, Murai, Tsuyoshi, Kurosawa, Takao, Hofmann, Alan F., Pandak, William M., Bajaj, Jasmohan S.
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LanguageEnglish
Published United States Elsevier Inc 01.05.2014
The American Society for Biochemistry and Molecular Biology
Elsevier
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Abstract We have developed a simple and accurate HPLC method for measurement of fecal bile acids using phenacyl derivatives of unconjugated bile acids, and applied it to the measurement of fecal bile acids in cirrhotic patients. The HPLC method has the following steps: 1) lyophilization of the stool sample; 2) reconstitution in buffer and enzymatic deconjugation using cholylglycine hydrolase/sulfatase; 3) incubation with 0.1 N NaOH in 50% isopropanol at 60°C to hydrolyze esterified bile acids; 4) extraction of bile acids from particulate material using 0.1 N NaOH; 5) isolation of deconjugated bile acids by solid phase extraction; 6) formation of phenacyl esters by derivatization using phenacyl bromide; and 7) HPLC separation measuring eluted peaks at 254 nm. The method was validated by showing that results obtained by HPLC agreed with those obtained by LC-MS/MS and GC-MS. We then applied the method to measuring total fecal bile acid (concentration) and bile acid profile in samples from 38 patients with cirrhosis (17 early, 21 advanced) and 10 healthy subjects. Bile acid concentrations were significantly lower in patients with advanced cirrhosis, suggesting impaired bile acid synthesis.
AbstractList We have developed a simple and accurate HPLC method for measurement of fecal bile acids using phenacyl derivatives of unconjugated bile acids, and applied it to the measurement of fecal bile acids in cirrhotic patients. The HPLC method has the following steps: 1) lyophilization of the stool sample; 2) reconstitution in buffer and enzymatic deconjugation using cholylglycine hydrolase/sulfatase; 3) incubation with 0.1 N NaOH in 50% isopropanol at 60°C to hydrolyze esterified bile acids; 4) extraction of bile acids from particulate material using 0.1 N NaOH; 5) isolation of deconjugated bile acids by solid phase extraction; 6) formation of phenacyl esters by derivatization using phenacyl bromide; and 7) HPLC separation measuring eluted peaks at 254 nm. The method was validated by showing that results obtained by HPLC agreed with those obtained by LC-MS/MS and GC-MS. We then applied the method to measuring total fecal bile acid (concentration) and bile acid profile in samples from 38 patients with cirrhosis (17 early, 21 advanced) and 10 healthy subjects. Bile acid concentrations were significantly lower in patients with advanced cirrhosis, suggesting impaired bile acid synthesis.We have developed a simple and accurate HPLC method for measurement of fecal bile acids using phenacyl derivatives of unconjugated bile acids, and applied it to the measurement of fecal bile acids in cirrhotic patients. The HPLC method has the following steps: 1) lyophilization of the stool sample; 2) reconstitution in buffer and enzymatic deconjugation using cholylglycine hydrolase/sulfatase; 3) incubation with 0.1 N NaOH in 50% isopropanol at 60°C to hydrolyze esterified bile acids; 4) extraction of bile acids from particulate material using 0.1 N NaOH; 5) isolation of deconjugated bile acids by solid phase extraction; 6) formation of phenacyl esters by derivatization using phenacyl bromide; and 7) HPLC separation measuring eluted peaks at 254 nm. The method was validated by showing that results obtained by HPLC agreed with those obtained by LC-MS/MS and GC-MS. We then applied the method to measuring total fecal bile acid (concentration) and bile acid profile in samples from 38 patients with cirrhosis (17 early, 21 advanced) and 10 healthy subjects. Bile acid concentrations were significantly lower in patients with advanced cirrhosis, suggesting impaired bile acid synthesis.
We have developed a simple and accurate HPLC method for measurement of fecal bile acids using phenacyl derivatives of unconjugated bile acids, and applied it to the measurement of fecal bile acids in cirrhotic patients. The HPLC method has the following steps: 1 ) lyophilization of the stool sample; 2 ) reconstitution in buffer and enzymatic deconjugation using cholylglycine hydrolase/sulfatase; 3 ) incubation with 0.1 N NaOH in 50% isopropanol at 60°C to hydrolyze esterified bile acids; 4 ) extraction of bile acids from particulate material using 0.1 N NaOH; 5 ) isolation of deconjugated bile acids by solid phase extraction; 6 ) formation of phenacyl esters by derivatization using phenacyl bromide; and 7 ) HPLC separation measuring eluted peaks at 254 nm. The method was validated by showing that results obtained by HPLC agreed with those obtained by LC-MS/MS and GC-MS. We then applied the method to measuring total fecal bile acid (concentration) and bile acid profile in samples from 38 patients with cirrhosis (17 early, 21 advanced) and 10 healthy subjects. Bile acid concentrations were significantly lower in patients with advanced cirrhosis, suggesting impaired bile acid synthesis.
We have developed a simple and accurate HPLC method for measurement of fecal bile acids using phenacyl derivatives of unconjugated bile acids, and applied it to the measurement of fecal bile acids in cirrhotic patients. The HPLC method has the following steps: 1) lyophilization of the stool sample; 2) reconstitution in buffer and enzymatic deconjugation using cholylglycine hydrolase/sulfatase; 3) incubation with 0.1 N NaOH in 50% isopropanol at 60°C to hydrolyze esterified bile acids; 4) extraction of bile acids from particulate material using 0.1 N NaOH; 5) isolation of deconjugated bile acids by solid phase extraction; 6) formation of phenacyl esters by derivatization using phenacyl bromide; and 7) HPLC separation measuring eluted peaks at 254 nm. The method was validated by showing that results obtained by HPLC agreed with those obtained by LC-MS/MS and GC-MS. We then applied the method to measuring total fecal bile acid (concentration) and bile acid profile in samples from 38 patients with cirrhosis (17 early, 21 advanced) and 10 healthy subjects. Bile acid concentrations were significantly lower in patients with advanced cirrhosis, suggesting impaired bile acid synthesis.
Author Kakiyama, Genta
Takei, Hajime
Kurosawa, Takao
Bajaj, Jasmohan S.
Muto, Akina
Murai, Tsuyoshi
Pandak, William M.
Hofmann, Alan F.
Nittono, Hiroshi
Author_xml – sequence: 1
  givenname: Genta
  surname: Kakiyama
  fullname: Kakiyama, Genta
  email: gkakiyama@vcu.edu
  organization: Division of Gastroenterology, Hepatology, and Nutrition, Virginia Commonwealth University and McGuire VA Medical Center, Richmond, VA 23249
– sequence: 2
  givenname: Akina
  surname: Muto
  fullname: Muto, Akina
  organization: Junshin Clinic Bile Acid Institute, Meguro-ku, Tokyo 152-0011, Japan
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  givenname: Hajime
  surname: Takei
  fullname: Takei, Hajime
  organization: Junshin Clinic Bile Acid Institute, Meguro-ku, Tokyo 152-0011, Japan
– sequence: 4
  givenname: Hiroshi
  surname: Nittono
  fullname: Nittono, Hiroshi
  organization: Junshin Clinic Bile Acid Institute, Meguro-ku, Tokyo 152-0011, Japan
– sequence: 5
  givenname: Tsuyoshi
  surname: Murai
  fullname: Murai, Tsuyoshi
  organization: Faculty of Pharmaceutical Sciences, Health Sciences University of Hokkaido, Ishikari-Tobetsu, Hokkaido 061-0293, Japan
– sequence: 6
  givenname: Takao
  surname: Kurosawa
  fullname: Kurosawa, Takao
  organization: Faculty of Pharmaceutical Sciences, Health Sciences University of Hokkaido, Ishikari-Tobetsu, Hokkaido 061-0293, Japan
– sequence: 7
  givenname: Alan F.
  surname: Hofmann
  fullname: Hofmann, Alan F.
  organization: Department of Medicine, University of California, San Diego, La Jolla, CA 92093
– sequence: 8
  givenname: William M.
  surname: Pandak
  fullname: Pandak, William M.
  organization: Division of Gastroenterology, Hepatology, and Nutrition, Virginia Commonwealth University and McGuire VA Medical Center, Richmond, VA 23249
– sequence: 9
  givenname: Jasmohan S.
  surname: Bajaj
  fullname: Bajaj, Jasmohan S.
  email: jasmohan@gmail.com
  organization: Division of Gastroenterology, Hepatology, and Nutrition, Virginia Commonwealth University and McGuire VA Medical Center, Richmond, VA 23249
BackLink https://www.ncbi.nlm.nih.gov/pubmed/24627129$$D View this record in MEDLINE/PubMed
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Issue 5
Keywords bile acid 24-phenacyl ester
gas chromatography-mass spectrometry
esterified bile acids
routine analysis
liquid chromatography-tandem mass spectrometry
high-performance liquid chromatography
derivatization
extraction
liver cirrhosis
Language English
License This is an open access article under the CC BY license.
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PublicationTitle Journal of lipid research
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Snippet We have developed a simple and accurate HPLC method for measurement of fecal bile acids using phenacyl derivatives of unconjugated bile acids, and applied it...
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StartPage 978
SubjectTerms bile acid 24-phenacyl ester
Bile Acids and Salts - analysis
Bile Acids and Salts - chemistry
Case-Control Studies
Chromatography, High Pressure Liquid - methods
derivatization
esterified bile acids
extraction
Feces - chemistry
Female
Fibrosis
Gas Chromatography-Mass Spectrometry
high-performance liquid chromatography
Humans
liquid chromatography-tandem mass spectrometry
liver cirrhosis
Male
Methods
Middle Aged
routine analysis
Title A simple and accurate HPLC method for fecal bile acid profile in healthy and cirrhotic subjects: validation by GC-MS and LC-MS[S]
URI https://dx.doi.org/10.1194/jlr.D047506
https://www.ncbi.nlm.nih.gov/pubmed/24627129
https://www.proquest.com/docview/1519839253
https://pubmed.ncbi.nlm.nih.gov/PMC3995475
https://doaj.org/article/26bdfabe4bd34b26b0e99fed0a23855f
Volume 55
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