A sensitive GC/MS detection method for analyzing microbial metabolites short chain fatty acids in fecal and serum samples

Gut microbiota and their major metabolites, short-chain fatty acids (SCFAs), are recognized as important players in gut homeostasis and metabolic disease occurance. A convenient and sensitive detection method is needed to profile SCFAs in limited and complex biological samples. The gas chromatograph...

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Veröffentlicht in:Talanta (Oxford) 2019-05, Vol.196, p.249-254
Hauptverfasser: Zhang, Shuming, Wang, Hongbin, Zhu, Mei-Jun
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Zhu, Mei-Jun
description Gut microbiota and their major metabolites, short-chain fatty acids (SCFAs), are recognized as important players in gut homeostasis and metabolic disease occurance. A convenient and sensitive detection method is needed to profile SCFAs in limited and complex biological samples. The gas chromatography/mass spectrometry (GC/MS) is the most common method for SCFAs profiling in biological samples. Trimethylsilyl (TMS) derivatization reagents such as N, O-bis(trimethyl-silyl)-trifluoroacetamide (BSTFA) are commonly used in GC/MS analysis to improve sensitivity and accuracy, but they were barely used in SCFA analysis due to their sensitivity to moisture and the volatility of SCFAs. Here, we developed a rapid, convenient and reliable method for SCFAs profiling in small amounts of fecal and serum samples by GC/MS using BSTFA in combination with sodium sulfate dehydration pretreatment. SCFAs were extracted with anhydrous ether from acidified fecal water extract or serum samples, followed by dehydration with sodium sulfate and BSTFA derivatization at a reduced temperature. Select ion monitoring mode was used for highly sensitive quantification of SCFAs by GC/MS. The derivation with BSTFA at 37 °C or 22 °C showed an excellent linearity (R2 > 0.999), good recoveries (81.27–128.42%), high repeatability (RSD < 2%) and low limit of detections (LODs) of different SCFAs ranging from 0.064 to 0.067 µM. All major SCFAs including acetic acid, propionic acid, isobutyric acid, butyric acid, isovaleric acid and valeric acid were identified and quantified accurately in fecal and serum samples. In conclusions, a reliable, convenient and sensitive method wasdeveloped for the measurement of SCFA and other volatile compounds in small biological samples using sodium sulfate dehydration pretreatment and BSTFA derivatization-based GC/MS analyses. [Display omitted] •A GC/MS SCFA profiling method combining BSTFA derivatization and Na2SO4 dehydration.•Na2SO4 dehydration breaks the moisture's limit on the use of BSTFA in SCFA analysis.•The method showed excellent performance and profiled mice fecal or serum SCFA.
doi_str_mv 10.1016/j.talanta.2018.12.049
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Wang, Hongbin ; Zhu, Mei-Jun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c511t-64bd0e541f1b6e35823d6d93ab71e787af9756bba280ec20f3557c428caeeccc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>acetic acid</topic><topic>Animals</topic><topic>blood serum</topic><topic>BSTFA</topic><topic>butyric acid</topic><topic>derivatization</topic><topic>detection limit</topic><topic>digestive system</topic><topic>Fatty Acids, Volatile - analysis</topic><topic>Fatty Acids, Volatile - chemistry</topic><topic>Feces - chemistry</topic><topic>gas chromatography-mass spectrometry</topic><topic>Gas Chromatography-Mass Spectrometry - methods</topic><topic>Gastrointestinal Microbiome - physiology</topic><topic>GC/MS</topic><topic>homeostasis</topic><topic>intestinal microorganisms</topic><topic>isobutyric acid</topic><topic>metabolic diseases</topic><topic>metabolites</topic><topic>Mice</topic><topic>monitoring</topic><topic>propionic acid</topic><topic>SCFAs</topic><topic>sodium sulfate</topic><topic>Sulfates - chemistry</topic><topic>temperature</topic><topic>Trimethylsilyl Compounds - chemistry</topic><topic>valeric acid</topic><topic>volatile compounds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Shuming</creatorcontrib><creatorcontrib>Wang, Hongbin</creatorcontrib><creatorcontrib>Zhu, Mei-Jun</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Talanta (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Shuming</au><au>Wang, Hongbin</au><au>Zhu, Mei-Jun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A sensitive GC/MS detection method for analyzing microbial metabolites short chain fatty acids in fecal and serum samples</atitle><jtitle>Talanta (Oxford)</jtitle><addtitle>Talanta</addtitle><date>2019-05-01</date><risdate>2019</risdate><volume>196</volume><spage>249</spage><epage>254</epage><pages>249-254</pages><issn>0039-9140</issn><eissn>1873-3573</eissn><abstract>Gut microbiota and their major metabolites, short-chain fatty acids (SCFAs), are recognized as important players in gut homeostasis and metabolic disease occurance. A convenient and sensitive detection method is needed to profile SCFAs in limited and complex biological samples. The gas chromatography/mass spectrometry (GC/MS) is the most common method for SCFAs profiling in biological samples. Trimethylsilyl (TMS) derivatization reagents such as N, O-bis(trimethyl-silyl)-trifluoroacetamide (BSTFA) are commonly used in GC/MS analysis to improve sensitivity and accuracy, but they were barely used in SCFA analysis due to their sensitivity to moisture and the volatility of SCFAs. Here, we developed a rapid, convenient and reliable method for SCFAs profiling in small amounts of fecal and serum samples by GC/MS using BSTFA in combination with sodium sulfate dehydration pretreatment. SCFAs were extracted with anhydrous ether from acidified fecal water extract or serum samples, followed by dehydration with sodium sulfate and BSTFA derivatization at a reduced temperature. Select ion monitoring mode was used for highly sensitive quantification of SCFAs by GC/MS. The derivation with BSTFA at 37 °C or 22 °C showed an excellent linearity (R2 &gt; 0.999), good recoveries (81.27–128.42%), high repeatability (RSD &lt; 2%) and low limit of detections (LODs) of different SCFAs ranging from 0.064 to 0.067 µM. All major SCFAs including acetic acid, propionic acid, isobutyric acid, butyric acid, isovaleric acid and valeric acid were identified and quantified accurately in fecal and serum samples. In conclusions, a reliable, convenient and sensitive method wasdeveloped for the measurement of SCFA and other volatile compounds in small biological samples using sodium sulfate dehydration pretreatment and BSTFA derivatization-based GC/MS analyses. 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subjects acetic acid
Animals
blood serum
BSTFA
butyric acid
derivatization
detection limit
digestive system
Fatty Acids, Volatile - analysis
Fatty Acids, Volatile - chemistry
Feces - chemistry
gas chromatography-mass spectrometry
Gas Chromatography-Mass Spectrometry - methods
Gastrointestinal Microbiome - physiology
GC/MS
homeostasis
intestinal microorganisms
isobutyric acid
metabolic diseases
metabolites
Mice
monitoring
propionic acid
SCFAs
sodium sulfate
Sulfates - chemistry
temperature
Trimethylsilyl Compounds - chemistry
valeric acid
volatile compounds
title A sensitive GC/MS detection method for analyzing microbial metabolites short chain fatty acids in fecal and serum samples
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