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首页> 外文期刊>Journal of Analytical Science and Technology >Method development for the quantitative determination of short chain fatty acids in microbial samples by solid phase extraction and gas chromatography with flame ionization detection
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Method development for the quantitative determination of short chain fatty acids in microbial samples by solid phase extraction and gas chromatography with flame ionization detection

机译:固相萃取-气相色谱-火焰电离检测定量测定微生物样品中短链脂肪酸的方法开发

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Background In order to quantitatively measure short chain fatty acids (SCFAs) in microbial samples, sample preparation and analytical conditions using gas chromatography with flame ionization detection (GC-FID) were established. Methods The extraction of SCFAs with ethyl ether-hexane (1:1, v / v ) followed by the aminopropyl solid phase extraction (SPE) was carried out. An acid-modified poly(ethylene glycol) GC column was used for the chromatographic separation of four volatile fatty acids. Results Good linearity was obtained with r ?>?0.999 in the calibration range. The limits of quantification (LOQs) of the analytical method were in the ranges of 5.71 to 11.20?μg/mL. The overall recoveries excluding acetic acid ranged between 96.51 and 108.83% with relative standard deviations (RSD) below 10% for the entire procedure from the results of matrix spiking experiments at three concentration levels. Conclusion The analytical method was validated in accordance with the requirements of the international guideline. The method enables the use of the most commonly used technology without derivatization and the elimination of interferences in the sample matrix.
机译:背景技术为了定量测量微生物样品中的短链脂肪酸(SCFA),建立了使用气相色谱和火焰离子化检测(GC-FID)的样品制备和分析条件。方法采用乙醚-己烷(1:1,v / v)萃取SCFA,然后进行氨丙基固相萃取(SPE)。酸改性的聚(乙二醇)GC色谱柱用于四种挥发性脂肪酸的色谱分离。结果在校正范围内,r≥0.999,可获得良好的线性。该分析方法的定量限(LOQ)在5.71至11.20μg/ mL的范围内。根据三种浓度水平的基质加标实验的结果,整个过程中不包括乙酸的总回收率在96.51至108.83%之间,相对标准偏差(RSD)低于10%。结论该分析方法已按照国际准则的要求进行了验证。该方法可以使用最常用的技术,而无需衍生化和消除样品基质中的干扰。

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