Tangerman A, Nagengast F M
Department of Gastroenterology and Hepatology, University Hospital Nijmegen, Nijmegen, 6500 HB, The Netherlands.
Anal Biochem. 1996 Apr 5;236(1):1-8. doi: 10.1006/abio.1996.0123.
A simple, reproducible, and rapid gas chromatographic method for short-chain fatty acid determination in human feces was developed. It involves direct injection of fecal supernatants into the gas chromatograph, without any pretreatment. Contamination of the gas chromatographic column with nonvolatile fecal material was prevented by the use of a glass liner in the injector. This liner, which acted as a precolumn, was stoppered with a glass wool plug at the lower end of the liner. Injection was performed against the glass wall of the liner, ensuring an immediate contact of the injected sample with the hot glass wall. More than 100 injections of fecal supernatants could be carried out before the liner had to be replaced by a new one. Peak tailing and ghosting was prevented by the use of formic acid in the fecal samples. The method gave sharp peaks with baseline separation for all the fatty acids.
开发了一种用于测定人粪便中短链脂肪酸的简单、可重复且快速的气相色谱法。该方法包括将粪便上清液直接注入气相色谱仪,无需任何预处理。通过在进样器中使用玻璃衬管,可防止气相色谱柱被非挥发性粪便物质污染。该衬管作为预柱,在其下端用玻璃棉塞堵住。进样是对着衬管的玻璃壁进行的,确保注入的样品立即与热玻璃壁接触。在必须更换新衬管之前,可以进行100多次粪便上清液的进样。通过在粪便样品中使用甲酸可防止峰拖尾和鬼峰。该方法对所有脂肪酸都给出了尖锐的峰且基线分离。