Dipartimento Neurofarba, University of Florence, via U. Schiff 6, Sesto Fiorentino, 50019 Firenze, Italy.
First Surgical Clinic Section, Department of Surgical, Oncological and Gastroenterological Sciences, University of Padua, via Nicolò Giustiniani 2, 35128 Padua, Italy.
J Pharm Biomed Anal. 2022 Jun 5;215:114762. doi: 10.1016/j.jpba.2022.114762. Epub 2022 Apr 8.
The targeted analysis of free fatty acids (FFAs) is attracting interest since several years with a plenty of studies. However, most of them are devoted to the solely determination of the short-chain fatty acids (SCFAs) arising from the symbiotic gut microbiota metabolism. Recently, the FFAs analysis highlighted changes in the plasma levels of octanoic and decanoic acids (medium-chain fatty acids or MCFAs) may be associated to gastrointestinal diseases, including colorectal cancer (CRC). Then, the simultaneous quantification of both SCFAs and MCFAs could be useful to put in evidence the interconnection between microbiota and metabolic alterations during hosts' disease. To this aim, it was developed an isotopic dilution gas-chromatography coupled mass spectrometry (ID/GC-MS) method for the targeted analysis of both linear and branched FFAs (SCFAs, MCFAs, and LCFAs) in human plasma samples as specific markers for both microbiota and host metabolic alterations. In order to minimize sample manipulation procedures, an efficient, sensible and low time-consuming procedure is presented, which relies in a simple liquid-liquid extraction before the determination of underivatized free acids (FFAs) by Single Ion Monitoring (SIM) acquisition. The reached detection limits (LODs) were less than 100 μg L for most of analytes, except for acetic, hexadecanoic and octadecanoic acids that showed a LOD > 1 mg L. Methods accuracy and precision, obtained by the analysis of the FFAs mixtures showed accuracy values between 84% and 100% and precision (RSD %) between 0.1% and 12.4% at the concentration levels tested. The proposed ID/GC-MS method was applied in a case study to evaluate the FFAs as specific markers for both microbiota and host alterations in CRC patients. Obtained results highlight the advantage of present method for its rapidity, simplicity, and robustness.
多年来,人们对游离脂肪酸 (FFAs) 的靶向分析产生了浓厚的兴趣,并且进行了大量的研究。然而,其中大多数研究都致力于单独测定共生肠道微生物代谢产生的短链脂肪酸 (SCFAs)。最近,FFAs 分析强调,血浆中辛酸和癸酸 (中链脂肪酸或 MCFAs) 水平的变化可能与胃肠道疾病有关,包括结直肠癌 (CRC)。因此,同时定量测定 SCFAs 和 MCFAs 可能有助于揭示微生物群和代谢改变之间的相互关系宿主疾病期间。为此,开发了一种同位素稀释气相色谱-质谱联用 (ID/GC-MS) 方法,用于靶向分析人血浆样品中的线性和支链 FFAs(SCFAs、MCFAs 和 LCFAs),作为微生物群和宿主代谢改变的特异性标志物。为了最大限度地减少样品处理程序,提出了一种高效、灵敏且耗时短的方法,该方法依赖于简单的液液萃取,然后通过单离子监测 (SIM) 采集来测定未衍生的游离酸 (FFAs)。大多数分析物的检测限 (LOD) 小于 100μg/L,除了乙酸、十六烷酸和十八烷酸,它们的 LOD 大于 1mg/L。通过分析 FFA 混合物获得的方法准确性和精密度,其准确度值在 84%至 100%之间,精密度(RSD%)在 0.1%至 12.4%之间,在测试浓度水平下。所提出的 ID/GC-MS 方法应用于病例研究,以评估 FFA 作为 CRC 患者微生物群和宿主改变的特异性标志物。结果强调了本方法快速、简单和稳健的优势。