Department of Applied Chemistry, Providence University, 200 Chungchi Road, Sha-Lu, Taichung Hsien 43301, Taiwan.
J Chromatogr A. 2011 Jan 21;1218(3):524-33. doi: 10.1016/j.chroma.2010.11.062. Epub 2010 Dec 9.
An effective method has been developed for quantitative determination of six bile acids including lithocholic acid (LCA), deoxycholic acid (DCA), chenodeoxycholic acid (CDCA), hydodeoxycholic acid (HDCA), cholic acid (CA) and ursodeoxycholic acid (UDCA) in biological tissues including pig liver, pig kidney and bovine liver by gas chromatography-chemical ionization/tandem mass spectrometry (GC-CI/MS/MS). Camphor-10-sulphonic acid (CSA) was proposed as effective catalyst for bile acid derivatization. Reactions were accelerated ultrasonically. The effects of different catalysts and reaction times on derivatization efficiency were evaluated and optimized. Bile acids were determined as methyl ester-trimethylsilyl ether and methyl ester-acetate derivatives. The efficiency of trimethylsilylation and acetylation was evaluated. Trimethylsilylation was done with N,O-bis(trimethylsilyl)trifluoroacetamide (BSTFA) as the trimethylsilyl donating reagent in a ultrasonic bath for 20 min. Acetylation was done in pyridine with acetic anhydride at 40-45°C for 4 h. The former reaction was faster than the latter. Thus, trimethylsilylation was employed for the quantitative analysis. Negligible interferences from sterols in biological matrices were observed when the biological samples were treated with solid phase extraction before GC-CI/MS/MS. The linearity, reproducibility, detection limit and recovery were evaluated under the optimized conditions. Satisfactory results were obtained when bile acid derivatives of LCA, CDCA, HDCA, and UDCA were determined with total ion chromatograms (TIC) while DCA and CA were determined with extracted ion chromatograms (EIC), respectively. The detection limits (S/N=3) for six bile acids in biological tissues were ranging from 0.40 to 1.6 ng/mL and the recoveries indicated that the proposed method was feasible for the determination of trace bile acids in the biological samples studied. The experimental results for the animal tissues purchased from five different markets were compared. Interestingly, all of the six bile acids were present in pig liver while only the dihydroxy bile acids, DCA, CDCA and HDCA were found in pig kidney. In addition to DCA and CDCA, trihydroxy bile acid, CA, are the major bile acids in bovine liver.
已开发出一种有效的方法,用于通过气相色谱-化学电离/串联质谱(GC-CI/MS/MS)定量测定包括鹅去氧胆酸(DCA)、石胆酸(LCA)、去氧胆酸(DCA)、鹅去氧胆酸(CDCA)、猪、牛的生物组织中的 6 种胆汁酸,包括猪肝、猪肾和牛肝。樟脑-10-磺酸(CSA)被提议作为胆汁酸衍生化的有效催化剂。反应在超声下加速。评估和优化了不同催化剂和反应时间对衍生化效率的影响。胆汁酸被确定为甲酯-三甲基硅醚和甲酯-乙酸酯衍生物。评估了三甲基硅烷化和乙酰化的效率。三甲基硅烷化是在超声浴中用 N,O-双(三甲基硅基)三氟乙酰胺(BSTFA)作为三甲基硅烷供体试剂进行的,反应时间为 20 分钟。乙酰化在 40-45°C 下用吡啶和乙酸酐进行 4 小时。前者的反应比后者快。因此,采用三甲基硅烷化进行定量分析。在 GC-CI/MS/MS 之前,用固相萃取处理生物基质时,观察到生物基质中的固醇几乎没有干扰。在优化条件下评估了线性、重现性、检测限和回收率。当用总离子色谱图(TIC)测定 LCA、CDCA、HDCA 和 UDCA 的胆汁酸衍生物,而 DCA 和 CA 分别用提取离子色谱图(EIC)测定时,得到了令人满意的结果。六种胆汁酸在生物组织中的检测限(S/N=3)范围为 0.40-1.6 ng/mL,回收率表明该方法适用于测定研究生物样品中的痕量胆汁酸。比较了从五个不同市场购买的动物组织的实验结果。有趣的是,六种胆汁酸均存在于猪肝中,而仅在猪肾中发现二羟基胆汁酸 DCA、CDCA 和 HDCA。除 DCA 和 CDCA 外,三羟基胆汁酸 CA 也是牛肝中的主要胆汁酸。