• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[尿液中有机酸的提取研究。气相色谱分离的初步步骤(作者译)]

[Study of the extraction of organic acids from urine. Preliminary step to their gas chromatographic separation (author's transl)].

作者信息

Boujet C, Drouet C, Decoux G, Favier A

出版信息

J Chromatogr. 1982 Mar 12;228:67-74.

PMID:7076776
Abstract

Ten organic acids are extracted from urine. Two extraction methods are used: anion exchange on DEAE-Sephadex columns and organic solvent extraction with five different solvents: diethyl ether, ethyl acetate, isopropyl chloride, light petroleum, and tetrahydrofuran. In order to quantify the extractions, the corresponding 14C-labeled acids are added to standard acid solutions and extraction rates are measured by a liquid scintillation counting system. The results show that: (1) The efficiency of anion exchange is generally good for all tested acids. (2) The extraction efficiency is not identical for the different solvents, one solvent being more efficient for a certain acid than another: tetrahydrofuran, which is generally a good solvent, is too hygroscopic to be usable. Isopropyl chloride and light petroleum are too specific with the most apolar molecules. Ethyl acetate and diethyl ether are similar and usable because of their acceptable solubilisation power as to the most polar molecules, their good solubilisation reproducibility and their readiness of use. (3) The solvent extraction method is not as time-consuming as the anion-exchange method which generally requires lengthy elution and extraction.

摘要

从尿液中提取出10种有机酸。采用了两种提取方法:一是在DEAE - 葡聚糖凝胶柱上进行阴离子交换,二是用5种不同溶剂进行有机溶剂萃取,这5种溶剂分别是:乙醚、乙酸乙酯、异丙基氯、轻质石油和四氢呋喃。为了对提取物进行定量分析,将相应的14C标记酸添加到标准酸溶液中,并通过液体闪烁计数系统测量提取率。结果表明:(1)阴离子交换效率对于所有测试酸来说总体良好。(2)不同溶剂的萃取效率不尽相同,一种溶剂对某一种酸的萃取效率高于另一种:四氢呋喃通常是一种良好的溶剂,但因其吸湿性太强而无法使用。异丙基氯和轻质石油对极性最小的分子选择性过高。乙酸乙酯和乙醚相似且可用,因为它们对极性最大的分子具有可接受的溶解能力、良好的溶解重现性且易于使用。(3)溶剂萃取法不像阴离子交换法那样耗时,阴离子交换法通常需要长时间的洗脱和萃取。

相似文献

1
[Study of the extraction of organic acids from urine. Preliminary step to their gas chromatographic separation (author's transl)].[尿液中有机酸的提取研究。气相色谱分离的初步步骤(作者译)]
J Chromatogr. 1982 Mar 12;228:67-74.
2
Solid-phase extraction with strong anion-exchange columns for selective isolation and concentration of urinary organic acids.
Clin Chem. 1988 Jun;34(6):1077-83.
3
Comparison of isolation methods of urinary organic acids by high-performance liquid chromatography.高效液相色谱法分离尿有机酸的方法比较
J Chromatogr. 1982 Mar 12;228:103-12. doi: 10.1016/s0378-4347(00)80423-5.
4
Isolation, identification and quantitation of urinary organic acids.尿有机酸的分离、鉴定和定量分析。
J Chromatogr. 1979 Mar 1;162(3):249-59. doi: 10.1016/s0378-4347(00)81512-1.
5
Automated metabolic profiling of organic acids in human urine. I. Description of methods.人尿中有机酸的自动代谢谱分析。I. 方法描述。
Clin Chem. 1978 Oct;24(10):1674-9.
6
[Gas chromatographic estimation of acidic urinary metabolites after separation on prepacked silica gel columns (author's transl)].在预装硅胶柱上分离后酸性尿代谢物的气相色谱法测定(作者译)
J Chromatogr. 1978 May 1;145(3):341-50.
7
Evaluation of continuous solvent extraction of organic acids from biological fluids.
Clin Biochem. 1978 Jun;11(3):126-30. doi: 10.1016/s0009-9120(78)90168-6.
8
Improved procedure for the anion-exchange isolation of urinary organic acids.
J Chromatogr. 1981 Mar 13;222(3):337-44. doi: 10.1016/s0378-4347(00)84133-x.
9
GC-MS determination of organic acids with solvent extraction after cation-exchange chromatography.阳离子交换色谱后溶剂萃取-气相色谱-质谱联用测定有机酸
Clin Chem. 1997 Dec;43(12):2256-61.
10
Compilation of gas chromatographic retention indices of 163 metabolically important organic acids, and their use in detection of patients with organic acidurias.
J Chromatogr. 1982 Apr 30;239:301-22. doi: 10.1016/s0021-9673(00)81990-1.