首页> 外文期刊>Analytical chemistry >Optically gated capillary electrophoresis ofo-phthalaldehyde/beta-mercaptoethanol derivatives of amino acids forchemical monitoring
【24h】

Optically gated capillary electrophoresis ofo-phthalaldehyde/beta-mercaptoethanol derivatives of amino acids forchemical monitoring

机译:邻苯二甲醛/β-巯基乙醇衍生物的光控毛细管电泳用于化学监测

获取原文
获取原文并翻译 | 示例
       

摘要

Optically gated capillary electrophoresis (CE) of amino acids derivatized with o-phthalaldehyde/beta-mercaptoethanol (OPA/beta-ME) was explored as a means to monitor amino acids with high temporal resolution. In agreement with a theoretical model described herein, 98% of a given concentration of OPA/beta-ME derivatives can be photobleached by a few milliwatts of the 350-nm line of an argon ion laser with just 0.7-ms exposure times in 5-mu m-i.d. capillaries. The low background from such high photobleaching efficiency allows detection limits in the low-nanomolar range for all amino acids tested. The short injection times possible with optical gating allow separation efficiencies of nearly 200000 plates to be achieved in less than 1 s under ideal conditions. Under mock in vivo conditions, separations were slower and had lower efficiency due to reduced electroosmotic flow associated with the high salt content. To demonstrate chemical monitoring, the optically gated CE system was interfaced to two different sampling probes with on-line derivatization with OPA/beta-ME. With microdialysis sampling, the optically gated CE system could assay the sample stream every 2 s but actual temporal resolution for monitoring was limited by band broadening in the dialysis probe to similar to 12 s. Optically gated CE was also interfaced to a 10-mu m-i.d. sampling capillary that continuously pulled samples into the separation capillary at 6.5 nL/min. This direct sampling probe allowed monitoring of multiple amino acids with 10-s temporal resolution with several advantages compared to microdialysis including improved detection limits and spatial resolution.
机译:探索了用邻苯二甲醛/β-巯基乙醇(OPA /β-ME)衍生的氨基酸的光学门控毛细管电泳(CE),以监测具有高时间分辨率的氨基酸。与本文所述的理论模型相一致,可以用几毫瓦的氩离子激光器的350 nm线以900毫秒的曝光时间对5毫瓦的氩离子激光器进行光漂白,以达到给定浓度的OPA /β-ME衍生物浓度的98%亩米毛细管。如此高的光漂白效率所带来的低本底允许所有测试氨基酸的检测限在低纳摩尔范围内。光学选通的可能短注入时间可在理想条件下在不到1 s的时间内实现近200000块板的分离效率。在模拟体内条件下,由于与高盐含量相关的电渗流减少,分离速度较慢且效率较低。为了演示化学监控,将光控CE系统连接到两个不同的采样探针,并使用OPA / beta-ME在线衍生化。通过微透析采样,光控CE系统可以每2 s检测一次样品流,但是由于透析探针中的谱带展宽至12 s,因此用于监测的实际时间分辨率受到限制。光学选通的CE也连接到10微米m.i.d.采样毛细管,以6.5 nL / min的速度将样品连续拉入分离毛细管。与微量透析相比,这种直接采样探针能够以10 s的时间分辨率监测多种氨基酸,与微透析相比具有多个优势,包括改进的检测限和空间分辨率。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号