Lacher Nathan A, Garrison Kenneth E, Lunte Susan M
Department of Pharmaceutical Chemistry, University of Kansas, Lawrence, KS, USA.
Electrophoresis. 2002 Jun;23(11):1577-84. doi: 10.1002/1522-2683(200206)23:11<1577::AID-ELPS1577>3.0.CO;2-4.
The use of capillary electrophoresis (CE) with on-capillary Cu(II) complexation for the determination of angiotensin and its metabolites is described. The resulting copper-peptide complexes can be detected using either UV or electrochemical (EC) detection. Optimal reaction and separation conditions for the angiotensin peptides were first determined using CE with UV detection. With UV detection, the limit of detection (signal-to noise ratio S/N = 3) for native angiotensin II was 18 microM, while the limit of detection (LOD) obtained for the copper-angiotensin II complex is 2 microM. CE with EC detection was then evaluated, yielding significantly lower LODs--2 microM for native angiotensin II and 200 nM for the copper-angiotensin II complex. The addition of copper to the run buffer improved the separation and sensitivity for both CE-UV and CE-EC detection. The method was demonstrated by monitoring the conversion of angiotensin I to angiotensin II in plasma via angiotensin-converting enzyme (ACE) and subsequent inhibition of ACE by captopril.
描述了使用毛细管电泳(CE)结合毛细管内铜(II)络合来测定血管紧张素及其代谢物的方法。生成的铜肽络合物可使用紫外(UV)检测或电化学(EC)检测进行检测。首先使用带紫外检测的CE确定血管紧张素肽的最佳反应和分离条件。对于紫外检测,天然血管紧张素II的检测限(信噪比S/N = 3)为18 μM,而铜 - 血管紧张素II络合物的检测限(LOD)为2 μM。然后评估了带EC检测的CE,得到了显著更低的检测限 - 天然血管紧张素II为2 μM,铜 - 血管紧张素II络合物为200 nM。向运行缓冲液中添加铜提高了CE - UV和CE - EC检测的分离度和灵敏度。通过监测血浆中血管紧张素I经血管紧张素转换酶(ACE)转化为血管紧张素II以及随后卡托普利对ACE的抑制作用,证明了该方法。