Vong Lilita, Laës Agathe, Blain Stéphane
Laboratoire d'Océanographie et de Biogéochimie, Université de la Méditerranée, Centre d'Oceanology de Marseille, Unité Mixte de Recherche CNRS 6535, Campus de Luminy, Case 901, 163, Avenue de Luminy, F-13288 Marseille Cedex 09, France.
Anal Chim Acta. 2007 Apr 11;588(2):237-44. doi: 10.1016/j.aca.2007.02.007. Epub 2007 Feb 12.
A new method for the non-specific determination of iron-porphyrin-like complexes in natural waters has been developed. It is based on the chemiluminescent oxidation of the luminol in the presence of dioxygen (O2) at pH 13. The method has been implemented in a FIA manifold that allowed the direct injection of seawater. The limit of detection is 0.11 nM of equivalent hemin (Fe-protoporphyrin IX). Fe2+, Fe3+, H2O2, siderophore (deferoxamin mesylate), humic acid and phytic acid did not interfere when they were present at the concentrations expected in seawater. Metal free porphyrin and Mg, Cu, Co porphyrin complexes did not induce a significant chemiluminescent signal. Poisoned unfiltered samples could be stored for several weeks before analyses. The new method was successfully applied to the determination of the Fe-porphyrin complexes contained in cultured phytoplankton and in natural samples.
一种用于非特异性测定天然水中类铁卟啉配合物的新方法已被开发出来。它基于在pH 13、存在双氧(O₂)的情况下鲁米诺的化学发光氧化反应。该方法已在流动注射分析(FIA)系统中实现,能够直接进样海水。检测限为0.11 nM等效血红素(铁原卟啉IX)。当Fe²⁺、Fe³⁺、H₂O₂、铁载体(去铁胺甲磺酸盐)、腐殖酸和植酸以海水中预期的浓度存在时,不会产生干扰。无金属卟啉以及镁、铜、钴卟啉配合物不会诱导显著的化学发光信号。经过预处理的未过滤样品在分析前可保存数周。该新方法已成功应用于测定培养的浮游植物和天然样品中所含的铁卟啉配合物。