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用于全血中锌原卟啉IX和原卟啉IX荧光定量的双波长激发

Dual-wavelength excitation for fluorescence-based quantification of zinc protoporphyrin IX and protoporphyrin IX in whole blood.

作者信息

Hennig Georg, Gruber Christian, Vogeser Michael, Stepp Herbert, Dittmar Stephan, Sroka Ronald, Brittenham Gary M

机构信息

Laser-Forschungslabor, LIFE Center, Klinikum der Universität München, Marchioninistr. 23, 81377 München, Germany.

出版信息

J Biophotonics. 2014 Jul;7(7):514-24. doi: 10.1002/jbio.201200228. Epub 2013 Mar 1.

Abstract

Quantification of erythrocyte zinc protoporphyrin IX (ZnPP) and protoporphyrin IX (PPIX), individually or jointly, is useful for the diagnostic evaluation of iron deficiency, iron-restricted erythropoiesis, lead exposure, and porphyrias. A method for simultaneous quantification of ZnPP and PPIX in unwashed blood samples is described, using dual-wavelength excitation to effectively eliminate background fluorescence from other blood constituents. In blood samples from 35 subjects, the results of the dual-wavelength excitation method and a reference high performance liquid chromatography (HPLC) assay were closely correlated both for ZnPP (rs = 0.943, p < 0.0001; range 37-689 μmol ZnPP/mol heme, 84-1238 nmol/L) and for PPIX (rs = 0.959, p < 0.0001; range 42-4212 μmol PPIX/mol heme, 93-5394 nmol/L). In addition, for ZnPP, the proposed method is compared with conventional single-wavelength excitation and with commercial front-face fluorimetry of washed erythrocytes and whole blood. We hypothesize that dual-wavelength excitation fluorimetry will provide a new approach to the suppression of background fluorescence in blood and tissue measurements of ZnPP and PPIX.

摘要

单独或联合定量红细胞锌原卟啉IX(ZnPP)和原卟啉IX(PPIX),对于缺铁、铁限制红细胞生成、铅暴露和卟啉病的诊断评估很有用。本文描述了一种在未洗涤血样中同时定量ZnPP和PPIX的方法,该方法使用双波长激发来有效消除其他血液成分的背景荧光。在35名受试者的血样中,双波长激发法与参考高效液相色谱(HPLC)测定法的结果在ZnPP(rs = 0.943,p < 0.0001;范围为37 - 689 μmol ZnPP/mol血红素,84 - 1238 nmol/L)和PPIX(rs = 0.959,p < 0.0001;范围为42 - 4212 μmol PPIX/mol血红素,93 - 5394 nmol/L)方面都密切相关。此外,对于ZnPP,将所提出的方法与传统单波长激发以及洗涤红细胞和全血的商业前表面荧光法进行了比较。我们假设双波长激发荧光法将为抑制血液和组织中ZnPP和PPIX测量的背景荧光提供一种新方法。

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