评估原卟啉作为炎症性肠病患者尿液中贫血症生物标记物的潜在用途

IF 3.1 3区 医学 Q2 CHEMISTRY, ANALYTICAL Journal of pharmaceutical and biomedical analysis Pub Date : 2024-09-02 DOI:10.1016/j.jpba.2024.116456
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引用次数: 0

摘要

原卟啉是具有环状结构的有机化合物,由多种生物合成。在人体的血液和尿液中都能检测到这些化合物,其中血液中的含量更高。目前正在研究它们作为贫血和其他疾病生物标志物的潜力,因为它们的含量会随着与疾病相关的生化过程而变化。最广泛使用的贫血生物标志物是血清铁蛋白,但它在炎症性肠病(IBD)患者中并不可靠,因为急性炎症和/或感染会改变铁蛋白的水平。因此,有必要寻找新的标记物来帮助诊断 IBD 患者的贫血。这项研究开发并验证了一种测定人体尿液中三种原卟啉的方法:原卟啉 IX (PPIX)、原卟啉 IX 与锌的复合物 (ZnPPIX) 和原卟啉 IX 与铁(II)的复合物 (FePPIX),后者也称为血红素。目的是评估它们作为确诊 IBD 患者贫血症生物标志物的潜力。拟议的分析方法基于高效液相色谱法(HPLC),并采用光电二极管阵列(PDA)和荧光(FD)双重检测。由于分散液-液微萃取(DLLME)的高效预富集和检测系统的灵敏度,可以在很低的浓度下对分析物进行定量。该方法通过线性(25-1000 纳克/毫升-1)、基质效应、灵敏度(定量限在 5-11 纳克/毫升-1 之间)、选择性、准确性、迁移量、稀释完整性、稳定性和精密度(12.1%)进行了验证。最后,对样本定量结果进行的统计分析显示,贫血和非贫血 IBD 患者的这三种标记物与五种临床标记物之间存在显著差异。
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Evaluation of the potential use of protoporphyrins as biomarkers of anemic disease in human urine from inflammatory bowel disease patients

Protoporphyrins are organic compounds with cyclic structure that are synthesised by a wide variety of organisms. In humans, these compounds are detected in blood and urine, with significantly higher levels in blood. Their potential as biomarkers of anemia and other diseases is currently being investigated, as their levels change according to the biochemical processes associated with the disease. The most widely used biomarker of anemia is serum ferritin, but it is unreliable in patients with inflammatory bowel disease (IBD) because its levels can be altered by acute inflammation and/or infections. There is therefore a need to look for new markers to help diagnose anemia in IBD patients. This work develops and validates a method for the determination of three protoporphyrins in human urine: protoporphyrin IX (PPIX), protoporphyrin IX complex with Zn (ZnPPIX) and protoporphyrin IX complex with Fe (II) (FePPIX), the latter also known as heme. The aim is to evaluate their potential as biomarkers of anemic disease in patients diagnosed with IBD. The proposed analytical method is based on high performance liquid chromatography (HPLC) with dual detection based on photodiode array (PDA) and fluorescence (FD). Quantification of the analytes at very low concentrations is possible due to the efficient preconcentration provided by dispersive liquid-liquid microextraction (DLLME) and the sensitivity of the detection systems. The method was validated by evaluating linearity (25–1000 ng mL−1), matrix effect, sensitivity (limits of quantification were between 5 and 11 ng mL−1), selectivity, accuracy, carry-over, dilution integrity, stability and precision (< 12.1 %). Finally, statistical analyses applied to the sample quantification results showed these three markers, together with five clinical markers, were significantly different between anemic and non-anemic IBD patients.

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来源期刊
CiteScore
6.70
自引率
5.90%
发文量
588
审稿时长
37 days
期刊介绍: This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome. Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.
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