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评估原卟啉作为炎症性肠病患者尿液中贫血疾病生物标志物的潜在用途。

Evaluation of the potential use of protoporphyrins as biomarkers of anemic disease in human urine from inflammatory bowel disease patients.

机构信息

Department of Analytical Chemistry, Faculty of Chemistry, University of Murcia, Regional Campus of International Excellence "Campus Mare Nostrum", Murcia E-30100, Spain.

Internal Medicine Service - Gastroenterology and Hepatology Section, Hospital General Universitario Rafael Méndez, 30813 Lorca, Spain.

出版信息

J Pharm Biomed Anal. 2024 Dec 15;251:116456. doi: 10.1016/j.jpba.2024.116456. Epub 2024 Sep 2.

Abstract

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), matrix effect, sensitivity (limits of quantification were between 5 and 11 ng mL), 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.

摘要

原卟啉是具有环状结构的有机化合物,广泛存在于各种生物体中。在人类体内,这些化合物可以在血液和尿液中被检测到,且血液中的含量显著更高。目前,人们正在研究其作为贫血和其他疾病生物标志物的潜力,因为其水平会根据与疾病相关的生化过程而发生变化。目前最广泛使用的贫血生物标志物是血清铁蛋白,但在炎症性肠病(IBD)患者中并不可靠,因为其水平可能会受到急性炎症和/或感染的影响而发生改变。因此,需要寻找新的标志物来帮助诊断 IBD 患者的贫血。本工作开发并验证了一种用于测定人尿中三种原卟啉的方法:原卟啉 IX(PPIX)、与 Zn 结合的原卟啉 IX(ZnPPIX)和与 Fe(II)结合的原卟啉 IX(FePPIX),后者也称为血红素。目的是评估它们作为诊断为 IBD 的贫血疾病患者的生物标志物的潜力。所提出的分析方法基于高效液相色谱法(HPLC),具有基于光电二极管阵列(PDA)和荧光(FD)的双重检测。由于分散液-液微萃取(DLLME)提供的高效浓缩和检测系统的灵敏度,可实现对非常低浓度分析物的定量。通过评估线性度(25-1000ng/mL)、基质效应、灵敏度(定量限在 5-11ng/mL 之间)、选择性、准确性、交叉污染、稀释完整性、稳定性和精密度(<12.1%)对方法进行了验证。最后,对样品定量结果进行的统计分析表明,这三种标志物与五种临床标志物一起,在贫血和非贫血的 IBD 患者之间存在显著差异。

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