A ratio luminescent europium organometallic gel for in vitro detection of hepatocellular carcinoma marker and cellular imaging

IF 6.1 1区 化学 Q1 CHEMISTRY, ANALYTICAL Talanta Pub Date : 2025-02-07 DOI:10.1016/j.talanta.2025.127708
Xiao Lian , Fang Chen , Yanmin Zhang , Juzhou Zhang , Bangben Yao , Helin Niu
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Abstract

Hepatocellular carcinoma is a particularly aggressive form of liver malignancy, representing one of the most formidable threats to human health and a major contributor to cancer-related deaths. Cholyglycine (CG), which plays a pivotal role in lipid metabolism, has garnered attention as a potential biomarker for hepatocellular carcinoma. Nevertheless, the structural resemblance of CG to various bile acids complicates the specific identification of CG. Therefore, the effective monitoring of CG in biological samples is still a challenge to be solved. In this study, a europium-based metal organic gel (Eu-MOG) with dual emission was synthesized and displayed an obvious luminescent color change from red to blue for CG. The synthesized Eu-MOG exhibits excellent selectivity towards CG, and enables the sensitive detection of CG in serum with LOD as 307 ppb. This character of Eu-MOG has also been validated in cell imaging for CG, which make this europium-based probe sufficient for clinical monitoring of CG to diagnosis hepatocellular carcinoma. The results of our experiments, corroborated by theoretical calculations, indicate that the high sensitivity of MOG to CG stems from the intermolecular N–H⋯O interaction between CG and the ligand H2NDC. This interaction facilitates intermolecular charge transfer, which in turn alters the luminescence of the europium-based metal-organic gel (Eu-MOG). This study provides a robust platform for the early diagnosis of hepatocellular carcinoma and contributes significantly to the evaluation of human hepatobiliary metabolic status.

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比值发光铕有机金属凝胶体外检测肝癌标志物及细胞显像
肝细胞癌是一种特别具有侵袭性的肝脏恶性肿瘤,是对人类健康最严重的威胁之一,也是癌症相关死亡的主要原因。甘氨酸(CG)在脂质代谢中起着关键作用,作为肝细胞癌的潜在生物标志物引起了人们的关注。然而,CG与各种胆汁酸的结构相似性使CG的具体鉴定变得复杂。因此,对生物样品中CG的有效监测仍然是一个有待解决的难题。本研究合成了一种具有双发射特性的铕基金属有机凝胶(Eu-MOG),该凝胶在CG上显示出明显的由红色到蓝色的发光变化。合成的Eu-MOG对CG具有良好的选择性,可在LOD为307ppb的情况下对血清中的CG进行灵敏检测。Eu-MOG的这一特征也在CG的细胞成像中得到了验证,这使得这种基于铕的探针足以用于临床监测CG以诊断肝细胞癌。我们的实验结果得到了理论计算的证实,表明MOG对CG的高灵敏度源于CG与配体H2NDC之间的分子间N-H⋯O相互作用。这种相互作用促进了分子间的电荷转移,从而改变了铕基金属有机凝胶(Eu-MOG)的发光。本研究为肝细胞癌的早期诊断提供了一个强大的平台,并对人类肝胆代谢状态的评估有重要意义。
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麦克林
ZnCl2
麦克林
CuCl2
麦克林
NaCl
麦克林
MgCl2
麦克林
KCl
麦克林
CaCl2
麦克林
glycine (Gly)
麦克林
histidine (His)
麦克林
isoleucine (Ile)
麦克林
valine (Val)
麦克林
threonine (Thr)
麦克林
serine (Ser)
麦克林
tryptophan (Trp)
麦克林
leucine (Leu)
麦克林
tyrosine (Tyr)
麦克林
phenylalanine (Phe)
麦克林
alanine (Ala)
麦克林
methionine (Met)
来源期刊
Talanta
Talanta 化学-分析化学
CiteScore
12.30
自引率
4.90%
发文量
861
审稿时长
29 days
期刊介绍: Talanta provides a forum for the publication of original research papers, short communications, and critical reviews in all branches of pure and applied analytical chemistry. Papers are evaluated based on established guidelines, including the fundamental nature of the study, scientific novelty, substantial improvement or advantage over existing technology or methods, and demonstrated analytical applicability. Original research papers on fundamental studies, and on novel sensor and instrumentation developments, are encouraged. Novel or improved applications in areas such as clinical and biological chemistry, environmental analysis, geochemistry, materials science and engineering, and analytical platforms for omics development are welcome. Analytical performance of methods should be determined, including interference and matrix effects, and methods should be validated by comparison with a standard method, or analysis of a certified reference material. Simple spiking recoveries may not be sufficient. The developed method should especially comprise information on selectivity, sensitivity, detection limits, accuracy, and reliability. However, applying official validation or robustness studies to a routine method or technique does not necessarily constitute novelty. Proper statistical treatment of the data should be provided. Relevant literature should be cited, including related publications by the authors, and authors should discuss how their proposed methodology compares with previously reported methods.
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