Enrichment and Quantitative Determination of Free 3,5- Diiodothyronine, 3′,5′-Diiodothyronine, and 3,5-Diiodothyronamine in Human Serum of Thyroid Cancer by Covalent Organic Hyper Cross-linked Poly-ionic Liquid

•We developed a novel hyper-cross-linked poly ionic liquid material based on covalent organic reaction.•The material has specific enrichment for three main compounds in T2s family.•We applied this material in quantitative determination of T2s in serum of thyroid cancer patients.•3,5- diiodothyronine...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of Chromatography A 2021-01, Vol.1637, p.461821, Article 461821
Hauptverfasser: Shao, Lili, Chen, Xi, Lyu, Jinxiu, Zhao, Meng, Li, Qing, Ji, Shuai, Sun, Qiang, Tang, Daoquan, Geng, Houfa, Guo, Mengzhe
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:•We developed a novel hyper-cross-linked poly ionic liquid material based on covalent organic reaction.•The material has specific enrichment for three main compounds in T2s family.•We applied this material in quantitative determination of T2s in serum of thyroid cancer patients.•3,5- diiodothyronine can act as potential biomarkers for “non-invasive” clinical diagnosis of thyroid cancer. The incidence of thyroid cancer is increasing worldwide. So far, still no non-invasive clinical test biomarkers were developed for the diagnosis of thyroid cancer. The diiodothyronines (T2s) are precursors and metabolites of thyroid hormone (T4). Some reports predict that T2s may be associated with several thyroid diseases, especially the thyroid cancer. Detecting free T2s in human serum may help the diagnosis of thyroid cancer. However, few works have reported the detection of T2s due to their trace amounts. Here we developed a novel hyper organic cross-linked poly ionic liquid (PIL) material for the enrichment of three main compounds in T2s family, including 3,5- diiodothyronine (3,5-T2), 3′,5′-diiodothyronine (3′,5′-T2), and 3,5-diiodothyronamine (3,5-T2AM). This PIL material provided specific enrichment superiority for three T2s. After enrichment, the signal intensity of 3,5-T2, 3′,5′-T2, and 3,5-T2AM increased 14, 132 and 1.6 folds, respectively, with LOQ of 76, 87, and 107 fM, respectively. Finally, we successfully applied PIL material coupled with HPLC-ESI-MS/MS in enrichment and quantitative determination of free 3,5-T2, 3′,5′-T2, and 3,5-T2AM in human serum of 45 thyroid cancer patients and 15 healthy people. We also used free thyroid hormone (FT4) as the calibration reference to eliminate individual differences. We found that the levels of 3,5-T2 (P < 0.001), and 3′,5′-T2 (P = 0.001) in patients with thyroid cancer were significantly higher than those in healthy people. Additionally, we further investigated the power of different T2 thyroid hormones divided FT4 to classify thyroid cancer patients and healthy people. And 3,5-T2/FT4 had the highest classification performance for discriminating thyroid cancer patients from healthy people at certain threshold, indicating that 3,5-T2/FT4 in human serum can act as potential biomarkers for “non-invasive” clinical diagnosis of thyroid cancer.
ISSN:0021-9673
1873-3778
DOI:10.1016/j.chroma.2020.461821