Iron(III)-Quercetin Complex: In Vivo Acute Toxicity and Biodistribution of Novel MRI Agent.

IF 6.5 2区 医学 Q1 NANOSCIENCE & NANOTECHNOLOGY International Journal of Nanomedicine Pub Date : 2025-01-31 eCollection Date: 2025-01-01 DOI:10.2147/IJN.S496015
Phattarawadee Innuan, Sarawut Kongkarnka, Atigan Thongtharb, Jiraporn Kantapan, Nathupakorn Dechsupa
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Abstract

Background: The iron(III)-quercetin complex, known as "IronQ", is an innovative MRI contrast agent composed of one Fe(III) ion and two quercetin molecules. IronQ is efficiently internalized by cells, enabling T1-weighted MRI tracking. It has demonstrated therapeutic benefits in reducing inflammation in an intracerebral hemorrhage (ICH) mouse model and offers a safer alternative to gadolinium-based agents by avoiding cytotoxicity and genotoxicity. These properties make IronQ a promising candidate for safe and effective MRI contrast enhancement.

Purpose: This study aims to further the development of IronQ as an MRI contrast agent by investigating its biodistribution, pharmacokinetics, and acute toxicity in a preclinical animal model.

Methods: The relaxivity of IronQ was measured in water and whole blood phantoms. Acute toxicity was evaluated in Sprague Dawley rats administered single intraperitoneal doses of IronQ (75, 150, and 225 µmol Fe/kg BW) over a 14-day period. Pharmacokinetic studies were performed at a dose of 150 µmol Fe/kg BW, with blood iron content analyzed using ICP-OES. For in vivo biodistribution, SD rats were administered an intravenous dose of IronQ (225 µmol Fe/kg BW), followed by MR imaging using a 1.5 T scanner and subsequent tissue-ICP analysis.

Results: The longitudinal relaxivity (r1) of IronQ was measured to be 2.17 mm⁻¹s⁻¹ in ultrapure water and 3.56 mm⁻¹s⁻¹ in whole blood. Acute toxicity studies showed no mortality, morbidity, or significant biochemical changes, with histopathology confirming no irreversible organ damage. Pharmacokinetics revealed peak blood iron content at 1.1 hours post-administration and clearance within 24 hours. MRI demonstrated enhanced T1 signal intensity, particularly in the liver and kidney.

Conclusion: These findings provide valuable insights into the safety, pharmacokinetics, and imaging efficacy of IronQ, highlighting its potential as a robust and biocompatible MRI contrast agent.

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铁(III)-槲皮素复合物:新型MRI试剂的体内急性毒性和生物分布。
背景:铁(III)-槲皮素复合物,被称为“IronQ”,是一种由一个铁(III)离子和两个槲皮素分子组成的新型MRI造影剂。IronQ被细胞有效内化,从而实现t1加权MRI跟踪。它在脑出血(ICH)小鼠模型中显示出减少炎症的治疗效果,并且通过避免细胞毒性和遗传毒性,为钆基药物提供了更安全的替代方案。这些特性使IronQ成为安全有效的MRI对比增强的有希望的候选者。目的:本研究旨在通过研究IronQ在临床前动物模型中的生物分布、药代动力学和急性毒性,进一步开发其作为MRI造影剂。方法:在水和全血模型中测定铁q的弛豫度。在14天的时间内,对Sprague Dawley大鼠进行单次腹腔注射IronQ(75、150和225µmol Fe/kg BW)的急性毒性评估。在150µmol Fe/kg BW剂量下进行药代动力学研究,并用ICP-OES分析血铁含量。对于体内生物分布,SD大鼠静脉注射IronQ(225µmol Fe/kg BW),然后使用1.5 T扫描仪进行MR成像,随后进行组织icp分析。结果:经测定,IronQ的纵向弛缓度(r1)在超纯水中为2.17 mm⁻¹s,在全血中为3.56 mm⁻¹s。急性毒性研究显示没有死亡率、发病率或显著的生化变化,组织病理学证实没有不可逆的器官损伤。药代动力学显示血铁含量在给药后1.1小时达到峰值,并在24小时内清除。MRI显示T1信号增强,尤其在肝脏和肾脏。结论:这些发现为IronQ的安全性、药代动力学和成像功效提供了有价值的见解,突出了其作为一种强大的生物相容性MRI造影剂的潜力。
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来源期刊
International Journal of Nanomedicine
International Journal of Nanomedicine NANOSCIENCE & NANOTECHNOLOGY-PHARMACOLOGY & PHARMACY
CiteScore
14.40
自引率
3.80%
发文量
511
审稿时长
1.4 months
期刊介绍: The International Journal of Nanomedicine is a globally recognized journal that focuses on the applications of nanotechnology in the biomedical field. It is a peer-reviewed and open-access publication that covers diverse aspects of this rapidly evolving research area. With its strong emphasis on the clinical potential of nanoparticles in disease diagnostics, prevention, and treatment, the journal aims to showcase cutting-edge research and development in the field. Starting from now, the International Journal of Nanomedicine will not accept meta-analyses for publication.
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