纳米金造影剂粒径对胃肠道及炎症性肠病CT成像的影响

IF 4 2区 化学 Q1 BIOCHEMICAL RESEARCH METHODS
Derick N Rosario-Berríos, Amanda Pang, Leening P Liu, Portia S N Maidment, Johoon Kim, Seokyoung Yoon, Lenitza M Nieves, Katherine J Mossburg, Andrew Adezio, Peter B Noël, Elizabeth M Lennon, David P Cormode
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引用次数: 0

摘要

溃疡性结肠炎是一种慢性炎症性肠病(IBD)。CT造影剂成像通常用于UC患者胃肠道的显像。增强成像性能的造影剂在这一领域非常有价值。最近的研究在开发用于胃肠道成像的纳米颗粒造影剂方面取得了重大进展。然而,纳米颗粒尺寸对这一应用的影响仍未被探索。金纳米颗粒(AuNPs)是研究纳米颗粒大小对胃肠道成像影响的理想模型,因为它们可以在很宽的尺寸范围内可控合成。在这项研究中,我们合成了核心尺寸在5到75 nm之间的AuNPs,以检验大小在这种情况下的影响。AuNPs包被聚乙二醇(PEG)以提高稳定性和生物相容性。体外实验表明,金纳米颗粒与巨噬细胞具有细胞相容性(约100%的细胞活力),在酸性条件下保持稳定,随着时间的推移没有明显的大小变化。使用临床CT扫描仪的幻影成像研究表明,纳米颗粒大小对CT造影剂的产生没有影响,正如之前所证明的那样。使用小鼠急性结肠炎模型的体内成像显示,所有测试的药物在整个胃肠道中产生强烈的造影剂。在大多数情况下,体内对比与AuNP大小无关,尽管AuNP优于iopamidol(一种临床批准的对照剂)。此外,在健康小鼠和结肠炎小鼠之间观察到衰减趋势的差异。我们还观察到所有测试的配方在24小时几乎完全清除(保留小于0.7% ID/g),支持它们作为研究纳米颗粒成像行为的模型平台的价值。总之,本研究强调了纳米颗粒作为UC胃肠道(GIT) CT成像有效造影剂的潜力。需要进一步的系统研究来探索造影剂,可以特异性地显示这种疾病的疾病过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Effect of the Size of Gold Nanoparticle Contrast Agents on CT Imaging of the Gastrointestinal Tract and Inflammatory Bowel Disease.

Ulcerative colitis (UC) is a chronic inflammatory bowel disease (IBD). CT imaging with contrast agents is commonly used for visualizing the gastrointestinal (GI) tract in UC patients. Contrast agents that provide enhanced imaging performance are highly valuable in this field. Recent studies have made significant progress in developing better contrast agents for imaging the gastrointestinal tract using nanoparticles. However, the impact of nanoparticle size on this application remains unexplored. Gold nanoparticles (AuNPs) serve as an ideal model to investigate the effect of nanoparticle size on imaging of the gastrointestinal tract due to their controllable synthesis across a broad size range. In this study, we synthesized AuNPs with core sizes ranging from 5 to 75 nm to examine the effect of the size in this setting. AuNPs were coated with poly(ethylene glycol) (PEG) to enhance stability and biocompatibility. In vitro tests show that gold nanoparticles are cytocompatible with macrophage cells (∼100% cell viability) and remain stable under acidic conditions, with no significant size changes over time. Phantom imaging studies using a clinical CT scanner indicated that there was no effect of nanoparticle size on CT contrast production, as previously demonstrated. In vivo imaging using a mouse model of acute colitis revealed a strong contrast generation throughout the GI tract for all agents tested. For the most part, in vivo contrast was independent of AuNP size, although AuNP outperformed iopamidol (a clinically approved control agent). In addition, differences in attenuation trends were observed between healthy and colitis mice. We also observed almost complete clearance at 24 h of all formulations tested (less than 0.7% ID/g was retained), supporting their value as a model platform for studying nanoparticle behavior in imaging. In conclusion, this study highlights the potential of nanoparticles as effective contrast agents for CT imaging of the gastrointestinal tract (GIT) in the UC. Further systemic research is needed to explore contrast agents that can specifically image disease processes in this disease setting.

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来源期刊
Bioconjugate Chemistry
Bioconjugate Chemistry 生物-化学综合
CiteScore
9.00
自引率
2.10%
发文量
236
审稿时长
1.4 months
期刊介绍: Bioconjugate Chemistry invites original contributions on all research at the interface between man-made and biological materials. The mission of the journal is to communicate to advances in fields including therapeutic delivery, imaging, bionanotechnology, and synthetic biology. Bioconjugate Chemistry is intended to provide a forum for presentation of research relevant to all aspects of bioconjugates, including the preparation, properties and applications of biomolecular conjugates.
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