翻译(生物学)
碘造影剂
对比度(视觉)
医学
静脉造影剂
药理学
放射科
化学
计算机断层摄影术
计算机科学
生物化学
人工智能
信使核糖核酸
基因
作者
Mohamed F. Attia,Ryan N. Marasco,Samuel Kwain,Charity Foxx,Daniel C. Whitehead,Alexander V. Kabanov,Yueh Z. Lee
出处
期刊:
[Cold Spring Harbor Laboratory]
日期:2024-08-29
被引量:1
标识
DOI:10.1101/2024.08.28.610138
摘要
Current clinical small molecule x-ray CT agents are effective but pose risks such as nephrotoxicity, short blood circulation time, limiting scan durations, potential thyroid impact, and immune responses. These challenges drive the development of kidney-safe x-ray nanoparticle (NP)-based contrast agents (CAs), though translation to clinical practice is hindered by chemical complexities and potential toxicity. We have engineered an intravenous, injectable, and safe blood pool NP-based CT CAs at a clinical-equivalent dose of ∼300 mgI/kg (∼2 mL/kg), ideal for vascular and hepatic imaging which are limited by clinical agents. Our iodinated lipid nanodroplet emulsions (ILNEs) contrast agent offers high x-ray attenuation thus improved contrast enhancement, extended stability, and exceptional batch-to-batch consistency. It also boasts a straightforward and scalable manufacturing process with minimal protein interaction, prolonged blood residency (∼4h), and hepatic clearance within 3 days, avoiding nephrotoxicity. Studies in vitro, in mice, and 16.6kg porcine animal model studies confirm its safety, cytocompatibility, and absence of tissue damage. Blood, and thyroid-stimulating hormone (TSH) analyses, and kidney and liver function tests, also support further toxicity evaluations for clinical translation.
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