Targeted Imaging of Renal Fibrosis Using Antibody-Conjugated Gold Nanoparticles in Renal Artery Stenosis

胶体金 马森三色染色 体内 肾动脉狭窄 共轭体系 PEG比率 肾脏疾病 病理 纳米粒子跟踪分析 纤维化 化学 医学 材料科学 肾动脉 纳米颗粒 内科学 纳米技术 生物化学 生物 聚合物 小RNA 微泡 生物技术 有机化学 财务 经济 基因
作者
Xiang-Yang Zhu,Xiangyu Zou,Rahul Mukherjee,Zhicong Yu,Christopher M. Ferguson,Wei Zhou,Cynthia H. McCollough,Lilach O. Lerman
出处
期刊:Investigative Radiology [Ovid Technologies (Wolters Kluwer)]
卷期号:53 (10): 623-628 被引量:19
标识
DOI:10.1097/rli.0000000000000476
摘要

The ability to determine the severity of renal fibrosis, which is involved in most chronic kidney diseases, may be beneficial for monitoring disease progression and management. The aim of this study was to assess a new method involving gold nanoparticles conjugated to an anti-collagen-I antibody (Co-I-AuNPs) as a computed tomography (CT) imaging contrast for the evaluation of renal fibrosis in situ.Gold nanoparticles conjugated to an anti-collagen-I antibody were prepared using gold chloride reduction with sodium citrate and coated with polyethylene glycol (PEG), and their size was determined by electron microscopy and nanoparticle tracking analysis. Anti-collagen-I antibody was then conjugated to PEG-SH/COOH on the AuNP surface. The success of antibody conjugation was tested in vitro using collagen-coated plate and mouse stenotic kidney sections and in vivo using micro-CT and multidetector CT imaging.Bare AuNPs were 18.7 ± 0.6 nm and PEG-coated AuNPs were 45.3 ± 0.1 nm in size. In vitro, Co-I-AuNPs specifically bound to both a collagen-coated plate and mouse fibrotic kidneys. Furthermore, the stenotic mouse kidney showed increased Co-I-AuNPs retention compared with the contralateral kidney (59.3 ± 5.1 vs 45.1 ± 1.7 HU, P = 0.05), which correlated with its collagen deposition. Micro-CT also detected gold signals in situ in the Co-I-AuNP-injected kidney, which colocalized with histological trichrome staining.Gold nanoparticles conjugated to an anti-collagen-I antibody are able to visualize kidney fibrosis in vitro and in situ and may be useful for nondestructive quantification of tissue fibrosis.

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