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Blood-Labyrinth Barrier Permeability in Menière Disease and Idiopathic Sudden Sensorineural Hearing Loss: Findings on Delayed Postcontrast 3D-FLAIR MRI.梅尼埃病和特发性突发性感音神经性听力损失中的血迷路屏障通透性:延迟增强三维液体衰减反转恢复磁共振成像的研究结果
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Facile Synthesis of Uniform-Sized Bismuth Nanoparticles for CT Visualization of Gastrointestinal Tract in Vivo.简便合成用于体内胃肠道 CT 可视化的均一尺寸铋纳米颗粒。
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T1-Weighted MR imaging of liver tumor by gadolinium-encapsulated glycol chitosan nanoparticles without non-specific toxicity in normal tissues.载钆壳聚糖纳米粒的 T1 加权 MR 成像在正常组织中无非特异性毒性的肝脏肿瘤
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开发靶向分子成像以确定感音神经性听力损失内耳缺陷的挑战和机遇。

Challenges and opportunities in developing targeted molecular imaging to determine inner ear defects of sensorineural hearing loss.

机构信息

Department of Otorhinolaryngology-Head & Neck Surgery, University of Pennsylvania School of Medicine, Philadelphia, PA.

Department of Radiology, University of Pennsylvania, Philadelphia, PA.

出版信息

Nanomedicine. 2018 Feb;14(2):397-404. doi: 10.1016/j.nano.2017.10.004. Epub 2017 Oct 24.

DOI:10.1016/j.nano.2017.10.004
PMID:29074310
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5844828/
Abstract

The development of inner ear gene carriers and delivery systems has enabled genetic defects to be repaired and hearing to be restored in mouse models. Today, promising advances in translational therapies provide confidence that targeted molecular therapy for inner ear diseases will be developed. Unfortunately, the currently available non-invasive modalities, such as Computerized Tomography scan or Magnetic Resonance Imaging provide insufficient resolution to identify most pathologies of the human inner ear, even when the current generation of contrast agents is utilized. The development of targeted contrast agents may play a critical role in determining the cause of, and treatment for, sensorineural hearing loss. Such agents should be able to pass through the cochlea barriers, possess minimal cytotoxicity, and easily conjugate to a targeting agent, without distorting the anatomic details. This review focuses on a series of contrast agents which may fit these criteria for potential clinical application.

摘要

内耳基因载体和输送系统的发展使基因缺陷得以修复,听力得以恢复在小鼠模型中。如今,转化治疗的有希望的进展提供了信心,即针对内耳疾病的靶向分子治疗将得到发展。不幸的是,目前可用的非侵入性方式,如计算机断层扫描或磁共振成像提供的分辨率不足以识别人类内耳的大多数病变,即使当前一代的造影剂被利用。靶向造影剂的发展可能在确定感音神经性听力损失的原因和治疗方面发挥关键作用。这些试剂应该能够穿过耳蜗屏障,具有最小的细胞毒性,并容易与靶向剂结合,而不会扭曲解剖细节。这篇综述集中讨论了一系列可能符合这些标准的造影剂,这些造影剂可能适用于潜在的临床应用。