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从微泡到生物源气体囊泡的超声造影剂

Ultrasound contrast agents from microbubbles to biogenic gas vesicles.

作者信息

Zeng Wenlong, Yue Xiuli, Dai Zhifei

机构信息

Department of Biomedical Engineering, College of Future Technology, Peking University, Beijing, China.

School of Environment, Harbin Institute of Technology, Harbin, China.

出版信息

Med Rev (2021). 2022 Oct 19;3(1):31-48. doi: 10.1515/mr-2022-0020. eCollection 2023 Feb.

Abstract

Microbubbles have been the earliest and most widely used ultrasound contrast agents by virtue of their unique features: such as non-toxicity, intravenous injectability, ability to cross the pulmonary capillary bed, and significant enhancement of echo signals for the duration of the examination, resulting in essential preclinical and clinical applications. The use of microbubbles functionalized with targeting ligands to bind to specific targets in the bloodstream has further enabled ultrasound molecular imaging. Nevertheless, it is very challenging to utilize targeted microbubbles for molecular imaging of extravascular targets due to their size. A series of acoustic nanomaterials have been developed for breaking free from this constraint. Especially, biogenic gas vesicles, gas-filled protein nanostructures from microorganisms, were engineered as the first biomolecular ultrasound contrast agents, opening the door for more direct visualization of cellular and molecular function by ultrasound imaging. The ordered protein shell structure and unique gas filling mechanism of biogenic gas vesicles endow them with excellent stability and attractive acoustic responses. What's more, their genetic encodability enables them to act as acoustic reporter genes. This article reviews the upgrading progresses of ultrasound contrast agents from microbubbles to biogenic gas vesicles, and the opportunities and challenges for the commercial and clinical translation of the nascent field of biomolecular ultrasound.

摘要

微泡凭借其独特特性,成为最早且应用最广泛的超声造影剂:比如无毒、可静脉注射、能够穿过肺毛细血管床,以及在检查期间显著增强回声信号,从而在临床前和临床应用中发挥重要作用。使用经靶向配体功能化的微泡与血流中的特定靶点结合,进一步实现了超声分子成像。然而,由于其尺寸原因,利用靶向微泡对血管外靶点进行分子成像极具挑战性。为突破这一限制,人们开发了一系列声学纳米材料。特别是,生物源气体囊泡,即来自微生物的充气蛋白质纳米结构,被设计成首批生物分子超声造影剂,为通过超声成像更直接地可视化细胞和分子功能打开了大门。生物源气体囊泡有序的蛋白质外壳结构和独特的气体填充机制赋予它们出色的稳定性和诱人的声学响应。此外,它们的基因可编码性使其能够充当声学报告基因。本文综述了超声造影剂从微泡到生物源气体囊泡的升级进展,以及生物分子超声这一新兴领域商业化和临床转化面临的机遇与挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51f/10471104/3cce29a7b9f2/j_mr-2022-0020_fig_001.jpg

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