Ultrasound targeted microbubbles for theranostic applications in liver diseases: from molecular imaging to targeted therapy.

IF 8.1 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Drug Delivery Pub Date : 2025-12-01 Epub Date: 2025-08-07 DOI:10.1080/10717544.2025.2541656
Chujun Zhang, Qiaoyu Zhang, Qiao Xu, Xinyi Jiang, Yao Ma, Chaoqi Liu, Chang Zhou, Rong Liu, Yun Zhao, Yun Liu
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Abstract

Liver diseases, particularly chronic conditions leading to cirrhosis and hepatocellular carcinoma, represent a major global health burden with high mortality rates, necessitating innovative diagnostic and therapeutic approaches. Ultrasound-targeted microbubble destruction (UTMD) technology has emerged as a promising theranostic platform, combining enhanced contrast imaging with targeted drug/gene delivery capabilities. When activated by ultrasound, these microbubbles exhibit unique biophysical behaviors that significantly improve drug penetration, tissue perfusion, and site-specific delivery. This review comprehensively examines recent advancements in UTMD-based strategies for liver disease management, including microbubble design and imaging-targeted functionalization, and mechanisms of ultrasound-enhanced drug delivery, especially emerging theranostic applications. We further discuss the underlying biophysical principles governing microbubble-ultrasound interactions and their translational potential, providing insights for developing next-generation precision medicine approaches for hepatic disorders.

Abstract Image

Abstract Image

Abstract Image

超声靶向微泡在肝脏疾病治疗中的应用:从分子成像到靶向治疗。
肝病,特别是导致肝硬化和肝细胞癌的慢性疾病,是全球主要的健康负担,死亡率很高,因此需要采用创新的诊断和治疗方法。超声靶向微泡破坏(UTMD)技术已成为一种有前途的治疗平台,将增强的对比成像与靶向药物/基因递送能力相结合。当超声激活时,这些微泡表现出独特的生物物理行为,显著改善药物渗透、组织灌注和部位特异性递送。本文综述了基于utmd的肝脏疾病管理策略的最新进展,包括微泡设计和成像靶向功能化,超声增强给药机制,特别是新兴的治疗应用。我们进一步讨论了控制微泡-超声相互作用的潜在生物物理原理及其转化潜力,为开发下一代肝脏疾病的精准医学方法提供了见解。
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来源期刊
Drug Delivery
Drug Delivery 医学-药学
CiteScore
11.80
自引率
5.00%
发文量
250
审稿时长
3.3 months
期刊介绍: Drug Delivery is an open access journal serving the academic and industrial communities with peer reviewed coverage of basic research, development, and application principles of drug delivery and targeting at molecular, cellular, and higher levels. Topics covered include all delivery systems including oral, pulmonary, nasal, parenteral and transdermal, and modes of entry such as controlled release systems; microcapsules, liposomes, vesicles, and macromolecular conjugates; antibody targeting; protein/peptide delivery; DNA, oligonucleotide and siRNA delivery. Papers on drug dosage forms and their optimization will not be considered unless they directly relate to the original drug delivery issues. Published articles present original research and critical reviews.
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