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靶向纳米医学:经验教训与未来方向。

Targeted nanomedicine: Lessons learned and future directions.

机构信息

Laboratory of Angiogenesis and Vascular Metabolism, Center for Cancer Biology (CCB), VIB, Department of Oncology, Leuven Cancer Institute, KU Leuven, Leuven 3000, Belgium.

Laboratory of Precision Nanomedicine, The Shmunis School of Biomedicine and Cancer Research, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel-Aviv, Israel.

出版信息

J Control Release. 2023 Mar;355:446-457. doi: 10.1016/j.jconrel.2023.02.010. Epub 2023 Feb 13.


DOI:10.1016/j.jconrel.2023.02.010
PMID:36773958
Abstract

Designing a therapeutic modality that will reach a certain organ, tissue, or cell type is crucial for both the therapeutic efficiency and to limit off-target adverse effects. Nanoparticles carrying various drugs, such as nucleic acids, small molecules and proteins, are promoting modalities to this end. Beyond the need to identify a target for a specific indication, an adequate design has to address the multiple biological barriers, such as systemic barriers, dilution and unspecific distribution, tissue penetration and intracellular trafficking. The field of targeted delivery has developed rapidly in recent years, with tremendous progress made in understating the biological barriers, and new technologies to functionalize nanoparticles with targeting moieties for an accurate, specific and highly selective delivery. Implementing new approaches like multi-functionalized nanocarriers and machine learning models will advance the field for designing safe, cell -specific nanoparticle delivery systems. Here, we will critically review the current progress in the field and suggest novel strategies to improve cell specific delivery of therapeutic payloads.

摘要

设计一种能够到达特定器官、组织或细胞类型的治疗方式对于提高治疗效果和限制非靶向不良反应至关重要。携带各种药物的纳米颗粒,如核酸、小分子和蛋白质,正在促进这一目标的实现。除了需要为特定适应症确定目标外,还需要设计出能够克服多种生物屏障的药物,如全身屏障、稀释和非特异性分布、组织穿透和细胞内运输。近年来,靶向递药领域发展迅速,在理解生物屏障方面取得了巨大进展,并开发了新技术来将靶向基团功能化到纳米颗粒上,以实现准确、特异和高度选择性的递药。实施多功能化纳米载体和机器学习模型等新方法将推动设计安全、细胞特异性纳米颗粒递药系统的领域发展。在这里,我们将批判性地回顾该领域的当前进展,并提出提高治疗有效载荷细胞特异性递药的新策略。

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