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外泌体治疗学:工程学、药代动力学及未来应用。

Exosomes in Therapy: Engineering, Pharmacokinetics and Future Applications.

机构信息

National Center for Global Health, Istituto Superiore di Sanità (ISS), Viale Regina Elena 299, 00161, Rome, Italy.

出版信息

Curr Drug Targets. 2019;20(1):87-95. doi: 10.2174/1389450119666180521100409.

Abstract

BACKGROUND

Eukaryotic cells release vesicles of different sizes under both physiological and pathological conditions. On the basis of the respective biogenesis, extracellular vesicles are classified as apoptotic bodies, microvesicles, and exosomes. Among these, exosomes are considered tools for innovative therapeutic interventions, especially when engineered with effector molecules. The delivery functions of exosomes are favored by a number of typical features. These include their small size (i.e., 50-200 nm), the membrane composition tightly similar to that of producer cells, lack of toxicity, stability in serum as well as other biological fluids, and accession to virtually any organ and tissue including central nervous system. However, a number of unresolved questions still affects the possible use of exosomes in therapy. Among these are the exact identification of both in vitro and ex vivo produced vesicles, their large-scale production and purification, the uploading efficiency of therapeutic macromolecules, and the characterization of their pharmacokinetics.

OBJECTIVE

Here, we discuss two key aspects to be analyzed before considering exosomes as a tool of delivery for the desired therapeutic molecule, i.e., techniques of engineering, and their in vivo biodistribution/ pharmacokinetics. In addition, an innovative approach aimed at overcoming at least part of the obstacles towards a safe and efficient use of exosomes in therapy will be discussed.

CONCLUSION

Several biologic features render exosomes an attractive tool for the delivery of therapeutic molecules. They will surely be a part of innovative therapeutic interventions as soon as few still unmet technical hindrances will be overcome.

摘要

背景

真核细胞在生理和病理条件下都会释放不同大小的囊泡。根据各自的生物发生情况,细胞外囊泡被分类为凋亡小体、微泡和外泌体。在这些囊泡中,外泌体被认为是创新治疗干预的工具,尤其是当它们被效应分子工程化时。外泌体的递药功能得益于一些典型特征。这些特征包括它们的小尺寸(即 50-200nm)、与产生细胞紧密相似的膜组成、缺乏毒性、在血清和其他生物流体中的稳定性以及几乎可以进入任何器官和组织,包括中枢神经系统。然而,一些悬而未决的问题仍然影响着外泌体在治疗中的可能应用。其中包括对体外和离体产生的囊泡的确切鉴定、它们的大规模生产和纯化、治疗性大分子的加载效率以及对其药代动力学的表征。

目的

在这里,我们讨论了在将外泌体视为所需治疗分子的递药工具之前需要分析的两个关键方面,即工程技术及其体内生物分布/药代动力学。此外,还将讨论一种旨在克服外泌体在治疗中安全有效应用的一些尚未满足的技术障碍的创新方法。

结论

外泌体具有许多生物学特征,使其成为递药治疗分子的有吸引力的工具。一旦克服了少数仍未满足的技术障碍,它们肯定将成为创新治疗干预的一部分。

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