a Department of Ultrasound Diagnostics , Tangdu Hospital Fourth Military Medical University , Xi'an, People's Republic of China.
b The State Laboratory of Cancer Biology, Department of Biochemistry and Molecular Biology , Fourth Military Medical University , Xi'an, People's Republic of China.
Drug Deliv. 2019 Dec;26(1):45-50. doi: 10.1080/10717544.2018.1534898.
Recently, exosomes have been emerged as promising drug delivery carriers, while certain tissues are intrinsically resistant to exosomes. Therapeutically improving the drug delivery efficiency in these tissues/organs would certainly broaden the potential application of exosomes in future. Ultrasound-targeted microbubble destruction (UTMD) is a promising technique for non-invasive, targeted drug delivery. In this study, we explore the possibility that UTMD assists exosome delivery in these intrinsically resistant tissues. Mice were subjected to tail vein injection of DiR-labeled exosomes together with/without UTMD of SonoVue, followed by in vivo and ex vivo tracking of the exosomes. As expected, heart, adipose tissue, and skeletal muscle were found reluctant to exosomes from different origins. Targeted destruction of the ultrasound microbubbles (SonoVue) in the heart and adipose tissue region significantly increased the exosome infiltration and endocytosis there, as revealed by fluorescence imaging and confocal laser scanning microscope (CLSM). UTMD treatment 1 h prior to exosome injection failed to facilitate the exosome endocytosis in the targeted region, indicating that the transient promoting effects of UTMD. Moreover, increases of UTMD (numerous pulses) did not linearly enhance the exosome delivery. Together, our study here has established a novel strategy for targeted delivery of exosomes in the reluctant tissues, by combining the advantages of ultrasound microbubbles and exosomes in drug delivery.
最近,外泌体作为有前途的药物递送载体而受到关注,然而某些组织对其天然具有抵抗性。如果能够提高这些组织/器官中外泌体的药物递送效率,将大大拓宽外泌体在未来的潜在应用。超声靶向微泡破坏(UTMD)是一种很有前途的非侵入性靶向药物递送技术。在这项研究中,我们探讨了 UTMD 辅助外泌体在这些固有抵抗性组织中递送的可能性。将 DiR 标记的外泌体与 SonoVue 的 UTMD 一起经尾静脉注射入小鼠体内,随后进行体内和体外追踪。正如预期的那样,心脏、脂肪组织和骨骼肌对来自不同来源的外泌体都有抵抗性。在心脏和脂肪组织区域靶向破坏超声微泡(SonoVue),显著增加了外泌体在这些部位的渗透和内吞作用,荧光成像和共聚焦激光扫描显微镜(CLSM)显示了这一点。在注射外泌体前 1 小时进行 UTMD 处理未能促进靶向区域的外泌体内吞,表明 UTMD 具有短暂的促进作用。此外,增加 UTMD(更多脉冲)并不能线性增强外泌体的递送。总之,本研究通过结合超声微泡和外泌体在药物递送方面的优势,建立了一种在抵抗性组织中靶向递送外泌体的新策略。