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微泡辅助超声产生的细胞外囊泡作为癌症治疗的药物纳米载体的潜在用途。

Potential Use of Extracellular Vesicles Generated by Microbubble-Assisted Ultrasound as Drug Nanocarriers for Cancer Treatment.

机构信息

Imaging Division, University Medical Center Utrecht, 3584 CX Utrecht, The Netherlands.

Department of Biomedical Engineering, TU Eindhoven, 5600 MB Eindhoven, The Netherlands.

出版信息

Int J Mol Sci. 2020 Apr 24;21(8):3024. doi: 10.3390/ijms21083024.

Abstract

Extracellular vesicles (EVs)-carrying biomolecules derived from parental cells have achieved substantial scientific interest for their potential use as drug nanocarriers. Ultrasound (US) in combination with microbubbles (MB) have been shown to trigger the release of EVs from cancer cells. In the current study, the use of microbubbles-assisted ultrasound (USMB) to generate EVs containing drug cargo was investigated. The model drug, CellTracker™ green fluorescent dye (CTG) or bovine serum albumin conjugated with fluorescein isothiocyanate (BSA FITC) was loaded into primary human endothelial cells in vitro using USMB. We found that USMB loaded CTG and BSA FITC into human endothelial cells (HUVECs) and triggered the release of EVs containing these compounds in the cell supernatant within 2 h after treatment. The amount of EV released seemed to be correlated with the increase of US acoustic pressure. Co-culturing these EVs resulted in uptake by the recipient tumour cells within 4 h. In conclusion, USMB was able to load the model drugs into endothelial cells and simultaneously trigger the release of EVs-carrying model drugs, highlighting the potential of EVs as drug nanocarriers for future drug delivery in cancer.

摘要

细胞外囊泡(EVs)是源自母细胞的生物分子,因其作为药物纳米载体的潜在用途而引起了广泛的科学关注。超声(US)联合微泡(MB)已被证明可以触发癌细胞释放 EVs。在本研究中,研究了使用微泡辅助超声(USMB)生成含有药物货物的 EVs。模型药物 CellTracker™ 绿色荧光染料(CTG)或与异硫氰酸荧光素(BSA FITC)偶联的牛血清白蛋白被加载到体外的原代人内皮细胞中使用 USMB。我们发现,USMB 将 CTG 和 BSA FITC 加载到人内皮细胞(HUVECs)中,并在处理后 2 小时内触发含有这些化合物的 EV 在细胞上清液中的释放。释放的 EV 量似乎与 US 声压的增加相关。将这些 EV 共培养,结果显示在 4 小时内被受体肿瘤细胞摄取。总之,USMB 能够将模型药物加载到内皮细胞中,并同时触发携带模型药物的 EV 释放,这突显了 EV 作为未来癌症药物递送的药物纳米载体的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/586f/7216118/0367ef7616de/ijms-21-03024-g001.jpg

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