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用于递送反义寡核苷酸的双相离子电渗疗法。

Dual-Phase Iontophoresis for the Delivery of Antisense Oligonucleotides.

作者信息

Gibson Daniel J, Tuli Sonal S, Schultz Gregory S

机构信息

1 Institute for Wound Research, University of Florida , Gainesville, Florida.

2 Department of Ophthalmology, University of Florida , Gainesville, Florida.

出版信息

Nucleic Acid Ther. 2017 Aug;27(4):238-250. doi: 10.1089/nat.2016.0654. Epub 2017 Apr 4.

Abstract

In support of ongoing research in the study of corneal and skin wound healing, we sought to improve on previously published results by using iontophoresis to deliver RNA interference-based oligonucleotides. By using a electromechanics-based approach, we were able to devise a two-phase solution that separated the buffering solution from the antisense oligonucleotide (ASO) solution. The separation was obtained by making the drug solution a higher density than the buffer, leading it to sink directly onto the tissue surface. This change immediately decreased the distance that the ASO would have to travel before delivery. The changes enabled delivery into ex vivo skin and corneas in 10 or fewer minutes and into in vivo corneas in 5 min. In vivo studies demonstrated short-term bioavailability of at least 24 h, a lack of chemical or thermal injury, a lack of interference in the healing of a corneal injury, and an antisense effect till at least day 7, but not day 14. The only side-effect observed was postdelivery edema that was not present when the vehicle alone was iontophoresed. This suggests that electro-osmotic flow from the delivery chamber was not the mechanism, but that the delivered solute likely increased the tissue's osmolarity. These results support the continued development and utilization of this ASO delivery approach in research-grade oligonucleotides to probe molecular biological pathways and in support of testing therapeutic ASOs in the skin and cornea.

摘要

为了支持正在进行的角膜和皮肤伤口愈合研究,我们试图通过离子电渗疗法递送基于RNA干扰的寡核苷酸来改进先前发表的结果。通过基于机电学的方法,我们能够设计出一种两相溶液,将缓冲溶液与反义寡核苷酸(ASO)溶液分开。通过使药物溶液的密度高于缓冲液来实现分离,使其直接沉降到组织表面。这种变化立即缩短了ASO在递送前必须行进的距离。这些变化使得在10分钟或更短时间内能够将其递送至离体皮肤和角膜,在5分钟内递送至体内角膜。体内研究表明,其短期生物利用度至少为24小时,不存在化学或热损伤,不干扰角膜损伤的愈合,并且反义效应至少持续到第7天,但第14天则没有。观察到的唯一副作用是递送后水肿,而单独对载体进行离子电渗疗法时则不存在这种水肿。这表明来自递送腔室的电渗流不是其机制,而是递送的溶质可能增加了组织的渗透压。这些结果支持在研究级寡核苷酸中继续开发和利用这种ASO递送方法,以探究分子生物学途径,并支持在皮肤和角膜中测试治疗性ASO。

相似文献

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Delivery of antisense oligonucleotide to the cornea by iontophoresis.通过离子电渗疗法将反义寡核苷酸递送至角膜。
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