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研究超声介导的全氟丁烷纳米液滴外渗模型药物。

Investigation of Ultrasound Mediated Extravasation of a Model Drug by Perfluorobutane Nanodroplets.

机构信息

Institute of Biomedical Engineering, Department of Engineering Science, University of Oxford, Oxford, UK.

Botnar Institute for Musculoskeletal Sciences, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences (NDORMS), University of Oxford, Oxford, UK.

出版信息

Ultrasound Med Biol. 2024 Oct;50(10):1573-1584. doi: 10.1016/j.ultrasmedbio.2024.06.016. Epub 2024 Jul 26.

Abstract

OBJECTIVE

Perfluorocarbon nanodroplets (NDs) have been widely investigated as both diagnostic and therapeutic agents. There remains, however, a challenge in generating NDs that do not vaporize spontaneously but can be activated at ultrasound pressures that do not produce unwanted bioeffects. In previous work, it has been shown that phospholipid-coated perfluorobutane (PFB) NDs can potentially overcome this challenge. The aim of this study was to investigate whether these NDs can promote drug delivery.

METHODS

A combination of high-speed optical imaging and passive cavitation detection was used to study the acoustic properties of the PFB-NDs in a tissue mimicking phantom. PFB-NDs were exposed to ultrasound at frequencies from 0.5 to 1.5 MHz and peak negative pressures from 0.5 to 3.5 MPa. In addition, the penetration depth of two model drugs (Nile Red and 200 nm diameter fluorescent polymer spheres) into the phantom was measured.

RESULTS

PFB NDs were found to be stable in aqueous suspension at both 4°C and 37°C; their size remaining unchanged at 215 ± 11 nm over 24 h. Penetration of both model drugs in the phantom was found to increase with increasing ultrasound peak negative pressure and decreasing frequency and was found to be positively correlated with the energy of acoustic emissions. Extravasation depths >1 mm were observed at 0.5 MHz with pressures <1 MPa.

CONCLUSION

The results of the study thus suggest that PFB NDs can be used both as drug carriers and as nuclei for cavitation to enhance drug delivery without the need for high intensity ultrasound.

摘要

目的

全氟碳纳米液滴(NDs)已被广泛研究作为诊断和治疗剂。然而,仍然存在一个挑战,即产生不会自发蒸发但可以在不会产生不良生物效应的超声压力下激活的 NDs。在以前的工作中,已经表明磷脂包被的全氟丁烷(PFB)NDs 有可能克服这一挑战。本研究的目的是研究这些 NDs 是否可以促进药物传递。

方法

高速光学成像和被动空化检测的组合用于研究组织模拟体模中 PFB-NDs 的声学特性。将 PFB-NDs 暴露于频率为 0.5 至 1.5 MHz 和峰值负压力为 0.5 至 3.5 MPa 的超声下。此外,还测量了两种模型药物(尼罗红和 200nm 直径荧光聚合物球)进入体模的穿透深度。

结果

PFB NDs 在 4°C 和 37°C 的水悬浮液中均稳定;在 24 小时内,其尺寸保持在 215±11nm 不变。发现两种模型药物在体模中的穿透深度随超声峰值负压力的增加和频率的降低而增加,并且与声发射能量呈正相关。在 0.5MHz 时,压力<1MPa 即可观察到超过 1mm 的漏出深度。

结论

因此,研究结果表明,PFB-NDs 可用作药物载体和空化核,以增强药物传递,而无需高强度超声。

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