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一种新的用于对比增强血管内超声成像的体外试剂:载药的聚氰基丙烯酸丁酯纳米颗粒。

A new agent for contrast-enhanced intravascular ultrasound imaging in vitro: polybutylcyanoacrylate nanoparticles with drug-carrying capacity.

机构信息

The Department of Cardiology, The Fourth Affiliated Hospital of Zhejiang University School of Medicine, Yiwu, Zhejiang, China.

出版信息

Artif Cells Nanomed Biotechnol. 2024 Dec;52(1):218-228. doi: 10.1080/21691401.2024.2334713. Epub 2024 Apr 22.

Abstract

This study prepared and evaluated polymeric polybutylcyanoacrylate (PBCA) nanoparticles (NPs) that can be used as a new agent for contrast-enhanced intravascular ultrasound (IVUS) imaging with drug delivery capacity. The nanoformulation was successfully developed using suspension polymerisation and characterised in terms of size, size distribution, zeta potential, morphology, stability, toxicity effects, imaging effects and drug release study. The results showed that the nanoparticles were round and hollow, with a particle diameter of 215.8 ± 25.3 nm and a zeta potential of -22.2 ± 4.1 mV. In vitro experiments, the nanoparticles were safe, non-toxic, and stable in nature with the capacity to carry and release drug (ant-miR-126). Moreover, the nanoparticles can match the high-frequency probe of commercially IVUS as a contrast agent to improve the resolution of imaging (the mean echo intensity ratio in the vascular wall increased significantly from 10.89 ± 1.10 at baseline, to 24.51 ± 1.91 during injection and 43.70 ± 0.88 after injection, respectively  < .0001). Overall, a new nano agent with drug-carrying capacity was prepared, which can be used in combination with IVUS for simultaneous diagnosis and targeted therapy of coronary atherosclerosis.

摘要

本研究制备并评价了具有药物递送能力的新型聚合物聚丁基氰基丙烯酸酯(PBCA)纳米颗粒(NPs),可作为对比增强血管内超声(IVUS)成像的新造影剂。该纳米制剂是通过悬浮聚合成功开发的,并在粒径、粒径分布、Zeta 电位、形态、稳定性、毒性作用、成像效果和药物释放研究方面进行了表征。结果表明,纳米颗粒为圆形空心结构,粒径为 215.8±25.3nm,Zeta 电位为-22.2±4.1mV。体外实验表明,纳米颗粒安全无毒,性质稳定,具有携带和释放药物(抗 miR-126)的能力。此外,纳米颗粒可以匹配商用 IVUS 的高频探头作为造影剂,以提高成像分辨率(血管壁的平均回波强度比从基线时的 10.89±1.10 显著增加到注射时的 24.51±1.91 和注射后的 43.70±0.88,均<.0001)。总之,制备了一种具有载药能力的新型纳米制剂,可与 IVUS 联合用于冠状动脉粥样硬化的同时诊断和靶向治疗。

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