活性氧响应型双锁脂质体协同光动力疗法用于减少射频导管消融术后的电传导复发

IF 5.2 2区 医学 Q1 PHARMACOLOGY & PHARMACY
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引用次数: 0

摘要

射频导管消融术(RFCA)是治疗心房颤动的首选技术,但消融术后的电传导恢复严重危害患者的健康。本研究旨在开发响应活性氧(ROS)的双锁脂质体协同光动力疗法(PDT),靶向消融区域,减少消融术后的电传导恢复。1H NMR和FT-IR证实了用苯硼酸频哪醇酯修饰的β-环糊精(OCD)的成功合成。此外,1H NMR 和质谱也证实了十八胺修饰的吲哚菁绿(ICG-ODA)的成功合成。ICG-ODA 被封装在脂质体中,生成了双锁混合脂质体(ICG-ODA@rNP),随后对其进行了表征。对 ICG-ODA@rNP 的多项特性进行了评估,包括药物释放、靶向能力和抑制电传导复发的能力。此外,为了进一步评估 ICG-ODA@rNP,还构建了兔子 RFCA 后的电传导阻断模型。此外,还对 ICG-ODA@rNP 进行了初步的安全性评估。粒径均匀的 ICG-ODA@rNP 显示出良好的储存稳定性。该纳米粒子能在 ROS 环境下灵敏释放药物,并表现出良好的光热效应。此外,ICG-ODA@rNP 还能在体内长期循环,并在消融区域大量积聚。在左心房阑尾(LAA)的起搏试验中,这些纳米颗粒与光热疗法相结合,降低了电传导恢复的比率,这一点在苏木精和伊红(H&E)试验中得到了证实。进一步的分子分析表明,ICG-ODA@rNP 可增加 RFCA 诱导的细胞凋亡和 ROS 水平。具体来说,ICG-ODA@rNP 能明显增加 Bax 和裂解的 caspase-3 的表达,降低 Bcl-2 的表达。此外,研究还验证了双锁纳米粒子具有良好的生物安全性。该研究证明,ICG-ODA@rNP 具有双锁特性和生物安全性,可对 RFCA 诱导的心脏损伤区域产生靶向作用,通过与光导治疗的协同作用进一步降低 RFCA 区域的电传导恢复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Reactive oxygen species responsive double-locked liposome collaborative photodynamic therapy for reducing electrical conduction recurrence after radiofrequency catheter ablation

Reactive oxygen species responsive double-locked liposome collaborative photodynamic therapy for reducing electrical conduction recurrence after radiofrequency catheter ablation

Radiofrequency catheter ablation (RFCA) is the preferred technique for the treatment of atrial fibrillation, but the recovery of electrical conduction after ablation seriously endangers the health of patients. This study aimed to develop reactive oxygen species (ROS) responsive double-locked liposome collaborative photodynamic therapy (PDT) to target the ablation area and reduce the recovery of electrical conduction after ablation. The successful synthesis of β-cyclodextrin modified with phenylboronic acid pinacol ester (OCD) was confirmed by 1H NMR and FT-IR. Furthermore, the successful synthesis of octadecylamine-modified indocyanine green (ICG-ODA) was confirmed by 1H NMR and mass spectrometry. The ICG-ODA was encapsulated in liposomes to generate a double-locked hybrid liposome (ICG-ODA@rNP), which was subsequently characterized. Several properties of ICG-ODA@rNP were evaluated, including the drug release, targeting ability and ability to inhibit electrical conduction recurrence. Moreover, a model was constructed for the blockage of electrical conduction after RFCA in rabbits to further evaluate ICG-ODA@rNP. The preliminary safety evaluation of ICG-ODA@rNP was also performed. The ICG-ODA@rNP with a uniform particle size showed excellent storage stability. The nanoparticle can sensitively release drugs under ROS environment, and exhibits excellent photothermal effects. Furthermore, ICG-ODA@rNP can circulate for a long time in vivo and accumulate significantly in the ablation area. In a pacing test with a left atrial appendage (LAA), these nanoparticles, combined with PDT, reduced the ratio of electrical conduction recovery, which was confirmed by a hematoxylin and eosin (H&E) test. Further molecular analysis revealed that ICG-ODA@rNP could increase RFCA-induced apoptosis and ROS levels. Specifically, ICG-ODA@rNP significantly increased the expression of Bax and cleaved caspase-3, and decreased the expression of Bcl-2. In addition, the excellent biosafety of the double-locked nanoparticle was verified. This study provides evidence that ICG-ODA@rNP, with the double lock characteristic and biosafety, which exhibits a targeting effect on RFCA-induced cardiac injury areas, which further reduce electrical conduction recovery in RFCA areas by collaborativing PDT.

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来源期刊
International Journal of Pharmaceutics: X
International Journal of Pharmaceutics: X Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
6.60
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0.00%
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32
审稿时长
24 days
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