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Circulating Magnetic Microbubbles for Localized Real-Time Control of Drug Delivery by Ultrasonography-Guided Magnetic Targeting and Ultrasound

机译:循环磁微泡通过超声引导下的磁性靶向和超声对药物输送进行局部实时控制

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Image-guided and target-selective modulation of drug delivery by external physical triggers at the site of pathology has the potential to enable tailored control of drug targeting. Magnetic microbubbles that are responsive to magnetic and acoustic modulation and visible to ultrasonography have been proposed as a means to realize this drug targeting strategy. To comply with this strategy in vivo, magnetic microbubbles must circulate systemically and evade deposition in pulmonary capillaries, while also preserving magnetic and acoustic activities in circulation over time. Unfortunately, challenges in fabricating magnetic microbubbles with such characteristics have limited progress in this field. In this report, we develop magnetic microbubbles (MagMB) that display strong magnetic and acoustic activities, while also preserving the ability to circulate systemically and evade pulmonary entrapment. Methods: We systematically evaluated the characteristics of MagMB including their pharmacokinetics, biodistribution, visibility to ultrasonography and amenability to magneto-acoustic modulation in tumor-bearing mice. We further assessed the applicability of MagMB for ultrasonography-guided control of drug targeting. Results: Following intravenous injection, MagMB exhibited a 17- to 90-fold lower pulmonary entrapment compared to previously reported magnetic microbubbles and mimicked circulation persistence of the clinically utilized Definity microbubbles (>10 min). In addition, MagMB could be accumulated in tumor vasculature by magnetic targeting, monitored by ultrasonography and collapsed by focused ultrasound on demand to activate drug deposition at the target. Furthermore, drug delivery to target tumors could be enhanced by adjusting the magneto-acoustic modulation based on ultrasonographic monitoring of MagMB in real-time. Conclusions: Circulating MagMB in conjunction with ultrasonography-guided magneto-acoustic modulation may provide a strategy for tailored minimally-invasive control over drug delivery to target tissues.
机译:在病理部位通过外部物理触发对药物输送进行图像引导和靶点选择性调节,有可能实现对药物靶向的定制控制。响应于磁和声调制并且对超声检查可见的磁性微泡已被提出作为实现该药物靶向策略的手段。为了在体内遵守该策略,磁性微泡必须系统性循环并逃避肺毛细血管中的沉积,同时还必须随着时间的流逝保持磁性和声学活动。不幸的是,制造具有这种特性的磁性微气泡的挑战限制了该领域的进展。在本报告中,我们开发了显示出强大的磁和声活动的磁性微气泡(MagMB),同时还保留了系统循环和逃避肺部夹带的能力。方法:我们系统地评估了MagMB的特征,包括其药代动力学,生物分布,超声图的可见性以及对荷瘤小鼠的磁声调制的适应性。我们进一步评估了MagMB在超声引导下控制药物靶向的适用性。结果:静脉注射后,与以前报道的磁性微气泡相比,MagMB的肺部包埋降低了17到90倍,并且模仿了临床​​使用的Definity微气泡的循环持久性(> 10分钟)。此外,MagMB可以通过磁性靶向在肿瘤脉管系统中积聚,通过超声检查进行监测,并根据需要通过聚焦超声使其塌陷,以激活靶标上的药物沉积。此外,可以通过基于MagMB的超声监测实时调整磁声调制来增强向目标肿瘤的药物递送。结论:结合超声引导的磁声调制,循环MagMB可以为针对目标组织的药物输送量身定制的微创控制提供策略。

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