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本文引用的文献

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Blood-Brain Barrier Opening in Primary Brain Tumors with Non-invasive MR-Guided Focused Ultrasound: A Clinical Safety and Feasibility Study.非侵入性磁共振引导聚焦超声打开原发性脑肿瘤的血脑屏障:一项临床安全性和可行性研究。
Sci Rep. 2019 Jan 23;9(1):321. doi: 10.1038/s41598-018-36340-0.
2
Middle-ear dexamethasone delivery via ultrasound microbubbles attenuates noise-induced hearing loss.通过超声微泡递送中耳地塞米松可减轻噪声性听力损失。
Laryngoscope. 2019 Aug;129(8):1907-1914. doi: 10.1002/lary.27713. Epub 2018 Dec 27.
3
Combining Microbubble Contrast Agent with Pulsed-Laser Irradiation for Transdermal Drug Delivery.微泡造影剂与脉冲激光照射相结合用于经皮给药
Pharmaceutics. 2018 Oct 3;10(4):175. doi: 10.3390/pharmaceutics10040175.
4
State-of-the-art of microbubble-assisted blood-brain barrier disruption.微泡辅助血脑屏障破坏的最新进展。
Theranostics. 2018 Aug 7;8(16):4393-4408. doi: 10.7150/thno.26869. eCollection 2018.
5
Franz Diffusion Cell Approach for Pre-Formulation Characterisation of Ketoprofen Semi-Solid Dosage Forms.用于酮洛芬半固体剂型处方前特性研究的Franz扩散池法
Pharmaceutics. 2018 Sep 5;10(3):148. doi: 10.3390/pharmaceutics10030148.
6
Insonation of Systemically Delivered Cisplatin-Loaded Microbubbles Significantly Attenuates Nephrotoxicity of Chemotherapy in Experimental Models of Head and Neck Cancer.全身递送的载顺铂微泡的超声检查可显著减轻头颈癌实验模型中化疗的肾毒性。
Cancers (Basel). 2018 Sep 5;10(9):311. doi: 10.3390/cancers10090311.
7
Adjuvant agents enhance round window membrane permeability to dexamethasone and modulate basal to apical cochlear gradients.佐剂增强圆窗膜对地塞米松的通透性,并调节基底到顶端耳蜗的梯度。
Eur J Pharm Sci. 2019 Jan 1;126:69-81. doi: 10.1016/j.ejps.2018.08.013. Epub 2018 Aug 11.
8
Ultrasound-Mediated EGF-Coated-Microbubble Cavitation in Dressings for Wound-Healing Applications.超声介导的 EGF 涂层微泡空化在敷料中的应用于伤口愈合。
Sci Rep. 2018 May 29;8(1):8327. doi: 10.1038/s41598-018-26702-z.
9
Optimized phospholipid-based nanoparticles for inner ear drug delivery and therapy.优化的基于磷脂的纳米粒用于内耳药物递送和治疗。
Biomaterials. 2018 Jul;171:133-143. doi: 10.1016/j.biomaterials.2018.04.038. Epub 2018 Apr 16.
10
Controlled drug release to the inner ear: Concepts, materials, mechanisms, and performance.内耳的药物控释:概念、材料、机制和性能。
Hear Res. 2018 Oct;368:49-66. doi: 10.1016/j.heares.2018.03.006. Epub 2018 Mar 9.

经耳内镜或经颅途径超声致微泡空化作用促进内耳药物递送。

Ultrasound-induced microbubble cavitation via a transcanal or transcranial approach facilitates inner ear drug delivery.

机构信息

Graduate Institute of Biomedical Engineering, National Taiwan University of Science and Technology, Taipei, Taiwan.

Department of Biomedical Engineering and.

出版信息

JCI Insight. 2020 Feb 13;5(3):132880. doi: 10.1172/jci.insight.132880.

DOI:10.1172/jci.insight.132880
PMID:31895697
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7098803/
Abstract

Ultrasound-induced microbubble (USMB) cavitation is widely used to promote drug delivery. Our previous study investigated USMB targeting the round window membrane by applying the ultrasound transducer to the tympanic bulla. In the present study, we further extended the use of this technology to enhance drug delivery to the inner ear by introducing the ultrasound transducer into the external auditory canal (EAC) or applying it to the skull. Using a 3-dimensional-printed diffusion apparatus mimicking the pathway for ultrasound passing through and reaching the middle ear cavity in vitro, the models simulating the transcanal and transcranial approach demonstrated 4.8-fold- and 3.7-fold-higher delivery efficiencies, respectively. In an in vivo model of guinea pigs, by filling tympanic bulla with microbubbles and biotin-FITC, USMB applied transcanally and transcranially induced 2.8-fold and 1.5-fold increases in biotin-FITC delivery efficiencies, respectively. In addition, the gentamicin uptake by cochlear and vestibular hair cells and gentamicin-induced hair cell loss were significantly enhanced following transcanal application of USMB. On the 28th day after transcanal USMB, safety assessment showed no significant changes in the hearing thresholds and the integrity of cochlea. These are the first results to our knowledge to demonstrate the feasibility and support the potential clinical application of applying USMB via EAC to facilitate drug delivery into the inner ear.

摘要

超声空化微泡(USMB)被广泛用于促进药物传递。我们之前的研究通过将超声换能器应用于耳鼓来研究针对圆窗膜的 USMB 靶向作用。在本研究中,我们通过将超声换能器引入外耳道(EAC)或应用于颅骨,进一步扩展了这项技术在增强内耳药物传递方面的应用。使用模拟超声通过并到达体外中耳腔的途径的 3D 打印扩散装置,模拟经耳道和经颅途径的模型分别显示出 4.8 倍和 3.7 倍的更高传递效率。在豚鼠的体内模型中,通过用微泡和生物素-FITC 填充耳鼓,经耳道和经颅应用 USMB 分别诱导生物素-FITC 传递效率增加了 2.8 倍和 1.5 倍。此外,经耳道应用 USMB 后,耳蜗和前庭毛细胞摄取庆大霉素和庆大霉素诱导的毛细胞损失显著增加。在经耳道 USMB 后的第 28 天,安全性评估显示听力阈值和耳蜗完整性没有显著变化。这些是我们所知的首次证明通过 EAC 应用 USMB 促进药物进入内耳的可行性和支持其潜在临床应用的结果。