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超声介导的胶束药物递送。

Ultrasound-mediated micellar drug delivery.

机构信息

Department of Bioengineering, University of Utah, Salt Lake City, Utah 84112, USA.

出版信息

Int J Hyperthermia. 2012;28(4):374-85. doi: 10.3109/02656736.2012.665567.


DOI:10.3109/02656736.2012.665567
PMID:22621738
Abstract

During the last decade, nanomedicine has emerged as a new field of medicine that utilises nanoscale materials for delivery of drugs, genes and imaging agents. The efficiency of drug delivery may be enhanced by the application of directed energy, which provides for drug targeting and enhanced intracellular uptake. In this paper, we present a review of recent advances in the ultrasound-mediated drug delivery with the emphasis on polymeric micelles as tumour-targeted drug carriers. This new modality of drug targeting to tumours is based on the drug encapsulation in polymeric micelles followed by a localised release at the tumour site triggered by focused ultrasound. The rationale behind this approach is that drug encapsulation in micelles decreases systemic concentration of free drug and provides for a passive drug targeting to tumours via the enhanced permeability and retention (EPR) effect, therefore reducing unwanted drug interactions with healthy tissues. Ultrasound affects micellar drug delivery on various levels. Mild hyperthermia induced by ultrasound may enhance micelle extravasation into tumour tissue; mechanical action of ultrasound results in drug release from micelles and enhances the intracellular uptake of both released and encapsulated drug. In addition, polymeric micelles sensitise multidrug resistant (MDR) cells to the action of drugs.

摘要

在过去的十年中,纳米医学作为一门新兴的医学领域,利用纳米级材料来输送药物、基因和成像剂。通过应用定向能量,可以提高药物输送的效率,从而实现药物靶向和增强细胞内摄取。本文综述了超声介导的药物输送的最新进展,重点介绍了作为肿瘤靶向药物载体的聚合物胶束。这种新的肿瘤药物靶向模式是基于将药物包裹在聚合物胶束中,然后在肿瘤部位通过聚焦超声触发局部释放。这种方法的基本原理是,药物包封在胶束中可以降低游离药物的全身浓度,并通过增强的通透性和保留(EPR)效应实现被动的肿瘤靶向,从而减少与健康组织的不必要的药物相互作用。超声在多个层面上影响胶束药物输送。超声诱导的温和热疗可增强胶束向肿瘤组织的外渗;超声的机械作用导致药物从胶束中释放,并增强释放和包裹药物的细胞内摄取。此外,聚合物胶束使多药耐药(MDR)细胞对药物的作用敏感。

相似文献

[1]
Ultrasound-mediated micellar drug delivery.

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[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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Expert Opin Drug Deliv. 2010-2

引用本文的文献

[1]
Acoustomechanically activatable liposomes for ultrasonic drug uncaging.

bioRxiv. 2023-10-25

[2]
Curcumin-Loaded PnBA--POEGA Nanoformulations: A Study of Drug-Polymer Interactions and Release Behavior.

Int J Mol Sci. 2023-2-27

[3]
Ultrasonic Microbubble Cavitation Enhanced Tissue Permeability and Drug Diffusion in Solid Tumor Therapy.

Pharmaceutics. 2022-8-6

[4]
Mechanistic Insights and Therapeutic Delivery through Micro/Nanobubble-Assisted Ultrasound.

Pharmaceutics. 2022-2-22

[5]
Ultrasound-Responsive Materials for Drug/Gene Delivery.

Front Pharmacol. 2020-1-31

[6]
Micro/nano-bubble-assisted ultrasound to enhance the EPR effect and potential theranostic applications.

Theranostics. 2020

[7]
Investigation of drug release modulation from poly(2-oxazoline) micelles through ultrasound.

Sci Rep. 2018-7-2

[8]
A review of low-intensity ultrasound for cancer therapy.

Ultrasound Med Biol. 2015-4

[9]
Nanodrug-enhanced radiofrequency tumor ablation: effect of micellar or liposomal carrier on drug delivery and treatment efficacy.

PLoS One. 2014-8-18

[10]
Multifunctional polymeric micelles for delivery of drugs and siRNA.

Front Pharmacol. 2014-4-25

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