Ultrasound-Mediated Antibiotic Delivery to In Vivo Biofilm Infections: A Review

被引:1
|
作者
Liu, Jamie D. [1 ]
Van Treeck, Kelly E. [2 ,3 ,4 ]
Marston, William A. [5 ]
Papadopoulou, Virginie [2 ,3 ,6 ]
Rowe, Sarah E. [1 ]
机构
[1] Univ N Carolina, Dept Microbiol & Immunol, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Joint Dept Biomed Engn, Chapel Hill, NC 27599 USA
[3] North Carolina State Univ, Chapel Hill, NC 27599 USA
[4] Univ N Carolina, Eshelman Sch Pharm, Chapel Hill, NC 27599 USA
[5] Univ N Carolina, Dept Surg, Chapel Hill, NC 27599 USA
[6] Univ N Carolina, Dept Radiol, Chapel Hill, NC 27599 USA
关键词
Ultrasound drug delivery; Cavitation; Sonobactericide; Persister cells; Antibiotic tolerance; BLOOD-BRAIN-BARRIER; ACOUSTIC DROPLET VAPORIZATION; SUB-INHIBITORY CONCENTRATIONS; STAPHYLOCOCCUS-AUREUS; PERSISTER CELLS; BACTERIAL PERSISTENCE; CHRONIC WOUNDS; DRUG-DELIVERY; MICROBUBBLES; VANCOMYCIN;
D O I
10.1002/cbic.202400181
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bacterial biofilms are a significant concern in various medical contexts due to their resilience to our immune system as well as antibiotic therapy. Biofilms often require surgical removal and frequently lead to recurrent or chronic infections. Therefore, there is an urgent need for improved strategies to treat biofilm infections. Ultrasound-mediated drug delivery is a technique that combines ultrasound application, often with the administration of acoustically-active agents, to enhance drug delivery to specific target tissues or cells within the body. This method involves using ultrasound waves to assist in the transportation or activation of medications, improving their penetration, distribution, and efficacy at the desired site. The advantages of ultrasound-mediated drug delivery include targeted and localized delivery, reduced systemic side effects, and improved efficacy of the drug at lower doses. This review scrutinizes recent advances in the application of ultrasound-mediated drug delivery for treating biofilm infections, focusing on in vivo studies. We examine the strengths and limitations of this technology in the context of wound infections, device-associated infections, lung infections and abscesses, and discuss current gaps in knowledge and clinical translation considerations.
引用
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页数:21
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