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Ultrasound-mediated antibiotic delivery to in vivo biofilm infections: A Review.
Liu, Jamie D; VanTreeck, Kelly E; Marston, William A; Papadopoulou, Virginie; Rowe, Sarah E.
Afiliação
  • Liu JD; University of North Carolina at Chapel Hill, Microbiology and Immunology, 125 Mason Farm Road, 27599, Chapel Hill, UNITED STATES.
  • VanTreeck KE; University of North Carolina at Chapel Hill, Pharmacoengineering and Molecular Pharmaceutics, 116 Manning Drive, 27599, Chapel Hill, UNITED STATES.
  • Marston WA; University of North Carolina at Chapel Hill, Surgery, 3024 Burnett-Womack Building, 27599, Chapel Hill, UNITED STATES.
  • Papadopoulou V; University of North Carolina at Chapel Hill, Biomedical Engineering, 116 Manning Drive, 27599, Chapel Hill, UNITED STATES.
  • Rowe SE; University of North Carolina at Chapel Hill, Microbiology and Immunology, 125 Mason Farm Road, 27599, Chapel Hill, UNITED STATES OF AMERICA.
Chembiochem ; : e202400181, 2024 Jun 25.
Article em En | MEDLINE | ID: mdl-38924307
ABSTRACT
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chembiochem Assunto da revista: BIOQUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chembiochem Assunto da revista: BIOQUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos