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Polymeric microbubbles as delivery vehicles for sensitizers in sonodynamic therapy

McEwan, C., Fowley, Colin, Nomikou, N., McCaughan, Bridgeen, McHale, AP and Callan, J (2014) Polymeric microbubbles as delivery vehicles for sensitizers in sonodynamic therapy. Langmuir, 30 (49). pp. 14926-14930. [Journal article]

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URL: http://www.scopus.com/inward/record.url?eid=2-s2.0-84918789034&partnerID=40&md5=f12b01b4e56b4a30a1e81db9bf0e1f6d

DOI: 10.1021/la503929c

Abstract

Microbubbles (MBs) have recently emerged as promising delivery vehicles for sensitizer drugs in sonodynamic therapy (SDT). The ability to selectively destroy the MB and activate the sensitizer using an external ultrasound trigger could provide a minimally invasive and highly targeted therapy. While lipid MBs have been approved for use as contrast agents in diagnostic ultrasound, the attachment of sensitizer drugs to their surface results in a significant reduction in particle stability. In this Article, we prepare both lipid and polymer (PLGA) MBs with rose bengal attached to their surface and demonstrate that PLGA MB conjugates are significantly more stable than their lipid counterparts. In addition, the improved stability offered by the PLGA shell does not hinder their selective destruction using therapeutically acceptable ultrasound intensities. Furthermore, we demonstrate that treatment of ectopic human tumors (BxPC-3) in mice with the PLGA MB-rose bengal conjugate and ultrasound reduced tumor volume by 34 4 days after treatment while tumors treated with the conjugate alone increased in volume by 48 over the same time period. Therefore, PLGA MBs may offer a more stable alternative to lipid MBs for the site specific delivery of sensitizers in SDT. (Graph Presented). © 2014 American Chemical Society.

Item Type:Journal article
Keywords:Copolymers; Diagnosis; Polymers; Tumors; Ultrasonics, Delivery vehicle; Diagnostic ultrasound; Minimally invasive; Particle stability; Selective destruction; Selectively destroy; Sonodynamic therapy; Ultrasound intensity, Drug therapy, coumarin; coumarin derivative, animal; cell line; cell survival; chemical structure; drug delivery system; female; HeLa cell line; human; microbubble; mouse; ultrasound; ultrasound therapy; Uterine Neoplasms, Animals; Cell Line; Cell Survival; Coumarins; Drug Delivery Systems; Female; HeLa Cells; Humans; Mice; Microbubbles; Molecular Structure; Ultrasonic Therapy; Ultrasonics; Uterine Neoplasms
Faculties and Schools:Faculty of Life and Health Sciences > School of Pharmacy and Pharmaceutical Science
Faculty of Life and Health Sciences
Research Institutes and Groups:Biomedical Sciences Research Institute
Biomedical Sciences Research Institute > Pharmacy & Pharmaceutical Sciences
ID Code:34136
Deposited By: Dr Bridgeen Callan
Deposited On:06 Apr 2016 13:42
Last Modified:06 Apr 2016 13:42

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