4.5 Article

Characterization of Brain-Targeted Drug Delivery Enhanced by a Combination of Lipid-Based Microbubbles and Non-Focused Ultrasound

Journal

JOURNAL OF PHARMACEUTICAL SCIENCES
Volume 109, Issue 9, Pages 2827-2835

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.xphs.2020.06.008

Keywords

Blood-brain barrier (BBB); Controlled delivery; Drug delivery system(s); Lipid-based formulation(s); Microparticle(s); Permeability; Targeted drug delivery; Theranostic; Ultrasound

Funding

  1. JSPS KAKENHI [JP15J10508, 17H07119, 19K20717]
  2. AMED [JP16dm0107115h0001]
  3. Grants-in-Aid for Scientific Research [17H07119, 19K20717] Funding Source: KAKEN

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The combination of focused ultrasound (FUS) and microbubbles, an ultrasound (US) contrast agent, has attracted much attention for its ability to open the blood brain barrier (BBB) and deliver drugs to the brain parenchyma. FUS can concentrate US energy in a restricted space, whereas non-focused US can affect a wide area of tissue. Non-focused US is also promising for drug delivery to the brain and other tissues. We have previously developed lipid-based microbubbles (LBs), and demonstrated that nonfocused US and LBs have potential for drug delivery to tumor tissues. In this study, to achieve efficient and safe brain-targeted drug delivery, we evaluated the characteristics of BBB opening using non-focused US and LBs. Our results indicated that LBs could induce BBB opening with non-focused US. US frequency and intensity affected the efficiency of BBB opening and brain damage, and showed that the dose of LBs was also related to the efficiency of BBB opening. Furthermore, the combination of non-focused US and LBs could deliver macromolecules at 2000 kDa to the brain, and the induction of BBB opening was found to be reversible. These results suggest that the combination of non-focused US and LBs has potential as a brain-targeted drug delivery system. (C) 2020 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved.

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