Brain Delivery of Cisplatin Using Microbubbles in Combination with Ultrasound as an Effective Therapy for Glioblastoma

Glioblastoma is a highly invasive and fatal disease. Temozolomide, a blood-brain barrier (BBB)-penetrant therapeutic agent currently used for glioblastoma, does not exhibit sufficient therapeutic effect. Cisplatin (CDDP), a versatile anticancer drug, is not considered a therapeutic option for gliobl...

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Main Authors: Fumiko Hagiwara (Author), Daiki Omata (Author), Lisa Munakata (Author), Saori Kageyama (Author), Kazuo Maruyama (Author), Nobuki Kudo (Author), Ryo Suzuki (Author)
Format: Book
Published: MDPI AG, 2023-11-01T00:00:00Z.
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001 doaj_c65ceb1e7dc246b4bbe5fb81aac8b045
042 |a dc 
100 1 0 |a Fumiko Hagiwara  |e author 
700 1 0 |a Daiki Omata  |e author 
700 1 0 |a Lisa Munakata  |e author 
700 1 0 |a Saori Kageyama  |e author 
700 1 0 |a Kazuo Maruyama  |e author 
700 1 0 |a Nobuki Kudo  |e author 
700 1 0 |a Ryo Suzuki  |e author 
245 0 0 |a Brain Delivery of Cisplatin Using Microbubbles in Combination with Ultrasound as an Effective Therapy for Glioblastoma 
260 |b MDPI AG,   |c 2023-11-01T00:00:00Z. 
500 |a 10.3390/ph16111599 
500 |a 1424-8247 
520 |a Glioblastoma is a highly invasive and fatal disease. Temozolomide, a blood-brain barrier (BBB)-penetrant therapeutic agent currently used for glioblastoma, does not exhibit sufficient therapeutic effect. Cisplatin (CDDP), a versatile anticancer drug, is not considered a therapeutic option for glioblastoma due to its low BBB permeability. We previously investigated the utility of microbubbles (MBs) in combination with ultrasound (US) in promoting BBB permeability and reported the efficacy of drug delivery to the brain using a minimally invasive approach. This study aimed to evaluate the feasibility of CDDP delivery to the brain using the combination of MBs and US for the treatment of glioblastoma. We used mice that were implanted with glioma-261 GFP-Luc cells expressing luciferase as the glioblastoma model. In this model, after tumor inoculation, the BBB opening was induced using MBs and US, and CDDP was simultaneously administered. We found that the CDDP concentrations were higher at the glioblastoma site where the US was applied, although CDDP normally cannot pass through the BBB. Furthermore, the survival was longer in mice treated with CDDP delivered via MBs and US than in those treated with CDDP alone or those that were left untreated. These results suggest that the combination of MBs and US is an effective antitumor drug delivery system based on BBB opening in glioblastoma therapy. 
546 |a EN 
690 |a blood-brain barrier 
690 |a microbubble 
690 |a ultrasound 
690 |a drug delivery system 
690 |a cisplatin 
690 |a glioblastoma 
690 |a Medicine 
690 |a R 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceuticals, Vol 16, Iss 11, p 1599 (2023) 
787 0 |n https://www.mdpi.com/1424-8247/16/11/1599 
787 0 |n https://doaj.org/toc/1424-8247 
856 4 1 |u https://doaj.org/article/c65ceb1e7dc246b4bbe5fb81aac8b045  |z Connect to this object online.