Effects of Focused-Ultrasound-and-Microbubble-Induced Blood-Brain Barrier Disruption on Drug Transport under Liposome-Mediated Delivery in Brain Tumour: A Pilot Numerical Simulation Study

Focused ultrasound (FUS) coupled with microbubbles (MB) has been found to be a promising approach to disrupt the blood-brain barrier (BBB). However, how this disruption affects drug transport remains unclear. In this study, drug transport in combination therapy of liposomes and FUS-MB-induced BBB di...

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Main Author: Wenbo Zhan (Author)
Format: Book
Published: MDPI AG, 2020-01-01T00:00:00Z.
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100 1 0 |a Wenbo Zhan  |e author 
245 0 0 |a Effects of Focused-Ultrasound-and-Microbubble-Induced Blood-Brain Barrier Disruption on Drug Transport under Liposome-Mediated Delivery in Brain Tumour: A Pilot Numerical Simulation Study 
260 |b MDPI AG,   |c 2020-01-01T00:00:00Z. 
500 |a 1999-4923 
500 |a 10.3390/pharmaceutics12010069 
520 |a Focused ultrasound (FUS) coupled with microbubbles (MB) has been found to be a promising approach to disrupt the blood-brain barrier (BBB). However, how this disruption affects drug transport remains unclear. In this study, drug transport in combination therapy of liposomes and FUS-MB-induced BBB disruption (BBBD) was investigated based on a multiphysics model. A realistic 3D brain tumour model extracted from MR images was applied. The results demonstrated the advantage of liposomes compared to free doxorubicin injection in further improving treatment when the BBB is opened under the same delivery conditions using burst sonication. This improvement was mainly due to the BBBD-enhanced transvascular transport of free doxorubicin and the sustainable supply of the drug by long-circulating liposomes. Treatment efficacy can be improved in different ways. Disrupting the BBB simultaneously with liposome bolus injection enables more free drug molecules to cross the vessel wall, while prolonging the BBBD duration could accelerate liposome transvascular transport for more effective drug release. However, the drug release rate needs to be well controlled to balance the trade-off among drug release, transvascular exchange and elimination. The results obtained in this study could provide suggestions for the future optimisation of this FUS-MB−liposome combination therapy against brain cancer. 
546 |a EN 
690 |a blood-brain barrier disruption 
690 |a brain tumour 
690 |a drug transport 
690 |a focused ultrasound 
690 |a liposome-mediated delivery 
690 |a mathematical model 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceutics, Vol 12, Iss 1, p 69 (2020) 
787 0 |n https://www.mdpi.com/1999-4923/12/1/69 
787 0 |n https://doaj.org/toc/1999-4923 
856 4 1 |u https://doaj.org/article/b51bfc00b80347449a850e00ce51a841  |z Connect to this object online.