Novel magnetic/ultrasound focusing system enhances nanoparticle drug delivery for glioma treatment.
Authors: Chen PY, Liu HL, Hua MY, Yang HW, Huang CY, Chu PC, Lyu LA, Tseng IC, Feng LY, Tsai HC, Chen SM, Lu YJ, Wang JJ, Yen TC, Ma YH, Wu T, Chen JP, Chuang JI, Shin JW, Hsueh C, Wei KC
Malignant glioma is a common and severe primary brain tumor with a high recurrence rate and an extremely high mortality rate within 2 years of diagnosis, even when surgical, radiological, and chemotherapeutic interventions are applied. Intravenously administered drugs have limited use because of their adverse systemic effects and poor blood-brain barrier penetration. Here, we combine 2 methods to increase drug delivery to brain tumors. Focused ultrasound transiently permeabilizes the blood-brain barrier, increasing passive diffusion. Subsequent application of an external magnetic field then actively enhances localization of a chemotherapeutic agent immobilized on a novel magnetic nanoparticle. Combining these techniques significantly improved the delivery of 1,3-bis(2-chloroethyl)-1-nitrosourea to rodent gliomas. Furthermore, the physicochemical properties of the nanoparticles allowed their delivery to be monitored by magnetic resonance imaging (MRI). The resulting suppression of tumor progression without damaging the normal regions of the brain was verified by MRI and histological examination. This noninvasive, reversible technique promises to provide a more effective and tolerable means of tumor treatment, with lower therapeutic doses and concurrent clinical monitoring.
Introduction
Purpose
Drug delivery with BBB opening
Study Objective
To determine whether combining focused ultrasound–induced blood–brain barrier permeabilization with magnetic targeting of drug-loaded magnetic nanoparticles enhances delivery and therapeutic efficacy of 1,3-bis(2-chloroethyl)-1-nitrosourea to rodent gliomas while enabling MRI monitoring.
Animal model / Human subject
Rodent (species not specified; strain not specified; age not specified; sex not specified)
Disease model
malignant glioma (rodent glioma model)
Cargo name and characteristics
1,3-bis(2-chloroethyl)-1-nitrosourea (BCNU), a small-molecule chemotherapeutic immobilized on a novel magnetic nanoparticle (MRI-visible)
Route of administration
intravenous
Outcomes and Safety
Summary of Outcomes
Combination of focused ultrasound to transiently open the blood–brain barrier and an external magnetic field to localize BCNU-loaded magnetic nanoparticles significantly increased drug delivery to rodent gliomas, suppressed tumor progression without damaging normal brain tissue, and allowed MRI monitoring of nanoparticle delivery; the paper does not report or compare multiple focused ultrasound parameter sets or specify which ultrasound parameters were found to be successful.
Safety-related matter
The authors report tumor suppression without damage to normal brain regions verified by MRI and histological examination, and describe the technique as noninvasive, reversible, and more tolerable with lower therapeutic doses, suggesting reduced systemic adverse effects.
Brain Region
Ultrasound Parameters
Focal Characteristics
Focal depth: None, Focal length: None, Aperture size: None
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