Pitt Shield

Nanoparticle-Based Combinational Strategies for Overcoming the Blood-Brain Barrier and Blood-Tumor Barrier.

Authors: Lim SH, Yee GT, Khang D

The blood-brain barrier (BBB) and blood-tumor barrier (BTB) pose substantial challenges to efficacious drug delivery for glioblastoma multiforme (GBM), a primary brain tumor with poor prognosis. Nanoparticle-based combinational strategies have emerged as promising modalities to overcome these barriers and enhance drug penetration into the brain parenchyma. This review discusses various nanoparticle-based combinatorial approaches that combine nanoparticles with cell-based drug delivery, viral drug delivery, focused ultrasound, magnetic field, and intranasal drug delivery to enhance drug permeability across the BBB and BTB. Cell-based drug delivery involves using engineered cells as carriers for nanoparticles, taking advantage of their intrinsic migratory and homing capabilities to facilitate the transport of therapeutic payloads across BBB and BTB. Viral drug delivery uses engineered viral vectors to deliver therapeutic genes or payloads to specific cells within the GBM microenvironment. Focused ultrasound, coupled with microbubbles or nanoparticles, can temporarily disrupt the BBB to increase drug permeability. Magnetic field-guided drug delivery exploits magnetic nanoparticles to facilitate targeted drug delivery under an external magnetic field. Intranasal drug delivery offers a minimally invasive avenue to bypass the BBB and deliver therapeutic agents directly to the brain via olfactory and trigeminal pathways. By combining these strategies, synergistic effects can enhance drug delivery efficiency, improve therapeutic efficacy, and reduce off-target effects. Future research should focus on optimizing nanoparticle design, exploring new combination strategies, and advancing preclinical and clinical investigations to promote the translation of nanoparticle-based combination therapies for GBM.

Introduction

Purpose Drug delivery with BBB opening
Study Objective To review nanoparticle-based combination strategies to overcome the blood–brain and blood–tumor barriers and enhance drug delivery for glioblastoma treatment.
Disease model glioblastoma multiforme (GBM)
Cargo name and characteristics Nanoparticles (various platforms) — used as carrier vehicles for therapeutic payloads to cross the BBB/BTB, including small‑molecule drugs, proteins/biologics, and gene therapies delivered via viral vectors (e.g., AAV); includes magnetic nanoparticles for magnetically guided delivery and nanoparticles paired with focused ultrasound or intranasal delivery.
Route of administration Intranasal; focused ultrasound-mediated BBB disruption (with microbubbles/nanoparticles); magnetic field-guided delivery of magnetic nanoparticles; cell-based carrier delivery; viral vector delivery

Outcomes and Safety

Summary of Outcomes Nanoparticle-based combination strategies (with focused ultrasound/microbubbles, magnetic-field guidance, cell- or viral-carriers, or intranasal delivery) increase BBB/BTB permeability and enhance targeted drug delivery and therapeutic efficacy against glioblastoma while reducing off-target effects. The paper is a review and did not report or test specific focused ultrasound parameter sets.
Safety-related matter The review highlights safety considerations including potential toxicity and long-term effects, immunogenicity of bacterial/viral vectors, and off-target/systemic toxicity, and states clinical trials aim to validate safety and dosing; no specific adverse effects are reported.

Brain Region

Visualization unavailable

Ultrasound Parameters

Focal Characteristics Focal depth: None; Focal length: None; Aperture size: None

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