Treatment failure is largely driven by the Blood-Brain Barrier (BBB), which restricts the delivery of most conventional therapeutics and shields invasive tumor regions from systemic drugs.
First-pass extracted concept
blood-brain barrier
Aliases
BBB
Evidence Snippets
Ultrasound-assisted drug delivery systems (US-DDS) leverage MB/NB cavitation effects to enhance chemotherapeutic agent delivery efficiency, overcome biological barriers, including the blood-brain barrier, and modulate immune responses.
Neurological gliomas, as the most common and deadly primary brain tumors, face two major therapeutic obstacles: the blockade of the blood-brain barrier (BBB) and high tumor heterogeneity.
The blood brain barrier (BBB) plays a critically important role in the regulation of central nervous system (CNS) homeostasis, but also represents a major limitation to treatments of brain pathologies.
These clots, blood cells but also blood derivatives in the perivascular space, destabilize the blood-brain barrier from the brain parenchyma side.
The review centers on translational brain barrier biology across the blood-brain barrier (BBB), blood-CSF barrier, neurovascular unit (NVU), transport biology, tight junctions, development, and imaging.
Supporting Sources
Linked Claims
In glioblastoma, treatment failure is largely driven by the blood-brain barrier because it restricts delivery of most conventional therapeutics and shields invasive tumor regions from systemic drugs.
Recent inorganic nanoparticles are designed to cross the blood-brain barrier and target glioblastoma.
Ultrasound-assisted drug delivery systems use microbubble or nanobubble cavitation to enhance chemotherapeutic delivery, overcome biological barriers including the blood-brain barrier, and modulate immune responses.
Ultrasound-assisted drug delivery systems (US-DDS) leverage MB/NB cavitation effects to enhance chemotherapeutic agent delivery efficiency, overcome biological barriers, including the blood-brain barrier, and modulate immune responses.
Gliomas face two major therapeutic obstacles: blood-brain barrier blockade and high tumor heterogeneity.
Blood cells and blood derivatives in the perivascular space are proposed to destabilize the blood-brain barrier and weaken the neurovascular unit after IVH/rt-PA-associated clot dissolution.
This review synthesizes translational research themes in brain barrier biology spanning the blood-brain barrier, blood-cerebrospinal fluid barrier, neurovascular unit, transport biology, tight junctions, development, and imaging.