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@ARTICLE{Vanbilloen:277870,
author = {W. J. F. Vanbilloen and J. S. Rechberger and J. B. Anderson
and L. F. Nonnenbroich$^*$ and L. Zhang and D. J. Daniels},
title = {{N}anoparticle {S}trategies to {I}mprove the {D}elivery of
{A}nticancer {D}rugs across the {B}lood-{B}rain {B}arrier to
{T}reat {B}rain {T}umors.},
journal = {Pharmaceutics},
volume = {15},
number = {7},
issn = {1999-4923},
address = {Basel},
publisher = {MDPI},
reportid = {DKFZ-2023-01538},
pages = {1804},
year = {2023},
abstract = {Primary brain and central nervous system (CNS) tumors are a
diverse group of neoplasms that occur within the brain and
spinal cord. Although significant advances in our
understanding of the intricate biological underpinnings of
CNS neoplasm tumorigenesis and progression have been made,
the translation of these discoveries into effective
therapies has been stymied by the unique challenges
presented by these tumors' exquisitely sensitive location
and the body's own defense mechanisms (e.g., the brain-CSF
barrier and blood-brain barrier), which normally protect the
CNS from toxic insult. These barriers effectively prevent
the delivery of therapeutics to the site of disease. To
overcome these obstacles, new methods for therapeutic
delivery are being developed, with one such approach being
the utilization of nanoparticles. Here, we will cover the
current state of the field with a particular focus on the
challenges posed by the BBB, the different nanoparticle
classes which are under development for targeted CNS tumor
therapeutics delivery, and strategies which have been
developed to bypass the BBB and enable effective
therapeutics delivery to the site of disease.},
subtyp = {Review Article},
keywords = {blood–brain barrier (Other) / brain tumor (Other) /
chemotherapy (Other) / drug delivery (Other) / extracellular
vesicle (Other) / glioma (Other) / liposome (Other) /
nanoparticle (Other) / targeted therapy (Other)},
cin = {B310 / HD01},
ddc = {610},
cid = {I:(DE-He78)B310-20160331 / I:(DE-He78)HD01-20160331},
pnm = {312 - Funktionelle und strukturelle Genomforschung
(POF4-312)},
pid = {G:(DE-HGF)POF4-312},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:37513992},
pmc = {pmc:PMC10383584},
doi = {10.3390/pharmaceutics15071804},
url = {https://inrepo02.dkfz.de/record/277870},
}