Abstract
By way of its intrinsic structural and physiological properties, the blood-brain barrier (BBB) represents a formidable obstacle to the delivery of drug to the central nervous system. The treatments of many diseases affecting the central nervous system is thereby complicated by the aspect of delivery, that is, insuring that the therapeutic molecule will reach the target cell in sufficient concentration, and in a suitable timing for the treatment to be effective. Although many different etiologic conditions will be affected by this delivery impediment, in no other condition has it been as extensively documented as in malignant brain tumors. Brain tumor is the prototypical situation through which one can best exemplify the problematic of delivery across the blood-brain barrier. We will therefore frequently refer to this particular problematic, acknowledging the fact that a lot of research endeavour in this field was undertaken as alternate strategies in the treatment of brain tumors. However, by no means will we imply that these strategies should be restricted to the treatment of cerebral malignancies.
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Abbreviations
- BAT:
-
brain adjacent to tumor
- BBB:
-
blood-brain barrier
- BBBD:
-
blood brain barrier disruption
- BCNU:
-
1,3-bis(2-chloroethyl)-1-nitrosourea
- BDT:
-
brain distant to tumor
- CNS:
-
central nervous system
- CSF:
-
cerebrospinal fluid
- CT:
-
computed tomography
- ICP:
-
intracranial pressure
- i.v.:
-
intravenous
- LH:
-
left hemisphere
- MRI:
-
magnetic resonance imaging
- PET:
-
positron emission tomographty
- SPECT:
-
single photon emission computed tomography
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Fortin, D. (2003). Altering the properties of the blood-brain barrier: disruption and permeabilization. In: Prokai, L., Prokai-Tatrai, K. (eds) Peptide Transport and Delivery into the Central Nervous System. Progress in Drug Research, vol 61. Birkhäuser, Basel. https://doi.org/10.1007/978-3-0348-8049-7_5
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DOI: https://doi.org/10.1007/978-3-0348-8049-7_5
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