SBIR-STTR Award

Development Of An Organotypic In-Vitro Model Of The Blood-Brain Barrier
Award last edited on: 7/19/10

Sponsored Program
SBIR
Awarding Agency
NIH : NINDS
Total Award Amount
$190,632
Award Phase
1
Solicitation Topic Code
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Principal Investigator
Thomas Neumann

Company Information

VisionGate Inc (AKA: Vision Gate Inc)

10220 South 51st Street Suite 2
Phoenix, AZ 85044
   (602) 368-2118
   info@visiongate3d.com
   www.visiongate3d.com
Location: Single
Congr. District: 09
County: Maricopa

Phase I

Contract Number: 1R43NS070440-01
Start Date: 4/1/10    Completed: 3/31/11
Phase I year
2010
Phase I Amount
$190,632
The blood-brain barrier (BBB) is a tight barrier formed by microvessels and capillaries controlling the passage of nutrients, fluids, metabolic products and drugs between the blood and the brain. Imbalance of the BBB is involved in a number of major pathologies afflicting the brain, such as Alzheimer's disease, stroke, and cancer. Although neurotherapeutics are among the largest and fastest growing markets in the pharmaceutical industry, progress is currently impaired by the lack of in-vitro assays that reliably predict in-vivo BBB permeability. None of the existing models adequately replicates the in-vivo organotypic microenvironment, which is seen as a key for achieving in-vivo-like functionality. We have previously developed a 3D model for the study of in-vitro angiogenesis, consisting of small fluidic devices with a collagen-filled chamber. We intend to advance our model into an organotypic in-vitro model of the blood-brain barrier with the following main attributes: (1) a tissue-engineered endothelial-cell microvessel, surrounded by pericytes and astrocytes arranged in physiological ratio and architecture; (2) direct contact between endothelial cells, pericytes, and astrocytes; (3) an extracellular matrix (ECM) that resembles the interstitial environment of the CNS; (4) luminal flow providing shear stress to the endothelium; (5) tightly-controlled physical and chemical conditions; (6) a mass- produced, disposable fluidic device that can be adapted for use in existing high-throughput analysis platforms. In Phase 1, we will establish the prototype of a model that comprises a central BBB-microvessel in a brain-specific extracellular matrix, surrounded by pericytes and astrocytes--cells that induce and maintain barrier tightness. In Phase 2 we will pursue the development of a commercial product, including the adaptation of the fluidic device to high- throughput analysis platforms. We predict that our model will facilitate a significant progress in the therapy of a number of devastating diseases.

Public Health Relevance:
A major obstacle to the successful development of drugs that treat diseases of the central nervous system (CNS) such as Alzheimer's, Parkinson's, stroke, brain cancers, and metastasis to the brain, is the inability of these drugs to cross the blood-brain barrier (BBB). This natural barrier, whose function is to protect CNS from potentially harmful molecules, unfortunately also prevents penetration of potentially beneficial drugs. The difficulty in assessing whether or not drugs will cross the BBB makes the development of new neurologic drugs a difficult and unusually unsuccessful task. For this reason, in- vitro models that successfully predict in vivo drug BBB-permeability are of paramount importance for the neuropharmaceutical industry. We propose the development of an in- vitro model that mimics the natural BBB architecture, including perfused microvessels This model promises to become a valuable system for drug developers as well as to CNS researchers in academia.

Thesaurus Terms:
3d Modeling; Academia; Adventitial Cell; Alzheimer; Alzheimer Disease; Alzheimer Sclerosis; Alzheimer Syndrome; Alzheimer's; Alzheimer's Disease; Alzheimers Dementia; Alzheimers Disease; Apoplexy; Architecture; Area; Astrocytes; Astrocytus; Astroglia; Blood; Blood - Brain Barrier Anatomy; Blood Capillaries; Blood-Brain Barrier; Brain; Cns Diseases; Cns Disorder; Cancer Of Brain; Cancers; Capillaries; Capillary; Capillary, Unspecified; Cell-Extracellular Matrix; Cells; Central Nervous System; Central Nervous System Diseases; Central Nervous System Disorders; Cerebral Stroke; Cerebrovascular Apoplexy; Cerebrovascular Stroke; Cerebrovascular Accident; Chemicals; Co-Culture; Cocultivation; Coculture; Coculture Techniques; Collagen; Dementia, Alzheimer Type; Dementia, Primary Senile Degenerative; Dementia, Senile; Development; Devices; Dextrans; Disease; Disorder; Drug Industry; Drugs; Ecm; Electrical Resistance; Encephalon; Encephalons; Endothelial Cells; Endothelium; Engineering / Architecture; Environment; Evaluation; Extracellular Matrix; Extravasation; Gel; Hemato-Encephalic Barrier; Human; Human, General; Idiopathic Parkinson Disease; In Vitro; Industry; Industry, Pharmaceutic; Investigators; Label; Leakage; Lewy Body Parkinson Disease; Liquid Substance; Malignant Neoplasms; Malignant Tumor; Malignant Tumor Of The Brain; Malignant Neoplasm Of Brain; Man (Taxonomy); Man, Modern; Marketing; Measurement; Measures; Medication; Metabolic; Metastasis; Metastasize; Metastatic Neoplasm; Metastatic Tumor; Methods; Methods And Techniques; Methods, Other; Microfluidic Device; Microfluidic Lab-On-A-Chip; Microfluidic Microchips; Modeling; Molecular Weight; Neoplasm Metastasis; Nervous System, Brain; Nervous System, Cns; Neuraxis; Neurologic; Neurological; Nutrient; Oregon; Paralysis Agitans; Parents; Parkinson; Parkinson Disease; Parkinson's; Parkinson's Disease; Parkinsons Disease; Pathology; Penetration; Pericapillary Cell; Pericytes; Perivascular Cell; Permeability; Pharmaceutic Preparations; Pharmaceutical Industry; Pharmaceutical Preparations; Phase; Physiologic; Physiological; Pressure; Pressure- Physical Agent; Primary Parkinsonism; Primary Senile Degenerative Dementia; Production; Protocol; Protocols Documentation; Research Personnel; Researchers; Resistance, Electric; Reticuloendothelial System, Blood; Rouget Cells; Secondary Neoplasm; Secondary Tumor; Spatial Distribution; Spillage; Stroke; Surface; System; System, Loinc Axis 4; Techniques; Testing; Tissue Engineering; Tumor Cell Migration; Vascular Accident, Brain; Angiogenesis; Brain Attack; Cancer Metastasis; Capillary; Cell Type; Cerebral Vascular Accident; Dementia Of The Alzheimer Type; Density; Design; Designing; Dextran; Disease/Disorder; Drug Development; Drug/Agent; Engineered Tissue; Fluid; High Throughput Analysis; In Vitro Assay; In Vitro Model; In Vivo; Interstitial; Liquid; Malignancy; Neoplasm/Cancer; Pressure; Prevent; Preventing; Primary Degenerative Dementia; Prototype; Public Health Relevance; Senile Dementia Of The Alzheimer Type; Shear Stress; Stroke; Three-Dimensional Modeling

Phase II

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
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Phase II Amount
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