USA flag logo/image

An Official Website of the United States Government

Ultrasound Contrast Agents for Inflammation and Angiogenesis

Award Information

Agency:
Department of Health and Human Services
Branch:
N/A
Award ID:
89095
Program Year/Program:
2008 / SBIR
Agency Tracking Number:
EB007857
Solicitation Year:
N/A
Solicitation Topic Code:
N/A
Solicitation Number:
N/A
Small Business Information
TARGESON, LLC
850 CARLINS WAY CHARLOTTESVILLE, VA 22903-7666
View profile »
Woman-Owned: No
Minority-Owned: No
HUBZone-Owned: No
 
Phase 1
Fiscal Year: 2008
Title: Ultrasound Contrast Agents for Inflammation and Angiogenesis
Agency: HHS
Contract: 1R43EB007857-01A1
Award Amount: $99,729.00
 

Abstract:

DESCRIPTION (provided by applicant): We propose to develop molecular imaging probes for imaging angiogenesis and inflammation using contrast-enhanced ultrasound. These probes are gas-encapsulated microbubbles that can be coated with ligands specific for mo lecular markers of disease using robust covalent coupling chemistries. The agents proposed here will be used to image the severity and spatial extent of disease in preclinical animal models, and have strong potential for clinical translation. We propose to develop microbubbles bearing versatile covalent ligand-coupling chemistries, which will allow preclinical users to couple their own ligands. Additionally, we will develop two pre-targeted agents bearing covalently bound ligands specific for biomarkers of inflammation and angiogenesis. Although site-targeted microbubble contrast agents are currently commercially available for preclinical research, these agents utilize time consuming and potentially immunogenic biotin/avidin ligand coupling chemistry. Covale nt coupling of the ligand to the agent surface eliminates the biotin/avidin system, greatly increasing the convenience and utility of the agents. The goals of this proposal are (1) to develop covalent ligand coupling strategies suitable for a variety of li gand classes, (2) to create ultrasound contrast agents bearing covalently bound ligands specific for biomarkers of inflammation and angiogenesis, and (3) to quantitatively test targeted adhesion of these ligand-bearing agents to relevant molecular targets in vitro. We will test two ligands for biomarkers of inflammation and angiogenesis, respectively: a selectin-binding oligosaccharide (sialyl Lewisx) and a VEGF receptor binding single-chain VEGF construct. The selectins are critically involved in numerous inflammatory disorders, and have been implicated in therapeutic and pathogenic angiogenesis. With the goal of producing convenient probes for imaging inflammation and angiogenesis, we propose to construct microbubbles bearing covalently bound sLex, a singl e-chain VEGF, or a combination of both ligands. These ligands are superior to antibodies commonly used as ligands due to the lack of immunogenicity, species-independence, and small size. Additionally, sLex possesses an excellent ability to mediate high-eff iciency retention of microparticles, even under conditions of rapid blood flow. We hypothesize that dual-targeted microbubbles bearing both scVEGF and sLex may exhibit synergistic adhesion resulting in enhanced microbubble retention to angiogenic endotheli um expressing E- selectin and VEGFR-2. The rapid bond kinetics of sLex can mediate initial tethering of the agent, and once localized at the endothelial surface scVEGF can mediate firm adhesion to VEGF receptors. Microbubbles bearing the sLex ligand alone will be useful for imaging a wide variety of inflammatory disorders, and VEGF- bearing microbubbles will be useful for imaging general angiogenic processes. The knowledge gained will serve to develop a universal targeted microbubble platform able to be con jugated to user-selected ligands using a robust covalent coupling system, and will provide a platform for subsequent pre-targeted formulations. Project Narrative Molecular imaging of biomarker expression can greatly accelerate the pace of drug discovery, a nd has tremendous potential for clinical translation. The development of microbubbles bearing a robust and versatile covalent ligand-coupling chemistry will expand the utility of these agents in preclinical research, and is necessary for subsequent clinica l implementation. Additionally, microbubbles pre-targeted to biomarkers of inflammation and angiogenesis will serve as a convenient and user-friendly product for preclinical molecular imaging.

Principal Investigator:

Joshua J. Rychak
4349770062
JOSHUA.RYCHAK@TARGESON.COM

Business Contact:


joshua.rychak@targeson.com
Small Business Information at Submission:

TARGESON, LLC
TARGESON, LLC 325 Barracks Hill Road CHARLOTTESVILLE, VA 22901

EIN/Tax ID: 127006058
DUNS: N/A
Number of Employees: N/A
Woman-Owned: No
Minority-Owned: No
HUBZone-Owned: No