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Potential Brain Therapeutics

Award Information
Agency: Department of Health and Human Services
Branch: National Institutes of Health
Contract: 4R44NS043948-02
Agency Tracking Number: NS043948
Amount: $832,041.00
Phase: Phase II
Program: SBIR
Solicitation Topic Code: N/A
Solicitation Number: N/A
Timeline
Solicitation Year: N/A
Award Year: 2003
Award Start Date (Proposal Award Date): N/A
Award End Date (Contract End Date): N/A
Small Business Information
AMERICAN BIOTECHNOLOGY RES CORP 424 E STATE PKY, STE 229
SCHAUMBURG, IL 60173
United States
DUNS: N/A
HUBZone Owned: No
Woman Owned: No
Socially and Economically Disadvantaged: No
Principal Investigator
 ANASTASIOS RAPTIS
 (847) 274-5618
 ANASTRAPTIS@AOL.COM
Business Contact
 BHAVNA VYAS
Phone: (847) 274-5618
Email: BVYASB@AOL.COM
Research Institution
N/A
Abstract

DESCRIPTION (provided by applicant): Use of botanical products such as
exogenous antioxidants has gained considerable momentum in the last few years
in therapy of human degenerative diseases. Among these antioxidants, tumeric,
neem, guggul, alpha-tocopherol, Beta-carotene, and ascorbic acid have been
shown to have a special relevance in maintaining the redox equilibrium in
various cell types, including those of the nervous system. They have a strong
commercial potential as dietary supplements or as potential pharmaceutical
agents in the treatment of various human degenerative diseases.

In Phase I of the project, our aim is to develop cell free in vitro assay
systems for the measurement of the biological activities of these compounds,
using biological molecules present in their free form as targets of reactive
oxygen species (ROS). In the development of these methods, we will take into
account the critical factors that may influence the results, for example: (a)
different types of ROS; (b) different systems for the generation of these ROS;
(c) different molecular targets of ROS, and (d) different methods for the
measurements of the molecular lesions produced by the ROS.

In Phase II of the proposed project, we will optimize assay systems in which
the target molecule is present as an integral part of the cell (intact-cell
systems). The intact-cell systems will use functional neurons and astrocytes in
which the effects of ROS and antioxidants will be measured by their effects on
the structural integrity of the mitochondrial DNA. Also, in Phase Il, we will
develop an approach for assigning antioxidant indices to mixtures of
antioxidants, using a minimum number of different assays.

* Information listed above is at the time of submission. *

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