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Development Of Bioelastic Matrices for Drug Delivery

Award Information
Agency: Department of Health and Human Services
Branch: N/A
Contract: N/A
Agency Tracking Number: 22320
Amount: $49,998.00
Phase: Phase I
Program: SBIR
Solicitation Topic Code: N/A
Solicitation Number: N/A
Timeline
Solicitation Year: N/A
Award Year: 1993
Award Start Date (Proposal Award Date): N/A
Award End Date (Contract End Date): N/A
Small Business Information
1075 South 13th Street
Birmingham, AL 35205
United States
DUNS: N/A
HUBZone Owned: No
Woman Owned: No
Socially and Economically Disadvantaged: No
Principal Investigator
 D Channe Gowda
 (205) 934-9510
Business Contact
Phone: () -
Research Institution
N/A
Abstract

The objective of this proposal is the development of degradable, transducible, biocompatible, elastomeric matrices to function as drug delivery systems. Despite continuing interest in the development of polymers, both synthetic and natural, (over a 25-year period), there is yet a need for suitable materials for drug delivery. Such materials would have significant and broad clinical applications including continuous and/or localized delivery of existing therapeutic agents as well as delivery systems for the new proteinaceous agents resulting from genetic engineering. The elastomeric polypeptides utilized in this work are a unique class of polymers designed from repeat sequences which occur in native elastin. These materials are particularly suited for this application since they are constructed of natural amino acids arranged in sequences which occur throughout the body. All data to date indicates the parent polypentapeptide and its gamma-irradiated cross-linked matrix to be biocompatible and totally innocuous. This current data includes the eleven recommended generic biological tests as well as muscle and intraperitoneal implant studies. Our understanding of the science of these materials has progressed to the point that polymers can be designed which exhibit a set of specified physical characteristics. Initial results indicate that the rate of degradation and/or swelling of these matrices could be modulated by the inclusion of various chemical clocks located both within the backbone and side chains. Phase I of this proposal will produce monolith slabs will extend the in vitro studies on controlling the rate of degradation and release of therapeutic agents from these matrices. Phase II will involve studies of degradation and agent release in animal models and biological testing of the materials developed in Phase I.

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

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