SBIR/STTR Research Award

Surface Modification to Improve Breast Prostheses

Award identifier bccd48192ec9d8a313748db3d2630fd8efda6e3d7e3fcb630e24671cfab92c45Awarding agency Department of Health and Human Services

Award amount

$750,000

Program and phase

SBIR · Phase II

Award year

1995

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Award details

Awarding agency
Department of Health and Human Services
Branch
Not reported
Recipient company
SURMODICS, INC.
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
Not reported
Topic code
Not reported

Research abstract

There are currently no rapid and reliable in vitro assays that measure the metastatic activity of cells. In this project, we will develop an improved Boyden chamber chemoinvasion assay. The Boyden chamber chemoinvasion assay will utilize Transwell¿ membranes with a defined basement membrane overlayer that will allow in vitro assays for metastatic cells to be conducted with greater speed, reproducability, and sensitivity than existing assays. The chemoinvasion assays evaluate the invasive activity of metastatic cells by quantitating their ability to respond to a chemoattractant by penetrating a layer of reconstituted basement membrane (RBM). Several recent papers which utilize Matrigel¿ as an RBM preparation have shown that this assay can be conducted in 6 hours and clearly discriminates between invasive and non-invasive cells. However, there is considerable assay variability, which is caused by l) variability in the Matrigel overlayer and 2) poor adherence of Matrigel to the polycarbonate membrane (resulting in gaps through which non-metastatic cells can migrate). During Phase I, patented BSI photochemistry will be used to covalently couple type IV collagen and heparin onto the polycarbonate membranes with the expectation of greatly improving the adherence of RBM to the membrane. Also, initial experiments will be conducted to develop a defined RBM preparation to replace Matrigel. Modified polycarbonate membranes overlaid with Matrigel and defined RBM compositions will be evaluated with metastatic and non-metastatic cell lines. Phase II studies will complete the development of a defined RBM preparation.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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