NOVEL TISSUE ENGINEERING MATRICES WITH CONTROLLED MICROS
NOVEL TISSUE ENGINEERING MATRICES WITH CONTROLLED MICROS
批准号:
2796493
负责人:
KRISTI S. ANSETH
金额:
$16.03万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1998
资助国家:
美国
项目状态:
已结题
起止时间:
1998-09-01 至 2001-06-30
关键词:
animal tissue biomaterial compatibility biomaterial development /preparation biomaterial evaluation cartilage transplantation cell proliferation chondrocytes collagen craniofacial extracellular matrix gel hydropathy photochemistry polymers polyvinyls tissue /cell culture tissue engineering tissue support frame
中文摘要
描述
英文摘要
DESCRIPTION
(Adapted from the applicant's abstract) The overall objective of this
proposal is to develop novel polymer networks for tissue engineering that
elicit desired physicochemical properties for the repair or replacement of
craniofacial and orthopaedic cartilage. In particular, this proposal
focuses on the development stage of intelligent matrices with controlled
architectures and gelling techniques that allow imprinting of the cellular
structure in the final network microstructure. The global hypothesis to be
tested is that matrix materials will provide superior performance in tissue
engineering cartilage when they are engineered to: 1) match the physical
and mechanical properties of native cartilage; 2) incorporate cellular
structural information in the hydrogel pores; and 3) allow easy structural
and chemical modification through photochemistry.
Specifically, the aims of the research are as follows. Specific Aim 1: to
develop hydrogel matrices based on poly (vinyl alcohol) (PVA) which have
controlled molecular architecture that allows intelligent engineering of
properties such as mesh size, mechanical behavior, hydrophilicity, and
degradability. Specific Aim 2: to modify further the aforementioned PVA
hydrogels with a novel photografting technique which facilitates initiator
free gelation and grafting of hydrophilic monomers to improve the
immunoprotective properties and mechanical stabilization. Specific Aim 3 to
evaluate these materials for their cellular compatibility (e.g., chondrocyte
proliferation and extracellular matrix formation) and their performance in
the correction of a cartilage defect to restore function (e.g., mechanical
and eventual integrated tissue formation).
期刊论文(0)
专著(0)
科研奖励(0)
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