SBIR/STTR Research Award

Electro-Mechanical Micro-Post Array to Detect In Vitro Muscle Contraction

Award identifier d1b3cce0abdd82f54fa46694ede993f7175aa59601010f2e1fddc8627fc1c8abAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$99,939

Program and phase

STTR · Phase I

Award year

2006

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Award details

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

Research abstract

DESCRIPTION (provided by applicant): Myomics? technology to be developed in this Phase 1 project is based upon an in vitro skeletal muscle tissue force measurement technique for high throughput screening (HTS) of compounds to attenuate muscle weakness. The technology, termed Patterned Micro-Post-Arrays (P-fPA), is comprised of bioengineered skeletal muscle tissue attached to micro-mechanical sensors in a ninety-six well format to detect muscle contractile forces. Miniature human BioArtificial Muscles (mBAMs) are three-dimensional (3-D) contractile tissues with organized striated skeletal muscle fibers which can generate directed force when electrically stimulated. Myomics? mBAM tissue/sensor composite is well suited for repetitive nondestructive force measurements long term i.e. weeks; the sensors provide physiological data regarding tissue function in response to a drug. Such long term studies can determine cumulative effects of drugs on 3-D tissues which are not apparent in shorter term single cell or monolayer HTS technologies. mBAMs have been successfully engineered to grow within the sensors and generate force using P-fPA prototypes. The purpose of this project is to expand these preliminary studies into reproducible quantitative muscle force measurements for up to 30 days. Briefly, Myomics will (1) determine the optimal micro-post geometry for measuring mBAM passive and active contractile forces; (2) test P-fPA with mBAMs chemically stimulated to contract; (3) incorporate in-plane electrodes into the P-fPA technology; and (4) test P-fPA with mBAMs electrically stimulated to contract. With Myomics? P-fPA technology, the physiological measurement of force generation by mBAMs will not be limited to any particular known biochemical pathway and the measurement of force will be the result of both positive and negative drug effects. Thus, the technology will not only screen compounds for positive muscle growth effects, but will more rapidly eliminate target compounds with adverse side effects. This will lead to a greater chance of success in follow-up preclinical animal and Phase 1 clinical studies. Musculoskeletal disorders affect greater than 60 million individuals in the U.S. today and the annual health care costs resulting from skeletal muscle weakness is hundreds of billions of dollars. Few drugs are currently available to treat these disorders and Myomics? high throughput drug screening technology using bioengineered muscle tissue is aimed at identifying new drugs candidates to attenuate skeletal muscle weakness including the sarcopenia associated with aging.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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