SBIR/STTR Research Award

Labtype to Preclinical Prototype VAD

Award identifier f4928fbf98c84120dab4e258673d5317b1e3f9997594afe70d576774fe3c0c15Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$257,631

Program and phase

SBIR · Phase I

Award year

2012

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Perfusion Solutions, Inc.
Proposal award date
Not reported
Contract end date
Not reported
UEI
TF8CUC65VLG5
Solicitation number
PA11-096
Topic code
NHLBI

Research abstract

DESCRIPTION (provided by applicant): Perfusion Solutions, Inc. (PSI) has licensed the MiniMixedFlow (M2F) pump technology from the Cleveland Clinic. This Fast-Track SBIR application is intended to overcome the remaining obstacles to major commercial investment leading to qualification for clinical use. The patent applied for configuration employs passive magnetic bearings, a miniature motor, and a mixed flow impeller to build a durable pump of high output relative to its size. The configuration is extremely flexible and adaptable. Hardware prototypes addressing multiple clinical niches have been built. Excellent bench results and very preliminary in vivo data have been obtained with labtype hardware built with shortcuts to enable expeditious evaluation of the most fundamental design questions. Hardware to date has shown good hydraulic performance, low hemolysis, very long life and preliminary in vivo results, compromised by construction shortcuts necessary in the lab program. The key remaining feasibility issue is freedom from deposition/embolic events under chronic implant conditions. PSI proposes to build a preclinical prototype pump using refined construction and finishing techniques. During phase I of this fast-track proposal, we will demonstrate:1) that the preclinica hardware maintains the basic performance and hemolysis results of the preliminary hardware; 2) that the durability shows no change relative to the labtype in the early stages of a new endurance test series; and, 3) good biocompatibility is shown in two 30-day in vivo studies. The success criteria for (1) and (2) are comparisons to the matching data of the lab- type pumps, while (3) will be judged by an absence of deposition in the pump or of thromboembolic complications downstream attributable to the pump. With acceptance from the NIH program officer of phase I results, phase II will build more pump hardware and a preclinical prototype console, launch an extended in vivo demonstration study and continue the bench endurance testing. With this data the last barrier to overcome in order to raise significant phase III commercial investment will have been breached. PUBLIC HEALTH RELEVANCE: Heart disease is a major source of mortality, loss of quality of life, and high medical costsfor treatment. Blood pumps have shown a potential to not only save lives, but to rehabilitate patients to a much higher level of function. However, present technology still has a significant number of limitations which cause death and disability as a result of the pump implant; the proposed project addresses many of these limitations.

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

8 SBIR/STTR records share this UEI (2009–2025). Reported award amounts total $1,912,540. Reported amounts are not federal obligations.

Phases: Phase I

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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