SBIR-STTR Award

Alternative to Heparin Anticoagulation
Award last edited on: 1/12/06

Sponsored Program
SBIR
Awarding Agency
NIH : NHLBI
Total Award Amount
$849,874
Award Phase
2
Solicitation Topic Code
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Principal Investigator
Kenneth A Solen

Company Information

ThromboVision Inc (AKA: Thrombodyne Inc)

8036 El Rio Street
Houston, TX 77054
   (713) 491-4449
   info@thrombovision.com
   thrombovision.com
Location: Single
Congr. District: 09
County: Harris

Phase I

Contract Number: 1R43HL065860-01A1
Start Date: 00/00/00    Completed: 00/00/00
Phase I year
2001
Phase I Amount
$99,938
Anticoagulation of blood is necessary for prevention of clotting and/or thromboembolism during extracorporeal circulation. Conventionally, anticoagulation is achieved by administering heparin and reversed by neutralizing with protamine. Both of these procedures may have potential pathological consequences. The applicants have conceived an approach that will obviate the need for heparin as well as protamine. They have developed a clotting factor filter, and through in-vitro studies, demonstrated that it is possible to reversibly bind to a solid substrate certain key clotting factors (prothrombin complex) and thus remove those factors from circulating blood. This renders the blood hypocoagulable. They have also worked out a strategy to harvest the bound clotting factors and return these autologous factors to the blood, thereby restoring its clotting function. This is a proposal to explore the possibility of using the clotting factor filter in an ex-vivo configuration, and thus test the feasibility of: i) rendering the circulating blood hypocoagulable in vivo and ii) establishing that bound clotting factors can be safely returned to the circulating blood in vivo. Success of the proposed experiments will lead to the development of a clotting factor filter for clinical application. PROPOSED COMMERCIAL APPLICATIONS: The proposed research will lead to the development of a simple device that may present an alternative to the current coagulation management with heparin for extracorporeal circulation. This device will obviate the need for both heparin and protamine.

Phase II

Contract Number: 2R44HL065860-02
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
2003
(last award dollars: 2004)
Phase II Amount
$749,936

Anticoagulation of blood is necessary for prevention of clotting and/or thromboembolism during cardiopulmonary bypass or other procedures that require extracorporeal circulation. Conventionally, anticoagulation is achieved by administering heparin and reversed by neutralizing heparin with protamine. Both of these procedures may have potential pathological consequences. A subpopulation of patients is known to be sensitive to protamine, and heparin itself has been shown to cause thrombocytopenia in a subpopulation of patients undergoing open heart surgery. This is proposal to refine and develop an alternative to the heparin-protamine strategy. A novel device, termed clotting factor filter (CFF) has been developed that will bind and transiently remove clotting factors from circulating blood. Blood from which clotting factors have been removed would neither form clots nor thromboemboli during extracorporeal circulation, thus achieving the same effect as intended with heparin. Hypocoagulable blood gradually returns to normal state when the procedure is stopped, or recovery can be accelerated and normal hemostasis restored immediately by transfusion of autologous blood or plasma. Preliminary Phase I studies have confirmed the safety and efficacy of CFF approach. The objective of this Phase II proposal include: optimization of the CFF, characterization and performance of the optimized system, and verification that the CFF is able to effect appropriate 'anticoagulation' safely during cardiopulmonary bypass in an animal model. For the active matrix, linkers and base substrates will be investigated. For the plasma-matrix contact system, optimal column geometry will be selected, and a high-flow plasma separator will be designed. The optimal CFF system will be characterized to ascertain required level of 'anticoagulation' that will eliminate thrombosis during ECC. Finally, a porcine CPB model will be utilized to test the safety and efficacy of the CFF approach for 'anticoagulation' of blood during bypass. This will include careful assessment of hematologic and cardiovascular parameters during the procedure and during long term survival of the animal to assure that CFF approach is efficacious and safe.

Thesaurus Terms:
biomedical equipment development, blood coagulation, blood filtration, clotting factor, embolism, extracorporeal circulation, heart /lung bypass, surgery material /equipment biomaterial compatibility, biomedical equipment safety, hemostasis, nonhuman therapy evaluation, surface coating, surface property bioengineering /biomedical engineering, swine