SBIR/STTR Research Award

THE PRIMARY TREATMENT FOR GALLSTONES IS SURGICAL REMOVAL.

Award identifier 96ff30c9dbc7a8ef1166102add08e805cf36d219ffb1879bb63b06b208481afaAwarding agency Department of Health and Human Services

Award amount

$34,000

Program and phase

SBIR · Phase I

Award year

1986

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Award details

Awarding agency
Department of Health and Human Services
Branch
Not reported
Recipient company
Lipid Specialties Inc
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
Not reported
Topic code
Not reported

Research abstract

THE PRIMARY TREATMENT FOR GALLSTONES IS SURGICAL REMOVAL. WITH A 1% MORTALITY RATE AND SUBSTANTIAL HOSPITALIZATION COSTS, A SEARCH FOR LESS EXPENSIVE AND SAFER TREATMENTS FOR GALLSTONE ELIMINATION IS WARRANTED. IT HAS BEEN SHOWN THAT GALLSTONES CONSIST PRIMARILY OF CHOLESTEROL AND THAT THEIR FORMATION IS A CONSEQUENCE OF EXCEEDING THE SOLUBILITY LIMITS OF CHOLESTEROL IN THE BILE. AS A RESULT, IT HAS BEENPROPOSED THAT ORAL TREATMENT WITH SUITABLE BILE ACIDS MAY ACT AS GALLSTONE DISSOLVING AGENTS, THEREBY ELIMINATING THE NEED FOR SURGERY. THE GOAL OF THIS PROJECT IS TO DEMON- STRATE THAT SHORT CHAIN ANALOGS OF HEAD GROUP MODIFIED PHOSPHATIDYLCHOLINES HAVE SUPERIOR SOLUBILIZING PROPERTIES WHEN COMPARED TO OTHER POTENTIAL CHOLESTEROL SOLUBILIZING AGENTS AND RELATIVE TO THE AMOUNT AND SPEED AT WHICH THEY CAN DISSOLVE PRE-EXISTING CHOLESTEROL CRYSTALS. SHOULD PHASE I STUDIES BE SUCCESSFUL, PHASE II STUDIES WOULD THEN CONCENTRATE ON THE ABILITY OF MODIFIED PHOSPHATIDYLCHOLINES TAKEN ORALLY TO ENTER INTO THE ENTEROHEPATIC CIRCULATION IN ANIMAL MODELS. FUTURE TESTING WOULD CONSIST OF PRELIMINARY HUMAN STUDIES.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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