SBIR/STTR Research Award
SOLID SITOSTANOL FORMULATIONS LOWER LDL-CHOLESTEROL
Award amount
$0Program and phase
SBIR · Phase IAward year
2002Award details
- Awarding agency
- Department of Health and Human Services
- Branch
- National Institutes of Health
- Recipient company
- LIFELINE TECHNOLOGIES, INC.
- Proposal award date
- Not reported
- Contract end date
- Not reported
- UEI
- Not reported
- Solicitation number
- Not reported
- Topic code
- Not reported
Research abstract
Incorporation of a new water-based sterol/stanol formulation system in foods and capsules lowers intestinal cholesterol absorption. This methodology is fat-free and provides a
distinct improvement over existing inflexible oil-based strategies that
increase the consumer's caloric load. A series of 14-week, double blind placebo
controlled trials will examine the effect of formulated sterols on
LDL-cholesterol reduction in mildly hypercholesterolemic adults maintained on
the American Heart Association Step I diet. Two dosing strategies will be
examined. In the first, formulated soy sterols will be dry blended with Instant
Breakfast to provide a convenient, once a day dosing regimen. In the second
strategy, soy stanols will be delivered in capsules to determine the optimum
dose and dosing regimen. Each of these methods will then be tested in subjects
who have problems with lipid management. Children who are not candidates for
statin therapy because of long-term safety concerns will be enrolled and their
LDL-cholesterol reduction monitored while consuming soy sterols in Instant
Breakfast. Similarly, adults on statin drugs who have not reached their target
LDL-cholesterol level will receive soy stanols in capsules to determine the
extent of LDL-cholesterol reduction using this adjunct therapy. Positive
results from these studies will provide a safe non-pharmaceutical approach to
cholesterol reduction.
Technology keywords
Not reported