SBIR/STTR Research Award

SYNTHESIS OF CONJUGATED METABOLITES OF BUPRENOPHINE

Award identifier 03b68cd08d072467afb2b8877bde107b0e4619927826632876e6549e08c5f698Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$93,816

Program and phase

SBIR · Phase I

Award year

2002

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
ElSohly Laboratories, Incorporated
Proposal award date
Not reported
Contract end date
Not reported
UEI
SQB7R3XYCW35
Solicitation number
Not reported
Topic code
Not reported

Research abstract

The development of maintenance treatment for subjects with addictive behavior is an important public health issue. Buprenorphine, a promising new drug for the treatment of opiates addition, has been widely abused since the mid-90's. Using drug testing for buprenorphine will become an important issue. The proposed research will focus on the preparation of the reference materials of two major urinary metabolites of buprenorphine, namely, buprenorphine-3-beta-D-glucuronide and buprenorphine-3-beta-D-glucuronide, which are not commercially available. The successful development of these two compounds will make it possible during the Phase II research to prepare the deuterated analogs of these metabolites and to achieve our long-term goals such as optimization of the analytical protocols, development of an efficient immunoassay technology, development of marketing of urine controls, and preparation of these standards and internal standards in bulk quantities for commercial marketing. Two possible synthetic routes as well as an enzymatic synthesis have been proposed for the synthesis. Route 1 has been tested on small scale and proved to be workable. Route 2 starts with a cheap starting material but requires multiple synthetic steps. The enzymatic synthesis will use either uridine diphosphate glucuronosyltransferase (UDPGT) in solution or immobilized UDPGT to catalyze the reactions. These processes will evaluated based on their efficiency and feasibility. Upon completion of the synthesis, the optimum enzymatic hydrolysis conditions will be assessed using different types of glucuronidases. PROPOSED COMMERCIAL APPLICATIONS: The products developed in this research will be marked as reference standard materials for analytical laboratories, hospitals, and drug testing research organizations. The products will also be used for preparation of urine controls for marketing purposes, and the deuterated analogs (to be prepared during Phase II) will be marked as internal standards to other analytical laboratories.

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.

Research funding history

17 SBIR/STTR records share this UEI (1986–2019). Reported award amounts total $4,150,945. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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