SBIR/STTR Research Award

BIODEGRADABLE INJECTABLE DELIVERY SYSTEM FOR NALTREXONE

Award identifier 04e2523843ef2c5c27dce5f363cc3d8fdba33e22e4cb90e1f2a2bf4fc80c8b65Awarding agency Department of Health and Human Services

Award amount

$49,900

Program and phase

SBIR · Phase I

Award year

1991

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Award details

Awarding agency
Department of Health and Human Services
Branch
Not reported
Recipient company
ATRIX LABORATORIES, INC.
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
Not reported
Topic code
Not reported

Research abstract

NALTREXONE IS AN EFFECTIVE NARCOTIC ANTAGONIST. HOWEVER, ITS EFFECTIVENESS IS LIMITED BY THE NEED FOR HIGH PATIENT COMPLIANCE, AS ORAL DOSAGES MUST BE TAKEN AT LEAST THREE TIMES WEEKLY. BY USING A PROPRIETARY DELIVERY SYSTEM, IT ISEXPECTED THAT NALTREXONE CAN BE DELIVERED AT A CONTROLLED RATE FOR ONE MONTH. THE DELIVERY SYSTEM TO STUDIED IS BIODEGRADABLE AND BIOCOMPATIBLE, AND HAS BEEN SHOWN TO CAUSENO ADVERSE TISSUE REACTIONS IN ANIMAL TESTING. IT HAS BEEN STUDIED IN VITRO FOR THE CONTROLLED RELEASE OF SEVERAL DRUGS AND IS CURRENTLY BEING STUDIED IN HUMANS UNDER A PHASEII IND. MOST IMPORTANTLY, IT CAN BE INJECTED USING STANDARDSYRINGES AND NEEDLES. NALTREXONE WILL BE INCORPORATED INTO THIS DELIVERY SYSTEM. THE EFFECT OF SEVERAL VARIABLES INCLUDING DRUG FORM AND POLYMER COMPOSITION, MOLECULAR WEIGHT AND CONCENTRATION, WILL BE STUDIED IN ORDER TO OBTAIN THE DESIRED RELEASE PROFILE OF 5 MG/DAY. THE MOST PROMISING FORMULATION WILL BETESTED IN RABBITS FOR TISSUE COMPATIBILITY. NALTREXONE IS AN EFFECTIVE NARCOTIC ANTAGONIST. HOWEVER, ITS EFFECTIVENESS IS LIMITED BY THE NEED FOR HIGH PATIENT COMPLIANCE, AS ORAL DOSAGES MUST BE TAKEN AT LEAST THREE TIMES WEEKLY. BY USING A PROPRIETARY DELIVERY SYSTEM, IT ISEXPECTED THAT NALTREXONE CAN BE DELIVERED AT A CONTROLLED RATE FOR ONE MONTH. THE DELIVERY SYSTEM TO STUDIED IS BIODEGRADABLE AND BIOCOMPATIBLE, AND HAS BEEN SHOWN TO CAUSENO ADVERSE TISSUE REACTIONS IN ANIMAL TESTING. IT HAS BEEN STUDIED IN VITRO FOR THE CONTROLLED RELEASE OF SEVERAL DRUGS AND IS CURRENTLY BEING STUDIED IN HUMANS UNDER A PHASEII IND. MOST IMPORTANTLY, IT CAN BE INJECTED USING STANDARDSYRINGES AND NEEDLES. NALTREXONE WILL BE INCORPORATED INTO THIS DELIVERY SYSTEM. THE EFFECT OF SEVERAL VARIABLES INCLUDING DRUG FORM AND POLYMER COMPOSITION, MOLECULAR WEIGHT AND CONCENTRATION, WILL BE STUDIED IN ORDER TO OBTAIN THE DESIRED RELEASE PROFILE OF 5 MG/DAY. THE MOST PROMISING FORMULATION WILL BETESTED IN RABBITS FOR TISSUE COMPATIBILITY.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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