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R43DA050384

Project Grant

Overview

Grant Description
Narcobond: Opioid targeted biomimetic nanosponges for treatment of opioid overdose.
Awardee
Funding Goals
NOT APPLICABLE
Place of Performance
Carlsbad, California 920087216 United States
Geographic Scope
Single Zip Code
Analysis Notes
Amendment Since initial award the End Date has been extended from 09/29/20 to 09/29/23 and the total obligations have increased 38% from $254,039 to $349,939.
Cibots was awarded Project Grant R43DA050384 worth $349,939 from National Institute on Drug Abuse in September 2019 with work to be completed primarily in Carlsbad California United States. The grant has a duration of 4 years and was awarded through assistance program 93.279 Drug Abuse and Addiction Research Programs. The Project Grant was awarded through grant opportunity HEAL Initiative: Americas Startups and Small Businesses Build Technologies to Stop the Opioid Epidemic (R43/R44 - Clinical Trial Optional).

SBIR Details

Research Type
SBIR Phase I
Title
NarcoBond: Opioid Targeted Biomimetic Nanosponges for Treatment of Opioid Overdose
Abstract
Abstract We propose to develop a broad acute/sub-acute opioid drug detoxifying treatment for opioid overdose that can complement andamp; compensate for the deficiencies in nalaxone, using opioid-targeted biomimetic “nanosponges” that absorb overdosed opioids in the body. (Note: if this proof-of-concept is successful here, the approach may be tailored to other drugs-of-abuse.) Called “NarcoBondTM” these 100 nm diameter nanospheres are assembled from a mixture of cholesterol andamp; synthetic choline-based phospholipids that mimic the lipid bilayer cell membranes. Its multifunctional surface displays an optimized milieu of human membrane proteins isolated from: a) erythrocytes to increase half-life in peripheral blood andamp; circulation, b) neurons to increase binding affinity for opioid receptor, andamp; c) purified Mu opioid receptors to bind opioids in circulation. The NarcoBondandapos;s repertoire of native opioid receptors broadly binds andamp; captures opioids from microenvironmental niches of cells in tissues andamp; will result in an antagonistic pharmacological effect by rapidly reducing the concentration of the overdosed opioid. Significance. Every 15 min. in the US, a person dies after overdosing on opioids.1 Naloxone, an opioid receptor antagonist, is, to date, the only life-saving treatment for opioid overdose based on its ability to reverse respiratory depression acutely.3 Yet the pharmacodynamic actions of naloxone last for a briefer period than all but the most short acting opioids;3-9 although the elimination half life of naloxone is similar to that of morphine (60–90andapos;)9 it is redistributed away from the brain more rapidly.3 Consequently, the patients may become renarcotised after naloxone treatment due to the continued presence of opioids in peripheral blood. In full development, NarcoBond offers a more broad alternative for cost effective andamp; longer lasting means to cleanse the peripheral blood of opioids, reducing the risk of renarcotisation, andamp; assisting in the life-saving reversal of overdose-induced respiratory depression. While prompting acute withdrawal syndrome (AWS) is always a risk in rapid opioid receptor blockade, without renarcotisationandapos;s acute risk of recurrent respiratory depression, clinicians will have more time to intervene with gradual weaning protocols to avoid AWS. In addition, NarcoBondandapos;s broad capability to mitigate against all opioids including highly potent synthetic acrylfentanyl (i.e., “naloxone resistant” chemical threat agents), addresses unmet need(s) for medical countermeasures in terrorism andamp; hostage scenarios.8,11Every 15 min. in the US, a person dies after overdosing on opioids.1 Naloxone, an opioid receptor antagonist, is, to date, the only life-saving treatment for opioid overdose based on its ability to reverse respiratory depression acutely.3 Yet the pharmacodynamic actions of naloxone last for a briefer period than all but the most short acting opioids;3-9 although the elimination half life of naloxone is similar to that of morphine (60–90andapos;)9 it is redistributed away from the brain more rapidly.3 Consequently, the patients may become renarcotised after naloxone treatment due to the continued presence of opioids in peripheral blood. To address this and other challenges of the opioid crisis, we propose to develop a broad acute/ sub-acute opioid drug detoxifying treatment for opioid overdose that can complement andamp; compensate for the deficiencies in nalaxone, using opioid-targeted biomimetic “nanosponges” that absorb overdosed opioids in the body. (Note: if this proof-of-concept is successful here, the approach may be tailored to other drugs-of-abuse.) Called “NarcoBondTM” these 100 nm diameter nanospheres are assembled from a mixture of cholesterol andamp; synthetic choline-based phospholipids that mimic the lipid bilayer cell membranes. In full development, NarcoBond offers a more broad alternative for cost effective andamp; longer lasting means to cleanse the peripheral blood of opioids, reducing the risk of renarcotisation, andamp; assisting in the life-saving reversal of overdose-induced respiratory depression. While prompting acute withdrawal syndrome (AWS) is always a risk in rapid opioid receptor blockade, without renarcotisationandapos;s acute risk of recurrent respiratory depression, clinicians will have more time to intervene with gradual weaning protocols to avoid AWS. In addition, NarcoBondandapos;s broad capability to mitigate against all opioids including highly potent synthetic acrylfentanyl (i.e., “naloxone resistant” chemical threat agents), addresses unmet need(s) for medical countermeasures in terrorism andamp; hostage scenarios.8,11
Topic Code
NIDA
Solicitation Number
PA18-591

Status
(Complete)

Last Modified 3/20/24

Period of Performance
9/30/19
Start Date
9/29/23
End Date
100% Complete

Funding Split
$349.9K
Federal Obligation
$0.0
Non-Federal Obligation
$349.9K
Total Obligated
100.0% Federal Funding
0.0% Non-Federal Funding

Activity Timeline

Interactive chart of timeline of amendments to R43DA050384

Transaction History

Modifications to R43DA050384

Additional Detail

Award ID FAIN
R43DA050384
SAI Number
R43DA050384-2990313727
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Small Business
Awarding Office
75N600 NIH NATIONAL INSITUTE ON DRUG ABUSE
Funding Office
75N600 NIH NATIONAL INSITUTE ON DRUG ABUSE
Awardee UEI
W6FWBNH967D5
Awardee CAGE
765S6
Performance District
CA-49
Senators
Dianne Feinstein
Alejandro Padilla

Budget Funding

Federal Account Budget Subfunction Object Class Total Percentage
National Institute on Drug Abuse, National Institutes of Health, Health and Human Services (075-0893) Health research and training Grants, subsidies, and contributions (41.0) $508,078 84%
Office of the Director, National Institutes of Health, Health and Human Services (075-0846) Health research and training Grants, subsidies, and contributions (41.0) $95,900 16%
Modified: 3/20/24