NarcoBond: Opioid Targeted Biomimetic Nanosponges for Treatment of Opioid Overdose
NarcoBond: Opioid Targeted Biomimetic Nanosponges for Treatment of Opioid Overdose
批准号:
10179237
负责人:
Babak Esmaeli-Azad
金额:
$9.59万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-09-30 至 2020-09-29
关键词:
ARNT geneAcuteAddressAffinityBindingBiodistributionBiological AssayBiomimeticsBloodBlood CirculationBrainCaliberCell membraneCellsCellular AssayCholesterolCholineClinicalCodeineComplementDerivation procedureDevelopmentErythrocytesFatty acid glycerol estersFentanylHalf-LifeHostageHumanHydrocodoneIn VitroIntravenousLegal patentLifeLipid BilayersLiquid substanceLiverLymphMembraneMembrane ProteinsMethadoneMorphineMusNaloxoneNanosphereNeuronsNociceptionNociceptorsOpioidOpioid AntagonistOpioid ReceptorOpioid Receptor BindingOverdoseOxycodonePatientsPersonsPharmaceutical PreparationsPharmacodynamicsPharmacologyPhasePhospholipidsProtocols documentationRecording of previous eventsRecurrenceResistanceRiskSavingsSerumSolidSubstance Withdrawal SyndromeSurfaceTerrorismTimeTissuesTranslatingUrineVaccinationVentilatory DepressionWeaningbasechemical threatclinical applicationcost effectivedrug of abusein vivoinduced pluripotent stem cellinnovationmedical countermeasuremu opioid receptorsnovelnovel strategiesopioid epidemicopioid injectionopioid misuseopioid overdoseopioid useperipheral bloodscreeningtool
中文摘要
摘要
我们建议开发一种广泛的急性/亚急性阿片类药物解毒治疗,
阿片类药物过量,可以补充和补偿纳洛酮的不足,
使用阿片类药物靶向的仿生“纳米海绵”,
身体(Note:如果这一概念验证在这里取得成功,该方法可以针对其他
药物滥用)。被称为“NarcoBondTM”的这些100纳米直径的纳米球组装
从胆固醇和合成胆碱基磷脂的混合物,
细胞膜它的多功能表面显示了优化的人体膜环境
分离自以下的蛋白质:a)红细胞,以增加外周血和循环中的半衰期,B)
c)纯化的Mu阿片受体,以结合
阿片类药物在循环。NarcoBond的天然阿片受体库广泛结合&
从组织细胞的微环境小生境中捕获阿片类药物,
拮抗药理作用,通过快速降低过量的
阿片类药物
意义在美国,每15分钟就有一个人在过量服用阿片类药物后死亡。
阿片受体拮抗剂,是迄今为止,唯一的挽救生命的治疗阿片类药物过量的基础
其逆转急性呼吸抑制的能力。3然而,
纳洛酮持续的时间比除最短作用的阿片类药物外的所有药物都要短;3-9,尽管
纳洛酮的消除半衰期与吗啡相似(60- 90 ')9,它被重新分布
3因此,患者可能会在术后发生再神经病变。
纳洛酮治疗由于阿片类药物在外周血中的持续存在。足额
发展,NarcoBond提供了一个更广泛的替代成本效益和更持久的
清除外周血中阿片类药物的方法,降低再麻醉的风险,
帮助挽救过量引起的呼吸抑制的逆转。而
促使急性戒断综合征(AWS)始终是快速阿片受体阻断的风险,
如果没有再麻醉的复发性呼吸抑制的严重风险,临床医生将
有更多的时间来干预逐步断奶协议,以避免AWS。此外,本发明还提供了一种方法,
NarcoBond的广泛能力,以减轻对所有阿片类药物,包括高效合成
丙烯酰芬太尼(即,“耐纳洛酮”化学威胁剂),解决了
恐怖主义和人质劫持事件中的医疗对策8,11
英文摘要
Abstract
We propose to develop a broad acute/sub-acute opioid drug detoxifying treatment for
opioid overdose that can complement & 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 & 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 & circulation, b)
neurons to increase binding affinity for opioid receptor, & c) purified Mu opioid receptors to bind
opioids in circulation. The NarcoBond's repertoire of native opioid receptors broadly binds &
captures opioids from microenvironmental niches of cells in tissues & 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 (60–90')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 & longer lasting
means to cleanse the peripheral blood of opioids, reducing the risk of renarcotisation, &
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 renarcotisation's acute risk of recurrent respiratory depression, clinicians will
have more time to intervene with gradual weaning protocols to avoid AWS. In addition,
NarcoBond'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 & hostage scenarios.8,11
期刊论文(0)
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会议论文
NarcoBond: Opioid Targeted Biomimetic Nanosponges for Treatment of Opioid Overdose
-
批准号:9912595
-
项目类别:
-
资助金额:$25.4万
-
财政年份:2019
-
负责人:Babak Esmaeli-Azad
-
依托单位:
Direct Conversion of Human Fibroblasts into Neuronal Cells by Small Molecules (hCiN)
-
批准号:9254639
-
项目类别:
-
资助金额:$22.4万
-
财政年份:2017
-
负责人:Babak Esmaeli-Azad
-
依托单位:
Human Chemically induced Pluripotent Stem Cells (CiPSC) generated Cardiomyocytes
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批准号:8059798
-
项目类别:
-
资助金额:$25.25万
-
财政年份:2011
-
负责人:Babak Esmaeli-Azad
-
依托单位:
Chemically Induced Pluripotent Stem (CiPS) Cells Alzheimer's Patient Specific Cel
-
批准号:7911334
-
项目类别:
-
资助金额:$24.72万
-
财政年份:2010
-
负责人:Babak Esmaeli-Azad
-
依托单位:
Clinically Relevant CiPS Cell Lines
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批准号:7672118
-
项目类别:
-
资助金额:$24.03万
-
财政年份:2009
-
负责人:Babak Esmaeli-Azad
-
依托单位:
HUMAN PROTEIN DIFFERENTIAL DISPLAY ASSAY ICAT-ULC-MS/MS
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批准号:6311048
-
项目类别:
-
资助金额:$14.31万
-
财政年份:2001
-
负责人:Babak Esmaeli-Azad
-
依托单位:
ONLINE 2D FUNCTIONAL PROTEOMICS
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批准号:2865578
-
项目类别:
-
资助金额:$10.0万
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财政年份:1999
-
负责人:Babak Esmaeli-Azad
-
依托单位:
Online 2-D Proteomics Differential Display
-
批准号:6540629
-
项目类别:
-
资助金额:$51.3万
-
财政年份:1999
-
负责人:Babak Esmaeli-Azad
-
依托单位:
Online 2-D Proteomics Differential Display
-
批准号:6338292
-
项目类别:
-
资助金额:$50.94万
-
财政年份:1999
-
负责人:Babak Esmaeli-Azad
-
依托单位:
海外基金