Antioxidant enzyme-loaded Pro-NP for treatment of TBI.
Antioxidant enzyme-loaded Pro-NP for treatment of TBI.
批准号:
10079980
负责人:
Forrest M Kievit
金额:
$25.99万
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
已结题
起止时间:
2020-09-30 至 2022-08-31
关键词:
AcuteAddressAnimalsAntioxidantsAttenuatedBiochemicalBiodistributionBiologicalBrainBrain InjuriesBrain imagingCause of DeathClinicalDNADataDevelopmentDoseDrug Delivery SystemsDrug KineticsEconomic BurdenEmergency department visitEventFoundationsHospitalizationHourHumanImpairmentIndividualInflammationInjuryInterruptionKineticsLegal patentLipid PeroxidationMagnetic Resonance ImagingMediatingMediator of activation proteinMonitorMusNanotechnologyNerve DegenerationOxidative StressPharmaceutical PreparationsPharmacologic SubstancePhasePreventionProcessProductionProteinsReactive Oxygen SpeciesRecoveryResearchRisk FactorsSafetySiteSmall Business Technology Transfer ResearchSuperoxide DismutaseSystemTBI treatmentTestingTherapeuticTimeTissuesToxic effectTranslationsTraumatic Brain InjuryTraumatic Brain Injury recoveryTreatment Efficacyantioxidant enzymebasebrain tissuecatalaseclinical translationconfocal imagingdisabilitydrug efficacydrug testingimprovedimproved outcomemortalitymouse modelnanoparticlenanoparticle deliveryneuroinflammationnovel therapeutic interventionoxidationpreclinical studypreventprotective effectresponsetreatment planning
中文摘要
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英文摘要
ABSTRACT
Traumatic brain injury (TBI) is one of the leading causes of death and disability worldwide and comes with a
significant economic burden associated with emergency room visits and hospitalizations. Oxidative stress-
mediated secondary injury post-TBI is a considerable risk factor for mortality and long-term impairment.
Immediately following TBI, a cascade of biological responses leads to increased production of reactive oxygen
species (ROS), a critical mediator of the subsequent pathophysiological events that manifest through lipid
peroxidation (LPO), oxidation of proteins and DNA, neuroinflammation, and neurodegeneration. While
technological and clinical advancements have improved the outcome for individuals suffering from TBI, there is
currently no effective neuroprotective therapy specific for the prevention and treatment of TBI-related secondary
injury associated with oxidative stress. Super antioxidants, superoxide dismutase (SOD), and catalase (Cat)
have the potential to attenuate the spread of inflammation and brain tissue damage if administered shortly after
a TBI. However, the activity of antioxidants is short-lived and rapidly cleared, limiting therapeutic strategies based
on exogenous delivery. ProTransit is developing an antioxidant-loaded nanoparticles (NP) delivery system, Pro-
NP™, for the treatment of TBI-related secondary injury, as (1) there is currently no effective neuroprotective
therapy specific for TBI-related secondary damage; (2) prior attempts have failed clinical translation due to
ineffectual drug delivery and retention, and unintended toxicity; and (3) super antioxidants like SOD and Cat are
effective but short-lived and rapidly cleared without a robust drug delivery system. The proposed research will
address and improve upon current approaches by providing a delivery system, Pro-NP™ that can (1) deliver
super antioxidants in a sustained manner, (2) rapidly accumulate and be retained in the damaged brain, and (3)
improve TBI recovery. Thus, this proposal will provide a therapeutic strategy for TBI-related secondary brain
damage, which is not available through current TBI treatment plans.
In contrast with current secondary TBI therapeutic strategies, Protransit’s core patented nanotechnology,
Pro-NP™, can deliver biologically active antioxidant enzymes, like SOD and Cat, with sustained release and
increased target engagement with the site of injury. With increased accumulation and retention in a damaged
brain, antioxidant-loaded Pro-NP™, can exert a protective effect and prevent the spread of biochemical
derangements to surrounding healthy brain, potentially providing a significant advantage over other tested
therapies. Overall, this Phase I STTR project will determine the feasibility of SOD/Cat-loaded Pro-NP™ to inhibit
the development of secondary injury related to TBI. Further, this project will lay the foundation for a Phase II
STTR in which we will investigate the pharmacokinetics, biodistribution, and safety profile of Pro-NP™ for the
treatment of TBI.
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Nanoparticle-mediated reduction of oxidative stress for the treatment of traumatic brain injury
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批准号:10676967
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项目类别:
-
资助金额:$43.94万
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财政年份:2019
-
负责人:Forrest M Kievit
-
依托单位:
Nanoparticle-mediated reduction of oxidative stress for the treatment of traumatic brain injury
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批准号:10222791
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项目类别:
-
资助金额:$44.66万
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财政年份:2019
-
负责人:Forrest M Kievit
-
依托单位:
Nanoparticle-mediated reduction of oxidative stress for the treatment of traumatic brain injury
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批准号:10454334
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项目类别:
-
资助金额:$43.72万
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财政年份:2019
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负责人:Forrest M Kievit
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依托单位:
海外基金