Nanoformulation of the BDNF for treatment of stroke
Nanoformulation of the BDNF for treatment of stroke
批准号:
9139992
负责人:
ALEXANDER V KABANOV
金额:
$37.21万
依托单位国家:
美国
项目类别:
财政年份:
2015
资助国家:
美国
项目状态:
已结题
起止时间:
2015-09-15 至 2018-08-31
关键词:
AcidsActive Biological TransportAddressAnimal ModelBiocompatibleBiological AvailabilityBlood - brain barrier anatomyBlood CirculationBrainBrain InjuriesBrain-Derived Neurotrophic FactorCellsChronicComplexContinuous Intravenous InfusionDevelopmentDrug KineticsEcosystemEnsureEnvironmentFormulationFutureGlutamatesGoalsHalf-LifeHealthHousingHumanInfarctionInflammationInjection of therapeutic agentInjuryIschemiaIschemic StrokeLeadLiposomesMiddle Cerebral Artery OcclusionModelingModificationMusNerve DegenerationNeuraxisNeuronal PlasticityNeuronsPenetrationProceduresProcessProteinsPublishingRattusReactive Oxygen SpeciesReceptor ActivationRecombinantsRecoveryReperfusion TherapyReportingResearchRouteSafetyScientistSensorimotor functionsSerumStagingStrokeSystemTherapeuticTherapeutic AgentsTherapeutic EffectTimeTranslational Researchantioxidant enzymeantioxidant therapyaqueousbiocompatible polymercopolymercopper zinc superoxide dismutasedrug candidatedrug developmentethylene glycolimprovedin vivoinnovationintravenous administrationmilligramnanonanoformulationnanoparticlenanoscaleneurogenesisneurological recoveryneuroprotectionnovelnovel therapeuticsparticlepolyionpolypeptidepost strokepre-clinicalproduct developmentreceptorrestorationstroke treatmenttherapeutic developmenttherapeutic proteintherapy developmentuptake
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): This project develops a formulation for the delivery of the brain-derived neurotrophic factor (BDNF) to the central nervous system and evaluates the drug candidate using this formulation for the treatment of ischemic stroke. BDNF has shown potential to exert neuroprotective and neurodegenerative effects when administered after stroke. However, the use of native BDNF as therapeutic agent for systemic administration is hindered by its poor brain accumulation. To address this problem we propose a novel yet simple and scalable polymeric nano-formulation of BDNF, nano-BDNF, in which BDNF is incorporated into polyion complexes with safe and biocompatible poly (ethylene glycol)-poly (L-glutamate) (PEG-PGA) block copolymer. The complexes are produced spontaneously in mild aqueous conditions upon mixing of native BDNF with the PEG-PGA block copolymer, which entraps the BDNF molecule in nanoscale size (<100 nm) core-shell particles. Preliminary studies suggest that nano-BDNF will strongly improve the brain uptake of BDNF and increase efficacy of BDNF treatment to elicit neuroprotection and neuro-restoration after stroke. We propose to advance nano-BDNF as a potential therapeutic agent for the treatment of brain injury in an animal model of stroke. This will be achieved by (1) producing in house the abundant amount of human recombinant BDNF and developing simple, scalable and robust procedure for nano-BDNF with optimized composition; (2) determining the brain pharmacokinetics of nano-BDNF after intravenous administration and identifying the best composition for efficacy studies; and (3) determining the therapeutic effect of nano-BDNF treatment on chronic recovery in an ischemia/reperfusion- induced mouse middle cerebral artery occlusion (MCAO) model. We use step-wise process; each step has its own go/no go criteria to identify a lead nano-BDNF candidate that will be taken forward into preclinical development. The plan for subsequent therapy development will implement the product development steps and result in the filing of IND.
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