Publication | Open Access
RVG29-modified microRNA-loaded nanoparticles improve ischemic brain injury by nasal delivery
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Citations
43
References
2020
Year
NanoparticlesEngineeringNose-to-brain DeliveryBiomedical EngineeringTherapeuticsCerebral Vascular RegulationNeuroinflammationNanomedicineTranslational MedicineNeurobiology Of DiseaseRvg29-modified Microrna-loaded NanoparticlesTherapeutic NanomaterialsBrain InjuryNeurologyIschemic SyndromePeg-plga/mirna-124 Nasal AdministrationVascular BiologyNeuroprotectionCerebral Blood FlowMicrorna DetectionReperfusion InjuryNeurological AssessmentCell BiologyNasal DeliveryNano-drug DeliveryNeuroscienceMedicine
Effective nose-to-brain delivery needs to be developed to treat neurodegenerative diseases. Regulating miR-124 can effectively improve the symptoms of ischemic brain injury and provide a certain protective effect from brain damage after cerebral ischemia. We used rat models of middle cerebral artery occlusion (t-MCAO) with ischemic brain injury, and we delivered RVG29-NPs-miR124 intranasally to treat neurological damage after cerebral ischemia. Rhoa and neurological scores in rats treated by intranasal administration of RVG29-PEG-PLGA/miRNA-124 were significantly lower than those in PEG-PLGA/miRNA-124 nasal administration and RVG29-PLGA/miRNA-124 nasal administration group treated rats. These results indicate that the nose-to-brain delivery of PLGA/miRNA-124 conjugated with PEG and RVG29 alleviated the symptoms of cerebral ischemia-reperfusion injury. Thus, nasal delivery of RVG29-PEG-PLGA/miRNA-124 could be a new method for treating neurodegenerative diseases.
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