6533b82efe1ef96bd1293cb4
RESEARCH PRODUCT
Ionizing radiation-engineered nanogels as insulin nanocarriers for the development of a new strategy for the treatment of Alzheimer's disease
Lorena Anna DittaLaura CristaldiPasquale PiconeDaniela GiacomazzaPier Luigi San BiagioClelia DispenzaClelia DispenzaValeria MilitelloMarta Di CarloDomenico NuzzoMaria Antonietta SabatinoMaria Laura Di Giacintosubject
Materials scienceIonizing radiation processingmedicine.medical_treatmentBiophysicsBioengineering02 engineering and technologyBlood–brain barrierNeuroprotectionBiomaterialsInsulin nanocarrier03 medical and health sciencesNanogel0302 clinical medicineDrug Delivery SystemsAlzheimer DiseaseCell Line TumorRadiation Ionizingmedicinenanogels; ionizing radiation processing; insulin nanocarriers; Alzheimer's Disease; targeted drug deliveryAnimalsHumansInsulinNanotechnologyProtein kinase BDrug CarriersTargeted drug deliverybiologyInsulinBrainPovidoneAlzheimer's disease021001 nanoscience & nanotechnologyReceptor InsulinCell biologyNanostructuresMice Inbred C57BLInsulin receptormedicine.anatomical_structureTargeted drug deliveryBiochemistryMechanics of MaterialsCeramics and Compositesbiology.proteinSettore CHIM/07 - Fondamenti Chimici Delle TecnologieNanocarriers0210 nano-technology030217 neurology & neurosurgeryNanogeldescription
A growing body of evidence shows the protective role of insulin in Alzheimer's disease (AD). A nanogel system (NG) to deliver insulin to the brain, as a tool for the development of a new therapy for Alzheimer's Disease (AD), is designed and synthetized. A carboxyl-functionalized poly(N-vinyl pyrrolidone) nanogel system produced by ionizing radiation is chosen as substrate for the covalent attachment of insulin or fluorescent molecules relevant for its characterization. Biocompatibility and hemocompatibility of the naked carrier is demonstrated. The insulin conjugated to the NG (NG-In) is protected by protease degradation and able to bind to insulin receptor (IR), as demonstrated by immunofluorescence measurements showing colocalization of NG-In(FITC) with IR. Moreover, after binding to the receptor, NG-In is able to trigger insulin signaling via AKT activation. Neuroprotection of NG-In against dysfunction induced by amyloid β (Aβ), a peptide mainly involved in AD, is verified. Finally, the potential of NG-In to be efficiently transported across the Blood Brain Barrier (BBB) is demonstrated. All together these results indicate that the synthesized NG-In is a suitable vehicle system for insulin deliver in biomedicine and a very promising tool to develop new therapies for neurodegenerative diseases.
year | journal | country | edition | language |
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2016-01-01 |