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Insulin Formulations of Enhanced Stability

Insulin Formulations of Enhanced Stability
稳定性增强的胰岛素制剂
批准号:
7188519
负责人:
MICHAEL Aaron WEISS
金额:
$30.75万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-03-01 至 2010-02-28
关键词:
AffectAfricaAlanineAmino AcidsAmyloidAnimalsAppendixApplied ResearchAreaAsiaBasic ScienceBindingBinding SitesBiochemistryBiologicalBiological AssayBiotechnologyC-terminalCaringCell NucleusChemicalsChemistryClinicalCollaborationsConditionDevelopmentDiabetes MellitusDiabetic AngiopathiesDiffuseDiseaseDisulfidesDrug FormulationsDrug IndustryDrug KineticsElectron MicroscopyElementsEndocrinologyEngineeringEpidemicExcipientsExhibitsFigs - dietaryFluorescence SpectroscopyFoundationsFutureGenomicsGlassGoalsHeatingHeelHelix (Snails)HeterosexualsHigh temperature of physical objectHistidineHumanHypoglycemiaImprove AccessIn VitroInflammationInjection of therapeutic agentInsulinInsulin ReceptorInvestigationIonsJournalsKidney FailureKineticsKnowledgeLettersLifeLogicMeasurementMedicalMedical EconomicsMembrane ProteinsMetal Binding SiteMethodsModelingModificationMolecularMolecular ConformationMolecular ModelsMonitorMutationN-terminalNMR SpectroscopyNumbersOceaniaPainPatientsPharmacologic SubstancePhenolsPolymersPositioning AttributePost-Translational Protein ProcessingPrecipitationPredispositionPrincipal InvestigatorPrionsProcessProductionPropertyProtein ChemistryProtein EngineeringProteinsPublishingRangeRattusRefrigerationRelative (related person)Replacement TherapyResearchResistanceResolutionResourcesRetinal DiseasesRiskSafetyScienceSeriesSideSocietiesSolventsSouth AmericaStandards of Weights and MeasuresStructureSubcutaneous InjectionsSurfaceTechnologyTemperatureTestingTherapeuticThermodynamicsTimeTranslatingTranslationsTropical ClimateUnited States Food and Drug AdministrationUnited States National Institutes of HealthUniversity HospitalsUpper armVariantVial deviceWomanWound HealingX-Ray CrystallographyZincamyloid formationamyloidogenesisanalogbaseclassical conditioningclinical applicationconceptcryogenicscytokinedaydeamidationdesignear helixfrontierglobular proteinglycemic controlimmunogenicimprovedin vivoinsightinterestmagnetic fieldmethyl groupminiproinsulinmonomernovelnovel strategiespeptide analogpolymerizationpreventprogramsprotein degradationprotein foldingprotein protein interactionreceptor bindingstructural biologysynthetic proteintherapeutic proteinthree dimensional structuretransmission process

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英文摘要
DESCRIPTION (provided by applicant): Insulin formulation chemistry represents a cross roads between protein science and applied biotechnology. In accord with the dual perspective of the NIH Roadmap, we propose to exploit general principles of protein engineering to improve the stability of insulin formulations. This application thus seeks clinical translation of basic insights into the folding and unfolding of proteins. Present insulin formulations must be stored in refrigerator and discarded after 28 days. In addition, patients are urged to monitor vials for discoloration, frosting of the glass, or precipitation: signs of chemical or physical degradation of the protein. Of principal concern is insulin fibrillation, a misfolding process analogous to amyloid formation. The Food & Drug Administration has set stringent standards to protect patients from inadvertent injection of insulin fibrils. We seek to develop novel insulin analogs and formulations that are highly active but resistant to fibrillation even after prolonged storage at elevated temperatures. Two novel design ideas are proposed based on preliminary studies of an insulin amyloidogenic intermediate: chiral stabilization of a B-chain ¿-turn by D-amino acids and introduction of an ancillary zinc-binding site in the A chain. Thermodynamic, kinetic and structural studies of these insulin analogues will be pursued to validate the design goals. The proposed studies, if successful, would represent the exciting application of structural principles to a problem of enormous medical and economic significance. Insulin formulations of prolonged stability and extended shelf life would be of particular advantage in the developing world where refrigeration is not consistently available. Our analog design strategies, although focused on structural features of insulin, employ concepts and principles of broad application in protein science. Accordingly, our strategy may generalize to enhance the utility of diverse protein pharmaceuticals in the post-genomic era.
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Biochemical Studies of a Transcription Factor
  • 批准号:
    8004618
  • 项目类别:
  • 资助金额:
    $9.91万
  • 财政年份:
    2010
  • 负责人:
    MICHAEL Aaron WEISS
  • 依托单位:
How Insulin Binds to the Insulin Receptor
  • 批准号:
    8003136
  • 项目类别:
  • 资助金额:
    $4.43万
  • 财政年份:
    2010
  • 负责人:
    MICHAEL Aaron WEISS
  • 依托单位:
Design of an Implantable Pump Insulin
  • 批准号:
    8003137
  • 项目类别:
  • 资助金额:
    $5.69万
  • 财政年份:
    2010
  • 负责人:
    MICHAEL Aaron WEISS
  • 依托单位:
Clinical Testing of an Insulin Analog
  • 批准号:
    7613905
  • 项目类别:
  • 资助金额:
    $25.5万
  • 财政年份:
    2009
  • 负责人:
    MICHAEL Aaron WEISS
  • 依托单位:
海外基金