Ureteral Stent Coatings
Ureteral Stent Coatings
批准号:
8454859
负责人:
Kristin S Taton
金额:
$17.29万
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-03-01 至 2016-02-29
关键词:
AchievementAddressAdhesivesAffectAnimal TestingBacteriaBindingBiocompatible Coated MaterialsBladderCalciumCalcium CarbonateCalcium OxalateCalculiCardiovascular systemCessation of lifeCitric AcidCrystal FormationCrystallizationDiseaseDrainage procedureEffectivenessEvaluationExcisionFibrosisFilmFlank PainGovernmentHandHeadHealedHematuriaHeparinIn VitroInjuryKidneyKidney CalculiKidney TransplantationLacerationLeftLongitudinal StudiesMagnesiumMalignant NeoplasmsMicrobial BiofilmsModelingMonitorPainPatientsPersonsPhasePolyurethanesPositioning AttributeProceduresProcessQuality of lifeReconstructive Surgical ProceduresSaltsSepsisSmall Business Innovation Research GrantSolutionsStentsSurfaceThickTimeTissuesTriclosanTwin Multiple BirthUreterUreteral obstructionUrinary tractUrineWorkantimicrobial drugbiomaterial compatibilitycalcium phosphatecombatconditioningdesignexperienceforgettinghealingin vivoinhibitor/antagonistinnovationnovelnovel strategiesosteopontinpreventpublic health relevancescaffoldurinaryurologic
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): This Phase I SBIR project is designed to develop new biodegradable hydrophilic coatings for ureteral stents. Ureteral stents are widely used to maintain drainage of the upper urinary tract and instrumental in management of stone disease, as well as in cases of other ureteral obstruction such as injury, fibrosis or malignancies. However, unlike cardiovascular stents, ureteral stents are recommended for use 3 months or less due to encrustation and biofilm formation. Over 75% of ureteral stents are encrusted at this 3 month time period, making removal difficult and causing patients pain. The best commercial coatings reduce encrustation thickness by 50% and extent of encrustion by only 22% over uncoated ureteral stents. This project focuses on novel biodegradable coatings which release agents designed to minimize encrustation. Two different agents will be evaluated; release and in vitro encrustation will be monitored over a four week period.
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