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Laboratory Core

Laboratory Core
实验室核心
批准号:
8289390
负责人:
Bernard J. Moncla
金额:
$46.27万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
关键词:
Adherent CultureAffectAnimalsAnti-Bacterial AgentsAnti-Retroviral AgentsBacteriaBacterial VaginosisBiological AssayBiopsyCatalogingCatalogsCell LineCell SurvivalCervicalChlamydia trachomatisClinical TrialsCollaborationsColony-forming unitsConfocal MicroscopyCulture TechniquesDevelopmentDiagnosticDrug FormulationsDrug InteractionsDrug KineticsEnrollmentEnsureEpithelialEpithelial CellsEpitheliumEscherichia coliEvaluationExcipientsExposure toFemaleFilmFreezingGelGenital systemGlycoproteinsGoalsGram&aposs stainGrantGrowthHIVHIV-1HealthHistologyHumanImmune systemIn VitroInfectionInfection preventionIrrigationLaboratoriesLactobacillusLightLiquid substanceLocal MicrobicidesMeasuresMicrobeMicrobiologyModelingMonitorMucinsNatural ImmunityNeisseria gonorrhoeaePap smearParticipantPharmaceutical PreparationsPharmacodynamicsPlacebo EffectPlacebosPreparationProcessProtozoaRecordsResidual stateResistanceRiskSafetySamplingScreening procedureSexual TransmissionSexually Transmitted DiseasesSimplexvirusStagingStaphylococcus aureusSwabTenofovirTestingTimeTissuesToxic effectTrichomonas vaginalisUC 781VaginaVaginal DouchingVirusWomanWorkantimicrobialcellulose sulfatedrug candidatedrug efficacydrug testingefficacy testinghigh throughput screeninghuman subjectin vitro Modelinclusion criteriainformation gatheringinnovationirradiationkillingsmeetingsmicrobialmicrobicidemonolayernonhuman primatenovelpathogenpreventrectal microbicideresearch clinical testingresearch studyroutine Bacterial stainsafety testingsimian human immunodeficiency virusstability testingsuccesstranscription mediated amplificationvaginal fluidvirologyvolunteer

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英文摘要
The Microbiology/Virology Core B of this IP/CP Grant "Alternative Formulations of Tenofovir and UC781" is fully integrated into this proposal providing support and interactions with all 4 projects. This Core brings several new innovations to the safety and efficacy testing of antiretroviral (ARVs) drugs, excipients, and formulations. Microbiology/Virology Core B will support the Formulations Project 1 by screening excipients and formulated films to ensure they are not active against Lactobacillus representative of normal vaginal flora and to screen for excipient activity against sexually transmitted pathogens (STPs). The normal vaginal flora is known to be important in the prevention of infection by HIV-1 and other STPs. This Core will provide standardized testing of formulated ARV safety using ecto-cervical explant and epithelial monolayer cultures in support of Projects 1, 2, 3 and 4. ARV film efficacy and coital timing testing will be performed using the ecto-cervical explant cultures supporting Projects 2, 3, and 4 while guiding formulations in Project 1. Core B will support the animal and human trials using ex vivo biopsies to demonstrate protection from SHIV/HIV-1 infection (supporting all projects). The effects of films and gel preparation used in Projects 2 and 3 will be monitored by culture work in the Core to monitor the microflora. In Project 3, this Core will screen subjects for STPs and normal floras to assure subjects meet inclusion criterion. Cervicovaginal lavages (CVLs) samples will be collected in Projects 2, 3 and 4 and for pharmacokinetic study. This Core will utilize those CVL to determine if the and/or formulation interfere with the natural innate immunity process by examining the effects of placebo and drug containing films and gels on the killing of HIV-1, HSV, and bacteria. Also, vaginal fluid contains factors known to kill HSV as well as some bacteria. An effective microbicide can not interfere with these processes and at the same time inactivate HIV-1 or prevent its' infection. Overall, this IP/CP seeks to develop a product which prevents HIV-1 infection safely without disturbing the normal flora or other natural defenses and this Core will ensure a successful microbicide candidate is created for further clinical evaluation.
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