Clinical Pharmacology Analytical Core
临床药理学分析核心
基本信息
- 批准号:7698887
- 负责人:
- 金额:$ 2.9万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2008
- 资助国家:美国
- 起止时间:2008-09-01 至 2013-08-31
- 项目状态:已结题
- 来源:
- 关键词:African AmericanAnimalsAntineoplastic AgentsAromatase InhibitorsArtsBackBasic ScienceBiological AssayCYP2D6 geneCYP3A4 geneCancer CenterCancer Center Support GrantCancer Control ResearchCaucasiansCaucasoid RaceCell ExtractsCellsChargeChildChildren&aposs Oncology GroupClinicClinicalClinical InvestigatorClinical PharmacologyCollaborationsCultured CellsDataDevelopmentDevelopmental Therapeutics ProgramDisease-Free SurvivalDoseDrug ExposureDrug InteractionsDrug KineticsEnsureEnzymesEquipmentExcretory functionExemestaneFluoxetineFundingGenetic PolymorphismGermanyGoalsGrantHeadHome environmentHospitalsHot flushesHousingHumanIn VitroIndianaIndividualItalyKoreaLabelLaboratoriesLaboratory ResearchLeadLetrozoleLightMaintenanceMalignant Childhood NeoplasmMalignant NeoplasmsMass Spectrum AnalysisMeasurementMedicineMenopausal hot flushesMentored Clinical Oncology AwardMentored Clinical Scientist AwardMentored Patient-Oriented Research Career Development AwardMetabolismNational Institute of General Medical SciencesNitrogenNorth Central Cancer Treatment GroupNumbersOperative Surgical ProceduresOutcomePTK787PaclitaxelParoxetinePatient CarePatientsPediatric OncologistPharmaceutical PreparationsPharmacogeneticsPharmacogenomicsPharmacology and ToxicologyPhasePhase III Clinical TrialsPlasmaPoliciesPreparationProtocols documentationPublicationsResearchResearch PersonnelResearch Project GrantsResourcesRetrospective StudiesRiskSaint Jude Children&aposs Research HospitalSamplingSchemeServicesShared Resource Cancer CenterSiteSpainStructureSupport of ResearchSystemTamoxifenTechnologyTimeTissue ExtractsToxic effectTranslationsUnited States Food and Drug AdministrationUniversitiesVariantVincristineWomanWorkabsorptionbasecancer therapycostcytochrome P450 3Adaydesigndosagegenetic variantin vivoinhibitor/antagonistinstrumentationmalignant breast neoplasmmembermicrobial alkaline proteinase inhibitorprogramsresearch studyresponsesmall moleculesuccesstrial comparingtumor
项目摘要
The Clinical Pharmacology Analytical Core (CPAC) assists Indiana University Simon Cancer Center (IUSCC)
investigators in support of research projects and scientific goals, CPAC has been in existence since
September 2004 and is the only laboratory on campus that provides investigators state-of-the-art technology
to quantify small molecules, drugs, and metabolites, to identify compounds based on their mass spectra, and
to analyze pharmacokinetic data. Access to state-of-the-art instrumentation for quantification of drugs and
metabolites is an invaluable resource for all cancer investigators in the IUSCC.
The CPAC develops and performs assays to identify and/or quantify drugs and metabolites from in vitro
(including tissue extracts, cell culture and cell extracts) and in vivo studies (including humans or other
animals). It also conducts pharmacokinetic analyses that describe drug (or metabolite) concentrations in the
body over a period of time, from absorption to excretion, and information on drug exposure. These services
ultimately assist investigators in the analysis of their research protocols regarding pharmacokinetics,
pharamacodynamics, pharmacogenetics, toxicity, tumor response and identification of appropriate
individualized therapies. This technology has allowed IUSCC investigators to make critical pharmacogenetic
observations that are already impacting patient care.
临床药理学分析核心(CPAC)协助印第安纳州西蒙大学癌症中心(IUSCC)
为了支持研究项目和科学目标,CPAC成立于
2004年9月,是校园里唯一一个为研究人员提供最先进技术的实验室
量化小分子、药物和代谢物,根据质谱鉴定化合物,
分析药代动力学数据。获得最先进的药物定量仪器,
代谢物是IUSCC所有癌症研究人员的宝贵资源。
CPAC开发并进行检测以识别和/或量化体外药物和代谢物
(包括组织提取物、细胞培养物和细胞提取物)和体内研究(包括人类或其他
动物)。它还进行药代动力学分析,描述药物(或代谢物)浓度,
身体在一段时间内,从吸收到排泄,以及药物暴露的信息。这些服务
最终协助研究者分析其关于药代动力学的研究方案,
药物动力学、药物遗传学、毒性、肿瘤反应和确定适当的
个性化治疗。这项技术使IUSCC研究人员能够进行关键的药物遗传学研究,
已经影响到病人护理的观察结果。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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David R. Jones其他文献
Determining the value of pulmonary metastasectomy.
确定肺转移瘤切除术的价值。
- DOI:
10.1093/ejcts/ezw181 - 发表时间:
2016 - 期刊:
- 影响因子:3.4
- 作者:
David R. Jones - 通讯作者:
David R. Jones
Assaying endogenous phosphatidylinositol-4-phosphate 5-kinase (PIP5K) activities.
测定内源性磷脂酰肌醇 4 磷酸 5 激酶 (PIP5K) 活性。
- DOI:
- 发表时间:
2009 - 期刊:
- 影响因子:0
- 作者:
Jonathan R. Halstead;M. Snel;Sarah Meeuws;David R. Jones;N. Divecha - 通讯作者:
N. Divecha
The Nonclinical Evaluation of Biotechnology‐Derived Pharmaceuticals, Moving on after the TeGenero Case*
生物技术衍生药物的非临床评估,在 TeGenero 案例之后继续进行*
- DOI:
- 发表时间:
2014 - 期刊:
- 影响因子:0
- 作者:
J. W. Laan;C. Herberts;David R. Jones;S. Thorpe;R. Stebbings;R. Thorpe - 通讯作者:
R. Thorpe
Critical analysis of carcinogenicity study outcomes. Relationship with pharmacological properties
致癌性研究结果的批判性分析。
- DOI:
10.3109/10408444.2016.1163664 - 发表时间:
2016 - 期刊:
- 影响因子:5.9
- 作者:
J. W. van der Laan;P. Kasper;B. Silva Lima;David R. Jones;M. Pasanen - 通讯作者:
M. Pasanen
Nonclinical Toxicological Support for Phase I Trials
I 期试验的非临床毒理学支持
- DOI:
10.1002/9781118820186.ch8 - 发表时间:
2014 - 期刊:
- 影响因子:3.2
- 作者:
David R. Jones;J. McBlane - 通讯作者:
J. McBlane
David R. Jones的其他文献
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{{ truncateString('David R. Jones', 18)}}的其他基金
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