Biodegradable macromolecular Blood pool contrast agents
Biodegradable macromolecular Blood pool contrast agents
批准号:
7260974
负责人:
ZHENG-RONG LU
金额:
$26.91万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-12-01 至 2011-02-28
关键词:
AbbreviationsAcidsAcuteAmidesAnimal ModelBiodistributionBloodBlood Circulation TimeBlood VesselsCardiovascular systemClinicalComplexContrast MediaCystamineCystineDetectionDevelopmentDiagnosisDiphosphatesDiseaseDrug KineticsEarly DiagnosisEarly treatmentElectron Transport Complex IIIEstersGadoliniumGadolinium DTPAGadopentetate DimeglumineGenerationsGlutathione DisulfideGoalsImageLeadLifeMS-325Macromolecular ComplexesMagnetic Resonance ImagingMalignant NeoplasmsMaximum Tolerated DoseModificationMolecular WeightN,N&apos-bis(pyridoxal-5-phosphate)ethylenediamine-N,N&apos-diacetic acidOsmolalitiesPatient CarePatientsPentetic AcidPharmacologic SubstancePhysiciansPlasmaPropertyRateResearchResearch PersonnelResearch Project GrantsSafetySodium ChlorideStructureTestingThermodynamicsTissuesToxic effectVascular Permeabilitiesalkyl groupbasecancer imagingchemical stabilityclinical applicationcopolymerdesigndiethylenetriaminepentaacetatedisulfide bondgadofosveset trisodiumhemodynamicsimprovedin vivomortalitynovelpre-clinicalprogramstumor
中文摘要
描述(由申请人提供):本研究项目的目的是设计和开发新型生物可降解大分子Gd(III)复合物作为安全、有效的磁共振成像(MRI)血池造影剂。聚二硫化物Gd(III)络合物是无毒的,具有延长的血液循环时间,可以降解并从体内快速消除,如动物模型中所示。它们有望用于进一步的临床前和临床开发。该研究将集中于优化聚二硫化物的结构,以开发新一代非离子聚二硫化物Gd(III)配合物,其具有可控的体内降解速率和药代动力学,以及改善的体内对比增强。新型非离子型药物具有最小的组织蓄积、低渗透压和广泛的临床应用。具体目标是设计、合成和表征具有可控降解速率和可控血浆药代动力学的新型非离子聚二硫化物Gd(III)络合物;研究它们的物理化学性质,包括Gd(III)螯合物的弛豫性、降解性和热力学稳定性以及大分子试剂的化学稳定性;研究新药的血浆药代动力学、消除和生物分布、血流动力学安全性、急性和亚急性耐受性以及最大耐受剂量;研究生物可降解大分子造影剂在动物模型中常规和动态增强MRI肿瘤成像的有效性;并鉴定具有可控降解速率、有效的对比增强最小的身体保留和最佳的安全性特征,用于进一步的临床前和临床开发。本项目的长期目标是开发一种安全、有效的可生物降解的大分子血池MRI造影剂,用于临床癌症成像。该研究项目旨在开发更有效的MRI造影剂,以提高早期诊断危及生命的疾病(包括癌症和心血管系统疾病)的准确性。早期发现和诊断将使护理这些患者的医生能够对这些疾病进行早期治疗,改善患者的生活质量,降低死亡率。
英文摘要
DESCRIPTION (provided by applicant): The objectives of this research project are to design and develop novel biodegradable macromolecular Gd(lll) complexes as safe, effective magnetic resonance imaging (MRI) blood pool contrast agents. Polydisulfide Gd(lll) complexes are non-toxic, have prolonged blood circulation time, can degrade and rapidly eliminate from the body as shown in animal models. They are promising for further preclinical and clinical development. The proposed research will focus on the optimization of the structure of polydisulfides to develop a new generation of non-ionic polydisulfide Gd(lll) complexes with controllable in vivo degradation rate and pharmacokinetics, and improved in vivo contrast enhancement. The novel non-ionic agents will have minimal tissue accumulation, low osmolality and broad applications in clinical practice. The specific aims are to design, synthesize and characterize novel non-ionic polydisulfide Gd(lll) complexes with controllable degradation rate and controllable plasma pharmacokinetics; to study their physicochemical properties including relaxivities, degradability and the thermodynamic stability of Gd(lll) chelates and chemical stability of the macromolecular agents; to investigate the plasma pharmacokinetics, elimination and biodistribution, hemodynamic safety, acute and subacute tolerance and maximum tolerated dose of the novel agents; to investigate efficacy of the biodegradable macromolecular contrast agents in tumor imaging in animal models with conventional and dynamic contrast enhanced MRI; and to identify a lead agent with controllable degradation rate, effective contrast enhancement, minimal body retention and optimal safety profiles for further preclinical and clinical development. The long-term goal of this project is to develop a safe, effective biodegradable macromolecular blood pool MRI contrast agent for clinical applications in cancer imaging. This research project is proposed to develop more effective MRI contrast agents to improve accuracy for the earlier diagnosis of life-threatening diseases including cancer and diseases in the cardiovascular systems. Earlier detection and diagnosis will allow the physicians caring these patients to pursue the earliest treatment of these diseases, improve the quality of the patients' life and reduce the mortality rate.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Smart nanoparticles regulating oncogenic IncRNA for breast cancer therapy
-
批准号:10307922
-
项目类别:
-
资助金额:$2.37万
-
财政年份:2021
-
负责人:ZHENG-RONG LU
-
依托单位:
Smart nanoparticles regulating oncogenic IncRNA for breast cancer therapy
-
批准号:10300425
-
项目类别:
-
资助金额:$35.02万
-
财政年份:2018
-
负责人:ZHENG-RONG LU
-
依托单位:
Smart nanoparticles regulating oncogenic IncRNA for breast cancer therapy
-
批准号:10524128
-
项目类别:
-
资助金额:$7.47万
-
财政年份:2018
-
负责人:ZHENG-RONG LU
-
依托单位:
Smart nanoparticles regulating oncogenic IncRNA for breast cancer therapy
-
批准号:10755865
-
项目类别:
-
资助金额:$7.54万
-
财政年份:2018
-
负责人:ZHENG-RONG LU
-
依托单位:
Smart nanoparticles regulating oncogenic IncRNA for breast cancer therapy
-
批准号:10532735
-
项目类别:
-
资助金额:$34.98万
-
财政年份:2018
-
负责人:ZHENG-RONG LU
-
依托单位:
Smart nanoparticles regulating oncogenic IncRNA for breast cancer therapy
-
批准号:10054176
-
项目类别:
-
资助金额:$35.78万
-
财政年份:2018
-
负责人:ZHENG-RONG LU
-
依托单位:
Targeted MRI contrast agents for differential diagnosis of prostate cancer
-
批准号:9327104
-
项目类别:
-
资助金额:$42.34万
-
财政年份:2017
-
负责人:ZHENG-RONG LU
-
依托单位:
Targeted MRI contrast agents for differential diagnosis of prostate cancer
-
批准号:9903251
-
项目类别:
-
资助金额:$42.62万
-
财政年份:2017
-
负责人:ZHENG-RONG LU
-
依托单位:
Image-guided EMT inhibition for treating metastatic breast cancer
-
批准号:9301500
-
项目类别:
-
资助金额:$47.39万
-
财政年份:2015
-
负责人:ZHENG-RONG LU
-
依托单位:
Biodegradable macromolecular CT contrast agents
-
批准号:8790640
-
项目类别:
-
资助金额:$19.37万
-
财政年份:2014
-
负责人:ZHENG-RONG LU
-
依托单位:
Biodegradable macromolecular CT contrast agents
-
批准号:8870352
-
项目类别:
-
资助金额:$23.3万
-
财政年份:2014
-
负责人:ZHENG-RONG LU
-
依托单位:
Polymer chelate conjugates for diagnostic cancer imaging
-
批准号:7910964
-
项目类别:
-
资助金额:$37.61万
-
财政年份:2009
-
负责人:ZHENG-RONG LU
-
依托单位:
Multifunctional Carriers for Systemic siRNA Delivery
-
批准号:7745571
-
项目类别:
-
资助金额:$13.76万
-
财政年份:2009
-
负责人:ZHENG-RONG LU
-
依托单位:
Minimally-Invasive Image-Guided Therapy for Cancer Treatment
-
批准号:7536104
-
项目类别:
-
资助金额:$14.96万
-
财政年份:2008
-
负责人:ZHENG-RONG LU
-
依托单位:
Polymer chelate conjugates for diagnostic cancer imaging
-
批准号:8133002
-
项目类别:
-
资助金额:$24.37万
-
财政年份:2004
-
负责人:ZHENG-RONG LU
-
依托单位:
Polymer chelate conjugates for Diagnostic cancer imaging
-
批准号:7023930
-
项目类别:
-
资助金额:$23.94万
-
财政年份:2004
-
负责人:ZHENG-RONG LU
-
依托单位:
Polymer chelate conjugates for Diagnostic cancer imaging
-
批准号:6853595
-
项目类别:
-
资助金额:$24.52万
-
财政年份:2004
-
负责人:ZHENG-RONG LU
-
依托单位:
Polymer chelate conjugates for diagnostic cancer imaging
-
批准号:7526210
-
项目类别:
-
资助金额:$24.08万
-
财政年份:2004
-
负责人:ZHENG-RONG LU
-
依托单位:
Polymer chelate conjugates for diagnostic cancer imaging
-
批准号:7918143
-
项目类别:
-
资助金额:$25.12万
-
财政年份:2004
-
负责人:ZHENG-RONG LU
-
依托单位:
Polymer chelate conjugates for Diagnostic cancer imaging
-
批准号:7195798
-
项目类别:
-
资助金额:$23.25万
-
财政年份:2004
-
负责人:ZHENG-RONG LU
-
依托单位:
国内基金
海外基金
登录
查看更多内容
具有抗癌活性的天然产物金霉酸(Aureolic acids)全合成与选择性构建2-脱氧糖苷键
-
批准号:22007039
-
项目类别:青年科学基金项目
-
资助金额:24.0万元
-
批准年份:2020
-
负责人:王黎明
-
依托单位:
海洋放线菌来源聚酮类化合物Pteridic acids生物合成机制研究
-
批准号:
-
项目类别:省市级项目
-
资助金额:10.0万元
-
批准年份:2019
-
负责人:朱义广
-
依托单位:
手性Lewis Acids催化的分子内串联1,5-氢迁移/环合反应及其在构建结构多样性手性含氮杂环化合物中的应用
-
批准号:21372217
-
项目类别:面上项目
-
资助金额:80.0万元
-
批准年份:2013
-
负责人:袁伟成
-
依托单位:
对空气稳定的新型的有机金属Lewis Acids催化剂制备、表征与应用研究
-
批准号:21172061
-
项目类别:面上项目
-
资助金额:30.0万元
-
批准年份:2011
-
负责人:许新华
-
依托单位:
钛及含钛Lewis acids促臭氧/过氧化氢体系氧化性能的广普性、高效性及其机制
-
批准号:21176225
-
项目类别:面上项目
-
资助金额:60.0万元
-
批准年份:2011
-
负责人:童少平
-
依托单位:
基于Zip Nucleic Acids引物对高度降解和低拷贝DNA检材的STR分型研究
-
批准号:81072511
-
项目类别:面上项目
-
资助金额:31.0万元
-
批准年份:2010
-
负责人:严江伟
-
依托单位:
海洋天然产物Makaluvic acids 的全合成及其对南海鱼虱存活的影响
-
批准号:30660215
-
项目类别:地区科学基金项目
-
资助金额:21.0万元
-
批准年份:2006
-
负责人:王世范
-
依托单位: