EX VIVO MODEL TO STUDY NANOPARTICLE UPTAKE FOR ORAL GENE DELIVERY
EX VIVO MODEL TO STUDY NANOPARTICLE UPTAKE FOR ORAL GENE DELIVERY
批准号:
7956911
负责人:
KAM W LEONG
金额:
$0.55万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-07-01 至 2010-06-30
关键词:
BiodistributionChitosanComputer Retrieval of Information on Scientific Projects DatabaseDNAExcisionFundingGastrointestinal tract structureGene DeliveryGenesGrantImageInstitutionIntestinesLabelMicroscopyModelingOralOral AdministrationPilot ProjectsQuantum DotsRattusResearchResearch PersonnelResourcesSourceSystemUnited States National Institutes of Healthdesignin vivonanoparticleuptake
中文摘要
这个子项目是许多研究子项目中利用
资源由NIH/NCRR资助的中心拨款提供。子项目和
调查员(PI)可能从NIH的另一个来源获得了主要资金,
并因此可以在其他清晰的条目中表示。列出的机构是
该中心不一定是调查人员的机构。
该项目旨在确定在闭合肠环模型中口服后,用量子点标记的聚合物纳米络合物的生物分布。作为一项试点研究,在远红区发射的量子点将被用来标记DNA,然后用DNA与壳聚糖形成纳米络合物。然后,将纳米颗粒注射到大鼠胃肠道(GIT)的分离部分,持续预定的时间。在切除了GIT的相关部分之后,我们建议通过柯达体内成像系统来确定纳米复合体的摄取。该系统将提供GIT中显示增强吸收我们的纳米复合体的特定部分的半定量鉴定。
这项研究将使我们能够更好地设计聚合基因载体和大分子制剂,进一步保护DNA和纳米复合体,以促进更有效的口服基因输送。
英文摘要
This subproject is one of many research subprojects utilizing the
resources provided by a Center grant funded by NIH/NCRR. The subproject and
investigator (PI) may have received primary funding from another NIH source,
and thus could be represented in other CRISP entries. The institution listed is
for the Center, which is not necessarily the institution for the investigator.
The project aims to determine the biodistribution of polymeric nanocomplexes labeled with quantum dots, following oral administration in a closed intestinal loop model. As a pilot study, quantum dots that emit in the far-red region will be used to label DNA, which is then used to form nanocomplexes with chitosan. The nanoparticles are then administered to isolated sections of rat gastrointestinal tract (GIT) for pre-determined durations. Following the excision of the relevant sections of the GIT, we propose to determine the uptake of the nanocomplexes by means of the Kodak In-Vivo Imaging System. The system would provide a semi-quantitative identification of the specific sections of the GIT that show enhanced uptake of our nanocomplexes.
Such a study would enable us to better design polymeric gene carriers and macroformulations that would further protect the DNA and nanocomplexesin order to facilitate more efficient oral gene delivery.
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