Novel Engineered Particle Platform for Endothelium Regeneration

用于内皮再生的新型工程颗粒平台

• 批准号: 9198993
• 负责人: Kytai Truong Nguyen
• 金额: $ 39.55万
• 依托单位: UNIVERSITY OF TEXAS ARLINGTON
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-01-01 至 2018-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9198993
• 关键词: Adherence; Adhesions; Angioplasty; Animal Model; Area; Arteries; Binding; Biocompatible Materials; Blood Circulation; Blood Platelets; Blood Vessels; Blood coagulation; CD34 Antigens; Cardiovascular Diseases; Cardiovascular system; Cause of Death; Cell Maturation; Cell Proliferation; Cell-Matrix Junction; Cells; Deposition; Development; Effectiveness; Endothelial Cells; Endothelium; Engineering; Evaluation; Family; Family suidae; Goals; Growth Factor; In Situ; In Vitro; Inflammation; Injectable; Injury; Intervention; Investigation; Ligands; Modality; Nanotechnology; Natural regeneration; Nature; Obstruction; Outcome; P-Selectin; Pathologic; Peptides; Physiological; Play; Polyesters; Polymers; Population; Prevention; Procedures; Property; Rattus; Reagent; Recruitment Activity; Research; Research Project Grants; Role; Site; Smooth Muscle Myocytes; Stem cells; Stents; Surface; System; Technology; Testing; Therapeutic; Thrombosis; Tissue Engineering; Toxic effect; Urethane; VWF gene; Vascular Diseases; Vascular Endothelial Cell; Vascular Endothelium; Work; base; biomaterial compatibility; cardiovascular disorder therapy; cell motility; economic impact; healing; improved; in vivo; in vivo regeneration; injured; innovation; mimicry; nanoparticle; novel; overexpression; particle; percutaneous coronary intervention; prevent; public health relevance; repaired; restenosis; scaffold; vascular tissue engineering

DESCRIPTION (provided by applicant): Although percutaneous coronary intervention (PCI) modalities such as angioplasty are often used as the standard procedure for treatment of cardiovascular disease, the number one cause of death in the U.S., they have many limitations including late restenosis and thrombosis. Delayed endothelium regeneration after vascular injury by PCI has been indicated as a major cause for these drawbacks, especially late thrombosis. Indeed, endothelium layer serves as a nature barrier for the artery and plays an important role in the prevention of platelet adhesion and smooth muscle cell proliferation and migration. Thus our long-term goal is to engineer novel multifunctional targeting nanoparticles (MTNs) that can bind specifically onto the injured arterial site to serve as a temporary barrier to prevent platelet adhesion and smooth muscle cell migration while recruiting stem cells such as endothelial progenitor cells (EPCs) for enhancing endothelium regeneration. The novel engineered MTNs will prevent platelet adhesion and encourage rapid endothelium healing at the injured site, allowing the potential of re-endothelialization in situ. To reach our goal, three specific aims are proposed: (1) To synthesize and characterize novel biodegradable, biocompatible, and hemo-compatible biomaterials including urethane-doped polyesters (UPEs) for vascular tissue engineering applications. (2) To formulate MTNs, which are made of UPEs, loaded with therapeutic reagents including growth factors, and conjugated with both the injured arterial wall targeting ligands and the EPC binding molecules. Various properties of MTNs including the effects of MTNs on platelet deposition and endothelium regeneration in vitro will be further investigated. (3) To determine the effectiveness of novel MTNs in vivo for endothelium regeneration in situ following PCI injury using animal models. There are several innovative aspects associated with this research. Our engineered MTNs, based on recent advances in both tissue engineering and nanotechnology, provide a unique strategy to promote endothelium regeneration and hence to stimulate vascular healing after PCI while preventing platelet adhesion. Another novel aspect of our research is that the engineered MTNs utilize the combination of (1) targeting injured arteries, (2) reducing platelet adhesion by serving as a temporary barrier, (3) capturing EPC at the targeted sites, which indirectly reduce platelet deposition on the damaged areas, and (4) promoting endothelium regeneration using engineered tissue nanoscaffolds. The proposed MTNs will bring in a significant improvement in the treatment of PCI-associated vascular injury and should generate highly scientific and economic impacts in cardiovascular disease therapy.

描述（由申请人提供）：虽然经皮冠状动脉介入治疗（PCI）方式，如血管成形术，经常被用作治疗心血管疾病的标准程序，心血管疾病是美国的头号死因，但它们有许多局限性，包括晚期再狭窄和血栓形成。经PCI血管损伤后内皮细胞再生延迟已被认为是这些缺陷的主要原因，尤其是晚期血栓形成。内皮层是动脉的天然屏障，在阻止血小板粘附和平滑肌细胞增殖和迁移方面发挥着重要作用。因此，我们的长期目标是设计一种新的多功能靶向纳米颗粒（mtn），它可以特异性地结合到受伤的动脉部位，作为暂时的屏障

项目成果

The critical chemical and mechanical regulation of folic acid on neural engineering.

• DOI: 10.1016/j.biomaterials.2018.03.059
• 发表时间: 2018-09
• 期刊: Biomaterials
• 影响因子: 14
• 作者: Kim GB;Chen Y;Kang W;Guo J;Payne R;Li H;Wei Q;Baker J;Dong C;Zhang S;Wong PK;Rizk EB;Yan J;Yang J
• 通讯作者: Yang J

Electrospun biodegradable elastic polyurethane scaffolds with dipyridamole release for small diameter vascular grafts.

• DOI: 10.1016/j.actbio.2014.07.031
• 发表时间: 2014-11
• 期刊: ACTA BIOMATERIALIA
• 影响因子: 9.7
• 作者: Punnakitikashem, Primana;Danh Truong;Menon, Jyothi U.;Nguyen, Kytai T.;Hong, Yi
• 通讯作者: Hong, Yi

Dual-responsive polymer-coated iron oxide nanoparticles for drug delivery and imaging applications.

• DOI: 10.1016/j.ijpharm.2014.03.016
• 发表时间: 2014-05-15
• 期刊: International journal of pharmaceutics
• 影响因子: 5.8
• 作者: Sundaresan V;Menon JU;Rahimi M;Nguyen KT;Wadajkar AS
• 通讯作者: Wadajkar AS

Highly photostable nanogels for fluorescence-based theranostics.

• DOI: 10.1016/j.bioactmat.2017.03.001
• 发表时间: 2018-03
• 期刊: Bioactive materials
• 影响因子: 18.9
• 作者: Gyawali D;Kim JP;Yang J
• 通讯作者: Yang J

Deep vein thrombosis: current status and nanotechnology advances.

• DOI: 10.1016/j.biotechadv.2012.08.004
• 发表时间: 2013-09
• 期刊: BIOTECHNOLOGY ADVANCES
• 影响因子: 16
• 作者: Wadajkar, Aniket S.;Santimano, Sonia;Rahimi, Maham;Yuan, Baohong;Banerjee, Subhash;Nguyen, Kytai T.
• 通讯作者: Nguyen, Kytai T.