Drug Delivery and Biomimetic Approaches for Optimal Stem Cell Therapy

最佳干细胞治疗的药物输送和仿生方法

• 批准号: 10995606
• 负责人: Ke Cheng
• 金额: $ 75.95万
• 依托单位: COLUMBIA UNIV NEW YORK MORNINGSIDE
• 依托单位国家: 美国
• 财政年份: 2021
• 资助国家: 美国
• 起止时间: 2021-04-01 至 2025-03-31
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10995606
• 关键词: Drug; Delivery; Biomimetic; Approaches; Optimal

PROJECT SUMMARY Numerous studies indicate that adult stem cells exert their functional benefits mainly through paracrine effects, i.e., secreted factors from stem cells promote cardiac regeneration and inhibit fibrosis and inflammation. However, two major challenges remain to efficiently delivery stem cell factors to the injured myocardium: 1) injected growth factors are quickly diffused, therefore sustained release is needed; 2) local injection is effective but requires open chest procedure, systemic injection is safe but cannot get sufficient dosage to the heart, therefore targeted delivery is needed. To overcome those challenges, we designed a platelet-inspired nano-cell (PINC) that has a core containing stem cell factors and a platelet membrane shell for injury binding. The core consists of therapeutic CSC-secreted factors encapsulated in a biodegradable poly (lactic-co-glycolic acid) (PLGA) nanoparticle for sustained release. The platelet membrane is conjugated with PGE2 which is expected to have targetability to cardiovascular cells and facilitate the endogenous repair through PGE2/EP receptor signaling after I/R injury. As a novel biomimetic therapeutic nanoparticle, PINC offers the following advantages compared to natural stem cells: (i) PINC is small enough for systemic administration: the nano size of PINC enables intravenous application; unlike stem cells, PINCs are less likely to be blocked by the lungs; (ii) PINC has dual targeting ability: the platelet membrane on PINCs targets injured blood vessels while the PGE2 targets injured cardiomyocytes in MI; (iii) PINC is stable during storage: unlike real stem cells, PINCs can be readily manipulated and cryopreserved since there are no living components. The Specific Aims are: AIM 1. Fabricate PINC particles functionalized with PGE2 and CSC secretome; Test the in vitro potency and cytotoxicity of PINC; AIM 2. Determine the safety, efficacy, and mechanism of PINC therapy in a rat model of ischemia-reperfusion (IR) injury; AIM 3. Translate the findings into a clinically-relevant porcine model of IR injury. Our study will form the foundation for an innovative and “off the shelf” therapy based on secreted factors and targeted nanomedicine that can be standardized from donor stem cell lines and xenogeneic cardiac tissues. The cell-free nature of our approach is more readily translatable to the clinic. Although this particular grant application targets the heart and cardiac stem cells, our approach represents a platform technology that can be applied to the creation of multiple types of synthetic stem cell and organ matrices for the repair of various other organs.

项目总结