Development of a modular, biocompatible thiolated gelatin microparticle platform for drug delivery and tissue engineering applications

被引:10
|
作者
Pearce, Hannah A. [1 ]
Kim, Yu Seon [1 ]
Watson, Emma [1 ]
Bahrami, Kiana [1 ]
Smoak, Mollie M. [1 ]
Jiang, Emily Y. [1 ]
Elder, Michael [1 ]
Shannon, Tate [1 ]
Mikos, Antonios G. [1 ]
机构
[1] Rice Univ, Dept Bioengn, 6500 Main St, Houston, TX 77030 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
gelatin microparticles; thiolated gelatin microparticles; click chemistry; cell delivery; drug delivery; tissue engineering; biomaterials; MESENCHYMAL STEM-CELLS; BIODEGRADABLE HYDROGEL COMPOSITES; CALCIUM-PHOSPHATE CEMENT; GROWTH-FACTOR DELIVERY; TRANSFORMING GROWTH-FACTOR-BETA-1; PHYSICOCHEMICAL CHARACTERIZATION; CHONDROGENIC DIFFERENTIATION; RELEASE KINETICS; CLICK REACTIONS; FUNCTIONALIZATION;
D O I
10.1093/rb/rbab012
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
The field of biomaterials has advanced significantly in the past decade. With the growing need for high-throughput manufacturing and screening, the need for modular materials that enable streamlined fabrication and analysis of tissue engineering and drug delivery schema has emerged. Microparticles are a powerful platform that have demonstrated promise in enabling these technologies without the need to modify a bulk scaffold. This building block paradigm of using microparticles within larger scaffolds to control cell ratios, growth factors and drug release holds promise. Gelatin microparticles (GMPs) are a well-established platform for cell, drug and growth factor delivery. One of the challenges in using GMPs though is the limited ability to modify the gelatin post-fabrication. In the present work, we hypothesized that by thiolating gelatin before microparticle formation, a versatile platform would be created that preserves the cytocompatibility of gelatin, while enabling post-fabrication modification. The thiols were not found to significantly impact the physicochemical properties of the microparticles. Moreover, the thiolated GMPs were demonstrated to be a biocompatible and robust platform for mesenchymal stem cell attachment. Additionally, the thiolated particles were able to be covalently modified with a maleimide-bearing fluorescent dye and a peptide, demonstrating their promise as a modular platform for tissue engineering and drug delivery applications.
引用
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页数:12
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