Injectable Supramolecular Hydrogel/Microgel Composites for Therapeutic Delivery

被引:83
作者
Chen, Minna H. [1 ]
Chung, Jennifer J. [2 ]
Mealy, Joshua E. [1 ]
Zaman, Samir [2 ]
Li, Elizabeth C. [2 ]
Arisi, Maria F. [2 ]
Atluri, Pavan [2 ]
Burdick, Jason A. [1 ]
机构
[1] Univ Penn, Dept Bioengn, 210 S 33rd St, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Surg, Div Cardiovasc Surg, Silverstein 6,3400 Spruce St, Philadelphia, PA 19104 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
composites; drug delivery; hydrogels; microgels; supramolecular; SHEAR-THINNING HYDROGELS; INFLAMMATORY RESPONSE; MYOCARDIAL-INFARCTION; PEPTIDE AMPHIPHILES; HEART-DISEASE; INTERLEUKIN-10; IL-10; SCAFFOLDS; MODULATE; PROTEIN;
D O I
10.1002/mabi.201800248
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Shear-thinning hydrogels are useful for biomedical applications, from 3D bioprinting to injectable biomaterials. Although they have the appropriate properties for injection, it may be advantageous to decouple injectability from the controlled release of encapsulated therapeutics. Toward this, composites of hydrogels and encapsulated microgels are introduced with microgels that are fabricated via microfluidics. The microgel cross-linker controls degradation and entrapped molecule release, and the concentration of microgels alters composite hydrogel rheological properties. For the treatment of myocardial infarction (MI), interleukin-10 (IL-10) is encapsulated in microgels and released from composites. In a rat model of MI, composites with IL-10 reduce macrophage density after 1 week and improve scar thickness, ejection fraction, cardiac output, and the size of vascular structures after 4 weeks when compared to saline injection. Improvements are also observed with the composite without IL-10 over saline, emphasizing the role of injectable hydrogels alone on tissue repair.
引用
收藏
页数:12
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