4.6 Article

Fibrillized peptide microgels for cell encapsulation and 3D cell culture

期刊

SOFT MATTER
卷 7, 期 13, 页码 6005-6011

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c1sm05504f

关键词

-

资金

  1. National Institutes of Health (NIBIB) [1R01EB009701, U54 CA151880]
  2. Chicago Biomedical Consortium
  3. National Science Foundation [CHE-0802286]
  4. NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING [R01EB009701] Funding Source: NIH RePORTER

向作者/读者索取更多资源

One of the advantages of materials produced by self-assembly is that in principle they can be formed in any given container to produce materials of predetermined shapes and sizes. Here, we developed a method for triggering peptide self-assembly within the aqueous phase of water-in-oil emulsions to produce spherical microgels composed of fibrillized peptides. Size control over the microgels was achieved by specification of blade type, speed, and additional shear steps in the emulsion process. Microgels constructed in this way could then be embedded within other self-assembled peptide matrices by mixing pre-formed microgels with un-assembled peptides and inducing gelation of the entire composite, offering a route towards multi-peptide materials with micron-scale domains of different peptide formulations. The gels themselves were cytocompatible, as was the microgel fabrication procedure, enabling the encapsulation of NIH 3T3 fibroblasts and C3H10T-1/2 mouse pluripotent stem cells with good viability.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据