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用于可注射组织构建体的微流体辅助制备明胶-二氧化硅核壳微凝胶

Microfluidics-assisted fabrication of gelatin-silica core-shell microgels for injectable tissue constructs.

作者信息

Cha Chaenyung, Oh Jonghyun, Kim Keekyoung, Qiu Yiling, Joh Maria, Shin Su Ryon, Wang Xin, Camci-Unal Gulden, Wan Kai-tak, Liao Ronglih, Khademhosseini Ali

机构信息

Harvard-MIT Division of Health Sciences and Technology, Division of Biomedical Engineering, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School , Cambridge, Massachusetts 02139, United States.

出版信息

Biomacromolecules. 2014 Jan 13;15(1):283-90. doi: 10.1021/bm401533y. Epub 2014 Jan 2.

Abstract

Microfabrication technology provides a highly versatile platform for engineering hydrogels used in biomedical applications with high-resolution control and injectability. Herein, we present a strategy of microfluidics-assisted fabrication photo-cross-linkable gelatin microgels, coupled with providing protective silica hydrogel layer on the microgel surface to ultimately generate gelatin-silica core-shell microgels for applications as in vitro cell culture platform and injectable tissue constructs. A microfluidic device having flow-focusing channel geometry was utilized to generate droplets containing methacrylated gelatin (GelMA), followed by a photo-cross-linking step to synthesize GelMA microgels. The size of the microgels could easily be controlled by varying the ratio of flow rates of aqueous and oil phases. Then, the GelMA microgels were used as in vitro cell culture platform to grow cardiac side population cells on the microgel surface. The cells readily adhered on the microgel surface and proliferated over time while maintaining high viability (∼90%). The cells on the microgels were also able to migrate to their surrounding area. In addition, the microgels eventually degraded over time. These results demonstrate that cell-seeded GelMA microgels have a great potential as injectable tissue constructs. Furthermore, we demonstrated that coating the cells on GelMA microgels with biocompatible and biodegradable silica hydrogels via sol-gel method provided significant protection against oxidative stress which is often encountered during and after injection into host tissues, and detrimental to the cells. Overall, the microfluidic approach to generate cell-adhesive microgel core, coupled with silica hydrogels as a protective shell, will be highly useful as a cell culture platform to generate a wide range of injectable tissue constructs.

摘要

微加工技术为工程化用于生物医学应用的水凝胶提供了一个高度通用的平台,具有高分辨率控制和可注射性。在此,我们提出了一种微流控辅助制备光交联明胶微凝胶的策略,同时在微凝胶表面提供保护性二氧化硅水凝胶层,最终生成明胶-二氧化硅核壳微凝胶,用作体外细胞培养平台和可注射组织构建体。利用具有流动聚焦通道几何结构的微流控装置生成含有甲基丙烯酸化明胶(GelMA)的液滴,随后进行光交联步骤以合成GelMA微凝胶。通过改变水相和油相的流速比,可以轻松控制微凝胶的尺寸。然后,将GelMA微凝胶用作体外细胞培养平台,在微凝胶表面培养心脏侧群细胞。细胞很容易附着在微凝胶表面并随时间增殖,同时保持高活力(约90%)。微凝胶上的细胞也能够迁移到其周围区域。此外,微凝胶最终会随时间降解。这些结果表明,接种细胞的GelMA微凝胶作为可注射组织构建体具有巨大潜力。此外,我们证明,通过溶胶-凝胶法用生物相容性和可生物降解的二氧化硅水凝胶包被GelMA微凝胶上的细胞,可提供显著的保护,防止在注射到宿主组织期间和之后经常遇到的、对细胞有害的氧化应激。总体而言,生成细胞粘附性微凝胶核心并结合二氧化硅水凝胶作为保护壳的微流控方法,作为一种细胞培养平台来生成各种可注射组织构建体将非常有用。

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