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壳聚糖/泊洛沙姆水凝胶中含有 bFGF/肝素,用于包封人真皮成纤维细胞。

Chitosan/pluronic hydrogel containing bFGF/heparin for encapsulation of human dermal fibroblasts.

机构信息

Department of Biomaterials Engineering, School of Bioscience and Bioengineering, Kangwon National University, Chuncheon, 200-701, South Korea.

出版信息

J Biomater Sci Polym Ed. 2013;24(2):210-23. doi: 10.1163/156856212X630267. Epub 2012 May 11.


DOI:10.1163/156856212X630267
PMID:23565598
Abstract

In order to act as a cell reservoir, a hydrogel has to have a suitable mechanical strength and should also enhance proliferation of cells. We have developed a hydrogel composed of chitosan and Pluronic containing a complex of basic fibroblast growth factor (bFGF) and heparin for cell encapsulation, and its ability as a scaffold for cells was evaluated. The hydrogel was composed of glycidyl methacrylated chitooligosaccharide (COS) and diacrylated Pluronic F127 (Pluronic) in various blend ratios. A mixture of COS and Pluronic was homogeneously mixed with cells, bFGF and heparin; then, the hydrogel precursor was photo-irradiated. With increasing amount of COS, the chemically cross-linked COS/Pluronic hydrogel showed an approx. 2-fold increase of its elastic modulus and a lower mass erosion rate than the hydrogel composed of only Pluronic after 28 days. The amount of bFGF was increased according to the presence of heparin within the hydrogel, but the amount of released bFGF was decreased by increasing the content of COS. The hydrogel containing bFGF with heparin showed higher proliferation of cells compared to the hydrogel without heparin at 20% COS. However, when the blend ratio of COS was 50%, the hydrogel showed less proliferation of cells than those with 20% COS. Therefore, the chemically cross-linked COS/Pluronic hydrogel be useful for a protein-delivery system and tissue-engineering scaffold.

摘要

为了充当细胞储存库,水凝胶必须具有合适的机械强度,并且还应增强细胞的增殖。我们已经开发出一种由壳聚糖和含有碱性成纤维细胞生长因子(bFGF)和肝素复合物的 Pluronic 组成的水凝胶,用于细胞包封,并评估了其作为细胞支架的能力。水凝胶由不同比例的甲基丙烯酰化壳寡糖(COS)和二丙烯酰化 Pluronic F127(Pluronic)组成。将 COS 和 Pluronic 的混合物与细胞,bFGF 和肝素均匀混合;然后,对水凝胶前体进行光照射。随着 COS 用量的增加,与仅由 Pluronic 组成的水凝胶相比,化学交联的 COS/Pluronic 水凝胶在 28 天后其弹性模量约增加了 2 倍,质量侵蚀率降低。根据水凝胶中肝素的存在,bFGF 的量增加,但随着 COS 含量的增加,释放的 bFGF 的量减少。与不含肝素的水凝胶相比,含有肝素的 bFGF 的水凝胶在 20%COS 下显示出更高的细胞增殖。但是,当 COS 的混合比为 50%时,水凝胶的细胞增殖率低于 20%COS 的水凝胶。因此,化学交联的 COS/Pluronic 水凝胶可用于蛋白质递送系统和组织工程支架。

相似文献

[1]
Chitosan/pluronic hydrogel containing bFGF/heparin for encapsulation of human dermal fibroblasts.

J Biomater Sci Polym Ed. 2012-5-11

[2]
Photo-crosslinkable and biodegradable Pluronic/heparin hydrogels for local and sustained delivery of angiogenic growth factor.

J Biomed Mater Res A. 2007-12-1

[3]
Pluronic/chitosan hydrogels containing epidermal growth factor with wound-adhesive and photo-crosslinkable properties.

J Biomed Mater Res A. 2010-11

[4]
Evaluation of hydrogel composing of Pluronic F127 and carboxymethyl hexanoyl chitosan as injectable scaffold for tissue engineering applications.

Colloids Surf B Biointerfaces. 2016-6-1

[5]
Cell survival and proliferation after encapsulation in a chemically modified Pluronic(R) F127 hydrogel.

J Biomater Appl. 2011-11-15

[6]
Heparin-functionalized chitosan-alginate scaffolds for controlled release of growth factor.

Int J Pharm. 2009-7-6

[7]
Development of bFGF-chitosan matrices and their interactions with human dermal fibroblast cells.

J Biomater Sci Polym Ed. 2009

[8]
Injectable glycosaminoglycan hydrogels for controlled release of human basic fibroblast growth factor.

Biomaterials. 2005-10

[9]
Fabrication and characterization of ophthalmically compatible hydrogels composed of poly(dimethyl siloxane-urethane)/Pluronic F127.

Colloids Surf B Biointerfaces. 2009-6-1

[10]
Cell affinity for bFGF immobilized heparin-containing poly(lactide-co-glycolide) scaffolds.

Biomaterials. 2011-5

引用本文的文献

[1]
Progress in Pluronic F127 Derivatives for Application in Wound Healing and Repair.

Int J Nanomedicine. 2023

[2]
Chitooligosaccharide Inhibits Scar Formation and Enhances Functional Recovery in a Mouse Model of Sciatic Nerve Injury.

Mol Neurobiol. 2016-5

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