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用于控制生长因子递送的纳米和微尺度硫酸软骨素颗粒的开发。

Development of nano- and microscale chondroitin sulfate particles for controlled growth factor delivery.

机构信息

W.H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, 313 Ferst Drive, Atlanta, GA 30332, USA.

出版信息

Acta Biomater. 2011 Mar;7(3):986-95. doi: 10.1016/j.actbio.2010.10.009. Epub 2010 Oct 20.

Abstract

Size scale plays an important role in the release properties and cellular presentation of drug delivery vehicles. Because negatively charged chondroitin sulfate (CS) is capable of electrostatically sequestering positively charged growth factors, CS-derived nanoscale micelles and microscale spheroids were synthesized as potential growth factor carriers to enhance differentiation of stem cells. Particles were characterized for morphology, size distribution, surface charge and cytocompatibility, as well as release of transforming growth factor-β1 (TGF-β1) and tumor necrosis factor-α (TNF-α). CS micelles were spherical and negatively charged with a bimodal distribution of 324.1±8.5 and 73.2±4.4 nm diameters, and CS microspheres possessed a rounded morphology and a diameter of 4.3±0.93 μm. Positively charged TGF-β1 demonstrated minimal release after loading in CS microspheres, while negatively charged TNF-α exhibited substantial release over the first 15 h, suggesting that TGF-β1 electrostatically complexed with CS. The micelles and microparticles were found to be cytocompatible at moderate concentrations with marrow stromal cell monolayers and within embryonic stem cell embryoid bodies. These synthesis techniques, which allow the formation of CS-based carriers over a variety of nano- and microscale sizes, offer versatility for tailored release of positively charged growth factors and controlled CS presentation for a variety of stem cell-based applications in tissue engineering and regenerative medicine.

摘要

尺寸比例在药物输送载体的释放特性和细胞呈现中起着重要作用。由于带负电荷的硫酸软骨素(CS)能够静电隔离带正电荷的生长因子,因此合成了源自 CS 的纳米级胶束和微球作为潜在的生长因子载体,以增强干细胞的分化。对颗粒的形态、粒径分布、表面电荷和细胞相容性以及转化生长因子-β1(TGF-β1)和肿瘤坏死因子-α(TNF-α)的释放进行了表征。CS 胶束呈球形,带负电荷,粒径分布呈双峰分布,分别为 324.1±8.5nm 和 73.2±4.4nm,CS 微球呈圆形,直径为 4.3±0.93μm。负载在 CS 微球中的带正电荷的 TGF-β1 释放很少,而带负电荷的 TNF-α在最初 15 小时内大量释放,表明 TGF-β1 与 CS 静电复合。在中等浓度下,这些胶束和微球与骨髓基质细胞单层和胚胎干细胞胚状体相容。这些合成技术允许在各种纳米和微尺度上形成基于 CS 的载体,为正电荷生长因子的定制释放和各种基于干细胞的组织工程和再生医学应用中 CS 的可控呈现提供了多功能性。

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