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从多孔静电喷涂沉积法制备的磷酸钙涂层中释放转化生长因子-β1 。

Transforming growth factor-beta1 release from a porous electrostatic spray deposition-derived calcium phosphate coating.

作者信息

Siebers Marijke C, Walboomers X Frank, Leewenburgh Sander C G, Wolke Joop C G, Boerman Otto C, Jansen John A

机构信息

Department of Periodontology and Biomaterials, Radboud University Nijmegen Medical Centre, Nijmegen, the Netherlands.

出版信息

Tissue Eng. 2006 Sep;12(9):2449-56. doi: 10.1089/ten.2006.12.2449.

Abstract

This study evaluated the utilization of a porous coating, derived with electrostatic spray deposition (ESD), as a carrier material for transforming growth factor-beta1 (TGF-beta1). A porous beta-tricalcium phosphate coating was deposited with ESD, and 10 ng of (125) I-labeled TGF-beta1 was loaded on the substrates. A burst release during the first hour of incubation of >90% was observed, in either culture medium or phosphate-buffered saline (PBS). Ninety-nine percent of the growth factor was released after 10 days of incubation. All samples were able to inhibit epithelial cell growth, indicating that the growth factor had remained bioactive after release. Thereafter, osteoblast-like cells were seeded upon substrates with or without 10 ng of TGF-beta1. While proliferation of osteoblast-like cells was increased on TGF-beta1-loaded substrates, differentiation was inhibited or delayed. In conclusion, a porous ESD-derived calcium phosphate coating can be used as a carrier material for TGF-beta1, when a burst release is desired.

摘要

本研究评估了通过静电喷涂沉积(ESD)获得的多孔涂层作为转化生长因子-β1(TGF-β1)载体材料的应用。采用ESD沉积多孔β-磷酸三钙涂层,并将10 ng的(125)I标记的TGF-β1负载在基底上。在培养基或磷酸盐缓冲盐水(PBS)中孵育的第一小时内观察到超过90%的药物突发释放。孵育10天后,99%的生长因子被释放。所有样品均能抑制上皮细胞生长,表明生长因子在释放后仍保持生物活性。此后,将成骨样细胞接种在含有或不含有10 ng TGF-β1的基底上。虽然在负载TGF-β1的基底上成骨样细胞的增殖增加,但分化受到抑制或延迟。总之,当需要突发释放时,多孔ESD衍生的磷酸钙涂层可作为TGF-β1的载体材料。

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