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Volume 6, Issue 8, Pages 3044-3055 (August 2010)


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Injectable oxidized hyaluronic acid/adipic acid dihydrazide hydrogel for nucleus pulposus regeneration

Wen-Yu Su, Yu-Chun Chen, Feng-Huei LinCorresponding Author Informationemail address

Received 24 August 2009; received in revised form 23 February 2010; accepted 23 February 2010. published online 02 March 2010.

Abstract 

Injectable hydrogel allows irregular surgical defects to be completely filled, lessens the risk of implant migration, and minimizes surgical defects due to the solution–gel state transformation. Here, we first propose a method for preparing oxidized hyaluronic acid/adipic acid dihydrazide (oxi-HA/ADH) injectable hydrogel by chemical cross-linking under physiological conditions. Fourier transform infrared spectrometry and trinitrobenzene sulfonate assay were used to confirm the oxidation of hyaluronic acid. Rheological properties were measured to evaluate the working ability of the hydrogel for further clinical application. The oxi-HA/ADH in situ forming hydrogel can transform from liquid form into a gel-like matrix within 3–8min, depending on the operational temperature. Furthermore, hydrogel degradation and cell assessment is also a concern for clinical application. Injectable oxi-HA/ADH8 hydrogel can maintain its gel-like state for at least 5weeks with a degradation percentage of 40%. Importantly, oxi-HA/ADH8 hydrogel can assist in nucleus pulposus cell synthesis of type II collagen and aggrecan mRNA gene expression according to the results of real-time PCR analysis, and shows good biocompatibility based on cell viability and cytotoxicity assays. Based on the results of the current study, oxi-HA/ADH hydrogel may possess several advantages for future application in nucleus pulposus regeneration.

Institute of Biomedical Engineering, National Taiwan University (NTU), No. 1, Sec. 4, Roosevelt Road, Taipei 106, Taiwan, ROC

Division of Medical Engineering Research, National Health Research Institutes, 35 Keyan Road, Zhunan, Miaoli County 350, Taiwan, ROC

Corresponding Author InformationCorresponding author. Tel.: +886 37 246166x37126; fax: +886 37 246166.

PII: S1742-7061(10)00111-X

doi:10.1016/j.actbio.2010.02.037


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