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[壳聚糖-胶原蛋白聚合物通过自生长方法诱导牙齿硬组织再矿化]

[Chitosan-collagen polymer induced remineralization of tooth hard tissue through self-growing methods].

作者信息

Xun Ren, Jing Yao, Qin Du, Chuhang Liao, Kun Tian

出版信息

Hua Xi Kou Qiang Yi Xue Za Zhi. 2014 Oct;32(5):519-24. doi: 10.7518/hxkq.2014.05.021.

Abstract

OBJECTIVE

To modify biomacromolecules, such as chitosan and collagen, to synthesize a mineralized template that will induce self-growing remineralization of tooth enamel.

METHODS

Natural polycation polysaccharide chitosan was modified through phosphorylation to synthesize the polyanion derivative ofphosphorylated chitosan. Parent hydrogels com- bined with chitosan and collagen I were built through peptide binding reaction using genipin as a crosslinker. The gels self- assembled on the tooth's inert surface, which was stimulated by ultraviolet radiation. The bionic saliva provided mineralized ion, and then the hydroxyapatite assembled and grew in situ on the tooth.

RESULTS

The functional group P04(3-) (3,446 cm(-1)) was grafted on chitosan as confirmed by the Fourier transform infrared spectroscopy. The porous polyelectrolyte complex hydrogel formed by the interaction between the polycation chitosan and the polyanion phosphorylated chitosan could induce hydroxyapatite crystal nucleation and growth on the hydrogel fiber surfaces. The neonatal crystal was hydroxyapatite as confirmed by X-ray diffraction and was tightly connected to the tooth. A continuous structure of column crystals with sizes ranging from 30 nm to 60 nm was observed. The structure was in parallel direction similar to the direction of the enamel rod, and its hardness was close to dentin.

CONCLUSION

The parent hydrogels that were easily obtained and controlled could mimic the template of the enamel mineralization and induce a self-growing hydroxyapatite, which is an important step in the structural bionics of enamel.

摘要

目的

对壳聚糖和胶原蛋白等生物大分子进行改性,合成一种能诱导牙釉质自生长再矿化的矿化模板。

方法

通过磷酸化对天然聚阳离子多糖壳聚糖进行改性,合成磷酸化壳聚糖的聚阴离子衍生物。以京尼平为交联剂,通过肽键结合反应构建壳聚糖与I型胶原蛋白复合的母体水凝胶。水凝胶在牙齿惰性表面自组装,通过紫外线辐射进行刺激。仿生唾液提供矿化离子,然后羟基磷灰石在牙齿上原位组装并生长。

结果

傅里叶变换红外光谱证实壳聚糖上接枝了官能团PO4(3-)(3446 cm(-1))。聚阳离子壳聚糖与聚阴离子磷酸化壳聚糖相互作用形成的多孔聚电解质复合水凝胶能诱导羟基磷灰石晶体在水凝胶纤维表面成核和生长。X射线衍射证实新生晶体为羟基磷灰石,且与牙齿紧密相连。观察到尺寸为30 nm至60 nm的柱状晶体连续结构。该结构的平行方向与釉柱方向相似,其硬度接近牙本质。

结论

易于获得和控制的母体水凝胶能够模拟釉质矿化模板并诱导自生长羟基磷灰石,这是釉质结构仿生学中的重要一步。

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