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核黄素修饰牙本质胶原基质的特性研究。

Characterization of riboflavin-modified dentin collagen matrix.

机构信息

Discipline of Oral Sciences, Faculty of Dentistry, National University of Singapore, 11 Lower Kent Ridge Road, Singapore, 119083, Singapore.

出版信息

J Dent Res. 2012 Nov;91(11):1049-54. doi: 10.1177/0022034512459053. Epub 2012 Aug 22.

Abstract

Crosslinking is considered a possible approach to increasing the mechanical and structural stability and biodegradation resistance of the dentin collagen matrix. The aim of this study was to investigate the mechanical and chemical variations and collagen degradation resistance associated with crosslinking of the dentin collagen matrix with UVA-activated riboflavin. Dentin collagen matrix specimens were treated with 0.1 and 1% riboflavin for 2 min and photo-activated with 7 mW/cm(2) UVA (368 nm) for 2 min. The structural change of the dentin collagen network with collagenase exposure was investigated by AFM and SEM at different time-points. The variations in surface/bulk mechanical properties and biodegradation resistance were characterized by nano-indentation, conventional mechanical testing, and hydroxyproline liberation at different time-points. Chemical changes associated with riboflavin/collagen-matrix interaction were analyzed by micro-Raman spectroscopy. UVA-activated riboflavin increased the mechanical properties, mechanical stability, and biodegradation resistance of the dentin collagen matrix. Higher collagen-network structural resistance against collagenolytic challenges was found with crosslinking. micro-Raman spectroscopy showed a strong dependency, in both intensity and wave-number, of certain Raman bands (1242-1667 cm(-1)) with crosslinking indicating the collagen/riboflavin interactions. UVA-activated riboflavin (1%) more efficiently crosslinked the dentin collagen matrix within a relatively clinically acceptable time-frame compared with 0.1% riboflavin.

摘要

交联被认为是提高牙本质胶原基质的机械和结构稳定性以及抗生物降解性的一种可行方法。本研究旨在研究与 UVA 激活核黄素交联相关的牙本质胶原基质的机械和化学变化以及胶原降解抗性。用 0.1%和 1%核黄素处理牙本质胶原基质标本 2 分钟,并以 7 mW/cm(2)UVA(368nm)照射 2 分钟进行光激活。用 AFM 和 SEM 在不同时间点研究胶原酶暴露下牙本质胶原网络的结构变化。用纳米压痕、常规力学测试和羟脯氨酸释放在不同时间点表征表面/体机械性能和抗生物降解性的变化。用微拉曼光谱分析与核黄素/胶原基质相互作用相关的化学变化。UVA 激活核黄素增加了牙本质胶原基质的机械性能、机械稳定性和抗生物降解性。交联后发现胶原网络结构对胶原酶挑战的阻力更高。微拉曼光谱显示某些拉曼带(1242-1667cm(-1))的强度和波数与交联具有很强的依赖性,表明胶原/核黄素相互作用。与 0.1%核黄素相比,UVA 激活的 1%核黄素在相对临床可接受的时间范围内更有效地交联牙本质胶原基质。

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