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在稀磷酸盐溶液中,硅酸盐(45S5)、硼酸盐和硼硅酸盐玻璃转化为羟基磷灰石的动力学及机制

Kinetics and mechanisms of the conversion of silicate (45S5), borate, and borosilicate glasses to hydroxyapatite in dilute phosphate solutions.

作者信息

Huang Wenhai, Day Delbert E, Kittiratanapiboon Kanisa, Rahaman Mohamed N

机构信息

Materials Research Center, University of Missouri-Rolla, 101 Straumanis Hall, Rolla, MO 65409, USA.

出版信息

J Mater Sci Mater Med. 2006 Jul;17(7):583-96. doi: 10.1007/s10856-006-9220-z.

Abstract

Bioactive glasses with controllable conversion rates to hydroxyapatite (HA) may provide a novel class of scaffold materials for bone tissue engineering. The objective of the present work was to comprehensively characterize the conversion of a silicate bioactive glass (45S5), a borate glass, and two intermediate borosilicate glass compositions to HA in a dilute phosphate solution at 37 degrees Celsius. The borate glass and the borosilicate glasses were derived from the 45S5 glass by fully or partially replacing the SiO(2) with B(2)O(3). Higher B(2)O(3) content produced a more rapid conversion of the glass to HA and a lower pH value of the phosphate solution. Whereas the borate glass was fully converted to HA in less than 4 days, the silicate (45S5) and borosilicate compositions were only partially converted even after 70 days, and contained residual SiO(2) in a Na-depleted core. The concentration of Na(+) in the phosphate solution increased with reaction time whereas the PO(4) (3-) concentration decreased, both reaching final limiting values at a rate that increased with the B(2)O(3) content of the glass. However, the Ca(2+) concentration in the solution remained low, below the detection limit of atomic absorption, throughout the reaction. Immersion of the glasses in a mixed solution of K(2)HPO(4) and K(2)CO(3) produced a carbonate-substituted HA but the presence of the K(2)CO(3) had little effect on the kinetics of conversion to HA. The kinetics and mechanisms of the conversion process of the four glasses to HA are compared and used to develop a model for the process.

摘要

具有可控羟基磷灰石(HA)转化率的生物活性玻璃可为骨组织工程提供一类新型支架材料。本研究的目的是全面表征一种硅酸盐生物活性玻璃(45S5)、一种硼酸盐玻璃以及两种中间硼硅酸盐玻璃组合物在37摄氏度的稀磷酸盐溶液中向HA的转化过程。硼酸盐玻璃和硼硅酸盐玻璃是通过用B₂O₃完全或部分替代45S5玻璃中的SiO₂而衍生得到的。较高的B₂O₃含量使玻璃向HA的转化更快,且磷酸盐溶液的pH值更低。硼酸盐玻璃在不到4天的时间内就完全转化为HA,而硅酸盐(45S5)和硼硅酸盐组合物即使在70天后也只是部分转化,并且在贫钠核心中含有残留的SiO₂。磷酸盐溶液中Na⁺的浓度随反应时间增加,而PO₄³⁻浓度降低,二者均以随玻璃中B₂O₃含量增加的速率达到最终极限值。然而,在整个反应过程中,溶液中的Ca²⁺浓度一直很低,低于原子吸收的检测限。将玻璃浸入K₂HPO₄和K₂CO₃的混合溶液中会产生碳酸取代的HA,但K₂CO₃的存在对向HA转化的动力学影响很小。比较了四种玻璃向HA转化过程的动力学和机制,并用于建立该过程的模型。

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