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Apatite-forming ability of polyglutamic acid hydrogels in a body-simulating environment

机译:在人体模拟环境中聚谷氨酸水凝胶的磷灰石形成能力

摘要

Artificial joints such as hip joint and knee joint have been popularly used for replacementofdamaged joints. To achieve a successful outcome offixation of the joints, surroundingbone tissues should have sufficient bone density. However bone density of elderlypatients is generally lower than that ofhealthy people due to diseases such as osteoporosis.This also makes it difficult to tightly fix the artificial joints to the bone. Thereforerecovery of the bone density is the important factor that governs success on theimplantation ofthe artificial joints. As a treatment to increase bone density ofthe patients,injectable bioactive filler with bone-bonding ability, Le. osteconductivity, can be anattractive candidate, since the osteoporosis can be recovered with minimal invasion. Sucha filler material should have not only osteoconductive property but also bioresorbabilityafter implantation in the bone tissue. It is known that osteoconduction on bioactive _materials is achieved by formation of biologically active hydroxyapatite (so-calledbone-like apatite) layer on their surfaces through chemical reaction with surroundingbody fluid. Heterogeneous nucleation of the hydroxyapatite is triggered by a catalyticeffect of specific functional groups on the material surfaces. In addition, release of Ca2+ions into the surrounding body fluids allows to enhance the apatite nucleation byincreasing degree of supersaturation with respect to the apatite. In this study, weattempted to develop injectable bioactive filler started from polyglutamic acid (pGA)through chemical cross-linkage, since PGA is abundant in carboxyl group that iseffective for inducing the apatite nucleation in body environments. The cross-linkage leadPGA hydrogel, whereas PGA without cross-linkage easily dissolved in aqueous media.The potential of the bone-like apatite formation was examined on the PGA gels due toexposure to a simulated body fluid (SBF) proposed by Kokubo and his colleagues. Aftersoaking in SBF for 7 days, trace amounts of particles were formed on the PGA gel, butwere not identified to bone-like apatite with X-ray diffraction. Formation of bone-likeapatite layer could be detected with X-ray diffraction on the PGAgels treated with CaChaqueous solution of 0.01 moldm-3 or more, followed by soaking in SBF for 7 days. Therate ofapatite formation increases with increasing concentration ofthe CaCh in the priortreatment. These results indicate that chemically cross-linked PGA gel has a potential toinduce the heterogeneous nucleation ofhydroxyapatite in body environment, and that thepotential would be remarkably enhanced by prior treatment ofthe gel with CaCh aqueoussolution.
机译:诸如髋关节和膝关节的人造关节已广泛用于替换受损的关节。为了成功完成关节固定,周围骨组织应具有足够的骨密度。然而,由于骨质疏松症等疾病,老年患者的骨密度通常低于健康人的骨密度,这也使得很难将人造关节牢固地固定在骨骼上。因此,骨密度的恢复是决定人工关节植入成功与否的重要因素。作为增加患者骨密度的一种治疗方法,可注射的具有骨结合能力的生物活性填充剂乐。由于骨质疏松可以以最小的侵袭得以恢复,因此骨传导性很强。这种填充材料不仅应具有骨传导性能,而且还应具有在植入骨组织后的生物吸收能力。已知通过与周围体液的化学反应在其表面上形成生物活性羟基磷灰石(所谓的骨样磷灰石)层来实现对生物活性材料的骨传导。羟基磷灰石的异质成核是由材料表面特定官能团的催化作用触发的。另外,Ca 2+离子向周围体液中的释放允许通过增加相对于磷灰石的过饱和度来增强磷灰石成核。在这项研究中,我们尝试通过化学交联从聚谷氨酸(pGA)开始开发可注射的生物活性填充剂,因为PGA中的羧基丰富,可在人体环境中诱导磷灰石成核。交联的是PGA水凝胶,而没有交联的PGA则很容易溶解在水性介质中。由于暴露于Kokubo及其同事提出的模拟体液(SBF),因此在PGA凝胶上检查了骨状磷灰石形成的潜力。 。在SBF中浸泡7天后,在PGA凝胶上形成了痕量的颗粒,但通过X射线衍射未鉴定为骨状磷灰石。用X射线衍射在0.01moldm-3或更高的CaChaqueous溶液处理过的PGAgels上检测X射线衍射,然后在SBF中浸泡7天。在预先处理中,磷灰石形成的速率随CaCh浓度的增加而增加。这些结果表明化学交联的PGA凝胶具有在身体环境中诱导羟基磷灰石异质成核的潜力,并且通过用CaCh水溶液预先处理凝胶可以显着增强该潜力。

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