硅磷酸鈣骨水泥的理化性質及其生物相容性研究
發(fā)布時間:2018-11-02 15:17
【摘要】:實驗目的:復合C3S和磷酸鈣系(磷酸氫鈣DCPA+磷酸四鈣TTCP)骨水泥,以期能改善骨水泥的降解性,提高其抗壓強度和力學性能,調節(jié)固化時間,提高骨水泥的生物相容性。 實驗方法:(1)用吉爾摩(Gilmore)雙針法測定復合骨水泥的固化時間;在Instron5567型萬能材料實驗機上測試抗壓強度;模擬體液(SBF)中浸泡后,骨水泥浸提液的pH值及其降解率隨時間的變化,并結合SEM和XRD微觀結構的觀察,對骨水泥理化性質的動態(tài)變化規(guī)律進行描述;(2)MTT實驗結合實時定量研究復合骨水泥的生物相容性。 實驗結果:(1)隨著C3S百分含量的增大,固化時間先增加后減少然后又增加。(2)隨著C3S百分含量的增加,骨水泥的抗壓強度先升高后降低,在C3S的含量為40%時,骨水泥的抗壓強度達到最大值21.6Mpa,比磷酸鈣系(TTCP+DCPA)骨水泥的強度稍高。(3)復合骨水泥具有較好降解性,而且隨著C3S百分含量的增加,骨水泥的降解率增大,在C3S的含量為40%時,骨水泥的降解率達到最大值10.26%,浸泡完成后復合骨水泥維持較高的抗壓強度,在浸泡到第7d時,抗壓強度達到最大值27.84MPa。復合骨水泥浸泡7d后浸泡液的pH值接近中性。(4)添加一定量的C3S骨水泥能刺激細胞的增殖,并提高CyclinD1、PCNA、SDH基因的表達。 實驗結論:C3S的引入延長了磷酸鈣系(TTCP+DCPA)骨水泥的固化時間,提高了骨水泥的降解性,在一定程度上提高了磷酸鈣系骨水泥的抗壓強度。制備的復合骨水泥克服了磷酸鈣系(TTCP+DCPA)骨水泥降解率低的缺點,,而且具有適宜的固化時間,較高的抗壓強度和良好的生物相容性和安全性,可作為一種潛在的骨水泥修復材料。
[Abstract]:Objective: to combine C3s with calcium phosphate (DCPA) tetracalcium phosphate (TTCP) bone cement in order to improve the degradation of bone cement, improve its compressive strength and mechanical properties, adjust the curing time, and improve the biocompatibility of bone cement. Methods: (1) the curing time of composite bone cement was determined by Gilmore (Gilmore) double needle method, and the compressive strength was measured on Instron5567 universal material experiment machine. After soaking in simulated body fluid (SBF), the pH value and degradation rate of bone cement extract changed with time. The dynamic changes of physical and chemical properties of bone cement were described by observing the microstructure of SEM and XRD. (2) the biocompatibility of composite bone cement was studied by MTT experiment and real time quantitative analysis. The results were as follows: (1) with the increase of C3s content, the curing time increased first, then decreased, and then increased. (2) with the increase of C3S content, the compressive strength of bone cement increased first and then decreased, when the content of C3S was 40%, The compressive strength of bone cement reached the maximum value of 21.6 Mpaa, which was slightly higher than that of calcium phosphate (TTCP DCPA) cement. (3) the composite bone cement had better degradability, and the degradation rate of bone cement increased with the increase of C3s content. The degradation rate of bone cement reached the maximum value of 10.26 when the content of C _ 3s was 40 and the compressive strength of composite bone cement was maintained after immersion. The compressive strength reached the maximum of 27.84 MPA at the 7th day after immersion. (4) adding a certain amount of C3s bone cement could stimulate cell proliferation and increase the expression of CyclinD1,PCNA,SDH gene. Conclusion: the introduction of C3S can prolong the curing time of calcium phosphate (TTCP DCPA) cement, improve the degradation of bone cement, and improve the compressive strength of calcium phosphate bone cement to some extent. The prepared composite bone cement overcomes the shortcoming of low degradation rate of calcium phosphate (TTCP DCPA) cement, and has the advantages of suitable curing time, high compressive strength, good biocompatibility and safety. It can be used as a potential bone cement repair material.
【學位授予單位】:河南師范大學
【學位級別】:碩士
【學位授予年份】:2012
【分類號】:R318.08
[Abstract]:Objective: to combine C3s with calcium phosphate (DCPA) tetracalcium phosphate (TTCP) bone cement in order to improve the degradation of bone cement, improve its compressive strength and mechanical properties, adjust the curing time, and improve the biocompatibility of bone cement. Methods: (1) the curing time of composite bone cement was determined by Gilmore (Gilmore) double needle method, and the compressive strength was measured on Instron5567 universal material experiment machine. After soaking in simulated body fluid (SBF), the pH value and degradation rate of bone cement extract changed with time. The dynamic changes of physical and chemical properties of bone cement were described by observing the microstructure of SEM and XRD. (2) the biocompatibility of composite bone cement was studied by MTT experiment and real time quantitative analysis. The results were as follows: (1) with the increase of C3s content, the curing time increased first, then decreased, and then increased. (2) with the increase of C3S content, the compressive strength of bone cement increased first and then decreased, when the content of C3S was 40%, The compressive strength of bone cement reached the maximum value of 21.6 Mpaa, which was slightly higher than that of calcium phosphate (TTCP DCPA) cement. (3) the composite bone cement had better degradability, and the degradation rate of bone cement increased with the increase of C3s content. The degradation rate of bone cement reached the maximum value of 10.26 when the content of C _ 3s was 40 and the compressive strength of composite bone cement was maintained after immersion. The compressive strength reached the maximum of 27.84 MPA at the 7th day after immersion. (4) adding a certain amount of C3s bone cement could stimulate cell proliferation and increase the expression of CyclinD1,PCNA,SDH gene. Conclusion: the introduction of C3S can prolong the curing time of calcium phosphate (TTCP DCPA) cement, improve the degradation of bone cement, and improve the compressive strength of calcium phosphate bone cement to some extent. The prepared composite bone cement overcomes the shortcoming of low degradation rate of calcium phosphate (TTCP DCPA) cement, and has the advantages of suitable curing time, high compressive strength, good biocompatibility and safety. It can be used as a potential bone cement repair material.
【學位授予單位】:河南師范大學
【學位級別】:碩士
【學位授予年份】:2012
【分類號】:R318.08
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