CAJ | 학술논문

背景：人们对壳聚糖/羟基磷灰石复合多孔生物支架在体内的降解过程并非十分清楚，而且有关其降解产物对成骨细胞的影响研究也较少。 　　目的：分析大鼠成骨细胞与壳聚糖/羟基磷灰石复合多孔生物支架降解产物的生物相容性。 　　方法：将培养的第2代大鼠成骨细胞分别在壳聚糖/羟基磷灰石复合支架降解产物浸提液和含体积分数10%胎牛血清的DMEM培养液中培养，培养第2，4，6，8，10天分别对两组细胞做MTT细胞计数，采用联合会推荐法测定细胞碱性磷酸酶活性，采用BCA蛋白定量法测定总蛋白。 　　结果与结论：在壳聚糖/羟基磷灰石复合多孔生物支架降解产物浸提液中培养的大鼠成骨细胞增殖速度、细胞碱性磷酸酶活性、细胞总蛋白合成及碱性磷酸酶与总蛋白的比值明显高于在体积分数为10%胎牛血清DMEM培养液中培养的细胞(P<0.05)。表明壳聚糖/羟基磷灰石复合多孔生物支架的降解产物不仅可促进大鼠成骨细胞的黏附、生长和增殖，还可增强其骨化功能，具有较好的生物相容性。
배경：인문대각취당/간기린회석복합다공생물지가재체내적강해과정병비십분청초，이차유관기강해산물대성골세포적영향연구야교소。 　　목적：분석대서성골세포여각취당/간기린회석복합다공생물지가강해산물적생물상용성。 　　방법：장배양적제2대대서성골세포분별재각취당/간기린회석복합지가강해산물침제액화함체적분수10%태우혈청적DMEM배양액중배양，배양제2，4，6，8，10천분별대량조세포주MTT세포계수，채용연합회추천법측정세포감성린산매활성，채용BCA단백정량법측정총단백。 　　결과여결론：재각취당/간기린회석복합다공생물지가강해산물침제액중배양적대서성골세포증식속도、세포감성린산매활성、세포총단백합성급감성린산매여총단백적비치명현고우재체적분수위10%태우혈청DMEM배양액중배양적세포(P<0.05)。표명각취당/간기린회석복합다공생물지가적강해산물불부가촉진대서성골세포적점부、생장화증식，환가증강기골화공능，구유교호적생물상용성。
BACKGROUND:The in vivo degradation process of chitosan/hydroxyapatite composite porous scaffolds is not very clear. Research on the effects of rat osteoblasts and degradation products is less. OBJECTIVE:To analyze the biocompatiblity of rat osteoblasts with degradation products of chitosan/hydroxyapatite composite porous scaffolds. METHODS:The second generation of cultured rat osteoblasts were respectively cultured in the extract of degradation products of chitosan/hydroxyapatite composite scaffolds (experimental group) and Dulbecco’s modified Eagle’s medium containing 10%fetal bovine serum (control group). At 2, 4, 6, 8, 10 days of culture, cel counting was measured by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. Alkaline phosphatase activity was measured by the recommended method of determination of the Federation, and total protein was determined by BCA method. RESULTS AND CONCLUSION:The proliferation speed, alkaline phosphatase activity, total cel ular protein synthesis and ratio of alkaline phosphatase to total protein in rat osteoblasts cultured in the experimental group were significantly higher than those in the control group (P<0.05). This experiment showed that the degradation products of chitosan/hydroxyapatite composite porous scaffolds cannot only promote rat osteoblast adhesion, growth and proliferation, but also enhance its ossification function, with good biocompatibility.