中国组织工程研究 ›› 2016, Vol. 20 ›› Issue (25): 3706-3712.doi: 10.3969/j.issn.2095-4344.2016.25.009

• 组织工程骨及软骨材料 tissue-engineered bone and cartilage materials • 上一篇    下一篇

体外构建复合软质再生颅骨修复材料填充修复颅骨缺损

张同星,高 华   

  1. 冀州市医院神经外科,河北省冀州市  053200
  • 收稿日期:2016-04-17 出版日期:2016-06-17 发布日期:2016-06-17
  • 作者简介:张同星,男,1973年生,河北省冀州市人,汉族,2005年河北医科大学毕业,主治医师,主要从事脑出血手术治疗方向的研究。

Soft composite materials for bone regeneration in vitro in skull repair

Zhang Tong-xing, Gao Hua   

  1. Department of Neurosurgery, Jizhou Hospital, Jizhou 053200, Hebei Province, China
  • Received:2016-04-17 Online:2016-06-17 Published:2016-06-17
  • About author:Zhang Tong-xing, Attending physician, Department of Neurosurgery, Jizhou Hospital, Jizhou 053200, Hebei Province, China

摘要:

 文章快速阅读:

 

文题释义:
骨形态发生蛋白7:
成熟的骨形态发生蛋白7由前体的多肽产物经酶水解后,2条含139个氨基酸组成的多肽链经二硫键结合后形成的同源二聚体糖蛋白组成,相对分子质量约为35 000,其空间结构形似“手掌”。天然骨形态发生蛋白7存在同源和异源二聚体形式,二聚体形式的骨形态发生蛋白7是其生物学活性主要形式。内源性骨形态发生蛋白7可以通过抑制性Smads途径来抑制信号传递蛋白Smads的转移,阻断转化生长因子β的信号转导,从而抵消转化生长因子β的活性,调节细胞外基质的合成与降解,发挥抗纤维化作用。骨形态发生蛋白7也是 P53家族的靶基因,能够调节与P53生理水平相关的细胞存活能力。
壳聚糖的生理活性:①控制胆固醇:壳聚糖具有强大的阴离子吸附力,既能阻止脂肪的吸收,又可以将人体血液内的胆固醇排泄掉。②抑制细菌活性:壳聚糖在弱酸溶剂中易于溶解,其溶液中含有氨基(NH2+),这些氨基通过结合负电子来抑制细菌。③预防和控制高血压:壳聚糖通过自身的氯离子和氨根离子之间的吸附作用,排泄氯离子,还能降低血管紧缩素Ⅱ表达,有助于防止高血压的发生。④吸附和排泄重金属:壳聚糖是高效的螯合物介质。壳聚糖的吸附能力的大小取决于其脱乙酰度。脱乙酰度越大,吸附能力越强。⑤免疫效果:壳聚糖表现出有选择性的高度抑制口腔链球菌生长的作用,同时并不影响其他有益细菌的生长。

 

摘要
背景:
临床进行骨缺损修复的过程中,自体骨和异体骨移植等均存在一定的不足和问题,无法获得理想的治疗效果。
目的:观察体外环境下构建的复合软质再生颅骨修复材料修复颅骨缺损的效果。
方法:①体外环境下以骨形态发生蛋白7衍生多肽、壳聚糖、纳米羟基磷灰石及胶原制备复合软质再生颅骨修复材料。②取24只SD大鼠,随机等分为对照组和实验组,均制备颅骨缺损模型。对照组和实验组分别予以单纯壳聚糖/纳米轻基磷灰石/胶原复合材料和复合软质再生颅骨修复材料修复缺损部位。
结果与结论:①构建的复合软质再生颅骨修复材料呈疏松多孔结构,体外环境下骨形态发生蛋白7衍生多肽的释放量呈现出不断上升的趋势。②与对照组相比,实验组大鼠颅骨缺损区骨密度较高,且与正常骨组织十分接近,植入材料发生降解明显,新骨形成面积较大。表明复合软质再生颅骨修复材料修复颅骨缺损效果良好。

  ORCID: 0000-0002-0954-9361(张同星)

关键词: 生物材料, 骨生物材料, 骨缺损, 颅骨缺损, 再生颅骨, 骨形态发生蛋白, 壳聚糖, 羟基磷灰石, 胶原

Abstract:

BACKGROUND: In the process of bone defect repair, as their respective shortcomings, both autograft and allograft cannot obtain satisfactory outcomes.div> OBJECTIVE: To observe the effect of soft composite materials for bone regeneration established in vitro in skull defect repair.

 

METHODS: Soft composite materials for bone regeneration (bone morphogenetic protein 7-derived polypeptide, chitosan, nano hydroxyapatite and collagen) were established in vitro. Twenty-four Sprague-Dwley rats were enrolled to prepare skull defect models, and were randomly equivalently divided into two groups. The rats were repaired with chitosan/nano hydroxyapatite/collagen composite materials as control group, and those repaired with soft composite materials of bone regeneration as experimental group.

 

RESULTS AND CONCLUSION: The soft composite material of bone regeneration exhibited a loose and porous structure and bone morphogenetic protein 7-derived polypeptide was released in a gradually rising trend. Compared with the control group, bone mineral density of the defect region in the experimental group was higher, which was similar with that of the normal bone tissue, and additionally numerous newborn bones could be found. These results show that the soft bone regeneration composite material exerts a better repair effect in skull defect.

 

 

 

Key words: Skull, Bone Morphogenetic Protein 7, Tissue Engineering

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